High-density lipoprotein cholesterol and cardiovascular disease. Four prospective American studies.
David Gordon,Jeffrey L. Probstfield,Robert J. Garrison,James D. Neaton,William P. Castelli,J. D. Knoke,David R. Jacobs,Shrikant I. Bangdiwala,H. A. Tyroler +8 more
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TL;DR: A consistent inverse relation of high-density lipoprotein cholesterol levels and coronary heart disease event rates was apparent in BRHS as well as in the four American studies.
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Abstract: The British Regional Heart Study (BRHS) reported in 1986 that much of the inverse relation of high-density lipoprotein cholesterol (HDLC) and incidence of coronary heart disease was eliminated by covariance adjustment. Using the proportional hazards model and adjusting for age, blood pressure, smoking, body mass index, and low-density lipoprotein cholesterol, we analyzed this relation separately in the Framingham Heart Study (FHS), Lipid Research Clinics Prevalence Mortality Follow-up Study (LRCF) and Coronary Primary Prevention Trial (CPPT), and Multiple Risk Factor Intervention Trial (MRFIT). In CPPT and MRFIT (both randomized trials in middle-age high-risk men), only the control groups were analyzed. A 1-mg/dl (0.026 mM) increment in HDLC was associated with a significant coronary heart disease risk decrement of 2% in men (FHS, CPPT, and MRFIT) and 3% in women (FHS). In LRCF, where only fatal outcomes were documented, a 1-mg/dl increment in HDLC was associated with significant 3.7% (men) and 4.7% (women) decrements in cardiovascular disease mortality rates. The 95% confidence intervals for these decrements in coronary heart and cardiovascular disease risk in the four studies overlapped considerably, and all contained the range 1.9-2.9%. HDLC levels were essentially unrelated to non-cardiovascular disease mortality. When differences in analytic methodology were eliminated, a consistent inverse relation of HDLC levels and coronary heart disease event rates was apparent in BRHS as well as in the four American studies.
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Citations
African American-White Differences in Lipids, Lipoproteins, and Apolipoproteins, by Educational Attainment, among Middle-aged Adults: The Atherosclerosis Risk in Communities Study
Patricia Metcalf,A. Richey Sharrett,Aaron R. Folsom,Bruce Bartholow Duncan,Wolfgang Patsch,Richard G. Hutchinson,Moyses Szklo,Clarence E. Davis,Herman A. Tyroler +8 more
TL;DR: African American-white differences in lipids, lipoproteins, and apolipoproteins across levels of educational attainment that were not explained by conventional nondietary lifestyle variables are confirmed.
Effects of different forms of hazelnuts on blood lipids and α-tocopherol concentrations in mildly hypercholesterolemic individuals.
Siew Ling Tey,Rachel Brown,Alexandra Chisholm,Conor M. Delahunty,Andrew R. Gray,Sheila M. Williams +5 more
TL;DR: The ingestion of three different forms of hazelnuts equally improved the lipoprotein profile and α-tocopherol concentrations in mildly hypercholesterolemic individuals and can therefore be incorporated into the usual diet as a means of reducing cardiovascular disease risk.
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Epidemiological aspects of high density lipoprotein cholesterol
TL;DR: The results from the BIRNH study also suggest that the relation between HDL cholesterol and CVD mortality is curvilinear as discussed by the authors and that raising HDL cholesterol is useful in primary and secondary prevention of CHD.
68
Postprandial lipemia: an under-recognized atherogenic factor in patients with diabetes mellitus.
TL;DR: Several other classes of medications as well as non-pharmacological interventions can be used to treat lipid and lipoprotein abnormalities associated with insulin resistance and type 2 diabetes and these type of interventions may be more appropriate to ameliorate postprandial dyslipidemia.
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Apoa-ii maintains hdl levels in part by inhibition of hepatic lipase : studies in apoa-ii and hepatic lipase double knockout mice
Wei Weng,Neal A. Brandenburg,Shaobin Zhong,Joanna Halkias,Lin Wu,Xian-Cheng Jiang,Alan R. Tall,Jan L. Breslow +7 more
TL;DR: The results strongly suggest that apoA-II is a physiological inhibitor of hepatic lipase and that this is at least part of the mechanism whereby apo A-II maintains HDL cholesterol levels.
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TL;DR: Results are in accord with two previous trials with different pharmacologic agents and indicate that modification of lipoprotein levels with gemfibrozil reduces the incidence of coronary heart disease in men with dyslipidemia.
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