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Hormone Therapy, Lipoprotein Subclasses, and Coronary Calcification: The Healthy Women Study.

Authors :
Mackey, Rachel H.
Kuller, Lewis H.
Sutton-Tyrrell, Kim
Evans, Rhobert W.
Holubkov, Richard
Matthews, Karen A.
Source :
Archives of Internal Medicine; 3/14/2004, Vol. 165 Issue 5, p510-515, 6p
Publication Year :
2005

Abstract

Background The Women’s Health Initiative (WHI) clinical trial found no reduction in coronary heart disease events among hormone therapy (HT) users despite an improvement in lipid levels. We hypothesized that a lack of benefit of HT on atherosclerosis would be better explained by the lipoprotein subclasses than by standard lipid levels. To test this hypothesis, we evaluated differences in coronary calcification, lipids, and lipoprotein subclasses among HT users and nonusers in a longitudinal study of the menopause. Methods Lipoprotein subclasses determined by nuclear magnetic resonance spectroscopy and coronary artery calcification (CAC) determined by electron beam computed tomography were compared between HT users (49%) and nonusers among 243 women, approximately 8 years postmenopausal, from the Healthy Women Study. Results The distribution of CAC scores was not significantly different between HT users and nonusers. As expected, HT users had higher levels of large high-density lipoprotein (HDL) particles and large very low-density lipoprotein (VLDL) particles. However, despite lower low-density lipoprotein (LDL) cholesterol levels among HT users, there were no significant differences between HT users and nonusers in any LDL subclass measures, including particle size or concentration. Regardless of HT use, women with CAC had higher levels of large VLDL and small LDL particles, higher LDL particle concentration, and smaller mean LDL size compared with women with no detectable CAC. Conclusions Compared with nonusers, HT users had higher levels of VLDL particles (triglycerides) and did not have a better LDL subclass distribution, which may explain the failure of HT to be associated with a difference in CAC in our study or with a reduction in coronary heart disease risk in randomized clinical trials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00039926
Volume :
165
Issue :
5
Database :
Complementary Index
Journal :
Archives of Internal Medicine
Publication Type :
Academic Journal
Accession number :
16401531
Full Text :
https://doi.org/10.1001/archinte.165.5.510