癌症诊断后动脉粥样硬化性心血管疾病的风险:来自三个前瞻性队列研究的结果

Qiang Liu, Qiaoli Wang, Kai Wang, Han Han, Molin Wang, Jing Wang, Mingyang Song, Edward Giovannucci
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摘要

研究背景:确定癌症诊断与后续ASCVD风险之间的关系,并研究癌症诊断后随时间推移的关系轨迹。方法前瞻性随访护士健康研究(NHS)(1984-2020)中的108,689名女性,NHSII(1991-2019)中的113,569名女性,卫生专业人员随访研究(HPFS)(1986-2016)中的45,328名男性,基线时无ASCVD和癌症。我们采用多变量调整时变Cox比例风险回归模型来评估个体癌症诊断后的ASCVD风险。在长达36年的随访中,49603例癌症病例中记录了4334例新发ASCVD事件。在调整共同的危险因素后,子宫颈癌(HR: 1.56;95%CI: 1.06-2.29)和霍奇金淋巴瘤(HR: 2.80;95%CI: 1.89-4.15)与ASCVD发病率增加相关,而前列腺癌与ASCVD发病率降低相关(HR: 0.91;95% ci: 0.85-0.97)。与无癌个体相比,乳腺癌幸存者在前7.5年的ASCVD风险较低,但之后逐渐增加(p非线性=0.01)。结直肠癌(P = 0.003)、肺癌(P = 0.002)和子宫内膜癌(P = 0.04)患者发生ASCVD的风险随着时间的推移而增加。口腔癌、咽喉癌、肉瘤、黑色素瘤、肾癌、甲状腺癌、白血病或卵巢癌与ASCVD风险无显著相关性。结论宫颈癌或霍奇金淋巴瘤与新发ASCVD的风险增加相关,独立于共同的危险因素,而与其他癌症没有发现风险增加。根据癌症类型,ASCVD风险轨迹在诊断后随时间变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of atherosclerotic cardiovascular disease after cancer diagnosis: findings from three prospective cohort studies
Background To determine the association between cancer diagnosis and subsequent risk of ASCVD, and to examine the trajectory of the association over time after cancer diagnosis. Methods We prospectively followed 108,689 women in the Nurses’ Health Study (NHS) (1984-2020), 113,569 women in the NHSII (1991-2019), and 45,328 men in the Health Professionals Follow-up Study (HPFS) (1986-2016) who were free of ASCVD and cancer at baseline. We conducted multivariable-adjusted time-varying Cox proportional hazards regression models to assess ASCVD risk following individual cancer diagnosis. Results During up to 36 years of follow-up, 4,334 new-onset ASCVD events among 49,603 incident cancer cases were documented. After adjusting for shared risk factors, cervical cancer (HR: 1.56; 95%CI: 1.06-2.29) and Hodgkin lymphoma (HR: 2.80; 95%CI: 1.89-4.15) was associated with increased risk of ASCVD incidence, while prostate cancer was associated with a lower ASCVD incidence (HR: 0.91; 95% CI: 0.85-0.97). Compared to cancer-free individuals, breast cancer survivors experienced lower ASCVD risk during the first 7.5 years but gradually increased afterwards (Pnon-linearity=0.01). The risk of ASCVD increased over time among patients with cancers of the colorectum (P = .003), lung (P = .002), and endometrium (P = .04). No significant association with ASCVD risk was observed for cancers of the oral cavity and pharynx, sarcoma, melanoma, kidney, thyroid, leukemia, or ovary. Conclusions Cervical cancer or Hodgkin lymphoma was associated with an increased risk of new-onset ASCVD, independent of shared risk factors, while no increased risk was found with other cancers. ASCVD risk trajectories varied over time after diagnosis according to cancer types.
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