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血清脂质、降脂药物与乳腺癌风险

Serum lipids, lipid-lowering drugs, and the risk of breast cancer.

作者信息

Eliassen A Heather, Colditz Graham A, Rosner Bernard, Willett Walter C, Hankinson Susan E

机构信息

Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Mass 02115, USA.

出版信息

Arch Intern Med. 2005 Oct 24;165(19):2264-71. doi: 10.1001/archinte.165.19.2264.

Abstract

BACKGROUND

Experimental evidence suggests that statins protect against breast carcinogenesis by interrupting cell cycle progression and promoting apoptosis. Evidence in humans is limited and inconsistent. The relation between serum cholesterol levels and breast cancer risk is itself unclear; because cholesterol is the precursor to sex steroid hormones, higher levels could plausibly increase risk.

METHODS

The associations of statins, general lipid-lowering drugs, and reported cholesterol levels with breast cancer risk were assessed in the Nurses' Health Study, with 6 to 12 years of follow-up. A total of 79,994 women aged 42 to 69 years and free of cancer were followed prospectively for up to 12 years. Current statin use, including duration, was assessed retrospectively in 2000 in 75,828 women. Self-reported serum cholesterol level was assessed prospectively between 1990 and 2000 in 71,921 women.

RESULTS

Overall, we documented 3177 incident cases of invasive breast cancer. Compared with nonusers, current lipid-lowering drug users experienced similar breast cancer risk (multivariate relative risk [RR], 0.99; 95% confidence interval [CI], 0.86-1.13). Current use of statins also was not significantly associated with breast cancer risk (RR, 0.91; 95% CI, 0.76-1.08). Associations by duration of current use were similarly null. Self-reported serum cholesterol levels were not associated with breast cancer risk in postmenopausal women with levels of 240 mg/dL or higher (> or = 6.22 mmol/L) compared with less than 180 mg/dL (< 4.66 mmol/L) (RR, 1.04; 95% CI, 0.91-1.17).

CONCLUSION

Overall, these data suggest that serum cholesterol levels and the use of lipid-lowering drugs in general and of statins in particular are not substantially associated with breast cancer risk.

摘要

背景

实验证据表明,他汀类药物可通过阻断细胞周期进程和促进细胞凋亡来预防乳腺癌发生。但人类研究证据有限且不一致。血清胆固醇水平与乳腺癌风险之间的关系本身尚不清楚;由于胆固醇是性类固醇激素的前体,较高水平的胆固醇可能会增加风险。

方法

在护士健康研究中评估他汀类药物、一般降脂药物以及报告的胆固醇水平与乳腺癌风险的关联,并进行6至12年的随访。共有79994名年龄在42至69岁且无癌症的女性接受了长达12年的前瞻性随访。2000年对75828名女性进行回顾性评估,了解她们目前使用他汀类药物的情况,包括使用时长。1990年至2000年期间对71921名女性进行前瞻性评估,了解她们自我报告的血清胆固醇水平。

结果

总体而言,我们记录了3177例浸润性乳腺癌新发病例。与未使用者相比,目前使用降脂药物的女性患乳腺癌的风险相似(多变量相对风险[RR]为0.99;95%置信区间[CI]为0.86 - 1.13)。目前使用他汀类药物也与乳腺癌风险无显著关联(RR为0.91;95%CI为0.76 - 1.08)。根据当前使用时长的关联同样无统计学意义。与血清胆固醇水平低于180mg/dL(<4.66mmol/L)的绝经后女性相比,自我报告的血清胆固醇水平在240mg/dL或更高(≥6.22mmol/L)的绝经后女性中与乳腺癌风险无关(RR为1.04;95%CI为0.91 - 1.17)。

结论

总体而言,这些数据表明血清胆固醇水平以及一般降脂药物尤其是他汀类药物的使用与乳腺癌风险无实质性关联。

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