Nuffield Department of Population Health, University of Oxford, Oxford, UK.
UK Biobank Ltd, Stockport, UK.
Alzheimers Dement. 2024 Jan;20(1):447-458. doi: 10.1002/alz.13439. Epub 2023 Sep 7.
The association between metabolic syndrome (MetS) and incident dementia remains inconclusive.
In 176,249 dementia-free UK Biobank participants aged ≥60 years at baseline, Cox proportional-hazards models were used to investigate the association between MetS and incident dementia. MetS was defined as the presence of ≥3 of the following: elevated waist circumference, triglycerides, blood pressure, blood glucose, and reduced high-density lipoprotein cholesterol.
Over 15 years of follow-up (median = 12.3), 5255 participants developed dementia. MetS was associated with an increased risk of incident dementia (hazard ratio [HR]: 1.12, 95% confidence interval [CI]: 1.06, 1.18). The association remained consistent when restricting to longer follow-up intervals: >5 to 10 years (HR: 1.17, 95% CI: 1.07, 1.27) and >10 years (HR: 1.22, 95% CI: 1.12, 1.32). Stronger associations were observed in those with ≥4 MetS components and in apolipoprotein-E (APOE)-ε4 non-carriers.
In this large population-based prospective cohort, MetS was associated with an increased risk of dementia.
MetS was associated with a 12% increased risk of incident all-cause dementia. Associations remained similar after restricting the analysis to those with longer follow-up. The presence of four or five MetS components was significantly associated with dementia. Stronger associations were observed in those with a low genetic risk for dementia.
代谢综合征(MetS)与痴呆症发病之间的关系仍不确定。
在 176,249 名基线时年龄≥60 岁且无痴呆的 UK Biobank 参与者中,使用 Cox 比例风险模型研究了 MetS 与痴呆症发病之间的关系。MetS 的定义为存在以下≥3 种情况:腰围升高、甘油三酯升高、血压升高、血糖升高和高密度脂蛋白胆固醇降低。
在 15 年的随访期间(中位数=12.3 年),有 5255 名参与者发生了痴呆症。MetS 与痴呆症发病风险增加相关(风险比 [HR]:1.12,95%置信区间 [CI]:1.06,1.18)。当限制随访间隔更长时,该关联仍然一致:>5 至 10 年(HR:1.17,95% CI:1.07,1.27)和>10 年(HR:1.22,95% CI:1.12,1.32)。在具有≥4 个 MetS 成分的患者和载脂蛋白-E(APOE)-ε4 非携带者中,观察到更强的关联。
在这项大型基于人群的前瞻性队列研究中,MetS 与痴呆症发病风险增加相关。
MetS 与全因痴呆症发病风险增加 12%相关。在限制分析仅限于随访时间较长的患者后,关联仍然相似。存在四个或五个 MetS 成分与痴呆症显著相关。在痴呆症遗传风险较低的患者中,观察到更强的关联。