Tuesday, October 21, 2008

Family history of Cardio Vasular Disease

A family history of CHD puts women and men at increased risk for CHD, probably from a combination of genetic and environmental factors.1A history of MI in one first-degree relative doubles, and in two or more first-degree relatives triples MI risk. MI risk is strongest when MI in relatives occurs before age 55 years but is still present when MI occurs after age 55 years. The risk associated with a positive family history is independent of other known CHD risk factors. In the Nurses Health Study, women with a family history of parental MI at or below 60 years of age had 2.8 times the risk of nonfatal MI, 5 times the risk of fatal CHD, and 3.4 times the risk for angina pectoris compared with women without a history of parental MI. For women with a history of parental MI after age 60 years, there was no increase in risk for nonfatal CHD, but risk for fatal CHD was increased 2.6 times, and for angina pectoris it was increased 1.9 times compared with women with no family history of CHD. In contrast, a study of older women found no increase in CHD risk with a family history of heart attack.

Twin studies shed further light on the influence of family history on CHD risk. In a study of male and female Swedish monozygotic and dizygotic twins, among male twins the relative risk of CHD for monozygotic twins was 8.1 and the relative risk for dizygotic twins was 3.8 when one twin died of CHD before age 55 years. Among female twins, the relative risk of CHD for monozygotic twins was 15 and the relative risk for dizygotic twins was 2.6 when one twin died of CHD before age 55 years. In both monozygotic and dizygotic twins, as the age at which one twin died increased, the risk for CHD among the remaining twin decreased

REFERENCES
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* Al-Khalili F, Eriksson M, Landgren BM et al: Effect of conjugated estrogen on peripheral flow-mediated vasodilation in postmenopausal women. Am J Cardiol 82: 215–218, 1998
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* Anastos K, Charney P, Charon RA et al: Hypertension in women: What is really known? The Women's Caucus, Working Group on Women's Health of the Society of General Internal Medicine. Ann Intern Med 115: 287–293, 1991
* Austin MA, Breslow JL, Hennekens CH et al: Low-density lipoprotein subclass patterns and risk of myocardial infarction. JAMA 260: 1917–1921, 1988
* Barrett-Connor E, Brown W, Turner J et al: Heart disease risk factors and hormone use in postmenopausal women. JAMA 241: 2167–2169, 1979
* Barrett-Connor E, Khaw KT, Wingard DL: A ten-year prospective study of coronary heart disease mortality among Rancho Bernardo women. In Eaker ED, Packard B, Wenger NK et al (eds): Coronary Heart Disease in Women, pp 117–121. New York, Haymarket Doyma, 1987
* Barrett-Connor E, Wingard DL: Sex differential in ischemic heart disease mortality in diabetics: A prospective population-based study. Am J Epidemiol 118: 489–496, 1983
* Barrett-Connor EL: Obesity, atherosclerosis, and coronary artery disease. Ann Intern Med 103: 1010–1019, 1985
* Barrett-Connor EL: Postmenopausal estrogen and prevention bias. Ann Intern Med 115: 455–456, 1991
* Bates CJ, Mansoor MA, van der Pols J et al: Plasma total homocysteine in a representative sample of 972 British men and women aged 65 and over. Eur J Clin Nutr 51: 691–697, 1997
* Beard DM, Fuster V, Annergers JF: Reproductive history in women with coronary heart disease: A case-control study. Am J Epidemiol 120: 108–114, 1984