References
- Mazer CD, Whitlock RP, Fergusson DA, et al. Restrictive or liberal red-cell transfusion for cardiac surgery. N Engl J Med. 2017;377(22):2133–2144. doi:https://doi.org/10.1056/NEJMoa1711818.
- Berger M, Schenning KJ, Brown CH, et al. Best practices for postoperative brain health: recommendations from the fifth international perioperative neurotoxicity working group. Anesth Analg. 2018;127(6):1406–1413. doi:https://doi.org/10.1213/ANE.0000000000003841.
- Trubnikova OA, Maleva OV, Tarasova IV, Mamontova AS, Uchasova EG, Barbarash OL. [Effect of statins on development of early cognitive dysfunction after coronary artery bypass grafting]. Kardiologiia. 2015;55(4):49–56. doi:https://doi.org/10.18565/cardio.2015.4.49-56.
- Newman MF, Mathew JP, Grocott HP, et al. Central nervous system injury associated with cardiac surgery. Lancet (London, England). 2006;368(9536):694–703. doi:https://doi.org/10.1016/S0140-6736(06)69254-4.
- Newman MF, Grocott HP, Mathew JP, et al. Report of the substudy assessing the impact of neurocognitive function on quality of life 5 years after cardiac surgery. Stroke. 2001;32(12):2874–2881. doi:https://doi.org/10.1161/hs1201.099803.
- Phillips-Bute B, Mathew JP, Blumenthal JA, et al. Association of neurocognitive function and quality of life 1 year after coronary artery bypass graft (CABG) surgery. Psychosomatic Medicine. 2006;68(3):369–375.
- Patel N, Minhas JS, Chung EM. Risk factors associated with cognitive decline after cardiac surgery: a systematic review. Cardiovasc Psychiatry Neurol. 2015;2015:370612. doi:https://doi.org/10.1155/2015/370612.
- Yi SQ, Yang M, Duan KM. Immune-mediated metabolic kynurenine pathways are involved in the postoperative cognitive dysfunction after cardiopulmonary bypass. Thorac Cardiovasc Surg. 2015;63(7):618–623. doi:https://doi.org/10.1055/s-0034-1393704.
- Wang C, Liu L, Zhu H, et al. MicroRNA expression profile of HCT-8 cells in the early phase of Cryptosporidium parvum infection. BMC Genomics 2019;20(1):37. doi:https://doi.org/10.1186/s12864-018-5410-6.
- Zhang J, Xu Y, Liu H, Pan Z. MicroRNAs in ovarian follicular atresia and granulosa cell apoptosis. Reprod Biol Endocrinol. 2019;17(1):9. doi:https://doi.org/10.1186/s12958-018-0450-y.
- Vuokila N, Lukasiuk K, Bot AM, et al. miR-124-3p is a chronic regulator of gene expression after brain injury. Cell Mol Life Sci. 2018;75(24):4557–4581. doi:https://doi.org/10.1007/s00018-018-2911-z.
- Zhou Y, Deng J, Chu X, Zhao Y, Guo Y. Role of post-transcriptional control of calpain by miR-124-3p in the development of Alzheimer's disease. JAD. 2019;67(2):571–581. doi:https://doi.org/10.3233/JAD-181053.
- Hartmann H, Hoehne K, Rist E, Louw AM, Schlosshauer B. miR-124 disinhibits neurite outgrowth in an inflammatory environment. Cell Tissue Res. 2015;362(1):9–20. doi:https://doi.org/10.1007/s00441-015-2183-y.
- Li L, Zhang Y, Luo H, et al. Systematic identification and analysis of expression profiles of mRNAs and IncRNAs in macrophage inflammatory response. Shock (Augusta, Ga). 2019;51(6):770–779. doi:https://doi.org/10.1097/SHK.0000000000001181.
- Do H, Kim W. Roles of oncogenic long non-coding RNAs in cancer development. Genomics Inform. 2018;16(4):e18. doi:https://doi.org/10.5808/GI.2018.16.4.e18.
- Tang LP, Ding JB, Liu ZH, Zhou GJ. LncRNA TUG1 promotes osteoarthritis-induced degradation of chondrocyte extracellular matrix via miR-195/MMP-13 axis. Eur Rev Med Pharmacol Sci. 2018;22(24):8574–8581. doi:https://doi.org/10.26355/eurrev_201812_16620.
- Wang B, Zhang J. Multiple linear regression analysis of lncRNA-disease association prediction based on clinical prognosis data. Biomed Res Int. 2018;2018:3823082. doi:https://doi.org/10.1155/2018/3823082.
- Chen S, Chen JZ, Zhang JQ, et al. Silencing of long noncoding RNA LINC00958 prevents tumor initiation of pancreatic cancer by acting as a sponge of microRNA-330-5p to down-regulate PAX8. Cancer Lett. 2019;446:49–61. doi:https://doi.org/10.1016/j.canlet.2018.12.017.
- Qiu YY, Wu Y, Lin MJ, Bian T, Xiao YL, Qin C. LncRNA-MEG3 functions as a competing endogenous RNA to regulate Treg/Th17 balance in patients with asthma by targeting microRNA-17/ RORγt. Biomed Pharmacother. 2019;111:386–394. doi:https://doi.org/10.1016/j.biopha.2018.12.080.
- Wu XS, Wang F, Li HF, et al. LncRNA-PAGBC acts as a microRNA sponge and promotes gallbladder tumorigenesis. EMBO Rep. 2017;18(10):1837–1853. doi:https://doi.org/10.15252/embr.201744147.
- Zhang Y, Liu YX, Xiao QX, et al. Microarray expression profiles of lncRNAs and mRNAs in postoperative cognitive dysfunction. Front Neurosci. 2018;12:694. doi:https://doi.org/10.3389/fnins.2018.00694.
- Steinmetz J, Christensen KB, Lund T, Lohse N, Rasmussen LS. Long-term consequences of postoperative cognitive dysfunction. Anesthesiology. 2009;110(3):548–555. doi:https://doi.org/10.1097/ALN.0b013e318195b569.
- Moller JT, Cluitmans P, Rasmussen LS, et al. Long-term postoperative cognitive dysfunction in the elderly ISPND1 study. ISPND investigators. International Study of Post-Operative Cognitive Dysfunction. Lancet (London, England). 1998;351(9106):857–861. doi:https://doi.org/10.1016/S0140-6736(97)07382-0.
- Ge Y, Ma Z, Shi H, Zhao Y, Gu X, Wei H. [Incidence and risk factors of postoperative cognitive dysfunction in patients underwent coronary artery bypass grafting surgery]. Zhong Nan da Xue Xue Bao Yi Xue Ban. 2014;39(10):1049–1055.
- Shaefi S, Marcantonio ER, Mueller A, et al. Intraoperative oxygen concentration and neurocognition after cardiac surgery: study protocol for a randomized controlled trial. Trials. 2017;18(1):600. doi:https://doi.org/10.1186/s13063-017-2337-1.
- Ozturk S, Sacar M, Baltalarli A, Ozturk I. Effect of the type of cardiopulmonary bypass pump flow on postoperative cognitive function in patients undergoing isolated coronary artery surgery. Anatol J Cardiol. 2016;16(11):875–880.
- Silva FP, Schmidt AP, Valentin LS, et al. S100B protein and neuron-specific enolase as predictors of cognitive dysfunction after coronary artery bypass graft surgery: a prospective observational study. Eur J Anaesthesiol. 2016;33(9):681–689. doi:https://doi.org/10.1097/EJA.0000000000000450.
- Altarabsheh SE, Deo SV, Rababa'h AM, et al. Off-pump coronary artery bypass reduces early stroke in octogenarians: a meta-analysis of 18,000 patients. Ann Thorac Surg. 2015;99(5):1568–1575. doi:https://doi.org/10.1016/j.athoracsur.2014.12.057.
- Godinho AS, Alves AS, Pereira AJ, Pereira TS. On-pump versus off-pump coronary-artery bypass surgery: a meta-analysis. Arq Bras Cardiol. 2012;98(1):87–94. doi:https://doi.org/10.1590/s0066-782x2012000100014.
- Baba T, Maekawa K, Otomo S, Tokunaga Y, Oyoshi T. [Postoperative cognitive dysfunction in off-pump versus on-pump coronary artery bypass surgery]. Masui. 2014;6 (11):1219–1227.
- Fink HA, Hemmy LS, MacDonald R, et al. AHRQ Technology Assessments. Cognitive Outcomes after Cardiovascular Procedures in Older Adults: A Systematic Review. Rockville, MD: Agency for Healthcare Research and Quality (US); 2014.
- Makeyev EV, Zhang J, Carrasco MA, Maniatis T. The MicroRNA miR-124 promotes neuronal differentiation by triggering brain-specific alternative pre-mRNA splicing. Mol Cell. 2007;27(3):435–448. doi:https://doi.org/10.1016/j.molcel.2007.07.015.
- Yeom KH, Mitchell S, Linares AJ, et al. Polypyrimidine tract-binding protein blocks miRNA-124 biogenesis to enforce its neuronal-specific expression in the mouse. Proc Natl Acad Sci USA. 2018;115(47):E11061–E11070. doi:https://doi.org/10.1073/pnas.1809609115.
- Kong Y, Wu J, Zhang D, Wan C, Yuan L. The role of miR-124 in Drosophila Alzheimer's disease model by targeting delta in notch signaling pathway. Curr Mol Med. 2015;15(10):980–989. doi:https://doi.org/10.2174/1566524016666151123114608.
- Arrant AE, Roberson ED. MicroRNA-124 modulates social behavior in frontotemporal dementia. Nat Med. 2014;20(12):1381–1383. doi:https://doi.org/10.1038/nm.3768.
- Veremeyko T, Siddiqui S, Sotnikov I, Yung A, Ponomarev ED. IL-4/IL-13-dependent and independent expression of miR-124 and its contribution to M2 phenotype of monocytic cells in normal conditions and during allergic inflammation. PLoS One. 2013;8(12):e81774. doi:https://doi.org/10.1371/journal.pone.0081774.
- Rosas-Ballina M, Olofsson PS, Ochani M, et al. Acetylcholine-synthesizing T cells relay neural signals in a vagus nerve circuit. Science. 2011;334(6052):98–101. doi:https://doi.org/10.1126/science.1209985.
- Gaudet AD, Fonken LK, Watkins LR, Nelson RJ, Popovich PG. MicroRNAs: roles in regulating neuroinflammation. Neuroscientist. 2018;24(3):221–245. doi:https://doi.org/10.1177/1073858417721150.
- Zhang T, Pang P, Fang Z, et al. Expression of BC1 impairs spatial learning and memory in Alzheimer's disease via APP translation. Mol Neurobiol. 2018;55(7):6007–6020. doi:https://doi.org/10.1007/s12035-017-0820-z.
- Gu C, Chen C, Wu R, et al. Long noncoding RNA EBF3-AS promotes neuron apoptosis in Alzheimer's disease. DNA Cell Biol. 2018;37(3):220–226. doi:https://doi.org/10.1089/dna.2017.4012.
- Wang J, Zhou T, Wang T, Wang B. Suppression of lncRNA-ATB prevents amyloid-β-induced neurotoxicity in PC12 cells via regulating miR-200/ZNF217 axis. Biomed Pharmacother. 2018;108:707–715. doi:https://doi.org/10.1016/j.biopha.2018.08.155.