Coronary heart disease: genetic aspects.

作者: H N Neufeld , U Goldbourt

DOI: 10.1161/01.CIR.67.5.943

关键词:

摘要: Morbidity and mortality differences between populations, ethnic groups individuals are not satisfactorily explained by the variation of risk factors. Differences in genetic susceptibility might be responsible for a part unexplained coronary heart disease (CHD) rates. Genetic factors also significant determining level individuals. Ample evidence links to levels serum cholesterol, blood pressure diabetes. Marked sex CHD indicate role heredity development disease. The male:female ratio varies widely different countries, as well groups. These variations difficult explain environmental behavioral males females alone. degree atherosclerosis varies, depending on anatomic location atherosclerosis. Inherited disorders metabolism variability patterns provide additional indications genetics. data accumulated Israeli Ischemic Heart Disease Study over 15 years reveal an coupled with remarkably larger Patterns incidence assessed national study histologic findings arteries infants from compatible hypothesis that early structural changes partly determine latter In conclusion, our studies review epidemiologic investigations genetics degree, time course severity atherosclerotic process occurrence symptomatic CHD. This important component is relevant preventive strategies offered tools reducing burden Research into determinants both or clinical manifestation individual response measures should encouraged.

参考文章(40)
JØRN NERUP, HLA studies in diabetes mellitus: a review. Advances in metabolic disorders. ,vol. 9, pp. 263- 277 ,(1978) , 10.1016/B978-0-12-027309-6.50018-5
W.P.U. JACKSON, Epidemiology of Diabetes in South Africa Advances in metabolic disorders. ,vol. 9, pp. 111- 146 ,(1978) , 10.1016/B978-0-12-027309-6.50012-4
William Insull, B. Christensen, I. Tamir, P. Kwiterovich, C. J. Glueck, D. C. Trost, R. Beaglehole, Plasma high-density lipoprotein cholesterol in children and young adults. The Lipid Research Clinics Program Prevalence Study. Circulation. ,vol. 62, ,(1980)
William Reichel, Rafael Garcia-Bunuel, Pathologic findings in progeria: myocardial fibrosis and lipofuscin pigment. American Journal of Clinical Pathology. ,vol. 53, pp. 243- 253 ,(1970) , 10.1093/AJCP/53.2.243
KELLY M. WEST, Diabetes in American Indians. Advances in metabolic disorders. ,vol. 9, pp. 29- 48 ,(1978) , 10.1016/B978-0-12-027309-6.50008-2
Jack H Medalie, Uri Goldbourt, Angina pectoris among 10,000 men The American Journal of Medicine. ,vol. 60, pp. 910- 921 ,(1976) , 10.1016/0002-9343(76)90921-9
Henry N. Neufeld, C.A. Wagenvoort, Patrick A. Ongley, Jesse E. Edwards, Hypoplasia of ascending aorta. An unusual form of supravalvular aortic stenosis with special reference to localized coronary arterial hypertension. American Journal of Cardiology. ,vol. 10, pp. 746- 751 ,(1962) , 10.1016/0002-9149(62)90251-5
Leonard C. Blieden, Robert J. Desnick, John B. Carter, William Krivit, James H. Moller, Harvey L. Sharp, Cardiac involvement in Sandhoff's disease: Inborn error of glycosphingolipid metabolism American Journal of Cardiology. ,vol. 34, pp. 83- 88 ,(1974) , 10.1016/0002-9149(74)90097-6
RICHARD J. HAVLIK, ROBERT J. GARRISON, SOLOMON H. KATZ, R. CURTIS ELLISON, MANNING FEINLEIB, NTINOS C. MYRIANTHOPOULOS, DETECTION OF GENETIC VARIANCE IN BLOOD PRESSURE OF SEVEN-YEAR-OLD TWINS American Journal of Epidemiology. ,vol. 109, pp. 512- 516 ,(1979) , 10.1093/OXFORDJOURNALS.AJE.A112708