使用抗抑郁药与卵巢癌风险:来自丹麦和瑞典全国范围内超过 14,000 个病例的研究证据

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Guoqiao Zheng , Louise Baandrup , Jiangrong Wang , Rasmus Hertzum-Larsen , Charlotte Gerd Hannibal , Lina S. Mørch , Mette Tuxen Faber , Karin Sundström , Susanne K. Kjær
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引用次数: 0

摘要

鉴于有关使用抗抑郁药与卵巢癌风险之间联系的证据并不明确,我们在丹麦和瑞典人口中开展了两项全国性的巢式病例对照研究,从而对这一研究问题进行了调查。方法采用风险集抽样法,将14121名患有上皮性卵巢癌的女性(30-84岁)(丹麦:2000-2019年确诊8976人,瑞典:2010-2018年确诊5145人)与564840名女性对照者(丹麦359040人,瑞典205800人)进行随机年龄匹配。我们采用条件逻辑回归法估算出带有 95 % 置信区间 (CI) 的几率比 (OR),并根据固定效应假设合并了估算值。结果抗抑郁药的使用与卵巢癌风险的总体降低有关(OR = 0.92,95% 置信区间:0.88-0.96),这种降低在绝经后妇女和长期使用者中更为明显。这种效应在浆液性卵巢肿瘤中最为明显(OR = 0.90,95%CI:0.86-0.95),但在其他亚型中也有观察到,尽管没有统计学意义。在不同类型的抗抑郁药中,选择性血清素再摄取抑制剂尤其是西酞普兰可显著降低卵巢癌风险(OR = 0.89,95%CI:0.82-0.96)。此外,使用口服避孕药和激素替代疗法可单独改变使用抗抑郁药与卵巢癌风险之间的关系。考虑到卵巢癌的发病率和死亡率,以及抗抑郁药使用量的增加,这些发现可能对癌症预防具有重要意义,应从机理上进行更详细的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antidepressant use and ovarian cancer risk: Evidence from nationwide studies with >14,000 cases from Denmark and Sweden

Objective

Given that the evidence regarding the link between antidepressant use and ovarian cancer risk is equivocal, we investigated this research question by conducting two nationwide nested case-control studies among the Danish and Swedish populations.

Methods

Altogether, 14,121 women with epithelial ovarian cancer (30–84 years old) (Denmark: 8976 diagnosed 2000–2019, Sweden: 5145 diagnosed 2010–2018) were randomly age-matched with 564,840 female controls (359,040 from Denmark, and 205,800 from Sweden) using risk set sampling. We used conditional logistic regression to estimate odds ratios (OR) with 95 % confidence intervals (CI) and combined the estimates based on the fixed-effect assumption. We also investigated potential effect modification by well-established risk factors for ovarian cancer.

Results

Antidepressant use was associated with an overall reduced risk of ovarian cancer (OR = 0.92, 95%CI: 0.88–0.96), and that reduction was more pronounced in postmenopausal women and long-term users. The effect was most pronounced for serous ovarian tumors (OR = 0.90, 95%CI: 0.86–0.95) but was also observed in other subtypes, although not statistically significant. Among different types of antidepressants, selective serotonin reuptake inhibitors in general and citalopram in particular exhibited a noteworthy reduction in ovarian cancer risk (OR = 0.89, 95%CI: 0.82–0.96). Additionally, use of oral contraceptives and hormone replacement therapy individually modified the association between antidepressant use and ovarian cancer risk.

Conclusions

Use of an antidepressant was associated with a slight, but statistically significant, decrease in ovarian cancer risk. Given the morbidity and mortality associated with ovarian cancer, and increasing use of antidepressants, these findings may be of significance to cancer prevention and should be studied in more detail mechanistically.

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CiteScore
7.20
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