虚弱状态变化与非肿瘤性消化系统疾病之间的关系:基于中国健康与退休纵向研究的队列研究

IF 4.3
Jingwei Che , Qiao Song , Chunyu Zhao , Yuan Yuan , Xiaohua Lyu
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引用次数: 0

摘要

虽然先前的研究将基线虚弱与特定的非肿瘤性消化系统疾病(NNDSD)联系起来,但虚弱状态转变的影响仍未得到充分研究。参与者来自中国健康与退休纵向研究(CHARLS),并使用由32个健康缺陷组成的虚弱指数(阈值为0.10和0.25)将其分类为健壮、体弱或体弱。最初随访时的虚弱状态作为基线,并使用第一次和第二次随访之间的变化来评估过渡。NNDSD的定义基于患者是否被医生诊断患有相关疾病的自我报告。使用Cox比例风险模型评估基线虚弱状态、虚弱转变和NNDSD之间的关系。最后,进行多重敏感性分析以验证结果的稳健性。结果6994名参与者(41%为女性)被纳入基线。被分类为体弱前(风险比[HR]: 1.55, 95%可信区间[CI]: 1.38-1.75)和体弱(风险比:2.39,95% CI: 1.99-2.89)的参与者表现出NNDSD发生率升高。最终的样本包括5299名参与者(41%是女性)。相对于身体健康的参与者,进展到体弱前(HR: 1.64, 95% CI: 1.30-2.10)和体弱(HR: 2.91, 95% CI: 1.72-4.90)与NNDSD风险相关。从前期体弱到体弱的进展(HR: 1.39 95% CI: 1.08-1.81)增加了NNDSD发病的风险。从虚弱前期恢复到强壮(HR: 0.73, 95% CI: 0.57-0.94)与NNDSD风险降低相关,敏感性结果证实了研究的稳健性。结论虚弱状态的改变与新发NNDSD风险呈正相关。虚弱的进展与风险增加有关,而逆转与风险降低有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between changes in frailty status and non-neoplastic digestive system diseases: A cohort study based on the China health and retirement longitudinal study

Background

While prior studies have linked baseline frailty to specific non-neoplastic digestive diseases (NNDSD), the impact of frailty status transitions remains understudied.

Method

Participants were sourced from the China Health and Retirement Longitudinal Study (CHARLS) and categorized as robust, pre-frail, or frail using a frailty index comprising 32 health deficits with thresholds of 0.10 and 0.25. The frailty status at initial follow-up served as the baseline, and transitions were assessed using changes between the first and second follow-ups. NNDSD was defined based on patients' self-reports of whether a physician diagnosed them with a relevant disease. Associations between baseline frailty status, frailty transitions and NNDSD were assessed using Cox proportional hazards modeling. Finally, multiple sensitivity analyses were performed to validate result robustness.

Results

A total of 6994 participants (41 % women) were included in the baseline. Participants classified as pre-frail (hazard ratio [HR]: 1.55, 95 % confidence interval [CI]: 1.38–1.75) and frail (HR: 2.39, 95 % CI: 1.99–2.89) exhibited elevated NNDSD incidence. The final sample comprised 5299 participants (41 % women). Progression to pre-frail (HR: 1.64, 95 % CI: 1.30–2.10) and frail (HR: 2.91, 95 % CI: 1.72–4.90) was associated with NNDSD risk relative to participants who remained robust. Progression from pre-frail to frail (HR: 1.39 95 % CI: 1.08–1.81) elevated the risk of NNDSD onset. Recovery from pre-frail to robust (HR: 0.73, 95 % CI: 0.57–0.94) was associated with reduced NNDSD risk, with sensitivity findings corroborating study robustness.

Conclusions

Changes in frailty status were positively associated with new-onset NNDSD risk. Frailty progression corresponded to elevated risk, whereas reversal was linked to risk reduction.
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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
CiteScore
6.70
自引率
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审稿时长
66 days
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