Abstract
Objective: The atheroprotective action of estrogen is mediated by estrogen receptors ( ESR) 1 and 2, expressed in atherosclerotic lesions. The effects of hormone replacement therapy (HRT) and ESR1 PvuII genotypes on atherosclerosis have not previously been studied prospectively in postmenopausal women. Methods: We investigated the effect of HRT on the progression of atherosclerosis in a 5-year follow-up study of 88 postmenopausal women aged 45–71 years at baseline allocated into three groups based on the use of HRT. The HRT-EVP group ( n=26) used sequential estradiol valerate (EV) plus progestin (P), the HRT-EV group EV alone ( n=32), and a control group ( n=30) was without HRT. The atherosclerosis severity score (AS) of the abdominal aorta and carotid arteries were determined by sonography and the ESR1 PvuII genotypes (P/P, P/p and p/p) by PCR. Results: HRT, time and ESR1 PvuII genotype had a statistically significant or borderline significant main effect on AS during 5-year follow-up ( P=0.004, P<0.001 and P=0.090, respectively), when analyzed by repeated measures analysis of variance. There was a significant genotype-by-treatment (HRT-EVP and control groups) interaction for AS ( P=0.034). In response to HRT-EVP, subjects with P/P, compared with those with P/p and p/p genotypes, had a less increase in AS (1.61±1.14 vs. 1.71±1.27 vs. 2.43±1.27). Baseline AS as covariate in similar model does not change the significant interaction effect between HRT-EVP and control groups ( P=0.036). But this effect was not found between HRT-EV and control groups. Conclusions: Our results suggest that the effect of HRT-EVP in postmenopausal women on progression of AS may be determined in part by the genotype of ESR1 PvuII.
Published Version
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