Metabolic syndrome and risk of incident all-cause dementia, Alzheimer's disease and vascular dementia: a systematic review and meta-analysis of longitudinal studies.

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Danial Qureshi, Naomi E Allen, Elżbieta Kuźma, Thomas J Littlejohns
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引用次数: 0

Abstract

Background: Metabolic syndrome (MetS) comprises several co-occurring vascular and cardiometabolic characteristics and might represent a novel modifiable risk factor for dementia, though findings remain inconsistent. To clarify this, we conducted a systematic review and meta-analysis of longitudinal studies investigating the association between MetS with risk of incident all-cause dementia, Alzheimer's disease and vascular dementia.

Methods: We searched Medline, Embase and PsycINFO databases (from inception to Feb 19th, 2024) for longitudinal cohort studies investigating the association of MetS with incident all-cause dementia or key subtypes, including Alzheimer's, vascular, Lewy Body or other dementias. Random-effects models were used to estimate pooled hazard ratios (pHR) and 95% confidence intervals (CI). Risk of bias was assessed using the Quality Assessment Tool for Quantitative Studies.

Results: Of 4,719 studies identified, fourteen studies met the eligibility criteria. These studies combined included 4,345,741 participants who were initially free of dementia. Pooled estimates showed that, compared to participants with no MetS, those with MetS had a significantly greater risk of incident all-cause dementia (4,307,830 participants, 27,708 cases, pHR: 1.12, 95% CI: 1.08-1.15, I2 = 12.0%). No significant association was observed for incident Alzheimer's disease (4,109,436 participants, 14,890 cases, pHR: 0.91, 95% CI: 0.72-1.15, I2: 41.0%) or vascular dementia (4,109,436 participants, 2,642 cases, pHR: 1.40, 95% CI: 0.96-2.06, I2: 59.0%). Associations remained similar in subgroup analyses restricted to studies reporting results for those aged 65 + years: all-cause dementia (pHR: 1.08, 95% CI: 1.00-1.16, I2: 15.0%), Alzheimer's disease (pHR: 0.85, 95% CI: 0.65-1.11, I2: 0.0%), and vascular dementia (pHR: 1.55, 95% CI: 0.71-3.39, I2: 75.0%).

Conclusions: Our findings demonstrate that MetS may be an important risk factor for developing dementia, and represent a potential target for prevention. Further studies are needed to understand the influence of MetS on specific dementia subtypes.

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代谢综合征与发生全因痴呆、阿尔茨海默病和血管性痴呆的风险:纵向研究的系统回顾和荟萃分析
背景:代谢综合征(MetS)包括几种同时发生的血管和心脏代谢特征,可能是痴呆的一种新的可改变的危险因素,尽管研究结果仍不一致。为了澄清这一点,我们对调查MetS与全因痴呆、阿尔茨海默病和血管性痴呆风险之间关系的纵向研究进行了系统回顾和荟萃分析。方法:我们检索Medline, Embase和PsycINFO数据库(从创建到2024年2月19日),以调查MetS与事件性全因痴呆或关键亚型(包括阿尔茨海默氏症,血管性,路易体或其他痴呆)之间关系的纵向队列研究。随机效应模型用于估计合并风险比(pHR)和95%置信区间(CI)。使用定量研究质量评估工具评估偏倚风险。结果:在4719项研究中,14项研究符合入选标准。这些研究总共包括4,345,741名最初没有痴呆症的参与者。汇总估计显示,与没有MetS的参与者相比,MetS患者发生全因痴呆的风险明显更高(4,307,830名参与者,27,708例,pHR: 1.12, 95% CI: 1.08-1.15, I2 = 12.0%)。未观察到阿尔茨海默病(4,109,436名参与者,14,890例,pHR: 0.91, 95% CI: 0.72-1.15, I2: 41.0%)或血管性痴呆(4,109,436名参与者,2,642例,pHR: 1.40, 95% CI: 0.96-2.06, I2: 59.0%)的发生率有显著相关性。在局限于报告结果的65岁以上研究的亚组分析中,相关性仍然相似:全因痴呆(pHR: 1.08, 95% CI: 1.00-1.16, I2: 15.0%)、阿尔茨海默病(pHR: 0.85, 95% CI: 0.65-1.11, I2: 0.0%)和血管性痴呆(pHR: 1.55, 95% CI: 0.71-3.39, I2: 75.0%)。结论:我们的研究结果表明,MetS可能是发生痴呆的重要危险因素,并代表了预防的潜在目标。需要进一步的研究来了解MetS对特定痴呆亚型的影响。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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