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生殖因素与胆囊癌,以及常见遗传变异对这些关联的影响:印度的一项病例对照研究。

Reproductive factors and gall-bladder cancer, and the effect of common genetic variants on these associations: a case-control study in India.

机构信息

Section of Molecular Epidemiology and Population Genetics, Centre for Cancer Epidemiology, Tata Memorial Centre, Kharghar, Navi Mumbai, India.

Homi Bhabha National Institute (HBNI), Mumbai, India.

出版信息

Int J Epidemiol. 2022 Jun 13;51(3):789-798. doi: 10.1093/ije/dyab197.

Abstract

BACKGROUND

In India, as elsewhere, the incidence of gall-bladder cancer (GBC) is substantially higher in women than in men. Yet, the relevance of reproductive factors to GBC remains poorly understood.

METHODS

We used logistic regression adjusted for age, education and area to examine associations between reproductive factors and GBC risk, using 790 cases of histologically confirmed GBC and group-matched 1726 visitor controls. We tested the interaction of these associations by genetic variants known to increase the risk of GBC.

RESULTS

Parity was strongly positively associated with GBC risk: each additional pregnancy was associated with an ∼25% higher risk {odds ratio [OR] 1.26 [95% confidence interval (95% CI) 1.17-1.37]}. After controlling for parity, GBC risk was weakly positively associated with later age of menarche [postmenopausal women, OR 1.11 (95% CI 1.00-1.22) per year], earlier menopause [OR 1.03 (95% CI 1.00-1.06) per year] and shorter reproductive lifespan [OR 1.04 (95% CI 1.01-1.07) per year], but there was little evidence of an association with breastfeeding duration or years since last pregnancy. Risk alleles of single-nucleotide polymorphisms in the ABCB4 and ABCB1 genetic regions had a multiplicative effect on the association with parity, but did not interact with other reproductive factors.

CONCLUSIONS

We observed higher GBC risk with higher parity and shorter reproductive lifespan, suggesting an important role for reproductive and hormonal factors.

摘要

背景

在印度,与其他地方一样,胆囊癌(GBC)的发病率在女性中明显高于男性。然而,生殖因素与 GBC 的相关性仍知之甚少。

方法

我们使用逻辑回归调整了年龄、教育程度和地区因素,以检查生殖因素与 GBC 风险之间的关联,研究对象包括 790 例经组织学证实的 GBC 病例和 1726 例匹配的就诊对照者。我们通过已知增加 GBC 风险的遗传变异来检验这些关联的交互作用。

结果

生育次数与 GBC 风险呈强正相关:每增加一次妊娠,风险增加约 25%{优势比(OR)1.26(95%置信区间(95%CI)1.17-1.37)}。在控制生育次数后,GBC 风险与初潮年龄较晚[绝经后妇女,每年增加 1.11(95%CI 1.00-1.22)]、绝经年龄较早[每年增加 1.03(95%CI 1.00-1.06)]和生殖寿命较短[每年增加 1.04(95%CI 1.01-1.07)]呈弱正相关,但与母乳喂养时间或上次妊娠后年数几乎没有关联。ABCB4 和 ABCB1 基因区域的单核苷酸多态性风险等位基因对生育次数与 GBC 风险的关联具有相乘作用,但与其他生殖因素没有相互作用。

结论

我们观察到生育次数越高和生殖寿命越短与 GBC 风险越高相关,这表明生殖和激素因素起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/711b/9189936/3fc04ba8eaec/dyab197f1.jpg

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