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Cancers (Basel). 2020 Feb 21;12(2):504. doi: 10.3390/cancers12020504.
3
Prescription of Chinese herbal products is associated with a decreased risk of uterine fibroids: A population-based cohort study.中药产品处方与子宫肌瘤风险降低相关:一项基于人群的队列研究。
Medicine (Baltimore). 2019 Dec;98(51):e18195. doi: 10.1097/MD.0000000000018195.
4
Uterine fibroids in menopause and perimenopause.绝经和围绝经期的子宫肌瘤。
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Alcohol Consumption and Risk of Uterine Fibroids.饮酒与子宫肌瘤风险的关系。
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The effects of exposure to air pollution on the development of uterine fibroids.暴露于空气污染对子宫肌瘤发展的影响。
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10
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台湾绝经前和绝经后妇女中 ESR1 rs2234693 单核苷酸多态性与子宫肌瘤的关联。

Association between ESR1 rs2234693 single nucleotide polymorphism and uterine fibroids in Taiwanese premenopausal and postmenopausal women.

机构信息

Department of Medical Imaging, Chung Shan Medical University Hospital, Taichung City, 40201, Taiwan.

School of Medicine, Chung Shan Medical University, Taichung City, 40201, Taiwan.

出版信息

J Health Popul Nutr. 2023 Mar 8;42(1):16. doi: 10.1186/s41043-023-00357-7.

DOI:10.1186/s41043-023-00357-7
PMID:36890612
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9993586/
Abstract

BACKGROUND

Uterine fibroids (UFs) are uterine smooth muscle neoplasms that affect women, especially during the reproductive stage. Both genetic and lifestyle factors affect the onset of the disease. We examined the association between the estrogen receptor 1 (ESR1) rs2234693 variant (whose genotypes are TT, TC, and CC) and UFs in Taiwanese premenopausal and postmenopausal women.

METHODS

We linked individual-level data of 3588 participants from the Taiwan Biobank to the National Health Insurance Research Database at the Health and Welfare Data Science Center. The association of the ESR1 rs2234693 variant and other variables with UFs was determined by multiple logistic regression, and the results were presented as odds ratios and 95% confidence intervals (CIs).

RESULTS

The 3588 participants comprised 622 cases and 2966 controls. In all the participants, the ESR1 rs2234693 TC and CC genotypes compared to the reference genotype (TT) were associated with a lower risk of UFs. However, the results were significant only for the CC genotype (OR; 95% CI = 0.70; 0.52-0.93). Noteworthy, the association of TC and CC with UFs was dose-dependent (p-trend = 0.012). Based on menopausal status, both TC and CC were significantly and dose-dependently associated with a lower risk of UFs in premenopausal women (OR; 95% CI = 0.76; 0.59-0.98 for TC and 0.64; 0.43-0.95 for CC: p-trend = 0.010).

CONCLUSION

The TC and CC genotypes of the ESR1 rs2234693 variant may reduce susceptibility to UFs, especially in premenopausal women.

摘要

背景

子宫肌瘤(UFs)是一种影响女性的子宫平滑肌肿瘤,尤其是在生育期。遗传和生活方式因素都影响疾病的发生。我们研究了雌激素受体 1(ESR1)rs2234693 变体(其基因型为 TT、TC 和 CC)与台湾绝经前和绝经后妇女 UF 之间的关系。

方法

我们将来自台湾生物库的 3588 名参与者的个体水平数据与健康与福利数据科学中心的国家健康保险研究数据库相关联。采用多因素逻辑回归分析 ESR1 rs2234693 变体与 UF 及其他变量的相关性,并以比值比(OR)及其 95%置信区间(CI)表示结果。

结果

3588 名参与者包括 622 例病例和 2966 例对照。在所有参与者中,ESR1 rs2234693 TC 和 CC 基因型与 TT 参考基因型相比,UF 风险降低。然而,仅 CC 基因型的结果具有统计学意义(OR;95%CI=0.70;0.52-0.93)。值得注意的是,TC 和 CC 与 UF 的关联呈剂量依赖性(p 趋势=0.012)。基于绝经状态,TC 和 CC 均与 UF 的低风险显著相关,且呈剂量依赖性(TC:OR;95%CI=0.76;0.59-0.98,p 趋势=0.010;CC:OR;95%CI=0.64;0.43-0.95)。

结论

ESR1 rs2234693 变体的 TC 和 CC 基因型可能降低 UF 的易感性,尤其是在绝经前女性中。