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采用简易精神状态检查评估认知功能与全因死亡率风险:一项基于社区的前瞻性队列研究。

Cognitive function assessed by Mini-mental state examination and risk of all-cause mortality: a community-based prospective cohort study.

机构信息

Medical School of Chinese PLA, 28 Fuxing Road, Haidian District, Beijing, 100853, China.

Department of Geriatrics, the Second Medical Centre, Chinese PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing, 100853, China.

出版信息

BMC Geriatr. 2021 Oct 2;21(1):524. doi: 10.1186/s12877-021-02471-9.

Abstract

BACKGROUND

The Mini-Mental State Examination (MMSE) is the most widely used instrument to test cognitive functioning. The present study prospectively investigated the association between MMSE scores, MMSE domains, and all-cause mortality.

METHODS

A total of 2134 participants aged 60 years or over, selected from one urban community-dwelling population in China, were enrolled in the study. The cognitive test was performed by use of the MMSE at baseline, and covariates were recorded simultaneously. Cox regression models were used for examining the cognitive function, expressed by different MMSE transformations, and all-cause mortality. After followed up for a median of 10.8 years (ranging from 1.0 to 11.3 years), loss to follow-up was 13.1% and 1854 individuals were finally included in the analyses.

RESULTS

The subjects had the mean (SD) age of 71.01 (7.00) years, and 754 (40.67%) of them were women. Per point increase on MMSE scores was associated a 4% decreased risk of all-cause mortality [hazard ratio (HR): 0.96; 95%confidence interval (CI): 0.93-0.98]; compared to MMSE scores of ≥24, MMSE scores of < 24 was associated with a 43% increased risk of all-cause mortality (HR: 1.43; 95% CI: 1.05-1.95); compared to MMSE scores of 30, MMSE scores of 27-29 (HR: 1.27; 95% CI: 0.89-1.82), 24-26 (HR: 1.30; 95% CI: 0.86-1.99), and < 24 (HR: 1.79; 95% CI: 1.15-2.77) had a graded increase in risk of all-cause mortality (p for trend =0.003). Of MMSE domains, orientation to time (HR: 2.00; 95% CI: 1.29-3.11), attention and calculation (HR: 1.49; 95% CI: 1.16-1.92), recall (HR: 2.59; 95% CI: 1.22-5.47), and language (HR: 1.68; 95% CI: 1.25-2.26) were significantly associated with all-cause mortality in the unadjusted model; for one increase in the number of impaired MMSE domains, the unadjusted HR (95% CI) of mortality is 1.51 (1.38, 1.65), and the HR (95% CI) of mortality is 1.12 (1.01, 1.25) with full adjustment; compared to 0 and 1 impaired MMSE domains, the HRs of all-cause mortality associated with 2, 3, 4, and ≥ 5 impaired MMSE domains were 1.14 (95% CI: 0.84-1.54), 1.50 (95% CI: 0.98-2.28), 2.14 (95% CI: 1.12-4.09) and 2.29 (95% CI: 1.24-5.04), respectively, and a dose-dependent relationship was significant (p for trend =0.003).

CONCLUSION

Cognitive impairment is associated with the increased risk of all-cause mortality in the Chinese elderly. Similarly, reduced MMSE scores, as well as impaired MMSE domains, are also associated with the increasing risk of all-cause mortality.

摘要

背景

简易精神状态检查(MMSE)是最广泛用于测试认知功能的工具。本研究前瞻性地调查了 MMSE 评分、MMSE 域与全因死亡率之间的关系。

方法

从中国一个城市社区居住人群中选择了 2134 名年龄在 60 岁或以上的参与者,在基线时使用 MMSE 进行认知测试,并同时记录协变量。使用 Cox 回归模型检查不同 MMSE 转换的认知功能与全因死亡率之间的关系。中位随访时间为 10.8 年(范围为 1.0 至 11.3 年),失访率为 13.1%,最终有 1854 人纳入分析。

结果

受试者的平均(SD)年龄为 71.01(7.00)岁,其中 754 人(40.67%)为女性。MMSE 评分每增加 1 分,全因死亡率的风险降低 4%[风险比(HR):0.96;95%置信区间(CI):0.93-0.98];与 MMSE 评分≥24 相比,MMSE 评分<24 与全因死亡率增加 43%相关(HR:1.43;95%CI:1.05-1.95);与 MMSE 评分 30 相比,MMSE 评分 27-29(HR:1.27;95%CI:0.89-1.82)、24-26(HR:1.30;95%CI:0.86-1.99)和<24(HR:1.79;95%CI:1.15-2.77)的全因死亡率呈递增风险(趋势检验 P=0.003)。在 MMSE 域中,定向时间(HR:2.00;95%CI:1.29-3.11)、注意力和计算(HR:1.49;95%CI:1.16-1.92)、回忆(HR:2.59;95%CI:1.22-5.47)和语言(HR:1.68;95%CI:1.25-2.26)与全因死亡率显著相关在未经调整的模型中;对于 MMSE 域中受损数量增加一个,死亡率的未经调整 HR(95%CI)为 1.51(1.38,1.65),而完全调整后的死亡率 HR(95%CI)为 1.12(1.01,1.25);与 0 和 1 个受损 MMSE 域相比,与 2、3、4 和≥5 个受损 MMSE 域相关的全因死亡率的 HR 分别为 1.14(95%CI:0.84-1.54)、1.50(95%CI:0.98-2.28)、2.14(95%CI:1.12-4.09)和 2.29(95%CI:1.24-5.04),且呈剂量依赖性关系显著(趋势检验 P=0.003)。

结论

认知障碍与中国老年人全因死亡率的增加风险相关。同样,MMSE 评分降低以及 MMSE 域受损也与全因死亡率的增加风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a075/8487495/958954cb419e/12877_2021_2471_Fig1_HTML.jpg

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