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代谢综合征与英国生物库中痴呆症发病风险的关系。

Association between metabolic syndrome and risk of incident dementia in UK Biobank.

机构信息

Nuffield Department of Population Health, University of Oxford, Oxford, UK.

UK Biobank Ltd, Stockport, UK.

出版信息

Alzheimers Dement. 2024 Jan;20(1):447-458. doi: 10.1002/alz.13439. Epub 2023 Sep 7.

Abstract

INTRODUCTION

The association between metabolic syndrome (MetS) and incident dementia remains inconclusive.

METHODS

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.

RESULTS

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.

DISCUSSION

In this large population-based prospective cohort, MetS was associated with an increased risk of dementia.

HIGHLIGHTS

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.

摘要

简介

代谢综合征(MetS)与痴呆症发病之间的关系仍不确定。

方法

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。

结果

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。

讨论

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。

重点

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c535/10916994/8d995bf39fb7/ALZ-20-447-g002.jpg

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