PMID- 28444966 OWN - NLM STAT- MEDLINE DCOM- 20180507 LR - 20210109 IS - 1932-8737 (Electronic) IS - 0160-9289 (Print) IS - 0160-9289 (Linking) VI - 40 IP - 8 DP - 2017 Aug TI - Correlation between genetic polymorphisms within the MAPK1/HIF-1/HO-1 signaling pathway and risk or prognosis of perimenopausal coronary artery disease. PG - 597-604 LID - 10.1002/clc.22708 [doi] AB - BACKGROUND: Mitogen-activated protein kinase-1 (MAPK1), as well as its downstream factors of hypoxia-inducible factor-1 (HIF-1) and heme oxygenase-1 (HO-1), have been documented to be involved in modulating development of coronary artery disease (CAD). HYPOTHESIS: Genetic mutations within the MAPK1/HIF-1/HO-1 signaling pathway could alter the risk of perimenopausal CAD in Chinese patients. METHODS: Peripheral blood samples were gathered from 589 CAD patients and 860 healthy controls, and 12 potential single-nucleotide polymorphisms (SNPs) were obtained from HapMap database and previously published studies. Genotyping of SNPs was implemented with the TaqMan SNP Genotyping Assays. Odds ratios (OR) and 95% confidence intervals (CI) were utilized to evaluate the correlations between SNPs and CAD risk. RESULTS: Regarding MAPK1 , rs6928 (OR: 1.71, 95% CI: 1.47-1.98, P < 0.05), rs9340 (OR: 0.85, 95% CI: 0.73-0.99, P < 0.05), and rs11913721 (OR: 0.70, 95% CI: 0.52-0.95, P < 0.05) were remarkably associated with susceptibility to perimenopausal CAD. Of these, rs9340 and rs11913721 were also regarded as protective factors for perimenopausal CAD patients. Moreover, results of HIF-1 indicated noticeable correlations between combined SNPs of rs1087314 and rs2057482 and risk of perimenopausal CAD (OR: 1.24, 95% CI: 1.01-1.53, P < 0.05; and OR: 0.71, 95% CI: 0.55-0.91, P < 0.05, respectively). Nonetheless, rs2071746 in HO-1 was found to be only associated with perimenopausal CAD risk (OR: 0.67, 95% CI: 0.58-0.78, P < 0.05). CONCLUSIONS: The genetic mutations within MAPK1 (rs6928, rs9340, rs11913721), HIF-1 (rs1087314, rs2057482), and HO-1 (rs2071746) could alter susceptibility to perimenopausal CAD in this Chinese population. CI - (c) 2017 Wiley Periodicals, Inc. FAU - Guo, Nan AU - Guo N AD - Department of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. FAU - Zhang, Nan AU - Zhang N AUID- ORCID: 0000-0002-4713-0908 AD - Department of Cardiothoracic Surgery, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. FAU - Yan, Liqiu AU - Yan L AD - Department of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. FAU - Cao, Xufen AU - Cao X AD - Department of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. FAU - Wang, Jiawang AU - Wang J AD - Department of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. FAU - Wang, Yunfei AU - Wang Y AD - Department of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China. LA - eng PT - Journal Article DEP - 20170426 PL - United States TA - Clin Cardiol JT - Clinical cardiology JID - 7903272 RN - 0 (Hypoxia-Inducible Factor 1) RN - EC 1.14.14.18 (HMOX1 protein, human) RN - EC 1.14.14.18 (Heme Oxygenase-1) RN - EC 2.7.11.24 (MAPK1 protein, human) RN - EC 2.7.11.24 (Mitogen-Activated Protein Kinase 1) SB - IM MH - Chi-Square Distribution MH - China MH - Coronary Angiography MH - Coronary Artery Disease/diagnostic imaging/enzymology/*genetics MH - Coronary Stenosis/diagnostic imaging/enzymology/*genetics MH - Female MH - Gene Frequency MH - Genetic Association Studies MH - Genetic Predisposition to Disease MH - Heme Oxygenase-1/*genetics MH - Humans MH - Hypoxia-Inducible Factor 1/*genetics MH - Mitogen-Activated Protein Kinase 1/*genetics MH - Odds Ratio MH - *Perimenopause MH - Phenotype MH - *Polymorphism, Single Nucleotide MH - Retrospective Studies MH - Risk Factors MH - Signal Transduction/*genetics PMC - PMC6490459 OTO - NOTNLM OT - Gene-Gene Interaction OT - MAPK1/HIF-1/HO-1 Signaling OT - Perimenopausal CAD OT - Single-Nucleotide Polymorphism OT - Susceptibility COIS- The authors declare no potential conflicts of interest. EDAT- 2017/04/27 06:00 MHDA- 2018/05/08 06:00 PMCR- 2017/04/26 CRDT- 2017/04/27 06:00 PHST- 2016/12/13 00:00 [received] PHST- 2017/02/27 00:00 [revised] PHST- 2017/02/28 00:00 [accepted] PHST- 2017/04/27 06:00 [pubmed] PHST- 2018/05/08 06:00 [medline] PHST- 2017/04/27 06:00 [entrez] PHST- 2017/04/26 00:00 [pmc-release] AID - CLC22708 [pii] AID - 10.1002/clc.22708 [doi] PST - ppublish SO - Clin Cardiol. 2017 Aug;40(8):597-604. doi: 10.1002/clc.22708. Epub 2017 Apr 26.