Methods applied to neonatal dried blood spot samples for secondary research purposes: a scoping review

Figures & data

Figure 1. PRISMA 2020 flow diagram.

From: Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71. doi: 10.1136/bmj.n71.

Table 1. Key characteristics of included studies.

References	Study title	Location	Number of individuals	Study design
Makowski et al. [13]	The effect of storage on Guthrie cards: implications for deoxyribonucleic acid amplification	USA	Not stated	Methodological
Haak et al. [14]	Archived unfrozen neonatal blood spots are amenable to quantitative gene expression analysis	USA	12	Methodological
Resau et al. [15]	Evaluation of sex-specific gene expression in archived dried blood spots (DBS)	USA	106	Methodological
Slaughter et al. [16]	High correlations in gene expression between paired umbilical cord blood and neonatal blood of healthy newborns on Guthrie cards	USA	7	Methodological
Ponnusamy et al. [17]	A study of microRNAs from dried blood spots in newborns after perinatal asphyxia: a simple and feasible biosampling method	UK	30	Methodological
Bybjerg-Grauholm et al. [18]	RNA sequencing of archived neonatal dried blood spots	Denmark	10	Methodological
Gauffin et al. [19]	Quantitation of RNA decay in dried blood spots during 20 years of storage	Sweden	25	Methodological
Grauholm et al. [20]	Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank	Denmark	20	Methodological
Chaisomchit et al. [21]	Stability of genomic DNA in dried blood spots stored on filter paper	Thailand	100	Methodological
Hardin et al. [22]	Whole genome microarray analysis, from neonatal blood cards	USA	24	Methodological
Klassen et al. [23]	Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots	Sweden	16	Methodological
Lane et al. [24]	Maximizing deoxyribonucleic acid yield from dried blood spots	USA	4,000	Methodological
Pedersen et al. [25]	The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders	Denmark	77,639	Case-control
Rajatileka et al. [26]	Isolation of human genomic DNA for genetic analysis from premature neonates: a comparison between newborn dried blood spots, whole blood and umbilical cord tissue	UK	115	Methodological
Sjöholm et al. [27]	Assessing quality and functionality of DNA from fresh and archival dried blood spots and recommendations for quality control guidelines	Denmark	30	Methodological
Sok et al. [28]	Utilization of archived neonatal dried blood spots for genome-wide genotyping	USA	399	Methodological
St. Julien et al. [29]	High quality genome-wide genotyping from archived dried blood spots without DNA amplification	USA	1,773	Methodological
Hannelius et al. [30]	Phenylketonuria screening registry as a resource for population genetic studies	Sweden	76	Methodological
Hollegaard et al. [31]	Genome-wide scans using archived neonatal dried blood spot samples	Denmark	24	Methodological
Hollegaard et al. [32]	High-throughput genotyping on archived dried blood spot samples	Denmark	29	Methodological
Hollegaard et al. [33]	Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA	Denmark	29	Methodological
Hollegaard et al. [34]	Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source	Denmark	4,641	Methodological
Auma et al. [35]	Using dried blood spots for a sero-surveillance study of maternally derived antibody against Group B Streptococcus	UK	450	Case-control
Mei et al. [36]	Effect of specimen storage conditions on newborn dried blood spots used to assess Toxoplasma gondii immunoglobulin M (IgM)	USA	858	Case-control
He et al. [37]	Metabolite stability in archived neonatal dried blood spots used for epidemiological research	USA	899	Methodological
Murphy et al. [38]	Metabolic profiles derived from residual blood spot samples: a longitudinal analysis	Canada	307	Methodological
Ottosson et al. [39]	Effects of long-term storage on the biobanked neonatal dried blood spot metabolome	Denmark	200	Methodological
Petrick et al. [40]	An untargeted metabolomics method for archived newborn dried blood spots in epidemiologic studies	USA	106	Methodological
Yu et al. [41]	Untargeted metabolomics profiling and hemoglobin normalization for archived newborn dried blood spots from a refrigerated biorepository	Sweden	15	Methodological
Asrani et al. [42]	DNA methylome profiling on the Infinium HumanMethylation450 Array from limiting quantities of genomic DNA from a single, small archived bloodspot	USA	1	Methodological
Cunningham-Burley et al. [43]	Feasibility and ethics of using data from the Scottish newborn blood spot archive for research	UK	56	Methodological
Ghantous et al. [44]	Optimized DNA extraction from neonatal dried blood spots: application in methylome profiling	USA	Not stated	Methodological
Ghantous et al. [45]	DNA methylation analysis from blood spots: increasing yield and quality for genome-wide and locus-specific methylation analysis	USA	Not stated	Methodological
Hollegaard et al. [46]	DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study	Denmark	2	Methodological
Zar Kyaw et al. [47]	The utility of post-test newborn blood spot screening cards for epigenetic association analyses: association between HIF3A methylation and birth weight-for-gestational age	Japan	300	Methodological
Bakhireva et al. [48]	The validity of phosphatidylethanol in dried blood spots of newborns for the identification of prenatal alcohol exposure	USA	60	Case-control
Bakhireva et al. [49]	Stability of phosphatidylethanol in dry blood spot cards	USA	5	Prospective cohort
Henderson et al. [50]	Radioimmunoassay screening of dried blood spot materials for benzoylecgonine	USA	>500	Prospective cohort
Spector et al. [51]	Detection of cotinine in newborn dried blood spots	USA	20	Case-control
Yang et al. [52]	Levels of cotinine in dried blood specimens from newborns as a biomarker of maternal smoking close to the time of delivery	USA	428	Methodological
Di Martino et al. [53]	EDTA is essential to recover lead from dried blood spots on filter paper	Italy	20	Methodological
Funk et al. [54]	Hemoglobin adducts of benzene oxide in neonatal and adult dried blood spots	USA	9	Methodological
Funk et al. [55]	Quantification of arsenic, lead, mercury and cadmium in newborn dried blood spots	USA	49	Methodological
Kato et al. [56]	Analysis of blood spots for polyfluoroalkyl chemicals	USA	98	Methodological
Kim et al. [57]	Method for the determination of iodide in dried blood spots from newborns by high performance liquid chromatography tandem mass spectrometry	USA	20	Methodological
Ma et al. [58]	Analysis of polyfluoroalkyl substances and bisphenol A in dried blood spots by liquid chromatography tandem mass spectrometry	USA	192	Methodological
Björkesten et al. [59]	Stability of proteins in dried blood spot biobanks	Sweden	5	Methodological
Dijkstra et al. [60]	Important lessons on long-term stability of amino acids in stored dried blood spots	The Netherlands	2,170	Retrospective cohort
Klamer et al. [61]	Adiponectin levels measured in dried blood spot samples from neonates born small and appropriate for gestational age	Denmark	122	Case-control
McGuire et al. [62]	Screening newborns for candidate biomarkers of type 1 diabetes	Denmark	162	Case-control
Mihalopoulos et al. [63]	Validity and reliability of perinatal biomarkers of adiposity after storage as dried blood spots on paper	USA	45	Methodological
Mineyko et al. [64]	Association of neonatal inflammatory markers and perinatal stroke subtypes	Canada	197	Ambi-directional cohort
Raha-Chowdhury et al. [65]	Blood ferritin concentrations in newborn infants and the sudden infant death syndrome	UK	82	Case-control
Samenuk et al. [66]	Rapid method towards proteomic analysis of dried blood spots by MALDI mass spectrometry	USA	10	Methodological
Skogstrand et al. [67]	Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology	Denmark	66	Methodological
Yano et al. [68]	Untargeted adductomics of Cys34 modifications to human serum albumin in newborn dried blood spots	USA	49	Retrospective cohort
Yeung et al. [69]	Newborn adipokines and birth outcomes	UA	3,625	Cross-sectional
Durie et al. [70]	Quantification of DNA in neonatal dried blood spots by adenine tandem mass spectrometry	Canada	501	Methodological
Bassaganyas et al. [71]	Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification	USA	24	Methodological
Ding et al. [72]	Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots	USA	29	Methodological
Nagy et al. [73]	Minimally invasive genetic screen for GJB2 related deafness using dried blood spots	Hungary	576	Methodological
Hollegaard et al. [74]	Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing	Denmark	2	Methodological
Poulsen et al. [75]	High-quality exome sequencing of whole-genome amplified neonatal dried blood spot DNA	Denmark	22	Methodological
Winkel et al. [76]	Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis	Denmark	10	Methodological
Needham et al. [77]	Maternal social disadvantage and newborn telomere length in archived dried blood spots from the Michigan Neonatal Biobank	USA	192	Retrospective cohort
Barco et al. [78]	A validated LC-MS/MS method for the quantification of piperacillin/tazobactam on dried blood spot	Italy	7	Methodological
Rovito et al. [79]	Impact of congenital cytomegalovirus infection on transcriptomes from archived dried blood spots in relation to long-term clinical outcome	The Netherlands	18	Methodological

Table 2. Summary of methods used in included studies.

Purpose	Analyte(s)	Storage		DBS puncture size	Method(s)	Limitation(s)	Conclusion(s)	References
		Duration	Temperature / Humidity
Amplification	DNA	1–30 months	Room	1 × 3 mm	Water-based extraction method to elute whole blood PCR inhibitors (protein, hemoglobin, iron) and retain nucleic acid, followed by PCR by direct amplification.	Nucleic acid may become “fixed” to filter paper matrix. Eluting natural PCR inhibitors (protein, hemoglobin and iron) can be used to overcome this.	Possible to amplify two regions encoding cystic fibrosis mutation from DBS samples stored up to 30 months at room temperature.	Makowski et al. [13]
Gene expression	RNA	≤9 years	Room	8 × 3 mm	Parallel microarray-based gene expression and quantitative PCR analyses of RNA.	DNA contamination may occur when using small amounts of RNA. Treatment with RNase-free DNase recommended for future experiments.	RNA isolated and amplified from DBS samples archived at room temperature for up to 9 years can be analyzed by microarray and quantitative PCR.	Haak et al. [14]
	RNA	2.5–15.6 years	Room	3 × 3 mm	Samples were homogenized before total RNA extraction using the illustra RNAspin Mini RNA Isolation Kit.	None stated	Sex-specific RNA gene expression is preserved in DBS stored at room temperature up to 15.6 years.	Resau et al. [15]
	mRNA	5 months	Room	3 × 3 mm	RNA isolation, copy DNA synthesis, and microarray procedures were conducted according to published protocols.	None stated	Abundant gene expression observed in newborn blood on Guthrie cards.	Slaughter et al. [16]
	miRNA	6 months	Room	1 × 6 mm	Total RNA isolation was carried out using the MirVana PARIS isolation kit.	Circulating RNases may have degraded large RNAs into small RNAs.	Candidate miRNAs were extractable from DBS samples stored at room temperature for up to 6 months.	Ponnusamy et al. [17]
	RNA	Not stated	−20 °C	2 × 3.2 mm	Next generation sequencing for RNA expression.	RNA input for sequencing library preparation was restricted to two 3.2 mm DBS punches for each sample, lessening library output.	Feasible to use DBS for RNA extraction and expression studies.	Bybjerg-Grauholm et al. [18]
	RNA	1–20 years	4 °C (since 1981); controlled humidity (since 1996)	5 × 3 mm	RNA was isolated from each sample, quantitated by spectrophotometry and reverse transcribed following DNase I treatment. Amplifiable copy DNA was subsequently detected by real-time PCR using primers specific for transcripts encoding b-actin.	None stated	No evidence of significant RNA decay in DBS samples stored up to 20 years.	Gauffin et al. [19]
	RNA	12–30 years	−20 °C and Room	2 × 3.2 mm	RNA amplification, whole transcriptome amplification and gene expression profiling analysis.	Use of multiple whole transcriptome amplification kits may introduce significant differences in expression. The use of a single kit is recommended.	Length of storage is secondary to the storage temperature; no significant differences between samples when stored at −20 °C. Storing DBS samples at −20 °C improves the preservation of RNA.	Grauholm et al. [20]
Genotyping	gDNA	4–14 years	28 °C; 70% humidity; stored in sealed plastic bags	1 × 4.8 mm	DNA extraction method involved two steps: (1) DBS treated with methanol and (2) Genomic DNA extracted with Tris buffer in a heat incubation step.	Ambient conditions may not be appropriate for DBS storage for more than 10 years if studying long DNA sequences.	DNA in DBS samples are stable under tropical conditions for at least 10 years.	Chaisomchit et al. [21]
	DNA	≥10 years	Room	2 × 3 mm	GenSolve technology was used in combination with standard DNA purification, followed by analysis on the Illumina 610 bead array microarray platform.	None stated	The larger surface area of 2 × 3 mm dia. punches or 1 × 6 mm dia. punch may be more dependable to produce enough DNA for microarray analysis. High quality DNA can be obtained from standard neonatal DBS samples stored dry for at least 10 years.	Hardin et al. [22]
	gDNA	>30 years	Room	2 × 3 mm	Visual automated fluorescence electrophoresis (VAFE).	Lack of systematic quality control for sample preparation and assessment.	Addition of VAFE measures in downstream quality control increases confidence in the validity of genetic data and allows cost-effective downstream analysis of gDNA. DBS is a good resource for DNA for genotyping studies.	Klassen et al. [23]
	DNA	>10 years	Room	2 × 5 mm	Standard methods used for DNA extraction and purification with a modified elution step. Linear array method was used for HLA (human leukocyte antigen) genotyping.	Residual DBS samples are nonrenewable. Thus, DNA yield should be maximized.	Inclusion of modified elution step increased DNA yield. Commercial extraction protocols can be modified to maximize DNA yield from stored DBS samples.	Lane et al. [24]
	DNA	13–37 years	−20 °C	2 × 3.2 mm	DNA was extracted from neonatal DBS samples using the Extract-N-Amp Blood PCR kit and genotyped using the Illumina PsychChip.	No DBS-specific limitations stated	Genotyping was successful for 90% of DBS samples using described method.	Pedersen et al. [25]
	gDNA	3–22 years	Room; stored in boxes	1–3 × 3.2 mm	DNA isolated using the QIAmp DNA Micro Kit following manufacturer’s guidelines.	None stated	Storage duration did not affect total amount of DNA recovered but significantly reduced purity over time.	Rajatileka et al. [26]
	DNA	3 months; 22 years; 26 years	−20 °C and Room	1 × 3 mm	EZNA method for DNA extraction, followed by multiple displacement amplification (MDA).	The degree of fragmentation of DNA extracted from archival DBS increased with increasing age of the samples.	Room temperature-stored DBS samples performed poorly (likely degradation of DNA during storage). DBS storage at −20 °C recommended to prevent DNA degradation.	Sjöholm et al. [27]
	DNA	9–25 years	21 °C, 35% humidity (for 12 years); room, 35% humidity (for 4 years)	6 × 3 mm	DNA extraction performed using GenTegra GenSolve Whole Blood DNA recovery kit according to manufacturer protocol.	Unable to evaluate quality of low frequency variants as in other genome-wide association studies due to limited sample size.	DBS samples stored in a temperature- and humidity-controlled environment yielded higher quality DNA. Storage duration negatively affected DNA quality regardless of environment. However, samples stored in an uncontrolled environment were acceptable for most genotyping applications.	Sok et al. [28]
	gDNA	Not specified	−20 °C	2–5 × 2 mm	Genome-wide genotyping of DNA isolated from DBS samples was done by Illumina using their Infinium single nucleotide extension SNP genotyping assay and a cytoSNP or Omni bead microarray.	None stated	The described method provides sufficient unamplified DNA for genome-wide genotyping.	St. Julien et al. [29]
	wgaDNA	10 years; 25 years	4 °C	1 × 3 mm	Saponin and chelex-100 based method and preamplified by improved primer preamplification.	None stated	Whole genome amplification makes large genetic epidemiological studies feasible, even using 25-year-old samples.	Hannelius et al. [30]
	wgaDNA	15–25 years	−24 °C	1–3 × 3.2 mm	DNA extraction and whole genome amplification methods using standard test kits.	Call-rate cutoff that would ensure reliable genotyping could not be clearly defined due to few samples being available to calculate correlation coefficient. Limited number of samples in each comparison group is a noted limitation.	WgaDNA from one 3.2 mm punch of DBS sample stored at −24 °C for more than 20 years is suited for reliable genotyping.	Hollegaard et al. [31]
	wgaDNA	19–27 years	−24 °C	1 × 3.2 mm	Genomic DNA was extracted and amplified using GPlex WGA kit (selected over AmpliQ Genomic Amplifier kit following pilot study).	The early storage policy, where DBS samples were stored at 4 °C for up to 1 year, may have caused some degradation of the gDNA.	WgaDNA from DBS samples for genotyping studies is feasible despite years of storage.	Hollegaard et al. [32]
	wgaDNA	3–25 years	−24 °C	1 × 3.2 mm	Extract-N-Amp kit and WGA reactions using GPlex kit.	WgaDNA made from DBSs may result in scattered genotype plots. This is probably due to poor quality and/or low amounts of input DNA resulting in an unequal amplification of the alleles.	Genotyping quality dependent upon extraction and amplification method. Storage duration did not appear to influence results. One 3.2 mm punch sufficient for multiple amplifications.	Hollegaard et al. [33]
	wgaDNA	5–29 years	−20 °C	2 × 3.2 mm	DNA extraction, whole genome amplification and SNP genotyping.	Sample set limited by difficulty obtaining neonatal-adult matched samples.	Next generation sequencing (NGS) of neonatal DBS samples does not compromise NGS accuracy. Archived DBS samples represent a reliable source of DNA for whole genome amplification. Two 3.2 mm DBS punches sufficient for whole genome amplification and subsequent sequencing.	Hollegaard et al. [34]
Maternally-derived antibodies	Invasive Group B Streptococcus	5 years	Room	2 × 3 mm	Multiplex immunoassay.	Poor sample storage conditions resulted in few viable DBS sample cards.	DBS storage at room temperature was stable for 3 months compared with storage from collection at −20 °C and rapidly degraded thereafter. Poor sample storage conditions resulted in few viable DBS samples. DBS samples must be stored at −20 °C for long term preservation of antibody.	Auma et al. [35]
	Toxoplasma gondii	3–13 years	−20 °C with desiccant; room temperature with no desiccant; −1 °C to 40 °C (no humidity control)	1 x full DBS (approx. 13 mm)	Time-resolved immunofluorometric assay.	Relatively small number of DBS samples tested. Due to limited number of punches available, not all analytes could be tested from the subset.	Ability to recover IgM and other biomarkers related to storage conditions, independent of sample age or storage time. When stored at −20 °C with desiccant, Toxo-IgM was found to be stable for at least 2 years in DBS.	Mei et al. [36]
Metabolomics	39 metabolites related to nutrition and health	∼30 years	−20 °C	1 × 5 mm	High-resolution metabolomics with untargeted LC-MS/MS.	Metabolite detection may be affected by sample-handling issues during collection, transport, extraction, storage and analysis, duration of storage, lipid content and hematocrit impacting stability of metabolites during spot drying and delivery, resolubilization/loss of metabolites due to free-radical polymerization and protein trapping.	Storage at −20 °C for almost 30 years did not affect the deterioration of most of the metabolites. Stability over the period was seen for 17 of the 39 selected metabolites. Degradation appears minimal for amino acids, likely due to storage temperature. Caffeine was detected in 82% of samples indicating breastfeeding-related exposures. Cotinine and hydroxycotinine remain detectable in DBS after storage for up to 29 years. Lipid metabolites appeared less stable.	He et al. [37]
	48 metabolites	2–12 months	Room	8 × 3.2 mm	High performance liquid chromatography; Immunoassays; electrospray ionization tandem mass spectrometry; quantitative polymerase chain reaction.	Effects of extreme environmental storage conditions were not explored. Samples providing negative screening used. Unclear if analytes exhibit similar rates of degradation in infants with congenital conditions.	Largest changes in analyte levels were observed after 12 months of storage. Duration of sample storage, independent of temperature and humidity affects newborn screening profiles and should be considered when using DBS samples for research purposes.	Murphy et al. [38]
	731 metabolites	1–10 years	−20 °C	1 × 3.2 mm	Untargeted LC-MS/MS.	Short term effects of storage (< 1 year) not investigated. Transportation and storage time may influence metabolome.	Majority (>71%) of DBS metabolome is stable during storage at −20 °C for up to 10 years. Untargeted metabolomics of DBS samples, with long-term storage, is suitable for retrospective epidemiological studies.	Ottosson et al. [39]
	1,107 metabolites	9–32 years	−20 °C	1 × 4.7 mm	Untargeted LC-HRMS.	Nuisance technical variation may occur. Measuring potassium in each DBS punch as a proxy for hematocrit, used to adjust for this.	Method allowed >1000 prevalent and robust features representing all of the major subclasses of metabolites to be measured.	Petrick et al. [40]
	137 metabolites	≤21 years	4 °C	1 × 5 mm	LC-MS.	Small sample size (N = 15). Unknown volumes of blood and hematocrit are noted issues. Further evaluations should utilize larger numbers of archived DBS and samples with extreme values of hematocrit.	39% of metabolite features were associated with storage year. Amino acids and peptides were particularly sensitive to storage duration.	Yu et al. [41]
Methylation	Methylated DNA	14–31 years	Frozen (temperature not stated)	1 × 2 mm	DNA methylation analysis on the Illumina 450k platform	None stated	DNA isolated from stored DBS sample yields methylation profiles adequate for methylation studies.	Asrani et al. [42]
	Methylated DNA	32–38 years	Room	6–8 × 3 mm	DNA methylation was profiled using the Infinium HumanMethylationEPIC v1.0 BeadChip.	None stated	Pilot studies demonstrated sufficient quantity and quality of DNA could be extracted for whole genome/exome sequencing from 94% of DBS cards. Genome-wide methylation data, along with baseline smoking behavior information, reflected maternal smoking.	Cunningham-Burley et al. [43]
	DNA	>20 years	Room	2 × 1 mm	10 different DNA extraction protocols were tested. GQ was found to be the most robust protocol. For GQ, Phase I method: GenSolve and Phase II method: QIAamp (DNA Micro kit). DNA quality was assessed by PCR (gel electrophoresis) and DNA integrity and size range (bioanalyser analyses).	None stated	GQ method was able to detect small methylation differences in a consistent manner and with low inter-replicate variation. This optimized method for DNA extraction has applications in methylation analyses for diagnostic and research purposes.	Ghantous et al. [44]
	DNA	>20 years	Room	2 × 1 mm	Lysis-based DNA extraction methods from DBS using combinations of in-house derived and modified commercial extraction kits were compared.	None stated	Both protocols were more efficient relative to other published methods, one protocol yields less DNA compared to the other, but shows improved quality.	Ghantous et al. [45]
	Methylated DNA	26–28 years	−20 °C	2 × 3.2 mm	DNA extraction and methylation, using standard kits and protocols.	None stated	Choice of DNA extraction method is important. Neonatal DBS samples stored for 26 to 28 years can be used for DNA methylome profiling, using only two 3.2 mm punches.	Hollegaard et al. 2013a [46]
	DNA	>3 years	−20 °C	8 × 3 mm	DNA bisulfite treatment, amplification, reverse transcription and cleavage, applied to a 384 SpectroCHIP, for mass-based fragment separation using a Matrix Assisted Laser Desorption-Ionization Time of Flight platform.	None stated	DBS samples retained sufficient quantity and quality of DNA to conduct both genome-wide and epigenome-wide studies.	Zar Kyaw et al. [47]
Prenatal substance use	Phosphatidyl-ethanol (PEth; ethanol metabolite)	2 weeks	Room	3 x size not specified	LC-MS/MS.	Unable to detect PEth beyond 2–3 weeks prior to delivery. No agreement regarding cutoff concentration for PEth when assessing prenatal alcohol exposure in newborns.	Specificity of PEth-DBS in this study was 100% and sensitivity was 32.1%, believed to reflect moderate alcohol consumption. DBS samples can be used to detect PEth for prenatal alcohol exposure analyses. The stability of PEth long-term remains unknown.	Bakhireva et al. [48]
	Phosphatidyl-ethanol (PEth; ethanol metabolite)	4 months	−80 °C	3 × 3.175 mm	LC-MS/MS.	Higher humidity can potentially accelerate PEth degradation, although not taken into account in study as DBS samples stored at −80 °C less likely to be affected by humidity.	Insignificant degradation of PEth after storage for 4 months at −80 °C. Can be used for prenatal alcohol exposure analyses but long-term stability of analyte is unknown.	Bakhireva et al. [49]
	Benzoylecgonine (BE; cocaine metabolite)	≥30 days	Room	1 × 6.35 mm	Modified commercial radioimmunoassay (RIA) kit.	None stated	DBS samples stored at ambient temperature and room humidity show no diminution in BE levels measured over 30 days.	Henderson et al. [50]
	Cotinine (tobacco-specific biomarker)	7 years	4 °C	¼ x DBS	GC-MS.	Factors that may affect cotinine levels in DBS include storage, handling and blood volume. It is also unclear whether cotinine may transfer between DBS stored adjacently without being individually sealed or whether handling of DBS by smokers could contaminate samples. Although study assumed a constant blood volume to calculate cotinine, in reality, the amount of blood may vary with spot size, punch location and filter paper batch.	Mean cotinine in newborn DBS of infants of smoking mothers was significantly higher than in those of infants with nonsmoking mothers (five-fold difference). The extent to which cotinine in DBS may degrade under improper storage conditions is not known.	Spector et al. [51]
	Cotinine (tobacco-specific biomarker)	7 months	−20 °C	1 × 6.35 mm	LC-MS/MS.	The accuracy of DBS cotinine in measurement of maternal smoking is expected to be lower with increasing time of collection after delivery because of cotinine metabolism in the newborn and may vary among racial/ethnic groups. Contamination is a theoretical concern though not documented previously as almost impossible for cotinine to migrate between samples.	Measurements of cotinine in DBS samples had high sensitivity (92.3%) and specificity (99.7%) in the prediction of maternal active smoking. Cotinine levels in DBS samples are an accurate biomarker of maternal smoking close to the time of delivery. Study could not prove the cotinine stability in DBS over long-term storage at room or refrigerator temperatures.	Yang et al. [52]
Prenatal environmental pollutant exposure	Lead	6 months	Room	1 × 6.3 mm	Furnace atomic absorption spectrophotometry.	None stated	Residual DBS samples could be useful tools for epidemiological survey of lead pollution. Lead must be extracted from DBS in the presence of optimal amounts of EDTA.	Di Martino et al. [53]
	Hemoglobin adducts of benzene oxide	30 days	Frozen (temperature not specified)	1 x DBS	GC-MS.	None stated	Levels in neonatal DBS comparable to adult DBS or fresh blood. Can be used as a measure of the air pollutant, benzene, in neonatal DBS samples.	Funk et al. [54]
	Arsenic, lead, mercury and cadmium	4–10 years	Room	½ x DBS	ICP-MS (inductively coupled plasma mass spectrometry).	Results suggest contamination may be an issue during blood collection and storage.	Arsenic concentrations were low in samples, with 82% of samples below the limit of detection. Lead was detectable in all samples. Mercury levels were all below the detection limit. Cadmium was detectable in 67% of samples after pair-wise subtraction. However, recovery does not appear to decrease over time and heavy metal concentrations are expected to be higher and above the detection threshold in exposed populations.	Funk et al. [55]
	PFCs; PFHS; PFOA; PFOS; perfluorononanoate	≤2 years	Room	1 x DBS	SPE-HPLC-MS/MS (solid phase extraction high performance liquid chromatography tandem mass spectrometry).	Different combinations of extraction procedures and amplification may impact performance.	PFOS and PFOA were detected in all DBS samples at concentration in the low ngml^-1 range.	Kato et al. [56]
	Iodide	≤8 years	4 °C	1 × 16 mm	Ultrasonic extraction and HPLC-ESI-MS/MS (high performance liquid chromatography electron spray ionization tandem mass spectrometry).	Actual volume of whole blood spotted on DBS is not known. Efforts to measure the actual volume of blood present are needed. Development of appropriate internal standards for iodide analysis required to eliminate the need for using a matrix-matched calibration method of quantification.	Iodide stability in DBS specimens was tested and determined to be sufficient at storage conditions of 4 °C.	Kim et al. [57]
	BPA (bisphenol A), PFOA, PFOS	2–5 years	4 °C	1 × 16 mm	Liquid-liquid extraction and HPLC-MS/MS.	Quantification of exact volume of blood in each DBS sample remains challenging, along with potential issues arising from background levels of contamination.	Method is reliable but dependent on volume of blood used which is difficult to quantify. Background levels of contamination may also cause issues.	Ma et al. [58]
Protein biomarkers	92 oncology-related proteins	0.5–40.5 years	Room temperature (for 5 years), then 4 °C at < 70% humidity (for 13 years), then 4 °C at < 30% humidity to present	Not specified	Multiplex PEA (proximity extension assay).	None stated	61 of 92 proteins investigated degraded when stored at 4 °C. Storage at −24 °C better preserves protein levels after 10 years in storage. Many proteins remained detectable even after 30 years of storage, but temperature is a major factor in detectability.	Björkesten et al. [59]
	23 amino acids	5 years	4 °C for 1 year, then room temperature for 4 years	1 × 3.2 mm	LC-MS/MS.	Short-term instability could not be investigated.	Amino acids in residual DBS stored at room temperature are subject to substantial degradation. Except for aspartate (stable for 4 years, all other amino acid concentrations significantly decreased within one year of storage.	Dijkstra et al. [60]
	Adiponectin	Not specified	−24 °C	2 x full DBS samples	Luminex Sandwich immunoassay.	None stated	Reliable quantification of adiponectin in stored DBS samples is feasible.	Klamer et al. [61]
	Untargeted proteomics	6 years	−25 °C	1 × 3.2 mm	SELDI-TOF-MS (surface enhanced laser desorption/ionization time of flight mass spectrometry)	Little sample volume means it was not possible to identify any other proteins.	Hemoglobin is the dominant protein in samples. Method developed allows for the depletion of hemoglobin to measure other proteins.	McGuire et al. [62]
	Adiponectin, leptin and insulin	≤6 months	Room	1 × 3.2 mm	Chip-based immunoaffinity capillary electrophoresis (CB-ICE) with on-line laser-induced fluorescence detection.	None stated	Strong correlations between serum and DBS measures of adiponectin, leptin and insulin for up to 6 months storage.	Mihalopoulos et al. [63]
	64 cytokines	7 years	Room	1 × 10 mm	Luminex multiplex assay.	Retrospective analysis of DBS samples may result in decay of cytokines.	Quantified measures of cytokines were consistently and reliably obtained from neonatal DBS samples. 91% of cytokines were measurable in samples stored up to 10 years.	Mineyko et al. [64]
	Ferritin	≥11 months	Room	1 x DBS punch	Ferritin eluted and assayed as per previously published method using a mouse monoclonal antibody directed against human spleen ferritin.	Small sample size.	Recovery of ferritin was very low from DBS samples stored for more than 6 months at room temperature. A recovery of about 25% expected from DBS samples stored for prolonged periods of time at room temperature.	Raha-Chowdhury et al. [65]
	25 proteins	2 years	Room	¼ x DBS punch	Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS).	Storage in less-than-ideal conditions may have caused certain protein to degrade.	Proteins were identified based on their respective peptide fragments following enzymatic digestion. Study suggests method can be used to analyze and identify certain proteins and other molecular species even after 2 years storage at room temperature.	Samenuk et al. [66]
	Inflammatory markers, neurotrophins, CRP and TREM-1	1 month − 23 years	−24 °C	2 × 3.2 mm	Luminex multiplex assay.	Interactions between analytes and blood proteins/cells may have affected recovery of some analytes	The measurable amounts of most cytokines were nearly constant in DBS samples stored up to 23 years. A marked decrease over time was observed in measurable concentrations of interleukin (IL)-1β, IL-8, soluble (s)IL-6rα, matrix metallopeptidase (MMP)-9, triggering receptor expressed on myeloid cells (TREM)-1, CRP, Brain Derived Neurotrophic Factor (BDNF) and neurotrophin (NT)-4 in stored DBS samples.	Skogstrand et al. [67]
	Cys34 adducts in human serum albumin (HAS)	14–32 years	−20 °C	1 × 4.7 mm	LC-MS.	Possible that some HSA modifications may be artifacts of sample processing or storage.	Significantly higher levels of the Cys34 cyanide adduct were detected among newborns whose mother’s smoked during pregnancy. DBS adductomics is suitable for investigating in utero exposures to reactive chemicals and metabolites, such as smoking, in the month prior to birth.	Yano et al. [68]
	Adipokines (adiponectin, adipsin, resistin, leptin, CRP, serpin E1)	8 months	4 °C	1 × 3.2 mm	Luminex Human obesity panel.	Difficulties in measuring leptin may be due to the use of multiplex, which has less sensitivity than ELISA. Initial cold storage prior to freezing may have contributed to low measures of leptin.	Leptin and CRP were too low to detect in majority of samples. Mean levels of DBS adipokines differ from previously reported levels using cord or venous blood in this study.	Yeung et al. [69]
Quantification (DNA)	DNA	3 months	Room	1 × 3.2 mm	Adenine tandem MS.	Method measures total DNA present in sample regardless of source, including by contamination with microbial or viral content. Likewise, degraded and/or fragmented DNA will yield similar measurements as higher molecular weight DNA.	Method provides reliable quantification of DNA from neonatal DBS samples in high throughput settings using instruments currently used in NBS laboratories.	Durie et al. [70]
Sequencing	DNA	>20 years	−20 °C (stored in containers with desiccant)	2 × 3.2 mm	Automated DNA extraction protocol without amplification.	None stated	Properly stored residual newborn DBS samples are a satisfactory source of DNA for genetic studies.	Bassaganyas et al. [71]
	DNA	≤20 years	Room (in a desiccator)	6–12 × 3 mm	Genomic DNA extraction and whole genome sequencing using a number of methods.	None stated	High quality DNA can be obtained from DBS samples stored up to 20 years without need to amplify.	Ding et al. [72]
	DNA	5–10 years	Room	1 × 4 mm	AS-PCR (allele-specific polymerase chain reaction).	Further investigation on DBS and corresponding whole-blood samples required.	Blood stored on Guthrie cards can be used to store DNA samples for at least 10 years. Even under suboptimal storage conditions the samples’ DNA remains intact for detecting 35delG mutation in GJB2 (Cx26) gene.	Nagy et al. [73]
	wgaDNA	27–29 years	−20 °C	2 × 3.2 mm	DNA extraction, whole genome amplification, then whole genome sequencing and exome sequencing	Small sample size noted.	Reliable DNA obtained for whole genome and exome sequencing using a small fraction of archived neonatal DBS sample.	Hollegaard et al. [74]
	wgaDNA	Not specified	−20 °C	2 × 1.6 mm; 2 × 3.2 mm	Samples were set up for library preparation using different kits in 3 x pilot studies, before sequencing and data analysis.	Overall exome coverage may be affected by reduced quality of input DNA used for WGA or amplification bias (due to WGA kit used of reduced quality input DNA).	WgaDNA of neonatal DBS samples performs with great accuracy and efficiency in exome sequencing and performed similarly to matched high-quality reference (whole blood DNA). No differences were observed substituting 2 × 3.2 mm with 2 × 1.6 mm punches, allowing for reduction of sample material.	Poulsen et al. [75]
	wgaDNA	≤28 years	−24 °C	2 × 3.2 mm	DNA was extracted using an "in-house" technique based on Extract-N-amp Blood PCR Kit. WGA was performed in triplicates by the multi-displacement amplification method using the REPLI-g kit. 20 ng/µL used for subsequent exon sequencing.	None stated	WgaDNA works well for exome sequencing, similar to gDNA.	Winkel et al. [76]
Telomere length	DNA	5–9 years	−20 °C and Room; humidity-controlled	6 × 3.175 mm	QIAamp DNA Investigator Kit, PCR and telomere length to standard ratio assessed.	Small sample size, cross-sectional design and lack of detailed information on time in storage.	Room temperature associated with degraded samples. −20 °C is a better temperature for storage. Year of birth associated with telomere length.	Needham et al. [77]
Therapeutic drug monitoring	Antibiotics (Piperacillin and Tazobactam)	16 days	4 °C (stored in sealed bag with desiccant)	1 × 3.2 mm	LC-MS/MS.	Hematocrit correction not considered.	Developed method allows simultaneous identification of piperacillin and tazobactam from a low volume of blood. Piperacillin and tazobactam resulted to be stable in DBS for prolonged storage at −20 °C, while a rapid degradation occurred at 25 °C. Shipment and storage of DBS must be performed at −20 °C.	Barco et al. [78]
Transcriptome analysis	RNA	8 years	Room	1 x full DBS	RNA extracted using the Nucleospin miRNA kit according to manufacturer’s instruction with minor modification (pre-incubating DBS with lysis buffer).	RNA degradation may result from ribonucleases, pH, humidity or UV light, although RNA contamination considered negligible in this study.	RNA assumed to be less prone to degradation and relatively stable for long periods of time at room temperature in this study.	Rovito et al. [79]

CRP = C-reactive protein; DBS = dried blood spot; DNA = deoxyribonucleic acid; DNase = deoxyribonuclease; GC-MS = gas chromatography-mass spectrometry; gDNA = genomic DNA; LC-MS/MS = liquid chromatography-mass spectrometry; LC-HRMS = liquid chromatography-high resolution mass spectrometry; mRNA = messenger RNA; miRNA = microRNA; PCR = polymerase chain reaction; PFCs = polyfluoroalkyl chemicals; PFHS = perfluorohexane sulfonate; PFOA = perfluorooctanoate; PFOS = perfluorooctane sulfonate; RNA = ribonucleic acid; RNase = ribonucleases; wgaDNA = whole genome amplified DNA; SNP = single nucleotide polymorphism.

Table 3. Summary of analytes successfully measured using neonatal dried blood spot (DBS) samples stored at varying temperatures and their maximum duration of storage as reported in the included studies.

			Maximum storage duration studied
Category	Analytes measured	Storage conditions	< 1 year	1 to 5 years	> 5 to 10 years	> 10 to 20 years	> 20 to 30 years	> 30 years
Genomic	DNA	Room
		Frozen
	gDNA	Room
	Methylated DNA	Room
		Frozen
	wgaDNA	Cold
	RNA	Room
		Cold
		Frozen
	mRNA	Room
	miRNA	Room
Proteins	Ferritin	Room
	Cytokines	Room
	Untargeted proteomics	Room
		Frozen
	Aspartate	Room
	Adiponectin	Room
		Frozen
	Leptin	Room
	Insulin	Room
	Adipokines	Cold
	Oncology-related	Cold
	Neurotrophins	Frozen
	Inflammatory markers	Frozen
	Toxoplasma gondii IgM	Frozen
Metabolites	Untargeted metabolomics	Room
		Cold
		Frozen
	Nutrition and health status-related	Frozen
Environmental pollutants	Lead	Room
	Arsenic	Room
	Cadmium	Room
	Polyfluoroalkyl chemicals	Room
		Cold
		Frozen
	Iodide	Cold
	Cys34 adducts of HSA	Frozen
	Hb adducts of benzene oxide	Frozen
Substance use in pregnancy	Phosphatidylethanol (PEth)	Room
		Frozen
	Benzoylecgonine	Room
	Cotinine	Cold
		Frozen
Medications	Piperacillin/tazobactam	Cold

DNA = deoxyribonucleic acid; gDNA = genomic DNA; Hb = hemoglobin; HSA = human serum albumin; IgM = immunoglobulin M; mRNA = messenger RNA; miRNA = microRNA; RNA = ribonucleic acid; wgaDNA = whole genome amplified DNA.

Table 4. Summary of studies directly comparing methods used on neonatal dried blood spot (DBS) samples.

References	Methods compared	Results	Conclusion(s)/Recommendation(s)
Grauholm et al. [20]	Study examined the effect on gene expression profiles (GEPs) when two different whole transcriptome amplification (WTA) kits were used on samples stored for ∼5 years at −20 °C.	Use of two different WTA kits (WT-Ovation Pico RNA amplification system and Signa-Aldrich’s complete WTA kit) resulted in a 13% variation in the principal component analysis.	Consistent use of a single WTA kit throughout a study is recommended to avoid introduction of significant differences in expression.
Klassen et al. [23]	The novel quality control (QC) technology, visual automated fluorescence electrophoresis (VAFE), was performed before and after whole genome amplification in parallel with traditional QC methods to compare quantity, quality, and integrity of nucleic acid from downstream genomic technologies.	VAFE QC data were correlated with subsequent sample performance in PCR, sequencing, and high-density comparative genome hybridization array.	Addition of VAFE measures in QC increases confidence in the validity of genetic data and allows cost-effective downstream analysis of gDNA for investigational and diagnostic applications.
Lane et al. [24]	Commercial methods of DNA extraction from DBS samples were compared with and without protocol modifications to assess if DNA yield is improved.	The addition of a purpose developed GenSolve reagent and a pre-warmed elution buffer and 70 °C soaking step increased DNA yield versus following the commercial protocol alone.	DNA yield can be improved with modifications to commercially available DNA extraction kits.
Hollegaard et al. [31]	Study assessed the quality of DNA obtained from different amplification protocols, comparing: two commercial DNA extraction procedures (Extract-N-Amp Blood PCR Kit [Sigma-Aldrich] or QIAamp DNA Blood Micro Kit [Qiagen]) and three WGA procedures (REPLI-g kit [Qiagen], GenomePlex® Complete WGA Kit [GPlex2, Sigma-Aldrich] or GenomePlex® Single Cell Whole Genome Amplification Kit [GPlex4, Sigma-Aldrich]), the effect of number of 3.2 mm DBS samples punches used and the effect of protein extraction prior to gDNA extraction.	The Extract-N-Amp Blood PCR Kit combined with the REPLI-g kit WGA featured the highest call-rates and the lowest conflict rates. Use of one or three DBS sample punches did not affect extraction. Protein extraction did not impair genotyping of the produced wgaDNA.	The Extract-N-Amp Blood PCR Kit is recommended for DNA extraction combined with GPlex2 or GPlex4 for WGA. Tests should be performed to determine the suitability of WGA procedures based on the given task, with one to three DBS sample punches being sufficient for analysis.
Hollegaard et al. [33]	Three DNA extraction methods were compared: QIAamp DNA Blood Mini Kit (Qiagen), Extract-N-Amp Blood PCR Kit (Sigma-Aldrich) and an ‘‘in-house’’ method based on Chelex 100 beads (Sigma-Aldrich). QIAamp and Extract-N-Amp DNA extractions were performed according to the kit instructions. The ‘‘in-house’’ gDNA extraction was carried out by adding 200 ml washing buffer (PBS, 0.5% TWEEN20) to each well, containing one 3.2 mm DBS punch. Four WGA kits and one re-amplification kit were used: REPLI-g (RepliG, Qiagen), AmpliQ Genomic Amplifier Kit (AmpliQ, Ampliqon), GenomePlexs Complete WGA Kit (GPlex2, Sigma-Aldrich), GenomePlexs Single Cell Whole Genome Amplification Kit (GPlex4, Sigma-Aldrich), and GenomePlexs WGA Reamplification Kit (GPlex3, Sigma-Aldrich). WGA reactions were performed according to the kit instructions.	Using the Extract-N-Amp kit for extraction of gDNA and performing the maximal number of WGA reactions on the extract using the GPlex kit will give a total yield of approximately 50 mg wgaDNA. The wgaDNA can be re-amplified, producing virtually infinite amounts of wgaDNA. The two OmniPlex kits, GPlex2 and GPlex4, performed well with all three extraction methods, indicating that they tolerated lower quality and smaller amounts of input gDNA better than the two multi-displacement amplification kits.	Genotyping performance is dependent on the combination of extraction procedure and amplification method.
Hollegaard et al. [34]	Genome-wide association studies using three different types of array were examined. The three studies, "610k", "Omni1"z, and "Axiom" used an Infinium Human610-Quad chip array (Illumina), an Infinium HD HumanOmni1-Quad chip array (Illumina) and an Axiom Genome-Wide CEU Array chip (Affymetrix), respectively.	Type of filter paper used for DBS samples was significantly associated with genotyping call rate (GCR) when using the “Omni1” array. Samples stored at −20 °C genotyped by the “Axiom” array had significantly higher GCRs than samples stored at 4 °C. Storage time and conditions did not affect the GCR when measured using the “610k” array.	Overall, of the three arrays tested, the Illumina “Omni1” array performed best. Compared with the other arrays, “Omni1” had the highest mean GCR, and the highest sample success rate. Although none of the arrays performed poorly and the effects of the different variables on the GCR were minimal, even when statistically significant. All three arrays should be considered usable for GWS of DBS samples.
Ghantous et al. [44]	A range of DNA extraction methods from neonatal DBS samples, individually or in combinations, were developed and tested. The DNA extraction protocol was split into two phases: phase I included blood extraction from DBS samples, cell lysis and protease digestion and phase II included DNA precipitation, purification and elution. Ten method combinations were tested to optimize DNA extraction.	Protocol GQ used the commercially available kits, GenSolve for phase I and QIAamp (DNA Micro Kit) for phase II. DNA yield was consistently better with less DNA degradation/fragmentation when using this protocol compared to others.	Protocol GQ appears to be the most robust among the tested methods across all tested DNA quantity and quality parameters.
Ghantous et al. [45]	Two robust and efficient protocols that increase DNA yield from DBS while minimizing DNA degradation were presented. One protocol, termed GenSolve-Qiagen, represents a combination of (a) GenSolve material in Phase I, (b) Qiagen material in Phase II and (c) in-house modifications. The other protocol, termed Qiagen-Ethanol, involves (a) Qiagen consumables in phases I and II, (b) ethanol as a precipitation buffer and (c) in-house modifications.	The Qiagen-Ethanol protocol extracted approximately twice the amount of DNA relative to the GenSolve-Qiagen protocol, although the latter protocol still represents a highly efficient protocol yielding quality DNA.	Either protocol could be used according to specific needs of the study, with both protocols being more efficient relative to other published methods.
Di Martino et al. [53]	Lead from DBS samples was measured using furnace atomic absorption spectrophotometry with or without the addition of 5 mmol/L EDTA to eluting solution.	The median optical density at 283.3 nm was significantly higher in DBS samples than controls in the presence of EDTA. When EDTA was absent from eluting solution, controls had a higher optical density than DBS samples.	Adding EDTA to the eluting solution is essential for the optimal recovery of lead during the extraction step from DBS samples.

Makowski GS, Davis EL, Hopfer SM. The effect of storage on Guthrie cards: implications for deoxyribonucleic acid amplification. Ann Clin Lab Sci. 1996;26(5):458–469.

 PubMed Web of Science ®Google Scholar

Haak PT, Busik JV, Kort EJ, et al. Archived unfrozen neonatal blood spots are amenable to quantitative gene expression analysis. Neonatology. 2009;95(3):210–216. doi: 10.1159/000155652.

 PubMed Web of Science ®Google Scholar

Resau JH, Ho NT, Dykema K, et al. Evaluation of sex-specific gene expression in archived dried blood spots (DBS). Int J Mol Sci. 2012;13(8):9599–9608. doi: 10.3390/ijms13089599.

 PubMed Web of Science ®Google Scholar

Slaughter J, Wei C, Korzeniewski SJ, et al. High correlations in gene expression between paired umbilical cord blood and neonatal blood of healthy newborns on Guthrie cards. J Matern Fetal Neonatal Med. 2013;26(18):1765–1767. doi: 10.3109/14767058.2013.804050.

 PubMed Web of Science ®Google Scholar

Ponnusamy V, Kapellou O, Yip E, et al. A study of microRNAs from dried blood spots in newborns after perinatal asphyxia: a simple and feasible biosampling method. Pediatr Res. 2016;79(5):799–805. doi: 10.1038/pr.2015.276.

 PubMed Web of Science ®Google Scholar

Bybjerg-Grauholm J, Hagen CM, Khoo SK, et al. RNA sequencing of archived neonatal dried blood spots. Mol Genet Metab Rep. 2016;10:33–37. doi: 10.1016/j.ymgmr.2016.12.004.

 PubMed Web of Science ®Google Scholar

Gauffin F, Nordgren A, Barbany G, et al. Quantitation of RNA decay in dried blood spots during 20 years of storage. Clin Chem Lab Med. 2009;47(12):1467–1469. doi: 10.1515/CCLM.2009.351.

 PubMed Web of Science ®Google Scholar

Grauholm J, Khoo SK, Nickolov RZ, et al. Gene expression profiling of archived dried blood spot samples from the Danish neonatal screening biobank. Mol Genet Metab. 2015;116(3):119–124. doi: 10.1016/j.ymgme.2015.06.011.

 PubMed Web of Science ®Google Scholar

Chaisomchit S, Wichajarn R, Janejai N, et al. Stability of genomic DNA in dried blood spots stored on filter paper. Southeast Asian J Trop Med Public Health. 2005;36(1):270–273.

 PubMedGoogle Scholar

Hardin J, Finnell RH, Wong D, et al. Whole genome microarray analysis, from neonatal blood cards. BMC Genet. 2009;10(1):38. doi: 10.1186/1471-2156-10-38.

 PubMedGoogle Scholar

Klassen TL, Drabek J, Tomson T, et al. Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots. J Mol Diagn. 2013;15(3):283–290. doi: 10.1016/j.jmoldx.2013.01.003.

 PubMed Web of Science ®Google Scholar

Lane JA, Noble JA. Maximizing deoxyribonucleic acid yield from dried blood spots. J Diabetes Sci Technol. 2010;4(2):250–254. doi: 10.1177/193229681000400204.

 PubMedGoogle Scholar

Pedersen CB, Bybjerg-Grauholm J, Pedersen MG, et al. The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders. Mol Psychiatry. 2018;23(1):6–14. doi: 10.1038/mp.2017.196.

 PubMed Web of Science ®Google Scholar

Rajatileka S, Luyt K, El-Bokle M, et al. Isolation of human genomic DNA for genetic analysis from premature neonates: a comparison between newborn dried blood spots, whole blood and umbilical cord tissue. BMC Genet. 2013;14(1):105. doi: 10.1186/1471-2156-14-105.

 PubMedGoogle Scholar

Sjöholm MI, Dillner J, Carlson J. Assessing quality and functionality of DNA from fresh and archival dried blood spots and recommendations for quality control guidelines. Clin Chem. 2007;53(8):1401–1407. doi: 10.1373/clinchem.2007.087510.

 PubMed Web of Science ®Google Scholar

Sok P, Lupo PJ, Richard MA, et al. Utilization of archived neonatal dried blood spots for genome-wide genotyping. PLoS One. 2020;15(2):e0229352. doi: 10.1371/journal.pone.0229352.

 PubMed Web of Science ®Google Scholar

St Julien KR, Jelliffe-Pawlowski LL, Shaw GM, et al. High quality genome-wide genotyping from archived dried blood spots without DNA amplification. PLoS One. 2013;8(5):e64710. doi: 10.1371/journal.pone.0064710.

 PubMed Web of Science ®Google Scholar

Hannelius U, Lindgren CM, Melén E, et al. Phenylketonuria screening registry as a resource for population genetic studies. J Med Genet. 2005;42(10):e60–e60. doi: 10.1136/jmg.2005.032987.

 PubMed Web of Science ®Google Scholar

Hollegaard MV, Grauholm J, Børglum A, et al. Genome-wide scans using archived neonatal dried blood spot samples. BMC Genomics. 2009a;10(1):297. doi: 10.1186/1471-2164-10-297.

 PubMedGoogle Scholar

Hollegaard MV, Grove J, Thorsen P, et al. High-throughput genotyping on archived dried blood spot samples. Genet Test Mol Biomarkers. 2009b;13(2):173–179. doi: 10.1089/gtmb.2008.0073.

 PubMed Web of Science ®Google Scholar

Hollegaard MV, Thorsen P, Norgaard-Pedersen B, et al. Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA. Electrophoresis. 2009c;30(14):2532–2535. doi: 10.1002/elps.200800655.

 PubMed Web of Science ®Google Scholar

Hollegaard MV, Grove J, Grauholm J, et al. Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source. BMC Genet. 2011;12(1):58. doi: 10.1186/1471-2156-12-58.

 PubMedGoogle Scholar

Auma E, Hall T, Chopra S, et al. Using dried blood spots for a Sero-Surveillance study of maternally derived antibody against group B Streptococcus. Vaccines (Basel). 2023;11(2):357. doi: 10.3390/vaccines11020357.

 PubMed Web of Science ®Google Scholar

Mei JV, Li L, Rasmussen SA, et al. Effect of specimen storage conditions on newborn dried blood spots used to assess Toxoplasma gondii immunoglobulin M (IgM). Clin Chim Acta. 2011;412(5-6):455–459. doi: 10.1016/j.cca.2010.11.028.

 PubMed Web of Science ®Google Scholar

He D, Yan Q, Uppal K, et al. Metabolite stability in archived neonatal dried blood spots used for epidemiological research. Am J Epidemiol. 2023;192(10):1720–1730. doi: 10.1093/aje/kwad122.

 PubMed Web of Science ®Google Scholar

Murphy MSQ, Hawken S, Cheng W, et al. Metabolic profiles derived from residual blood spot samples: a longitudinal analysis. Gates Open Res. 2018;2:28. doi: 10.12688/gatesopenres.

 PubMedGoogle Scholar

Ottosson F, Russo F, Abrahamsson A, et al. Effects of long-term storage on the biobanked neonatal dried blood spot metabolome. J Am Soc Mass Spectrom. 2023;34(4):685–694. doi: 10.1021/jasms.2c00358.

 PubMed Web of Science ®Google Scholar

Petrick L, Edmands W, Schiffman C, et al. An untargeted metabolomics method for archived newborn dried blood spots in epidemiologic studies. Metabolomics. 2017;13(3):27. doi: 10.1007/s11306-016-1153-z.

 PubMed Web of Science ®Google Scholar

Yu M, Dolios G, Yong-Gonzalez V, et al. Untargeted metabolomics profiling and hemoglobin normalization for archived newborn dried blood spots from a refrigerated biorepository. J Pharm Biomed Anal. 2020;191:113574. doi: 10.1016/j.jpba.2020.113574.

 PubMed Web of Science ®Google Scholar

Asrani K, Shaw GM, Rine J, et al. DNA methylome profiling on the infinium HumanMethylation450 array from limiting quantities of genomic DNA from a single, small archived bloodspot. Genet Test Mol Biomarkers. 2017;21(8):516–519. doi: 10.1089/gtmb.2017.0019.

 PubMed Web of Science ®Google Scholar

Cunningham-Burley S, McCartney DL, Campbell A, et al. Feasibility and ethics of using data from the scottish newborn blood spot archive for research. Commun Med (Lond). 2022;2(1):126. doi: 10.1038/s43856-022-00189-2.

 PubMedGoogle Scholar

Ghantous A, Saffery R, Cros MP, et al. Optimized DNA extraction from neonatal dried blood spots: application in methylome profiling. BMC Biotechnol. 2014;14(1):60. doi: 10.1186/1472-6750-14-60.

 PubMedGoogle Scholar

Ghantous A, Hernandez-Vargas H, Herceg Z. DNA methylation analysis from blood spots: increasing yield and quality for genome-wide and locus-specific methylation analysis. Methods Mol Biol. 2018;1708:605–619. doi: 10.1007/978-1-4939-7481-8_31.

 PubMedGoogle Scholar

Hollegaard MV, Grauholm J, Nørgaard-Pedersen B, et al. DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study. Mol Genet Metab. 2013a;108(4):225–231. doi: 10.1016/j.ymgme.2013.01.016.

 PubMed Web of Science ®Google Scholar

Zar Kyaw T, Yamaguchi S, Imai C, et al. The utility of post-test newborn blood spot screening cards for epigenetic association analyses: association between HIF3A methylation and birth weight-for-gestational age. J Hum Genet. 2019;64(8):795–801. doi: 10.1038/s10038-019-0621-5.

 PubMed Web of Science ®Google Scholar

Bakhireva LN, Leeman L, Savich RD, et al. The validity of phosphatidylethanol in dried blood spots of newborns for the identification of prenatal alcohol exposure. Alcohol Clin Exp Res. 2014;38(4):1078–1085. doi: 10.1111/acer.12349.

 PubMed Web of Science ®Google Scholar

Bakhireva LN, Shrestha S, Gutierrez HL, et al. Stability of phosphatidylethanol in dry blood spot cards. Alcohol Alcohol. 2016;51(3):275–280. doi: 10.1093/alcalc/agv120.

 PubMed Web of Science ®Google Scholar

Henderson LO, Powell MK, Hannon WH, et al. Radioimmunoassay screening of dried blood spot materials for benzoylecgonine. J Anal Toxicol. 1993;17(1):42–47. doi: 10.1093/jat/17.1.42.

 PubMed Web of Science ®Google Scholar

Spector LG, Hecht SS, Ognjanovic S, et al. Detection of cotinine in newborn dried blood spots. Cancer Epidemiol Biomarkers Prev. 2007;16(9):1902–1905. doi: 10.1158/1055-9965.

 PubMed Web of Science ®Google Scholar

Yang J, Pearl M, Jacob P, 3rd, et al. Levels of cotinine in dried blood specimens from newborns as a biomarker of maternal smoking close to the time of delivery. Am J Epidemiol. 2013;178(11):1648–1654. doi: 10.1093/aje/kwt182.

 PubMed Web of Science ®Google Scholar

Di Martino MT, Michniewicz A, Martucci M, et al. EDTA is essential to recover lead from dried blood spots on filter paper. Clin Chim Acta. 2004;350(1-2):143–150. doi: 10.1016/j.cccn.2004.07.019.

 PubMed Web of Science ®Google Scholar

Funk WE, Waidyanatha S, Chaing SH, et al. Hemoglobin adducts of benzene oxide in neonatal and adult dried blood spots. Cancer Epidemiol Biomarkers Prev. 2008;17(8):1896–1901. doi: 10.1158/1055-9965.EPI-08-0356.

 PubMed Web of Science ®Google Scholar

Funk WE, McGee JK, Olshan AF, et al. Quantification of arsenic, lead, mercury and cadmium in newborn dried blood spots. Biomarkers. 2013;18(2):174–177. doi: 10.3109/1354750X.2012.750379.

 PubMed Web of Science ®Google Scholar

Kato K, Wanigatunga AA, Needham LL, et al. Analysis of blood spots for polyfluoroalkyl chemicals. Anal Chim Acta. 2009;656(1–2):51–55. doi: 10.1016/j.aca.2009.10.007.

 PubMed Web of Science ®Google Scholar

Kim UJ, Kannan K. Method for the determination of iodide in dried blood spots from newborns by high performance liquid chromatography tandem mass spectrometry. Anal Chem. 2018;90(5):3291–3298. doi: 10.1021/acs.analchem.7b04827.

 PubMed Web of Science ®Google Scholar

Ma W, Kannan K, Wu Q, et al. Analysis of polyfluoroalkyl substances and bisphenol a in dried blood spots by liquid chromatography tandem mass spectrometry. Anal Bioanal Chem. 2013;405(12):4127–4138. doi: 10.1007/s00216-013-6787-3.

 PubMed Web of Science ®Google Scholar

Björkesten J, Enroth S, Shen Q, et al. Stability of proteins in dried blood spot biobanks. Mol Cell Proteomics. 2017;16(7):1286–1296. doi: 10.1074/mcp.RA117.000015.

 PubMed Web of Science ®Google Scholar

Dijkstra AM, de Blaauw P, van Rijt WJ, et al. Important lessons on long-term stability of amino acids in stored dried blood spots. Int J Neonatal Screen. 2023;9(3):34. doi: 10.3390/ijns9030034.

 PubMed Web of Science ®Google Scholar

Klamer A, Skogstrand K, Hougaard DM, et al. Adiponectin levels measured in dried blood spot samples from neonates born small and appropriate for gestational age. Eur J Endocrinol. 2007;157(2):189–194. doi: 10.1530/EJE-06-0710.

 PubMed Web of Science ®Google Scholar

McGuire JN, Eising S, Wägner AM, et al. Screening newborns for candidate biomarkers of type 1 diabetes. Arch Physiol Biochem. 2010;116(4-5):227–232. doi: 10.3109/13813455.2010.501801.

 PubMedGoogle Scholar

Mihalopoulos NL, Phillips TM, Slater H, et al. Validity and reliability of perinatal biomarkers of adiposity after storage as dried blood spots on paper. Am J Hum Biol. 2011;23(5):717–719. doi: 10.1002/ajhb.21199.

 PubMed Web of Science ®Google Scholar

Mineyko A, Nettel-Aguirre A, de Jesus P, et al. Association of neonatal inflammatory markers and perinatal stroke subtypes. Neurology. 2020;95(9):e1163–e1173. doi: 10.1212/WNL.0000000000010309.

 PubMed Web of Science ®Google Scholar

Raha-Chowdhury R, Moore CA, Bradley D, et al. Blood ferritin concentrations in newborn infants and the sudden infant death syndrome. J Clin Pathol. 1996;49(2):168–170. doi: 10.1136/jcp.49.2.168.

 PubMed Web of Science ®Google Scholar

Samenuk GM, Kelley AR, Perry G, et al. Rapid method towards proteomic analysis of dried blood spots by MALDI mass spectrometry. Clin Mass Spectrom. 2019;12:30–36. doi: 10.1016/j.clinms.2019.03.002.

 PubMedGoogle Scholar

Skogstrand K, Thorsen P, Nørgaard-Pedersen B, et al. Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology. Clin Chem. 2005;51(10):1854–1866. doi: 10.1373/clinchem.2005.052241.

 PubMed Web of Science ®Google Scholar

Yano Y, Grigoryan H, Schiffman C, et al. Untargeted adductomics of Cys34 modifications to human serum albumin in newborn dried blood spots. Anal Bioanal Chem. 2019;411(11):2351–2362. doi: 10.1007/s00216-019-01675-8.

 PubMed Web of Science ®Google Scholar

Yeung EH, McLain AC, Anderson N, et al. Newborn adipokines and birth outcomes. Paediatr Perinat Epidemiol. 2015;29(4):317–325. doi: 10.1111/ppe.12203.

 PubMed Web of Science ®Google Scholar

Durie D, Yeh E, McIntosh N, et al. Quantification of DNA in neonatal dried blood spots by adenine tandem mass spectrometry. Anal Chem. 2018;90(1):801–806. doi: 10.1021/acs.analchem.7b03265.

 PubMed Web of Science ®Google Scholar

Bassaganyas L, Freedman G, Vaka D, et al. Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification. Hum Mutat. 2018;39(1):167–171. doi: 10.1002/humu.23356.

 PubMed Web of Science ®Google Scholar

Ding Y, Owen M, Le J, et al. Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots. NPJ Genom Med. 2023;8(1):5. doi: 10.1038/s41525-023-00349-w.

 PubMed Web of Science ®Google Scholar

Nagy AL, Csáki R, Klem J, et al. Minimally invasive genetic screen for GJB2 related deafness using dried blood spots. Int J Pediatr Otorhinolaryngol. 2010;74(1):75–81. doi: 10.1016/j.ijporl.2009.10.021.

 PubMed Web of Science ®Google Scholar

Hollegaard MV, Grauholm J, Nielsen R, et al. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing. Mol Genet Metab. 2013b;110(1-2):65–72. doi: 10.1016/j.ymgme.2013.06.004.

 PubMed Web of Science ®Google Scholar

Poulsen JB, Lescai F, Grove J, et al. High-quality exome sequencing of whole-genome amplified neonatal dried blood spot DNA. PLoS One. 2016;11(4):e0153253. doi: 10.1371/journal.pone.0153253.

 PubMed Web of Science ®Google Scholar

Winkel BG, Hollegaard MV, Olesen MS, et al. Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis. BMC Med Genet. 2011;12(1):22. doi: 10.1186/1471-2350-12-22.

 PubMedGoogle Scholar

Needham BL, Hicken MT, Govia IO, et al. Maternal social disadvantage and newborn telomere length in archived dried blood spots from the Michigan neonatal biobank. Biodemography Soc Biol. 2017;63(3):221–235. doi: 10.1080/19485565.2017.1300520.

 PubMed Web of Science ®Google Scholar

Barco S, Risso FM, Bruschettini M, et al. A validated LC-MS/MS method for the quantification of piperacillin/tazobactam on dried blood spot. Bioanalysis. 2014;6(21):2795–2802. doi: 10.4155/bio.14.205.

 PubMed Web of Science ®Google Scholar

Rovito R, Warnatz HJ, Kiełbasa SM, et al. Impact of congenital cytomegalovirus infection on transcriptomes from archived dried blood spots in relation to long-term clinical outcome. PLoS One. 2018;13(7):e0200652. doi: 10.1371/journal.pone.0200652.

 PubMed Web of Science ®Google Scholar