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重症 COVID-19 的遗传易感性通过免疫途径增加了 HER2 阳性乳腺癌的风险:一项孟德尔随机化研究。

Genetic liability to critically ill COVID-19 increased risk of HER2-positive breast cancer through the immune pathway: A Mendelian randomization study.

作者信息

Chen Jianfeng, Xin Bingyan, Tan Wenwen, Chen Zhilian, Zhang Lan, Zhu Xiaochuan

机构信息

Department of Toxicology II, Hunan Prevention and Treatment Institute for Occupational Diseases (Affiliated Prevention and Treatment Institute for Occupational Diseases of University of South China), Changsha, China.

Department of Occupational Lung Diseases II, Hunan Institute of Occupational Disease Prevention, Changsha, China.

出版信息

Medicine (Baltimore). 2025 May 9;104(19):e42372. doi: 10.1097/MD.0000000000042372.

Abstract

The clinical management of patients with both coronavirus disease 2019 (COVID-19) and breast cancer remains a complex and unresolved issue that despite extensive discussion has not reached a consensus. In contemporary literature, the association between COVID-19 and HER2-positive breast cancer has received minimal attention. Genetic instruments for severe acute respiratory syndrome coronavirus 2 infection (N = 2,597,856), hospitalized COVID-19 (N = 2,095,324), and critically ill COVID-19 (N = 1,086,211) were obtained from the COVID-19 Host Genetics Initiative genome-wide association study (GWAS) meta-analysis. A total of 103,530 HER2-positive breast cancer cases from GWAS were enrolled in our study. The summary GWAS statistics of 731 immune cells (N = 3757) were obtained from the MRCEU open database. Causal associations were evaluated by applying Mendelian randomization (MR) including inverse variance weighting, MR-Egger regression, and weighted-median analysis. Sensitivity analyses were employed, including Cochran Q test, MR-Egger intercept test, MR Pleiotropy Residual Sum and Outlier, and leave-one-out analysis, to examine the robustness of these findings. Genetic liability to critically ill COVID-19 was significantly causally associated with the increased risk of HER2-positive breast cancer (odds ratios = 1.086, 95% confidence intervals = 1.015-1.162, P = .016). No causal associations between severe acute respiratory syndrome coronavirus 2 infection or hospitalized COVID-19 and HER2-positive breast cancer were observed. Additionally, genetic liabilities to critically ill COVID-19 were significantly positively associated with 9 immune cells. IgD- CD27- AC and CD27 on IgD+ CD38- unsw mem (memory B cells) were identified as potential mediators of the causal relationship between critically ill COVID-19 and HER2-positive breast cancer. Genetic liability to critically ill COVID-19 is associated with an increased risk of HER2-positive breast cancer possibly through the immune pathway. Future studies are essential to elucidate the mechanisms underlying this causal relationship, aiming to develop therapeutic strategies to mitigate the immune cell-mediated impact on HER2-positive breast cancer risk.

摘要

2019冠状病毒病(COVID-19)合并乳腺癌患者的临床管理仍然是一个复杂且未解决的问题,尽管进行了广泛讨论,但尚未达成共识。在当代文献中,COVID-19与HER2阳性乳腺癌之间的关联很少受到关注。严重急性呼吸综合征冠状病毒2感染(N = 2,597,856)、住院COVID-19(N = 2,095,324)和危重症COVID-19(N = 1,086,211)的遗传工具来自COVID-19宿主遗传学倡议全基因组关联研究(GWAS)的荟萃分析。我们的研究纳入了来自GWAS的103,530例HER2阳性乳腺癌病例。731种免疫细胞(N = 3757)的汇总GWAS统计数据来自MRCEU开放数据库。通过应用孟德尔随机化(MR)评估因果关联,包括逆方差加权、MR-Egger回归和加权中位数分析。采用敏感性分析,包括Cochran Q检验、MR-Egger截距检验、MR多效性残差和离群值分析以及留一法分析,以检验这些发现的稳健性。危重症COVID-19的遗传易感性与HER2阳性乳腺癌风险增加显著因果相关(比值比 = 1.086,95%置信区间 = 1.015 - 1.162,P = 0.016)。未观察到严重急性呼吸综合征冠状病毒2感染或住院COVID-19与HER2阳性乳腺癌之间存在因果关联。此外,危重症COVID-19的遗传易感性与9种免疫细胞显著正相关。IgD-CD27-AC和IgD+CD38-非转换记忆B细胞上的CD27被确定为危重症COVID-19与HER2阳性乳腺癌因果关系的潜在介导因素。危重症COVID-19的遗传易感性可能通过免疫途径与HER2阳性乳腺癌风险增加相关。未来的研究对于阐明这种因果关系的潜在机制至关重要,旨在制定治疗策略以减轻免疫细胞介导的对HER2阳性乳腺癌风险的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a7d/12074039/a30a6837e6b4/medi-104-e42372-g001.jpg

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