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Arteriosclerosis, Thrombosis, and Vascular Biology. 1996;16:918-925

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(Arteriosclerosis, Thrombosis, and Vascular Biology. 1996;16:918-925.)
© 1996 American Heart Association, Inc.


Articles

Apolipoprotein E Polymorphism in American Indians and Its Relation to Plasma Lipoproteins and Diabetes

The Strong Heart Study

Shinkuro Kataoka; David C. Robbins; Linda D. Cowan; Oscar Go; Jeunliang L. Yeh; Richard B. Devereux; Richard R. Fabsitz; Elisa T. Lee; Thomas K. Welty; Barbara V. Howard; for the Strong Heart Study Investigators

the Second Department of Internal Medicine, Hiroshima University School of Medicine, Hiroshima, Japan (S.K.); the Department of Biostatistics and Epidemiology, University of Oklahoma, Oklahoma City (L.D.C., E.T.L.); the Center for Epidemiologic Research, University of Oklahoma Health Sciences Center, Oklahoma City (J.L.Y., O.G.); Medlantic Research Institute, Washington, DC (D.C.R., B.V.H.); Cornell Medical Center, New York, NY (R.B.D.); the National Heart, Lung, and Blood Institute, Bethesda, Md (R.R.F.); and the Aberdeen Area Indian Health Service, Rapid City, SD (T.K.W.).

Correspondence to Dr Barbara V. Howard, Medlantic Research Institute, 108 Irving St, NW, Washington, DC 20010-2933.

Apo E is an important genetic factor in the development of cardiovascular disease, which is the leading cause of death among American Indians. We investigated the occurrence of the apo E alleles and the relation between apo E polymorphism and blood lipoproteins and apoproteins in members of 13 American Indian communities in three geographic areas. The frequencies of the {epsilon}2 alleles in American Indians are significantly lower than those in white Americans, with the lowest frequencies of {epsilon}2 in American Indians who reside in Arizona. Levels of LDL cholesterol and apo B were highest in those with {epsilon}4 and lowest in those with {epsilon}2. Concentrations of HDL cholesterol and apo A-I, however, tended to be lowest in {epsilon}4 and highest in {epsilon}2. Concentrations of total and VLDL triglycerides were lowest in the {epsilon}3 group and higher in groups {epsilon}2 and {epsilon}4. Differences in concentrations of LDL cholesterol, HDL cholesterol, apo B, and apo A-I with apo E polymorphism were greater in women than in men, and differences in total and VLDL triglyceride concentrations by apo E phenotype were greater in men. Relations of total and VLDL triglycerides with apo E phenotype were stronger in women after menopause. In addition, differences in nearly all lipid and apoprotein concentrations between postmenopausal women and premenopausal women were greater if they had {epsilon}2. Relations between apo E phenotype and lipoproteins were seen in individuals with diabetes mellitus as well as in nondiabetics. Apo E was significantly related to glucose control in diabetic women; those with {epsilon}3 had higher glucose and hemoglobin A1C concentrations. Our findings show that (1) American Indians have low frequencies of apo {epsilon}2; (2) apo E phenotype can influence levels of VLDL, LDL, HDL, apo B, and apo A-I; (3) the associations of apo E polymorphisms with lipid parameters differ between men and women; and (4) the associations in women of apo E polymorphisms with lipid parameters are modified by menopausal status.


Key Words: lipoprotein • apolipoprotein E • diabetes • cholesterol • American Indians




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