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Clinical: Research Communication

Alpha-1 chain of human haptoglobin as viability marker of in vitro fertilized human embryos: information beyond morphology

, , , , &
Pages 174-180 | Received 03 Jan 2018, Accepted 26 Aug 2018, Published online: 17 Sep 2018
 

ABSTRACT

Only one third of the in vitro fertilization treatments result in successful delivery following morphological viability assessment worldwide. A paper by Montskó et al. (2015) describes the identification of the alpha-1 chain of human haptoglobin as a potential marker of embryo viability. Using mass spectrometry, the concentration of the haptoglobin alpha-1 chain was determined in spent culture media samples of in vitro fertilized embryos and correlation was found with the outcome of the respective transfer. In the present study we investigated, whether the concentration of haptoglobin alpha-1 chain shows any correlation with morphological scores to clarify whether levels of the alpha-1 chain provide additional information on embryo viability unnoticed by the morphological assessment. In the study, pregnancy and live birth rates were examined in 143 transferred samples of 86 patients, retrospectively. Two sample groups were created. The control group contained embryos classified as ‘good’ or ‘fair’ based on the Istanbul Consensus Criteria System, while the double-assay group contained embryos assessed as ‘good’ or ‘fair’ by the morphological evaluation and as ‘viable’ by the haptoglobin assay. Clinical pregnancy rate was 30.2% in the control group, while 47.6% in the group scored parallel with morphological criteria and proteomic analysis (p < 0.05). The increased clinical pregnancy rate observed in the double-assayed group can be attributed to decreased false-positivity of the double assay.

Abbreviations: IVF: in vitro fertilization; SEC: spent embryo culture medium; HSA: human serum albumin; Hpt: haptoglobin; HptA1: haptoglobin alpha-1 chain; ICCS: Istanbul Consensus Criteria System; BMI: body mass index; ICSI: intracytoplasmic sperm injection

Disclosure statement

No potential conflict of interest was reported by the authors.

Supplementary material

Supplemental data for this article can be accessed on the publisher’s website.

Additional information

Funding

The presented work was funded by NKFI-EPR K/115394/2015/HU ‘Early biochemical indicators of embryo viability’ and EDIOP-2.3.2-15-2016-00021. ‘The use of chip-technology in increasing the effectiveness of human in vitro fertilization’ and by the ÚNKP-17-4-III ‘New National Excellence Program of the Ministry of Human Capacities’ grants [ÚNKP-17-4-III]; National Research, Development and Innovation Office, Hungary [EDIOP-2.3.2-15-2016-00021, NKFI-EPR K/115394/2015/HU].

Notes on contributors

Gábor L. Kovács

Performed HptA1 assay, the statistics and prepared the manuscript: GM, RH. Performed the culturing of embryos, the morphological viability assessment and collected the samples: KG. Supervised the clinical protocol and prepared the sections of the manuscript describing oocyte collection, fertilization and embryo transfer procedures: ÁV, BJ. Supervised the preparation of the manuscript the statistical analysis and the corresponding author of the manuscript: GLK.

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