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血清胰岛素和 C 肽浓度与乳腺癌:一项荟萃分析。

Serum insulin and C-peptide concentration and breast cancer: a meta-analysis.

机构信息

International Prevention Research Institute, 95 cours Lafayette, 69006, Lyon, France.

出版信息

Cancer Causes Control. 2013 May;24(5):873-83. doi: 10.1007/s10552-013-0164-6. Epub 2013 Feb 14.

Abstract

PURPOSE

Chronic hyperinsulinemia may play a role in breast cancer etiology. We performed a meta-analysis examining whether serum concentrations of insulin and C-peptide are associated with increased breast cancer risk.

METHODS

We restricted our analyses to prospective studies. After a systematic literature search, we computed summary relative risks (SRRs) and 95 % confidence intervals (95 % CIs) using random effect models applied to the relative risk associated with the highest versus lowest quantile of serum concentrations. We also graphically examined results in order to identify whether dose-response relationships were present.

RESULTS

Six articles including 1,890 cases were retrieved for serum insulin levels and five for serum C-peptide levels including 1,759 cases. SRR and 95 % CI were 1.08 (0.66-1.78) for insulin and 1.04 (0.77-1.41) for C-peptide. Heterogeneity of results between studies was high for insulin and inexistent for C-peptide. Restricting the analysis to women diagnosed with breast cancer before or after menopause did not alter results. In insulin studies, SRR computed from relative risks not adjusted for body mass index (and other risk factors) was 1.22 (0.91-1.63). The SRR fell to 1.02 (0.53-1.97) in studies that adjusted for body mass index and other factors. Similar drops occurred in C-peptide studies, from 1.11 (0.87-1.41) to 1.06 (0.70-1.61). No consistent dose-response relationship was apparent in either pre- or post-menopausal cancers.

CONCLUSIONS

Our meta-analysis of observational studies found no evidence of an association between serum insulin or C-peptide concentrations and breast cancer risk. Increased risk found by some studies may have been due to inadequate control for adiposity.

摘要

目的

慢性高胰岛素血症可能在乳腺癌发病机制中发挥作用。我们进行了一项荟萃分析,以检验血清胰岛素和 C 肽浓度是否与乳腺癌风险增加有关。

方法

我们将分析仅限于前瞻性研究。经过系统的文献检索,我们使用随机效应模型计算了与血清浓度最高与最低定量值相关的相对风险的汇总相对风险 (SRR) 和 95%置信区间 (95%CI)。我们还通过图形检查结果,以确定是否存在剂量反应关系。

结果

共检索到 6 篇关于血清胰岛素水平的文章,包括 1890 例病例,5 篇关于血清 C 肽水平的文章,包括 1759 例病例。胰岛素的 SRR 和 95%CI 为 1.08(0.66-1.78),C 肽为 1.04(0.77-1.41)。研究之间胰岛素结果的异质性很高,而 C 肽则不存在。将分析仅限于绝经前或绝经后诊断为乳腺癌的女性并未改变结果。在胰岛素研究中,未根据体重指数 (和其他危险因素) 调整的相对风险计算的 SRR 为 1.22(0.91-1.63)。在调整体重指数和其他因素的研究中,SRR 降至 1.02(0.53-1.97)。C 肽研究也出现类似的下降,从 1.11(0.87-1.41)降至 1.06(0.70-1.61)。在绝经前或绝经后癌症中均未出现一致的剂量反应关系。

结论

我们对观察性研究的荟萃分析没有发现血清胰岛素或 C 肽浓度与乳腺癌风险之间存在关联的证据。一些研究发现的风险增加可能是由于对肥胖的控制不足。

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