Jiang Xiaqing, Bahorik Amber L, Dintica Christina S, Yaffe Kristine
Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, 94107, USA.
Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, 94107, USA.
J Prev Alzheimers Dis. 2025 May;12(5):100112. doi: 10.1016/j.tjpad.2025.100112. Epub 2025 Mar 4.
Cardiovascular-Kidney-Metabolic Syndrome (CKM) has profound impacts on cardiovascular events and mortality, yet its association with dementia risk remains poorly understood.
To investigate associations between CKM and dementia risk.
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.
The population-based study took place in two US communities in Memphis, Tennessee, and Pittsburgh, Pennsylvania.
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.
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.
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.
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-肾脏-代谢综合征(CKM)对心血管事件和死亡率有深远影响,但其与痴呆风险的关联仍知之甚少。
研究CKM与痴呆风险之间的关联。
前瞻性队列研究纳入了健康、衰老和身体成分研究,该研究于1997年至1998年招募参与者,并对新发痴呆进行了15年的随访。
这项基于人群的研究在美国田纳西州孟菲斯和宾夕法尼亚州匹兹堡的两个社区进行。
最初纳入的3075名70至79岁的参与者中,14名因缺乏基线认知评估被排除,308名因基线认知障碍被排除,4名因失访被排除,108名因缺少CKM数据被排除,最终2641名纳入分析。
CKM分期依据美国心脏协会框架最近的定义,基于包括功能失调性肥胖、代谢风险因素、慢性肾脏病(CKD)和心血管疾病(CVD)的指标构建。痴呆通过医院记录、痴呆药物处方和整体认知测试来确定。使用调整后的Cox和Fine-Gray比例风险模型来估计痴呆风险并考虑死亡的竞争风险。
2641名参与者基线时的平均(标准差)年龄为74(2.8)岁;53%为女性,36%为黑人,基线CKM情况各异:3%为0期(无CKM),4%为1期(肥胖/功能失调性肥胖),26%为2期(代谢风险因素),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了50%(风险比1.50,95%可信区间1.20至1.86)。在分别或共同对代谢风险因素、CVD和CKD进行额外调整后,这种关联仍然显著。考虑死亡的竞争风险得出了类似的结果。
在社区居住的老年人中,晚期CKM与痴呆风险增加相关。患有CKM的老年人可能需要密切随访以关注不良认知结局,并且应积极管理可改变的风险因素。