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高敏C反应蛋白与全因死亡率之间关联的性别和年龄差异:一项为期12年的前瞻性队列研究。

Sex and age differences in the association between high sensitivity C-reactive protein and all-cause mortality: A 12-year prospective cohort study.

作者信息

Bafei Solim Essomandan Clémence, Yang Song, Chen Changying, Gu Xincheng, Mu Jialing, Liu Fangyuan, Sun Junxiang, Zhuang Qian, Wei Pengfei, Zhao Xianghai, Chen Yanchun, Yin Yunjie, Xie Hankun, Shen Chong

机构信息

Department of Epidemiology, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China.

Department of Cardiology, Affiliated Yixing People's Hospital of Jiangsu University, People's Hospital of Yixing City, Yixing 214200, China.

出版信息

Mech Ageing Dev. 2023 Apr;211:111804. doi: 10.1016/j.mad.2023.111804. Epub 2023 Mar 24.

Abstract

To explore the influence of age on hs-CRP among men and women and investigate the impact of hs-CRP on all-cause death, this prospective cohort enrolled 4128 community adults from 2009 to 2022 for all-cause death. Age and sex-specific hs-CRP percentile curves were generated using the GAMLSS method. Cox-proportional hazard regression analysis was applied to estimate the hazard ratios (HRs) and 95 % confidence intervals (CIs). During the follow-up with a median of 12.59 years, 701 cases of all-cause death were identified. Among men, the smoothed centile curves of hs-CRP gradually increased from age 35 onwards whereas, the smoothed centile curves of hs-CRP continuously increased as age increased among women. Compared with the reference group, the adjusted HR of the association between elevated hs-CRP and all-cause death was 1.33 (95 % CI: 1.11-1.61). The adjusted HRs of the associations between elevated hs-CRP and all-cause death were higher in women [1.40 (95 % CI: 1.07-1.83)] than men [1.28 (95 % CI: 0.99-1.65) and in subjects aged < 65 years [1.77 (95 % CI: 1.19-2.62)] than in subjects aged ≥ 65 years [1.27 (95 % CI: 1.03-1.57)]. Our findings highlight the need of investigating sex and age differences in biological pathways that link inflammation and mortality.

摘要

为探讨年龄对男性和女性超敏C反应蛋白(hs-CRP)的影响,并研究hs-CRP对全因死亡的影响,本前瞻性队列研究在2009年至2022年期间纳入了4128名社区成年人以研究全因死亡情况。使用广义相加模型稳健估计法(GAMLSS)生成了按年龄和性别划分的hs-CRP百分位数曲线。采用Cox比例风险回归分析来估计风险比(HRs)和95%置信区间(CIs)。在中位随访时间为12.59年期间,共确定了701例全因死亡病例。在男性中,hs-CRP的平滑百分位数曲线从35岁起逐渐上升,而在女性中,hs-CRP的平滑百分位数曲线随年龄增长持续上升。与参照组相比,hs-CRP升高与全因死亡之间关联的校正后HR为1.33(95%CI:1.11 - 1.61)。hs-CRP升高与全因死亡之间关联的校正后HR在女性中[1.40(95%CI:1.07 - 1.83)]高于男性[1.28(95%CI:0.99 - 1.65)],且在年龄<65岁的受试者中[1.77(95%CI:1.19 - 2.62)]高于年龄≥65岁的受试者[1.27(95%CI:1.03 - 1.57)]。我们的研究结果强调了调查连接炎症和死亡率的生物学途径中性别和年龄差异的必要性。

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