Genetics of cardiovascular disease: Importance of sex and ethnicity.

Sex differences in incidence and prevalence of and morbidity and mortality from cardiovascular disease are well documented. However, many studies examining the genetic basis for cardiovascular disease fail to consider sex as a variable in the study design, in part, because there is an inherent difficulty in studying the contribution of the sex chromosomes in women due to X chromosome inactivation. This paper will provide general background on the X and Y chromosomes (including gene content, the pseudoautosomal regions, and X chromosome inactivation), discuss how sex chromosomes have been ignored in Genome-wide Association Studies (GWAS) of cardiovascular diseases, and discuss genetics influencing development of cardiovascular risk factors and atherosclerosis with particular attention to carotid intima-medial thickness, and coronary arterial calcification based on sex-specific studies. In addition, a brief discussion of how ethnicity and hormonal status act as confounding variables in sex-based analysis will be considered along with methods for statistical analysis to account for sex in cardiovascular disease.

[1]  D. Mozaffarian,et al.  Heart disease and stroke statistics--2014 update: a report from the American Heart Association. , 2014, Circulation.

[2]  I-Min Lee,et al.  A randomized trial of low-dose aspirin in the primary prevention of cardiovascular disease in women , 2005 .

[3]  K. Taylor,et al.  Association of androgen receptor CAG repeat polymorphism and polycystic ovary syndrome. , 2008, The Journal of clinical endocrinology and metabolism.

[4]  Tanya M. Teslovich,et al.  Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids , 2010, Nature.

[5]  Jennifer F. Hughes,et al.  Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators , 2014, Nature.

[6]  Maria Gutierrez-Arcelus,et al.  Sex-biased genetic effects on gene regulation in humans , 2012, Genome research.

[7]  James M. Eales,et al.  Male-Specific Region of the Y Chromosome and Cardiovascular Risk: Phylogenetic Analysis and Gene Expression Studies , 2013, Arteriosclerosis, thrombosis, and vascular biology.

[8]  Barry J. Davis,et al.  Efficacy and safety of LDL-lowering therapy among men and women: meta-analysis of individual data from 174 000 participants in 27 randomised trials , 2015, The Lancet.

[9]  F. Collins,et al.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.

[10]  C. Langefeld,et al.  Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS). , 2006, American heart journal.

[11]  Tom R. Gaunt,et al.  Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. , 2012, American journal of human genetics.

[12]  S. Moon,et al.  Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome. , 2008, Fertility and sterility.

[13]  Tom H. Pringle,et al.  The human genome browser at UCSC. , 2002, Genome research.

[14]  S. Schwartz,et al.  Clonal architecture of normal and atherosclerotic aorta: implications for atherogenesis and vascular development. , 1998, The American journal of pathology.

[15]  B. Ning,et al.  Common genetic polymorphisms in the 5′-flanking Region of the SULT1A1 gene: haplotypes and their association with platelet enzymatic activity , 2005, Pharmacogenetics and genomics.

[16]  K. Taylor,et al.  Association of the diabetes gene calpain-10 with subclinical atherosclerosis: the Mexican-American Coronary Artery Disease Study. , 2005, Diabetes.

[17]  D. Levy,et al.  Vascular Stiffness and Genetic Variation at the Endothelial Nitric Oxide Synthase Locus: The Framingham Heart Study , 2007, Hypertension.

[18]  T. Buchanan,et al.  Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families. , 2008, Atherosclerosis.

[19]  S. Kardia,et al.  Sex steroid hormone polymorphisms, high-density lipoprotein cholesterol, and apolipoprotein A-1 from the Study of Women's Health Across the Nation (SWAN). , 2006, The American journal of medicine.

[20]  Z. Rahimi,et al.  AT2R -1332 G:A polymorphism and its interaction with AT1R 1166 A:C, ACE I/D and MMP-9 -1562 C:T polymorphisms: risk factors for susceptibility to preeclampsia. , 2014, Gene.

[21]  P. Donnelly,et al.  Inference of population structure using multilocus genotype data. , 2000, Genetics.

[22]  Y. Gong,et al.  β‐Adrenergic Receptor Gene Polymorphisms and β‐Blocker Treatment Outcomes in Hypertension , 2008, Clinical pharmacology and therapeutics.

[23]  M. Link,et al.  Gender-related differences in the clinical presentation and outcome of hypertrophic cardiomyopathy. , 2005, Journal of the American College of Cardiology.

[24]  S. Juo Genetics of carotid atherosclerosis. , 2009, Frontiers in bioscience.

[25]  Louis Richer,et al.  Functional Variation in the Androgen-Receptor Gene Is Associated With Visceral Adiposity and Blood Pressure in Male Adolescents , 2010, Hypertension.

[26]  B. Horne,et al.  Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids. , 2011, Journal of clinical & experimental cardiology.

[27]  J. Nathans,et al.  Cellular Resolution Maps of X Chromosome Inactivation: Implications for Neural Development, Function, and Disease , 2014, Neuron.

[28]  C. Albert,et al.  Epidemiology and genetics of sudden cardiac death. , 2012, Circulation.

[29]  D. Page,et al.  Functional coherence of the human Y chromosome. , 1997, Science.

[30]  K. Korach,et al.  Endothelial dysfunction in a man with disruptive mutation in oestrogen-receptor gene , 1997, The Lancet.

[31]  T. Graves,et al.  The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes , 2003, Nature.

[32]  N. Woods,et al.  Polymorphisms in the estrogen synthesis and metabolism pathways and symptoms during the menopausal transition: observations from the Seattle Midlife Women's Health Study , 2006, Menopause.

[33]  R. Weinshilboum,et al.  Human phenol sulfotransferases SULT1A2 and SULT1A1: genetic polymorphisms, allozyme properties, and human liver genotype-phenotype correlations. , 1999, Biochemical pharmacology.

[34]  C. Rajkumar Effectiveness of intermittent pneumatic compression in reduction of risk of deep vein thrombosis in patients who have had a stroke (CLOTS 3): a multicentre randomised controlled trial , 2013 .

[35]  Xu Li Sex chromosomes and sex chromosome abnormalities. , 2011, Clinics in laboratory medicine.

[36]  J. Gimble,et al.  Bisphenol A enhances adipogenic differentiation of human adipose stromal/stem cells. , 2014, Journal of molecular endocrinology.

[37]  Shane J. Neph,et al.  A comparative encyclopedia of DNA elements in the mouse genome , 2014, Nature.

[38]  K. Korach,et al.  Premature coronary artery disease associated with a disruptive mutation in the estrogen receptor gene in a man. , 1997, Circulation.

[39]  R. Collins,et al.  Newly identified loci that influence lipid concentrations and risk of coronary artery disease , 2008, Nature Genetics.

[40]  A. Folsom,et al.  Carotid wall thickness is predictive of incident clinical stroke: the Atherosclerosis Risk in Communities (ARIC) study. , 2000, American journal of epidemiology.

[41]  Tanya M. Teslovich,et al.  Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes , 2012, Nature Genetics.

[42]  Tomas W. Fitzgerald,et al.  Genetic basis of Y-linked hearing impairment. , 2013, American journal of human genetics.

[43]  D. Schaid,et al.  Human SULT1A1 gene: copy number differences and functional implications. , 2007, Human molecular genetics.

[44]  P. Wolf,et al.  Genetic and Environmental Contributions to Atherosclerosis Phenotypes in Men and Women: Heritability of Carotid Intima-Media Thickness in the Framingham Heart Study , 2003, Stroke.

[45]  C. Disteche,et al.  Genes that escape from X inactivation , 2011, Human Genetics.

[46]  H. Markus,et al.  The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis , 2006, Journal of Medical Genetics.

[47]  S. Teutsch,et al.  NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older. , 2003, Diabetes.

[48]  J. Marchini,et al.  Fast and accurate genotype imputation in genome-wide association studies through pre-phasing , 2012, Nature Genetics.

[49]  Vera Regitz-Zagrosek,et al.  Gender differences in the metabolic syndrome and their role for cardiovascular disease , 2006, Clinical Research in Cardiology.

[50]  J. Manson,et al.  Estrogen therapy and coronary-artery calcification. , 2007, The New England journal of medicine.

[51]  Paul M Ridker,et al.  Inflammation in atherosclerosis: from pathophysiology to practice. , 2009, Journal of the American College of Cardiology.

[52]  Mark D. Huffman,et al.  AHA Statistical Update Heart Disease and Stroke Statistics — 2012 Update A Report From the American Heart Association WRITING GROUP MEMBERS , 2010 .

[53]  Ross M. Fraser,et al.  Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits , 2013, PLoS genetics.

[54]  K. Kohara,et al.  Association Between Risk Factors for Atherosclerosis and Mechanical Forces in Carotid Artery , 2000, Stroke.

[55]  J. Murabito,et al.  Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study , 2007, BMC Medical Genetics.

[56]  L. Mosca Sex, statins, and statistics , 2015, The Lancet.

[57]  R. Sacco,et al.  Segment-Specific Genetic Effects on Carotid Intima-Media Thickness: The Northern Manhattan Study , 2008, Stroke.

[58]  R. Krauss,et al.  Relationship of Sex to Diabetes Risk in Statin Trials , 2013, Diabetes Care.

[59]  M. Fornage,et al.  Matrix Gla protein and osteopontin genetic associations with coronary artery calcification and bone density: the CARDIA study , 2005, Human Genetics.

[60]  Chong Shen,et al.  Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease , 2012, Nature Genetics.

[61]  C. Kooperberg,et al.  Estrogen Receptor Polymorphisms and the Vascular Effects of Hormone Therapy , 2011, Arteriosclerosis, thrombosis, and vascular biology.

[62]  A. Dominiczak,et al.  Y is there a risk to being male? , 2003, Trends in Endocrinology & Metabolism.

[63]  J. Graves Review: Sex chromosome evolution and the expression of sex-specific genes in the placenta. , 2010, Placenta.

[64]  Doris A Taylor,et al.  Proceedings from the Scientific Symposium: Sex Differences in Cardiovascular Disease and Implications for Therapies , 2010 .

[65]  J. Broderick,et al.  The X-Chromosome Has a Different Pattern of Gene Expression in Women Compared With Men With Ischemic Stroke , 2012, Stroke.

[66]  N. Samani,et al.  Coronary artery disease predisposing haplogroup I of the Y chromosome, aggression and sex steroids--genetic association analysis. , 2014, Atherosclerosis.

[67]  Christian Gieger,et al.  Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts , 2009, Nature Genetics.

[68]  S. Kardia,et al.  Sex steroid hormone pathway genes and health-related measures in women of 4 races/ethnicities: the Study of Women's Health Across the Nation (SWAN). , 2006, The American journal of medicine.

[69]  Fabian J Theis,et al.  Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers , 2011, PLoS genetics.

[70]  Stacey J Winham,et al.  Gene-environment interactions in genome-wide association studies: current approaches and new directions. , 2013, Journal of child psychology and psychiatry, and allied disciplines.

[71]  A. Dyer,et al.  Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat. , 2012, Journal of andrology.

[72]  S. Juo,et al.  Sex-differential genetic effect of phosphodiesterase 4D (PDE4D) on carotid atherosclerosis , 2010, BMC Medical Genetics.

[73]  M. P. van den Berg,et al.  Sex differences in cardiomyopathies , 2014, European journal of heart failure.

[74]  Joseph B Hiatt,et al.  Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster , 2011, Nature Genetics.

[75]  Patrick Royston,et al.  Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension , 2002, Arteriosclerosis, thrombosis, and vascular biology.

[76]  R. Sacco,et al.  Fine Mapping Study Reveals Novel Candidate Genes for Carotid Intima-Media Thickness in Dominican Republican Families , 2012, Circulation. Cardiovascular genetics.

[77]  J. Manson,et al.  Using Basic Science to Design a Clinical Trial: Baseline Characteristics of Women Enrolled in the Kronos Early Estrogen Prevention Study (KEEPS) , 2009, Journal of cardiovascular translational research.

[78]  K. Bailey,et al.  Alterations in Platelet Function and Cell-Derived Microvesicles in Recently Menopausal Women: Relationship to Metabolic Syndrome and Atherogenic Risk , 2011, Journal of cardiovascular translational research.

[79]  Christian Gieger,et al.  Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk , 2011, Nature.

[80]  D. Clayton,et al.  Testing for association on the X chromosome , 2008, Biostatistics.

[81]  T. Graves,et al.  Independent specialization of the human and mouse X chromosomes for the male germline , 2013, Nature Genetics.

[82]  K. Matthews,et al.  Symptoms, myocardial ischaemia and quality of life in women: results from the NHLBI-sponsored WISE Study. , 2003, European heart journal.

[83]  I. Zineh,et al.  Adrenergic gene polymorphisms and cardiovascular risk in the NHLBI-sponsored Women's Ischemia Syndrome Evaluation , 2008, Journal of Translational Medicine.

[84]  Carolyn J. Brown,et al.  A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome , 1991, Nature.

[85]  Takeshi Matsumura,et al.  Statins Activate Peroxisome Proliferator-Activated Receptor γ Through Extracellular Signal-Regulated Kinase 1/2 and p38 Mitogen-Activated Protein Kinase–Dependent Cyclooxygenase-2 Expression in Macrophages , 2007, Circulation research.

[86]  J. Stephens,et al.  The structure of common genetic variation in United States populations. , 2007, American journal of human genetics.

[87]  J. Mckinlay,et al.  The androgen receptor gene CAG repeat polymorphism does not predict increased risk of heart disease: longitudinal results from the Massachusetts Male Ageing Study , 2006, Clinical endocrinology.

[88]  R. Camerini-Otero,et al.  The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation , 2004, Nature Genetics.

[89]  Faha,et al.  Aha Guideline Effectiveness-based Guidelines for the Prevention of Cardiovascular Disease in Women—2011 Update a Guideline from the American Heart Association Executive Writing Committee Expert Panel Members Cvd Risk Assessment Table 1. Class Iii Interventions (not Useful/effective and May Be Harmfu , 2022 .

[90]  Q. Z. Li,et al.  Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family , 2004, Journal of Medical Genetics.

[91]  C. H. Liu,et al.  Heritability of Subclinical Atherosclerosis in Latino Families Ascertained Through a Hypertensive Parent , 2002, Arteriosclerosis, thrombosis, and vascular biology.

[92]  Jennifer G. Robinson,et al.  Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Disease Risk in Adults: Synopsis of the 2013 American College of Cardiology/American Heart Association Cholesterol Guideline , 2014, Annals of Internal Medicine.

[93]  Robin Lovell-Badge,et al.  A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif , 1990, Nature.

[94]  K. Taylor,et al.  A Genome-Wide Scan for Carotid Artery Intima-Media Thickness: The Mexican-American Coronary Artery Disease Family Study , 2005, Stroke.

[95]  Hynek Pikhart,et al.  HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials , 2015, The Lancet.

[96]  R. Detrano,et al.  Ethnic Differences in Coronary Calcification: The Multi-Ethnic Study of Atherosclerosis (MESA) , 2005, Circulation.

[97]  R. Wild,et al.  Characterizing Cardiovascular Risk in Women with Polycystic Ovary Syndrome: More than the Sum of Its Parts? , 2009, Seminars in reproductive medicine.

[98]  D. Thomas,et al.  Gene–environment-wide association studies: emerging approaches , 2010, Nature Reviews Genetics.

[99]  David L. Steffen,et al.  The DNA sequence of the human X chromosome , 2005, Nature.

[100]  B. Lejeune,et al.  Effects of beta1-adrenoceptor genetic polymorphisms on resting hemodynamics in patients undergoing diagnostic testing for ischemia. , 2001, The American journal of cardiology.

[101]  S. Crawford,et al.  Vasomotor symptom prevalence is associated with polymorphisms in sex steroid-metabolizing enzymes and receptors. , 2006, The American journal of medicine.

[102]  E M Wijsman,et al.  Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women. , 1996, American journal of human genetics.

[103]  Nilesh J Samani,et al.  Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome , 2012, The Lancet.

[104]  H. Sprecher,et al.  Estrogen-induced Production of a Peroxisome Proliferator-activated Receptor (PPAR) Ligand in a PPARγ-expressing Tissue* , 1998, The Journal of Biological Chemistry.

[105]  T. Manolio,et al.  eXclusion: toward integrating the X chromosome in genome-wide association analyses. , 2013, American journal of human genetics.

[106]  E. Bleecker,et al.  Common Estrogen Receptor Polymorphism Augments Effects of Hormone Replacement Therapy on E-Selectin but Not C-Reactive Protein , 2002, Circulation.

[107]  C. Disteche Dosage compensation of the sex chromosomes. , 2012, Annual review of genetics.

[108]  Michael Zitzmann,et al.  The CAG repeat polymorphism within the androgen receptor gene and maleness. , 2003, International journal of andrology.

[109]  Michael Lehrke,et al.  The Many Faces of PPARγ , 2005, Cell.

[110]  C. Clancy,et al.  Effects of Sex Hormones on Cardiac Repolarization , 2010, Journal of Cardiovascular Pharmacology.

[111]  E. Bleecker,et al.  Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease. , 2002, The New England journal of medicine.

[112]  D. Page,et al.  Four evolutionary strata on the human X chromosome. , 1999, Science.

[113]  J. Hanover,et al.  Chromosome Imbalance as a Driver of Sex Disparity in Disease , 2014, Journal of genomics.

[114]  David N. Rider,et al.  Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study. , 2013, Physiological genomics.

[115]  H. Willard,et al.  X-inactivation profile reveals extensive variability in X-linked gene expression in females , 2005, Nature.

[116]  J. Blangero,et al.  Effects of genotype‐by‐sex interaction on quantitative trait linkage analysis , 1997, Genetic epidemiology.

[117]  Stephen R. Williams,et al.  Genome-Wide Meta-Analysis of Homocysteine and Methionine Metabolism Identifies Five One Carbon Metabolism Loci and a Novel Association of ALDH1L1 with Ischemic Stroke , 2014, PLoS genetics.

[118]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[119]  Thomas Meitinger,et al.  Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution , 2010, Nature Genetics.

[120]  Kathleen F. Kerr,et al.  Genetics of coronary artery calcification among African Americans, a meta-analysis , 2013, BMC Medical Genetics.

[121]  M. Turner,et al.  Which Sry Locus Is the Hypertensive Y Chromosome Locus? , 2009, Hypertension.