Cardiovascular-kidney-metabolic syndrome and incidence of dementia among older adults.

IF 4.3 Q2 BUSINESS
Xiaqing Jiang, Amber L Bahorik, Christina S Dintica, Kristine Yaffe
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引用次数: 0

Abstract

Background: Cardiovascular-Kidney-Metabolic Syndrome (CKM) has profound impacts on cardiovascular events and mortality, yet its association with dementia risk remains poorly understood.

Objectives: To investigate associations between CKM and dementia risk.

Design: The prospective cohort study is within the Health, Aging, and Body Composition study, which enrolled participants from 1997 to 1998, with a 15-year follow-up for incident dementia.

Setting: The population-based study took place in two US communities in Memphis, Tennessee, and Pittsburgh, Pennsylvania.

Participants: Of the 3,075 participants aged 70 to 79 years initially enrolled, 14 were excluded for lacking baseline cognitive assessment, 308 for baseline cognitive impairment, 4 for missing follow-up, and 108 for missing CKM data, resulting in 2,641 in the analysis.

Measurements: CKM staging, as defined recently by the American Heart Association framework, was based on constructs comprising dysfunctional adiposity, metabolic risk factors, chronic kidney disease (CKD), and cardiovascular disease (CVD). Dementia was identified using hospital records, prescriptions for dementia medication, and a test of global cognition. Adjusted Cox and Fine-Gray proportional hazards models were used to estimate dementia risk and account for competing risk of death.

Results: The 2,641 participants had a mean (SD) age of 74 (2.8) years at baseline; 53 % were female, 36 % were of Black race, and had a range of baseline CKM: 3 % Stage 0 (no CKM), 4 % Stage 1 (excess/dysfunctional adiposity), 26 % Stage 2 (metabolic risk factors), 24 % Stage 3 (subclinical CVD and CKD), and 43 % Stage 4 (clinical CVD and CKD). Compared to participants with CKM Stages 0-2, those with CKM Stages 3-4 had a 50 % increase in dementia risk (hazard ratio 1.50, 95 % CI 1.20 to 1.86) in the fully adjusted model. The association remained significant after additional adjustment for metabolic risk factors, CVD, and CKD, both separately and together. Accounting for competing risk of death yielded similar results.

Conclusions: Among community-dwelling older adults, advanced CKM is associated with an increased risk of dementia. Older adults with CKM may need to be followed closely for adverse cognitive outcomes, and modifiable risk factors should be managed proactively.

心血管-肾-代谢综合征与老年人痴呆的发病率。
背景:心血管肾代谢综合征(CKM)对心血管事件和死亡率有深远的影响,但其与痴呆风险的关系尚不清楚。目的:探讨CKM与痴呆风险之间的关系。设计:前瞻性队列研究是健康、衰老和身体组成研究的一部分,该研究从1997年到1998年招募了参与者,并对痴呆事件进行了15年的随访。背景:这项以人群为基础的研究在田纳西州孟菲斯和宾夕法尼亚州匹兹堡两个美国社区进行。参与者:在最初入组的3075名年龄在70 - 79岁的参与者中,14人因缺乏基线认知评估而被排除,308人因基线认知障碍而被排除,4人因缺少随访,108人因缺少CKM数据而被排除,总共有2641人被排除。测量方法:最近由美国心脏协会框架定义的CKM分期是基于功能失调性肥胖、代谢危险因素、慢性肾脏疾病(CKD)和心血管疾病(CVD)构成的。痴呆症是通过医院记录、痴呆症药物处方和全球认知测试来确定的。校正Cox和Fine-Gray比例风险模型用于估计痴呆风险和考虑竞争死亡风险。结果:2641名参与者的基线平均(SD)年龄为74(2.8)岁;53%为女性,36%为黑人,基线CKM范围为:3%为0期(无CKM), 4%为1期(过度/功能失调肥胖),26%为2期(代谢危险因素),24%为3期(亚临床CVD和CKD), 43%为4期(临床CVD和CKD)。在完全调整模型中,与CKM 0-2期的参与者相比,CKM 3-4期的参与者痴呆风险增加50%(风险比1.50,95% CI 1.20至1.86)。在对代谢危险因素、CVD和CKD单独或共同进行调整后,这种关联仍然显著。考虑到相互竞争的死亡风险也得出了类似的结果。结论:在社区居住的老年人中,晚期CKM与痴呆风险增加相关。老年CKM患者可能需要密切跟踪不良认知结果,并应主动管理可改变的风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
发文量
0
期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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