Skip to main content
Top
Published in: BMC Cardiovascular Disorders 1/2020

Open Access 01-12-2020 | Arterial Diseases | Research article

Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)

Authors: Jyotdeep Kour Raina, Minakashee Sharma, Rakesh Kumar Panjaliya, Vikas Dogra, Ashok Bakaya, Parvinder Kumar

Published in: BMC Cardiovascular Disorders | Issue 1/2020

Login to get access

Abstract

Background

Coronary artery disease (CAD) is a complex disease resulting from the cumulative and interactive effects of large number of genes along with environmental exposure. Therefore, the present study was envisaged as an effort to study the association of candidate genes ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with the risk of CAD, targeting the populations of Jammu (JandK).

Method

A total of 400 confirmed CAD patients and 400 healthy controls were enrolled for the present study. Genotyping was done by polymerase chain reaction- restriction fragment length polymorphism (PCR-RFLP).

Results

ESR1 gene (rs9340799) polymorphism was found to be associated with CAD in all the genetic models. The haplotype analysis of ESR1 (rs2234693 and rs9340799) gene revealed that C-G haplotype was conferring approximately 5-fold risk and T-A haplotype was adding 1.4-fold risk towards the disease. ‘T’ allele of MTHFR rs1801133 SNP was observed to be responsible for development of CAD in our study population (p < 0.0001). In case of MTHFR (rs1801133 and rs2274976) gene, the haplotype T-G was observed to confer 4.7-fold risk towards CAD whereas haplotype C-G provided nearly a 1.7 fold protection towards development of CAD. For MS gene, rs185087 was also found to be associated with CAD in a co-dominant (p = 0.003 and p = 0.03), dominant (p = 0.001) and allelic models (p = 0.001). The gene-gene interaction revealed strong epistasis between single nucleotide polymorphisms (SNPs), ESR1 rs9340799 and MTHFR rs2274976. Furthermore, the dendrogram for gene-environment dataset indicated moderately synergistic interaction between CETP rs708272 and physical inactivity.

Conclusion

In the study under reference, a significant association of ESR1-XbaI (rs9340799), MTHFR C677T (rs1801133) and MS A2756G (rs185087) gene polymorphisms with the susceptibility of CAD in the population of Jammu region (JandK) has been observed.
Literature
2.
go back to reference Ardeshna DR, Bob-Manuel T, Nanda A, Sharma A, et al. Asian-Indians: a review of coronary artery disease in this understudied cohort in the United States. Ann Transl Med. 2018;6(1):12.PubMedPubMedCentral Ardeshna DR, Bob-Manuel T, Nanda A, Sharma A, et al. Asian-Indians: a review of coronary artery disease in this understudied cohort in the United States. Ann Transl Med. 2018;6(1):12.PubMedPubMedCentral
3.
go back to reference Liu H, Pedram A, Kim JK. Oestrogen prevents cardiomyocyte apoptosis by suppressing p38α-mediated activation of p53 and by down-regulating p53 inhibition on p38β. Cardiovasc Res. 2011;89(1):119–28.PubMed Liu H, Pedram A, Kim JK. Oestrogen prevents cardiomyocyte apoptosis by suppressing p38α-mediated activation of p53 and by down-regulating p53 inhibition on p38β. Cardiovasc Res. 2011;89(1):119–28.PubMed
4.
go back to reference Gao HH, Gao LB, Wen JM. Genetic polymorphisms in the ESR1 gene and cerebral infarction risk: a meta-analysis. DNA Cell Biol. 2014;33:605–15.PubMed Gao HH, Gao LB, Wen JM. Genetic polymorphisms in the ESR1 gene and cerebral infarction risk: a meta-analysis. DNA Cell Biol. 2014;33:605–15.PubMed
6.
go back to reference Schuit SCE, Oei HHS, Witteman JCM, van Kessel CHG, et al. Estrogen receptor α gene polymorphisms and risk of myocardial infarction. JAMA. 2004;291:2969–77.PubMed Schuit SCE, Oei HHS, Witteman JCM, van Kessel CHG, et al. Estrogen receptor α gene polymorphisms and risk of myocardial infarction. JAMA. 2004;291:2969–77.PubMed
7.
go back to reference Kjaergaard AD, Ellervik C, Tybjærg-Hansen A, Axelsson CK, Grønholdt MLM, Grande P, et al. Estrogen receptor α polymorphism and risk of cardiovascular disease, cancer, and hip fracture cross-sectional, cohort and case-control studies and a meta-analysis. Circulation. 2007;115:861–71.PubMed Kjaergaard AD, Ellervik C, Tybjærg-Hansen A, Axelsson CK, Grønholdt MLM, Grande P, et al. Estrogen receptor α polymorphism and risk of cardiovascular disease, cancer, and hip fracture cross-sectional, cohort and case-control studies and a meta-analysis. Circulation. 2007;115:861–71.PubMed
8.
go back to reference Hassanzadeh T, Firoozrai M, Zonouz AE, Zavarehee A, Paoli M. Taq1B polymorphism of cholesteryl ester transfer protein (CETP) gene in primary combined hyperlipidaemia. Indian J Med Res. 2009;129:293–8.PubMed Hassanzadeh T, Firoozrai M, Zonouz AE, Zavarehee A, Paoli M. Taq1B polymorphism of cholesteryl ester transfer protein (CETP) gene in primary combined hyperlipidaemia. Indian J Med Res. 2009;129:293–8.PubMed
9.
go back to reference Raina JK, Sharma M, Panjaliya RK, Bhagat M, Sharma R, Bakaya A, Kumar P. Methylenetetrahydrofolate reductase C677T and methionine synthase A2756G gene polymorphisms and associated risk of cardiovascular diseases: a study from Jammu region. Indian Heart J. 2016a;168:421–30. Raina JK, Sharma M, Panjaliya RK, Bhagat M, Sharma R, Bakaya A, Kumar P. Methylenetetrahydrofolate reductase C677T and methionine synthase A2756G gene polymorphisms and associated risk of cardiovascular diseases: a study from Jammu region. Indian Heart J. 2016a;168:421–30.
10.
go back to reference WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. 2004;363:157–63. WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. 2004;363:157–63.
11.
go back to reference Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP). Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA. 2001;285:2486–97. Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP). Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA. 2001;285:2486–97.
12.
go back to reference Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jones DW, et al. The seventh report of the joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure: the JNC 7 report. JAMA. 2003;289:2560–72.PubMed Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jones DW, et al. The seventh report of the joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure: the JNC 7 report. JAMA. 2003;289:2560–72.PubMed
13.
go back to reference Sambrook J, Russell DW. Molecular cloning, a laboratory manual. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press; 2001. Sambrook J, Russell DW. Molecular cloning, a laboratory manual. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press; 2001.
14.
go back to reference Skol AD, Scott LJ, Abecasis GR, Boehnke M. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet. 2006;38:209–13.PubMed Skol AD, Scott LJ, Abecasis GR, Boehnke M. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet. 2006;38:209–13.PubMed
15.
go back to reference Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, Moore JH. Multifactor dimensionality reduction reveals high-order interactions among estrogen metabolism genes in sporadic breast cancer. Am J Hum Genet. 2001;69:138–47.PubMedPubMedCentral Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, Moore JH. Multifactor dimensionality reduction reveals high-order interactions among estrogen metabolism genes in sporadic breast cancer. Am J Hum Genet. 2001;69:138–47.PubMedPubMedCentral
16.
go back to reference Zhao T, Zhang D, Liu Y, Zhou D, Chen Z, Yang Y, et al. Association between ESR1 and ESR2 gene polymorphisms and hyperlipidemia in Chinese Han postmenopausal women. J Hum Genet. 2010;55:50–4.PubMed Zhao T, Zhang D, Liu Y, Zhou D, Chen Z, Yang Y, et al. Association between ESR1 and ESR2 gene polymorphisms and hyperlipidemia in Chinese Han postmenopausal women. J Hum Genet. 2010;55:50–4.PubMed
17.
go back to reference Panjaliya RK, Gupta D, Raina JK, Bhardwaj R, Gupta A, Kumar P. Study of genetic variation of Alu CD4, LPL-PvuII and ESR1-PvuII in different population groups of Jammu region (JandK). Int J Biol Biomed Sci. 2013;2(9):026–30. Panjaliya RK, Gupta D, Raina JK, Bhardwaj R, Gupta A, Kumar P. Study of genetic variation of Alu CD4, LPL-PvuII and ESR1-PvuII in different population groups of Jammu region (JandK). Int J Biol Biomed Sci. 2013;2(9):026–30.
18.
go back to reference Saini JS, Kumar A, Matharoo K, Sokhi J, Badaruddoza BAJS. Genomic diversity and affinities in population groups of north West India: an analysis of Alu insertion and a single nucleotide polymorphism. Gene. 2012;511:293–9.PubMed Saini JS, Kumar A, Matharoo K, Sokhi J, Badaruddoza BAJS. Genomic diversity and affinities in population groups of north West India: an analysis of Alu insertion and a single nucleotide polymorphism. Gene. 2012;511:293–9.PubMed
19.
go back to reference Koch W, Hoppmann P, Pfeufer A, Mueller JC, Schömig A, Kastrati A. No replication of association between estrogen receptor α gene polymorphisms and susceptibility to myocardial infarction in a large sample of patients of European descent. Circulation. 2005;112:2138–42.PubMed Koch W, Hoppmann P, Pfeufer A, Mueller JC, Schömig A, Kastrati A. No replication of association between estrogen receptor α gene polymorphisms and susceptibility to myocardial infarction in a large sample of patients of European descent. Circulation. 2005;112:2138–42.PubMed
20.
go back to reference Boroumand M, Ghaedi M, Mohammadtaghvaei N, Pourgholi L, Anvari MS, Davoodi G, et al. Association of estrogen receptor α gene polymorphism with the presence of coronary artery disease documented by coronary angiography. Clin Biochem. 2009;42:835–9.PubMed Boroumand M, Ghaedi M, Mohammadtaghvaei N, Pourgholi L, Anvari MS, Davoodi G, et al. Association of estrogen receptor α gene polymorphism with the presence of coronary artery disease documented by coronary angiography. Clin Biochem. 2009;42:835–9.PubMed
21.
go back to reference Wu MM, Hsieh YC, Lien LM, Chen WH, Bai CH, Chiu HC, et al. Association of estrogen receptor (alpha) genotypes/haplotypes with carotid intima-media thickness in Taiwanese women. Angiology. 2010;61:275–82.PubMed Wu MM, Hsieh YC, Lien LM, Chen WH, Bai CH, Chiu HC, et al. Association of estrogen receptor (alpha) genotypes/haplotypes with carotid intima-media thickness in Taiwanese women. Angiology. 2010;61:275–82.PubMed
22.
go back to reference Boroumand M, Ghasemi Y, Shirani S, Pourgholi L, Anvari MS, Sepehriseresht S, et al. Association between estrogen receptor-alpha PvuII and XbaI gene polymorphisms with extracranial carotid stenosis. Labmedicine. 2011;42(11):663–7. Boroumand M, Ghasemi Y, Shirani S, Pourgholi L, Anvari MS, Sepehriseresht S, et al. Association between estrogen receptor-alpha PvuII and XbaI gene polymorphisms with extracranial carotid stenosis. Labmedicine. 2011;42(11):663–7.
23.
go back to reference Rebelo AC, Verlengia R, Kunz V, Tamburus N, Cerda A, Hirata R, et al. Lack of association of estrogen receptor alpha gene polymorphisms with cardiorespiratory and metabolic variables in young women. Int J Mol Sci. 2012;13:13691–703.PubMedPubMedCentral Rebelo AC, Verlengia R, Kunz V, Tamburus N, Cerda A, Hirata R, et al. Lack of association of estrogen receptor alpha gene polymorphisms with cardiorespiratory and metabolic variables in young women. Int J Mol Sci. 2012;13:13691–703.PubMedPubMedCentral
24.
go back to reference Jiang N, Yang G, Peng CL. ESR1 gene polymorphisms PvuII (rs2234693T>C) and XbaI (rs9340799A>G) may not be directly correlated with cardiovascular disease risk. Genet Mol Res. 2015;14(4):13932–44.PubMed Jiang N, Yang G, Peng CL. ESR1 gene polymorphisms PvuII (rs2234693T>C) and XbaI (rs9340799A>G) may not be directly correlated with cardiovascular disease risk. Genet Mol Res. 2015;14(4):13932–44.PubMed
25.
go back to reference Mariah RA, Baghdadi H, El-din Ahmed K, Mostafa N, Ayat MMA, Nansour T, et al. Frequency of estrogen receptor-1 (ESR-1) gene polymorphism (PvuII and XbaI) in patients with coronary artery disease. Am J Med Biol Res. 2016;4(1):5–9. Mariah RA, Baghdadi H, El-din Ahmed K, Mostafa N, Ayat MMA, Nansour T, et al. Frequency of estrogen receptor-1 (ESR-1) gene polymorphism (PvuII and XbaI) in patients with coronary artery disease. Am J Med Biol Res. 2016;4(1):5–9.
26.
go back to reference Huang Q, Wang TH, Lu WS, Mu PW, Yang YF, Liang WW, et al. Estrogen receptor alpha gene polymorphism associated with type 2 diabetes mellitus and the serum lipid concentration in Chinese women in Guangzhou. Chin Med J. 2006;119(21):1794–801.PubMed Huang Q, Wang TH, Lu WS, Mu PW, Yang YF, Liang WW, et al. Estrogen receptor alpha gene polymorphism associated with type 2 diabetes mellitus and the serum lipid concentration in Chinese women in Guangzhou. Chin Med J. 2006;119(21):1794–801.PubMed
27.
go back to reference Yilmaz A, Menevse S, Erkan AF, Ergun MA, Ilhan MN, Cengel A, et al. The relationship of the ESR1 gene polymorphisms with the presence of coronary artery disease determined by coronary angiography. Genet Test. 2007;11(4):367–71.PubMed Yilmaz A, Menevse S, Erkan AF, Ergun MA, Ilhan MN, Cengel A, et al. The relationship of the ESR1 gene polymorphisms with the presence of coronary artery disease determined by coronary angiography. Genet Test. 2007;11(4):367–71.PubMed
28.
go back to reference Munshi A, Sharma V, Kaul S, Al-Hazzani A, Alshatwi AA, Manohar VR, et al. Estrogen receptor α genetic variants and the risk of stroke in a south Indian population from Andhra Pradesh. Clin Chim Acta. 2010;411(21–22):1817–21.PubMed Munshi A, Sharma V, Kaul S, Al-Hazzani A, Alshatwi AA, Manohar VR, et al. Estrogen receptor α genetic variants and the risk of stroke in a south Indian population from Andhra Pradesh. Clin Chim Acta. 2010;411(21–22):1817–21.PubMed
29.
go back to reference Wei CD, Zheng HY, Wu W, Dai W, Tong YQ, Wang M, et al. Meta-analysis of the association of the rs2234693 and rs9340799 polymorphisms of estrogen receptor alpha gene with coronary heart disease risk in Chinese Han population. Int J Med Sci. 2013;10(4):457–66.PubMedPubMedCentral Wei CD, Zheng HY, Wu W, Dai W, Tong YQ, Wang M, et al. Meta-analysis of the association of the rs2234693 and rs9340799 polymorphisms of estrogen receptor alpha gene with coronary heart disease risk in Chinese Han population. Int J Med Sci. 2013;10(4):457–66.PubMedPubMedCentral
30.
go back to reference Goulart AC, Zee RYL, Rexrode KM. Estrogen receptor 1 gene polymorphisms and decreased risk of obesity in women. Metabolism. 2009;58(6):759–64.PubMedPubMedCentral Goulart AC, Zee RYL, Rexrode KM. Estrogen receptor 1 gene polymorphisms and decreased risk of obesity in women. Metabolism. 2009;58(6):759–64.PubMedPubMedCentral
31.
go back to reference Molvarec A, Ver A, Fekete A, Rosta K, Derzbach L, Derzsy Z, et al. Association between estrogen receptor α (ESR1) gene polymorphisms and severe preeclampsia. Hypertens Res. 2007;3:205–11. Molvarec A, Ver A, Fekete A, Rosta K, Derzbach L, Derzsy Z, et al. Association between estrogen receptor α (ESR1) gene polymorphisms and severe preeclampsia. Hypertens Res. 2007;3:205–11.
32.
go back to reference Dixit M, Mittal B. Frequencies of CETP gene TaqI B and D442G polymorphisms in north Indian population. Curr Sci. 2005;88(12):1973–6. Dixit M, Mittal B. Frequencies of CETP gene TaqI B and D442G polymorphisms in north Indian population. Curr Sci. 2005;88(12):1973–6.
33.
go back to reference Padmaja N, Kumar MR, Soya SS, Adithan C. Common variants of cholesteryl ester transfer protein gene and their association with lipid parameters in healthy volunteers of Tamilian population. Clin Chim Acta. 2007;375:140–6.PubMed Padmaja N, Kumar MR, Soya SS, Adithan C. Common variants of cholesteryl ester transfer protein gene and their association with lipid parameters in healthy volunteers of Tamilian population. Clin Chim Acta. 2007;375:140–6.PubMed
34.
go back to reference Tantray JA, Kumar YS, Jamil K. Pharmacogenomic studies of cholesteryl ester transfer protein (CETP) genotypes in suspected CAD patients. Int J Pharm Sci Res. 2013;4(10):3910–6. Tantray JA, Kumar YS, Jamil K. Pharmacogenomic studies of cholesteryl ester transfer protein (CETP) genotypes in suspected CAD patients. Int J Pharm Sci Res. 2013;4(10):3910–6.
35.
go back to reference Gundogdu F, Gurlertop Y, Pirim I, Sevimli S, Dogan H, Arslan S, et al. The relationship between genetic variations of the cholesteryl ester transfer protein gene and coronary artery disease in Turkish subjects. Eurasian J Med. 2009;41:32–8.PubMedPubMedCentral Gundogdu F, Gurlertop Y, Pirim I, Sevimli S, Dogan H, Arslan S, et al. The relationship between genetic variations of the cholesteryl ester transfer protein gene and coronary artery disease in Turkish subjects. Eurasian J Med. 2009;41:32–8.PubMedPubMedCentral
36.
go back to reference Kaestner S, Patsouras N, Spathas DH, Flordellis CS, Manolis AS. Lack of association between the cholesteryl ester transfer protein gene-TaqIB polymorphism and coronary restenosis following percutaneous transluminal coronary angioplasty and stenting: a pilot study. Angiology. 2010;61(4):338–43.PubMed Kaestner S, Patsouras N, Spathas DH, Flordellis CS, Manolis AS. Lack of association between the cholesteryl ester transfer protein gene-TaqIB polymorphism and coronary restenosis following percutaneous transluminal coronary angioplasty and stenting: a pilot study. Angiology. 2010;61(4):338–43.PubMed
37.
go back to reference Lu Y, Tayebi N, Li H, Saha N, Yang H, Heng CK. Association of CETP Taq1B and -629C > a polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population. Lipids Health Dis. 2013;12:85.PubMedPubMedCentral Lu Y, Tayebi N, Li H, Saha N, Yang H, Heng CK. Association of CETP Taq1B and -629C > a polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population. Lipids Health Dis. 2013;12:85.PubMedPubMedCentral
38.
go back to reference Bhanushali AA, Das BR. Genetic variants at the APOE, lipoprotein lipase (LpL), cholesteryl ester transfer protein (CETP), and endothelial nitric oxide (eNOS) genes and coronary artery disease (CAD): CETP Taq1 B2B2 associates with lower risk of CAD in Asian Indians. J Community Genet. 2010;1:55–62.PubMedPubMedCentral Bhanushali AA, Das BR. Genetic variants at the APOE, lipoprotein lipase (LpL), cholesteryl ester transfer protein (CETP), and endothelial nitric oxide (eNOS) genes and coronary artery disease (CAD): CETP Taq1 B2B2 associates with lower risk of CAD in Asian Indians. J Community Genet. 2010;1:55–62.PubMedPubMedCentral
39.
go back to reference Rahimi Z, Nourozi-Rad R, Rahimi Z, Parsian A. Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus. Human Genomics. 2012;6(20):1–5. Rahimi Z, Nourozi-Rad R, Rahimi Z, Parsian A. Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus. Human Genomics. 2012;6(20):1–5.
40.
go back to reference Kaman D, İlhan N, İlhan N, Akbulut M. TaqIB and severity of coronary artery disease in the Turkish population: a pilot study. Bosn J Basic Med Sci. 2015;15(1):9–13.PubMedPubMedCentral Kaman D, İlhan N, İlhan N, Akbulut M. TaqIB and severity of coronary artery disease in the Turkish population: a pilot study. Bosn J Basic Med Sci. 2015;15(1):9–13.PubMedPubMedCentral
41.
go back to reference Iwanicka J, Iwanicki T, Niemiec P, Balcerzyk A, Krauze J, Gorczyńska-Kosiorz S, et al. Relationship between CETP gene polymorphisms with coronary artery disease in polish population. Mol Biol Rep. 2018;45:1929–35.PubMedPubMedCentral Iwanicka J, Iwanicki T, Niemiec P, Balcerzyk A, Krauze J, Gorczyńska-Kosiorz S, et al. Relationship between CETP gene polymorphisms with coronary artery disease in polish population. Mol Biol Rep. 2018;45:1929–35.PubMedPubMedCentral
42.
go back to reference Ilhan N, Kucuksu M, Kaman D, Ilhan N, Ozbay Y. The 677 C/T MTHFR polymorphism is associated with essential hypertension, coronary artery disease, and higher homocysteine levels. Arch Med Res. 2008;39:125–30.PubMed Ilhan N, Kucuksu M, Kaman D, Ilhan N, Ozbay Y. The 677 C/T MTHFR polymorphism is associated with essential hypertension, coronary artery disease, and higher homocysteine levels. Arch Med Res. 2008;39:125–30.PubMed
43.
go back to reference Markan S, Sachdeva M, Sehrawat BS, Kumari S, Jain S, Khullar M. MTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension in Indians. Mol Cell Biochem. 2007;302:125–31.PubMed Markan S, Sachdeva M, Sehrawat BS, Kumari S, Jain S, Khullar M. MTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension in Indians. Mol Cell Biochem. 2007;302:125–31.PubMed
44.
go back to reference Lakshmi SVV, Naushad SM, Rupasree Y, Rao DS, Kutala VK. Interactions of 5′ UTR Thymidylate synthase polymorphism with 677 C/T methylene Tetrahydrofolate Reductase and 66 a/G Methyltetrahydrofolate Homocysteine methyl- Transferase Reductase polymorphisms determine susceptibility to coronary artery disease. J Atheroscler Thromb. 2011;18(1):56–64. Lakshmi SVV, Naushad SM, Rupasree Y, Rao DS, Kutala VK. Interactions of 5′ UTR Thymidylate synthase polymorphism with 677 C/T methylene Tetrahydrofolate Reductase and 66 a/G Methyltetrahydrofolate Homocysteine methyl- Transferase Reductase polymorphisms determine susceptibility to coronary artery disease. J Atheroscler Thromb. 2011;18(1):56–64.
46.
go back to reference Raina JK, Panjaliya RK, Sharma M, Bhardwaj R, Bakaya A, Kumar P. Methylenetetrahydrofolate reductase C677T gene polymorphism and predisposition to essential hypertension. Int J Genetics. 2016b;8(5):207–10. Raina JK, Panjaliya RK, Sharma M, Bhardwaj R, Bakaya A, Kumar P. Methylenetetrahydrofolate reductase C677T gene polymorphism and predisposition to essential hypertension. Int J Genetics. 2016b;8(5):207–10.
47.
go back to reference Dhar S, Chatterjee S, Ray S, Dutta A, Sengupta B, Chakrabarti S. Polymorphisms of methylenetetrahydrofolate reductase gene as the genetic predispositions of coronary artery diseases in eastern India. J Cardiovasc Dis Res. 2010;1(3):152–7.PubMedPubMedCentral Dhar S, Chatterjee S, Ray S, Dutta A, Sengupta B, Chakrabarti S. Polymorphisms of methylenetetrahydrofolate reductase gene as the genetic predispositions of coronary artery diseases in eastern India. J Cardiovasc Dis Res. 2010;1(3):152–7.PubMedPubMedCentral
48.
go back to reference Latheef K, Rajasekhar D, Vanajakshamma V, Aparna BR, Chaudhury A, Sarma PVGK. Association of MTHFR, IL-6 and ICAM-1 gene polymorphisms with coronary artery disease in south-Indian ethnic subset: a case-control study. J Cardiovasc Disease Res. 2018;9(3):115–22. Latheef K, Rajasekhar D, Vanajakshamma V, Aparna BR, Chaudhury A, Sarma PVGK. Association of MTHFR, IL-6 and ICAM-1 gene polymorphisms with coronary artery disease in south-Indian ethnic subset: a case-control study. J Cardiovasc Disease Res. 2018;9(3):115–22.
49.
go back to reference Butler S, Young A, Akam EC, Sinha N, Agrawal S, Mastana S. Association of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms with coronary artery disease (CAD) in a north Indian population. Cogent Med. 2018;5:1478477. Butler S, Young A, Akam EC, Sinha N, Agrawal S, Mastana S. Association of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms with coronary artery disease (CAD) in a north Indian population. Cogent Med. 2018;5:1478477.
50.
go back to reference Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, et al. Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, 1793G>a. Am J Med Genet. 2002;107(2):162–8.PubMed Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, et al. Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, 1793G>a. Am J Med Genet. 2002;107(2):162–8.PubMed
51.
go back to reference Trifonova EA, Spiridonova MG, Gabidulina TV, Urnov FD, Puzyrev VP, Stepanov VA. Analysis of the MTHFR gene linkage disequilibrium structure and association of polymorphic gene variants with coronary atherosclerosis. Russ J Genet. 2012;48(10):1035–47. Trifonova EA, Spiridonova MG, Gabidulina TV, Urnov FD, Puzyrev VP, Stepanov VA. Analysis of the MTHFR gene linkage disequilibrium structure and association of polymorphic gene variants with coronary atherosclerosis. Russ J Genet. 2012;48(10):1035–47.
52.
go back to reference Neto AIM, de Moura Júnior JR, Persuhn DC. Frequency of MTHFR G1793A polymorphism in individuals with early coronary artery disease: cross-sectional study. Sao Paulo Med J. 2013;131(5):296–300.PubMed Neto AIM, de Moura Júnior JR, Persuhn DC. Frequency of MTHFR G1793A polymorphism in individuals with early coronary artery disease: cross-sectional study. Sao Paulo Med J. 2013;131(5):296–300.PubMed
53.
go back to reference Eghlim FF, Ashavaid TF, Nair KG. Genetic determinants of hyperhomocysteinemia in atherosclerosis. Indian J Clin Biochem. 2006;21(2):4–11.PubMedPubMedCentral Eghlim FF, Ashavaid TF, Nair KG. Genetic determinants of hyperhomocysteinemia in atherosclerosis. Indian J Clin Biochem. 2006;21(2):4–11.PubMedPubMedCentral
54.
go back to reference Jemaa R, Achouri A, Kallel A, Ali SB, Mourali S, Feki M, et al. Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients. Clin Chem Lab Med. 2008;46(10):1364–8.PubMed Jemaa R, Achouri A, Kallel A, Ali SB, Mourali S, Feki M, et al. Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients. Clin Chem Lab Med. 2008;46(10):1364–8.PubMed
55.
go back to reference Iyer UM, Bhoite RM, Shah T. Risk factor analysis in coronary heart diseases and identifying at risk patients using a simple risk score test. Asian J Exp Biol Sci. 2011;2(1):40–6. Iyer UM, Bhoite RM, Shah T. Risk factor analysis in coronary heart diseases and identifying at risk patients using a simple risk score test. Asian J Exp Biol Sci. 2011;2(1):40–6.
56.
go back to reference Raina JK, Sharma M, Sethi S, Panjaliya RK, Bakaya A, Kumar P. A pilot study on recognition and prevalence of risk factors for cardiovascular diseases in north Indian populace of Jammu and Kashmir. J Hum Ecol. 2018;62(1–3):47–57. Raina JK, Sharma M, Sethi S, Panjaliya RK, Bakaya A, Kumar P. A pilot study on recognition and prevalence of risk factors for cardiovascular diseases in north Indian populace of Jammu and Kashmir. J Hum Ecol. 2018;62(1–3):47–57.
57.
go back to reference Kalra S, Narain S, Karki P, Ansari JA, Ranabhat K, Basnet N. Prevalence of risk factors for coronary artery disease in the community in eastern Nepal- a pilot study. JAPI. 2011;59:1–2. Kalra S, Narain S, Karki P, Ansari JA, Ranabhat K, Basnet N. Prevalence of risk factors for coronary artery disease in the community in eastern Nepal- a pilot study. JAPI. 2011;59:1–2.
59.
go back to reference Koju R, Humagain S, Khanal K. Association of cardiovascular risk factors and coronary artery lesion among coronary artery disease patients. Kathmandu Univ Med J. 2014;46(2):137–40. Koju R, Humagain S, Khanal K. Association of cardiovascular risk factors and coronary artery lesion among coronary artery disease patients. Kathmandu Univ Med J. 2014;46(2):137–40.
Metadata
Title
Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)
Authors
Jyotdeep Kour Raina
Minakashee Sharma
Rakesh Kumar Panjaliya
Vikas Dogra
Ashok Bakaya
Parvinder Kumar
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Cardiovascular Disorders / Issue 1/2020
Electronic ISSN: 1471-2261
DOI
https://doi.org/10.1186/s12872-020-01618-7

Other articles of this Issue 1/2020

BMC Cardiovascular Disorders 1/2020 Go to the issue