Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease

被引:5
作者
Huang, Xiaoli [1 ]
Cheng, Yimin [2 ]
Wang, Na [1 ]
机构
[1] Xian Hosp Tradit Chinese Med, Dept Cardiovascol, 69 Fengcheng Eighth Rd, Xian 710021, Peoples R China
[2] Hosp Xian Shiyou Univ, Dept Obstet & Gynecol, Xian 710065, Peoples R China
关键词
Coronary heart disease; Polymorphisms; Susceptibility; Gene; POLYMORPHISMS; RISK;
D O I
10.1186/s12920-022-01307-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Genetic factors are important risk factors to develop coronary heart disease (CHD). In this study, we mainly explored whether CYP11B1 mutations influence CHD risk among Chinese Han population. Methods Six variants were genotyped using Agena MassARRAY system from 509 CHD patients and 509 healthy controls. The correlations between CYP11B1 mutations and CHD risk were assessed using odds ratio (OR) and 95% confidence interval (95% CI) by logistic regression. The haplotype analysis and were ultifactor dimensionality reduction (MDR) were conducted. Results In the overall analysis, CYP11B1 polymorphisms were not correlated with CHD susceptibility. In the stratified analysis, we found that rs5283, rs6410, and rs4534 are significantly associated with susceptibility to CHD dependent on age and gender (p < 0.05). Moreover, we also observed that rs5283 and rs4534 could affect diabetes/hypertension risk among CHD patients (p < 0.05). In addition, the C(rs4736312)A(rs5017238)C(rs5301)G(rs5283)T(rs6410)C(rs4534) haplotype of CYP11B1 reduce the susceptibility to CHD (p < 0.05). Conclusions We found that rs4534, rs6410 and rs5283 in CYP11B1 gene influence the susceptibility to CHD, which depend on age and gender.
引用
收藏
页数:11
相关论文
共 31 条
  • [1] The potential of targeting CYP11B
    Bernhardt, Rita
    [J]. EXPERT OPINION ON THERAPEUTIC TARGETS, 2016, 20 (08) : 923 - 934
  • [2] Development of CYP11B1 and CYP11B2 assays utilizing homogenates of adrenal glands: Utility of monkey as a surrogate for human
    Cerny, Matthew A.
    Csengery, Alexander
    Schmenk, Jennifer
    Frederick, Kosea
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2015, 154 : 197 - 205
  • [3] Large-scale association analysis identifies new risk loci for coronary artery disease
    Deloukas, Panos
    Kanoni, Stavroula
    Willenborg, Christina
    Farrall, Martin
    Assimes, Themistocles L.
    Thompson, John R.
    Ingelsson, Erik
    Saleheen, Danish
    Erdmann, Jeanette
    Goldstein, Benjamin A.
    Stirrups, Kathleen
    Koenig, Inke R.
    Cazier, Jean-Baptiste
    Johansson, Asa
    Hall, Alistair S.
    Lee, Jong-Young
    Willer, Cristen J.
    Chambers, John C.
    Esko, Tonu
    Folkersen, Lasse
    Goel, Anuj
    Grundberg, Elin
    Havulinna, Aki S.
    Ho, Weang K.
    Hopewell, Jemma C.
    Eriksson, Niclas
    Kleber, Marcus E.
    Kristiansson, Kati
    Lundmark, Per
    Lyytikainen, Leo-Pekka
    Rafelt, Suzanne
    Shungin, Dmitry
    Strawbridge, Rona J.
    Thorleifsson, Gudmar
    Tikkanen, Emmi
    Van Zuydam, Natalie
    Voight, Benjamin F.
    Waite, Lindsay L.
    Zhang, Weihua
    Ziegler, Andreas
    Absher, Devin
    Altshuler, David
    Balmforth, Anthony J.
    Barroso, Ines
    Braund, Peter S.
    Burgdorf, Christof
    Claudi-Boehm, Simone
    Cox, David
    Dimitriou, Maria
    Do, Ron
    [J]. NATURE GENETICS, 2013, 45 (01) : 25 - U52
  • [4] A Family-Based Association Study of CYP11A1 and CYP11B1 Gene Polymorphisms With Autism in Chinese Trios
    Deng, Hong-Zhu
    You, Cong
    Xing, Yu
    Chen, Kai-Yun
    Zou, Xiao-Bing
    [J]. JOURNAL OF CHILD NEUROLOGY, 2016, 31 (06) : 733 - 737
  • [5] Di Angelantonio Emanuele, 2011, IARC Sci Publ, P363
  • [6] Does altered glucocorticoid homeostasis increase cardiovascular risk?
    Girod, JP
    Brotman, DJ
    [J]. CARDIOVASCULAR RESEARCH, 2004, 64 (02) : 217 - 226
  • [7] CYP11B1 variants influence skeletal maturation via alternative splicing
    Grgic, Olja
    Gazzara, Matthew R.
    Chesi, Alessandra
    Medina-Gomez, Carolina
    Cousminer, Diana L.
    Mitchell, Jonathan A.
    Prijatelj, Vid
    de Vries, Jard
    Shevroja, Enisa
    McCormack, Shana E.
    Kalkwarf, Heidi J.
    Lappe, Joan M.
    Gilsanz, Vicente
    Oberfield, Sharon E.
    Shepherd, John A.
    Kelly, Andrea
    Mahboubi, Soroosh
    Faucz, Fabio R.
    Feelders, Richard A.
    de Jong, Frank H.
    Uitterlinden, Andre G.
    Visser, Jenny A.
    Ghanem, Louis R.
    Wolvius, Eppo B.
    Hofland, Leo J.
    Stratakis, Constantine A.
    Zemel, Babette S.
    Barash, Yoseph
    Grant, Struan F. A.
    Rivadeneira, Fernando
    [J]. COMMUNICATIONS BIOLOGY, 2021, 4 (01)
  • [8] Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders
    Han, Lin
    Chen, Meilin
    Wang, Yazhe
    Wu, Huidan
    Quan, Yingting
    Bai, Ting
    Li, Kuokuo
    Duan, Guiqin
    Gao, Yan
    Hu, Zhengmao
    Xia, Kun
    Guo, Hui
    [J]. MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (07):
  • [9] Forecasting the Future of Cardiovascular Disease in the United States A Policy Statement From the American Heart Association
    Heidenreich, Paul A.
    Trogdon, Justin G.
    Khavjou, Olga A.
    Butler, Javed
    Dracup, Kathleen
    Ezekowitz, Michael D.
    Finkelstein, Eric Andrew
    Hong, Yuling
    Johnston, S. Claiborne
    Khera, Amit
    Lloyd-Jones, Donald M.
    Nelson, Sue A.
    Nichol, Graham
    Orenstein, Diane
    Wilson, Peter W. F.
    Woo, Y. Joseph
    [J]. CIRCULATION, 2011, 123 (08) : 933 - 944
  • [10] Synonymous mutations make dramatic contributions to fitness when growth is limited by a weak-link enzyme
    Kristofich, JohnCarlo
    Morgenthaler, Andrew B.
    Kinney, Wallis R.
    Ebmeier, Christopher C.
    Snyder, Daniel J.
    Old, William M.
    Cooper, Vaughn S.
    Copley, Shelley D.
    [J]. PLOS GENETICS, 2018, 14 (08):