抗糖尿病药物与2型糖尿病患者痴呆风险:观察性研究和随机对照试验的系统回顾和网络荟萃分析

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2024-12-23 DOI:10.1186/s13195-024-01645-y
Zonglin Li, Chu Lin, Xiaoling Cai, Fang Lv, Wenjia Yang, Linong Ji
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引用次数: 0

摘要

目的:探讨抗糖尿病药物与2型糖尿病(T2D)患者痴呆风险的关系。方法:检索1995年1月至2024年10月PubMed、Embase、Cochrane Central Register of Controlled Trials和Clinicaltrial.gov的文献。T2D患者的观察性研究和随机对照试验(RCTs),将抗糖尿病药物或与安慰剂进行比较,并报告痴呆的发病率。对这些研究进行了常规和网络荟萃分析。结果显示为优势比(OR)或风险比(RR), 95%置信区间(CI)。结果:共纳入41项观察性研究(3,307,483名受试者)和23项随机对照试验(155,443名受试者)。在观察性研究的网络meta分析中,与未使用该药物的患者相比,葡萄糖共转运蛋白-2抑制剂钠(SGLT-2i) (OR = 0.56, 95%CI, 0.45至0.69)、胰高血糖素样肽-1受体激动剂(GLP-1RA) (OR = 0.58, 95%CI, 0.46至0.73)、噻唑烷二酮(TZD) (OR = 0.68, 95%CI, 0.57至0.81)和二甲双胍(OR = 0.89, 95%CI, 0.80至0.99)治疗均与T2D患者痴呆风险降低相关。根据累积排序曲线(SUCRA)评估,在认知益处方面,排名顺序为SGLT-2i > GLP-1RA > TZD >二肽基肽酶-4抑制剂(DPP-4i) >二甲双胍> α-葡萄糖苷酶抑制剂(AGI) >葡萄糖激酶激活剂(GKA) >磺酰脲类>格列尼德斯>胰岛素。同时,与非使用者相比,SGLT-2i (OR = 0.43, 95%CI, 0.30至0.62)、GLP-1RA (OR = 0.54, 95%CI, 0.30至0.96)和DPP-4i (OR = 0.73, 95%CI, 0.57至0.93)与阿尔茨海默病风险降低相关,而接受SGLT-2i (OR = 0.42, 95%CI, 0.22至0.80)和TZD (OR = 0.52, 95%CI, 0.36至0.75)治疗的患者患血管性痴呆的风险较低。在随机对照试验的网络荟萃分析中,抗糖尿病药物和安慰剂的痴呆风险相当。结论:与未服用者相比,SGLT-2i、GLP-1RA、TZD和二甲双胍与T2D患者痴呆风险降低相关。SGLT-2i和GLP-1RA可能是改善T2D患者认知预后的最佳选择。
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Anti-diabetic agents and the risks of dementia in patients with type 2 diabetes: a systematic review and network meta-analysis of observational studies and randomized controlled trials.

Objective: To evaluate the association between anti-diabetic agents and the risks of dementia in patients with type 2 diabetes (T2D).

Methods: Literature retrieval was conducted in PubMed, Embase, the Cochrane Central Register of Controlled Trials and Clinicaltrial.gov between January 1995 and October 2024. Observational studies and randomized controlled trials (RCTs) in patients with T2D, which intercompared anti-diabetic agents or compared them with placebo, and reported the incidence of dementia were included. Conventional and network meta-analyses of these studies were implemented. Results were exhibited as the odds ratio (OR) or risk ratio (RR) with 95% confidence interval (CI).

Results: A total of 41 observational studies (3,307,483 participants) and 23 RCTs (155,443 participants) were included. In the network meta-analysis of observational studies, compared with non-users, sodium glucose cotransporter-2 inhibitor (SGLT-2i) (OR = 0.56, 95%CI, 0.45 to 0.69), glucagon-like peptide-1 receptor agonist (GLP-1RA) (OR = 0.58, 95%CI, 0.46 to 0.73), thiazolidinedione (TZD) (OR = 0.68, 95%CI, 0.57 to 0.81) and metformin (OR = 0.89, 95%CI, 0.80 to 0.99) treatments were all associated with reduced risk of dementia in patients with T2D. The surface under the cumulative ranking curve (SUCRA) evaluation conferred a rank order as SGLT-2i > GLP-1RA > TZD > dipeptidyl peptidase-4 inhibitor (DPP-4i) > metformin > α-glucosidase inhibitor (AGI) > glucokinase activator (GKA) > sulfonylureas > glinides > insulin in terms of the cognitive benefits. Meanwhile, compared with non-users, SGLT-2i (OR = 0.43, 95%CI, 0.30 to 0.62), GLP-1RA (OR = 0.54, 95%CI, 0.30 to 0.96) and DPP-4i (OR = 0.73, 95%CI, 0.57 to 0.93) were associated with a reduced risk of Alzheimer's disease while a lower risk of vascular dementia was observed in patients receiving SGLT-2i (OR = 0.42, 95%CI, 0.22 to 0.80) and TZD (OR = 0.52, 95%CI, 0.36 to 0.75) treatment. In the network meta-analysis of RCTs, the risks of dementia were comparable among anti-diabetic agents and placebo.

Conclusion: Compared with non-users, SGLT-2i, GLP-1RA, TZD and metformin were associated with the reduced risk of dementia in patients with T2D. SGLT-2i, and GLP-1RA may serve as the optimal choice to improve the cognitive prognosis in patients with T2D.

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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.
期刊最新文献
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