Gerontology Research Programme, Department of Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Singapore 138648, Singapore.
Aging (Albany NY). 2020 Nov 6;12(21):22139-22151. doi: 10.18632/aging.104076.
Human evidence for the role of continuous antigenic stimulation from persistent latent infections in frailty is limited. We conducted a nested case-control study (99 deceased and 43 survivors) of participants aged 55 and above in a longitudinal ageing cohort followed up from 2003 to 2017. Using blood samples and baseline data collected in 2003-2004, we examined the association of pathogenic load (PL) count of seropositivity to 10 microbes (viruses, bacteria and mycoplasma) with cumulated deficit-frailty index (CD-FI) and the physical frailty (PF) phenotype, and mortality. Controlling for age, sex, education, smoking and alcohol histories, high PL (7-9) versus low PL (3-6) was associated with an estimated increase of 0.035 points in the CD-FI (Cohen's D=0.035 / 0.086, or 0.41). High PL was associated with 8.5 times odds of being physically frail (p=0.001), 2.8 times odds of being weak (p=0.010), 3.4 times odds of being slow (p=0.024), and mortality hazard ratio of 1.53 (p=0.046). There were no significant associations for specific pathogens, except marginal associations for Epstein-Barr virus and Chikungunya. Conclusion: A high pathogenic load of latent infections was associated with increased risks of frailty and mortality.
人体证据表明,持续潜伏感染的持续抗原刺激在衰弱中起作用,但证据有限。我们对 2003 年至 2017 年期间随访的纵向老龄化队列中年龄在 55 岁及以上的参与者进行了一项嵌套病例对照研究(99 例死亡和 43 例存活)。使用 2003-2004 年收集的血液样本和基线数据,我们检查了血清阳性的致病负荷(PL)计数与累积缺陷-衰弱指数(CD-FI)和身体衰弱(PF)表型以及死亡率之间的关联。在控制年龄、性别、教育程度、吸烟和饮酒史后,高 PL(7-9)与低 PL(3-6)相比,CD-FI 估计增加 0.035 分(Cohen's D=0.035 / 0.086,或 0.41)。高 PL 与身体虚弱的可能性增加 8.5 倍相关(p=0.001),与虚弱的可能性增加 2.8 倍相关(p=0.010),与缓慢的可能性增加 3.4 倍相关(p=0.024),与死亡率的危险比为 1.53(p=0.046)。除了 Epstein-Barr 病毒和基孔肯雅热病毒存在边缘关联外,特定病原体之间没有显著关联。结论:潜伏感染的高致病负荷与衰弱和死亡风险的增加相关。