Hu Peifeng, Greendale Gail A, Palla Shana L, Reboussin Beth A, Herrington David M, Barrett-Connor Elizabeth, Reuben David B
Multicampus Program in Geriatric Medicine and Gerontology, UCLA School of Medicine, 10945 Le Conte Avenue, Suite 2339, Los Angeles, CA 90095-1687, USA.
Atherosclerosis. 2006 Apr;185(2):347-52. doi: 10.1016/j.atherosclerosis.2005.06.011. Epub 2005 Jul 14.
The objective of this study was to determine whether oral conjugated equine estrogen (CEE) alone or with one of the three progestin regimens causes changes in biomarkers predictive of adverse cardiovascular events: C-reactive protein (CRP), interleukin-6 (IL-6), intercellular adhesion molecule (ICAM) and matrix metalloproteinase-9 (MMP-9).
The analysis included 271 postmenopausal women from the postmenopausal estrogen progestin intervention (PEPI) trial. Plasma levels of biomarkers were measured on frozen samples obtained at baseline, 1- and 3-year follow-up visits. Multivariable linear mixed effects models were used to estimate changes in CRP, IL-6, ICAM and MMP-9 levels from baseline to follow-up visits by treatment groups. Women assigned to CEE only or CEE plus a progestin had 121 and 150% 1-year increase in CRP levels, respectively. In contrast, these treatments caused no significant change in IL-6 levels. Women assigned to CEE with or without a progestin had a 6-8% decline in ICAM and a 26-33% decline in MMP-9.
The linkage between CEE alone or with a progestin and increased cardiovascular events may be associated with a rise in CRP level, but not through the mechanisms of IL-6-mediated inflammation, endothelial dysfunction or increased MMP activity.
本研究的目的是确定单独口服共轭马雌激素(CEE)或与三种孕激素方案之一联合使用是否会导致预测不良心血管事件的生物标志物发生变化:C反应蛋白(CRP)、白细胞介素-6(IL-6)、细胞间黏附分子(ICAM)和基质金属蛋白酶-9(MMP-9)。
分析纳入了绝经后雌激素孕激素干预(PEPI)试验中的271名绝经后女性。在基线、1年和3年随访时采集的冷冻样本上测量生物标志物的血浆水平。使用多变量线性混合效应模型来估计各治疗组从基线到随访时CRP、IL-6、ICAM和MMP-9水平的变化。单独服用CEE或CEE加孕激素的女性CRP水平在1年时分别升高了121%和150%。相比之下,这些治疗对IL-6水平没有显著影响。服用CEE无论是否加用孕激素的女性ICAM水平下降了6 - 8%,MMP-9水平下降了26 - 33%。
单独使用CEE或与孕激素联合使用与心血管事件增加之间的联系可能与CRP水平升高有关,但不是通过IL-6介导的炎症、内皮功能障碍或MMP活性增加的机制。