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American Journal of Epidemiology Vol. 142, No. 10: 1011-1019
Copyright © 1995 by The Johns Hopkins University School of Hygiene and Public Health


other

Estrogen Replacement Therapy and Progression of Intimal-Medial Thickness in the Carotid Arteries of Postmenopausal Women

Mark A. Espeland1, William Applegate2, Curt D. Furberg1, David Lefkowitz3, Linda Rice4, Donald Hunninghake5 and the ACAPS Investigators

1Department of Public Health Sciences, Bowman Gray School of Medicine Winston-Salem, NC
2Department of Preventive Medicine, University of Tennessee Memphis, TN
3Department of Neurology, Bowman Gray School of Medicine Winston-Salem, NC
4Division of Neurosurgery, University of Kentucky Medical Center Lexington, KY
5Departments of Medicine and Pharmacology, University of Minnesota Health Center Minneapolis, MN

The effect of estrogen replacement therapy (ERT) on 3-year changes in carotid intimal-medial thickness (IMT) was explored using serial B-mode ultrasound measurements collected during 1989–1993 as part of the Asymptomatic Carotid Atherosclerotic Progression Study (ACAPS). Eligibility included increased IMT and elevated low density lipoprotein cholesterol. Of the 186 postmenopausal ACAPS women randomly assigned to receive either placebo or lovastatin, 34% reported use of ERT. Users tended to be younger than nonusers by an average of 3 years, to have more favorable high and low density lipoprotein cholesterol levels, and to be more likely to have had hysterectomies. Baseline blood pressure, body mass index, and cross-sectional IMT were similar among ERT users and nonusers. In the placebo group, IMT tended to progress among ERT nonusers but to regress among ERT users: Mean covariate-adjusted progression rates were 0.015 ± 0.007 mm/year versus –0.012 ± 0.012 mm/year, respectively (p = 0.05). This difference appeared to be independent of lipoprotein concentrations. Lovastatin was associated with an approximately 25% lowering of low density lipoprotein cholesterol among both ERT users and nonusers and had a marked impact on IMT progression (p = 0.004) in these women. ERT appeared to have little additional effect on IMT in women assigned to lovastatin. ERT may reduce or halt the progression of early atherosclerosis in women not receiving active lipid-lowering medication. Am J Epidemiol 1995;142:1011–19.

atherosclerosis; lipids; ultrasonography


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