基于药效学的GLP-1受体激动剂和SGLT2抑制剂对神经退行性疾病的预防作用:来自网络meta分析的证据

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Ping-Tao Tseng, Bing-Yan Zeng, Chih-Wei Hsu, Chao-Ming Hung, Andre F Carvalho, Brendon Stubbs, Yen-Wen Chen, Tien-Yu Chen, Wei-Te Lei, Jiann-Jy Chen, Kuan-Pin Su, Yow-Ling Shiue, Chih-Sung Liang
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引用次数: 0

摘要

背景:胰高血糖素样肽-1(GLP-1)受体激动剂和钠-葡萄糖共转运体 2(SGLT2)抑制剂是新一代降糖药物,其作用机制与传统糖尿病治疗方法不同。除了代谢作用外,这些药物还在临床前研究中表现出神经保护特性。虽然临床试验探索了这些药物在神经退行性疾病中的治疗潜力,但它们在疾病预防中的作用仍不明确。我们进行了一项网络荟萃分析(NMA),以全面评估这些药物对多种神经退行性疾病的预防作用,并确定最有前景的预防策略:我们系统地检索了 PubMed、Embase、ClinicalKey、Cochrane CENTRAL、ProQuest、ScienceDirect、Web of Science 和 ClinicalTrials.gov(截至 2024 年 10 月 24 日)中有关 GLP-1 受体激动剂或 SGLT2 抑制剂的随机对照试验 (RCT)。我们的主要研究结果是七种主要神经退行性疾病的发病率:帕金森病、阿尔茨海默病、路易体痴呆、多发性硬化、肌萎缩侧索硬化、额颞叶痴呆和亨廷顿病。次要结果包括通过辍学率评估的安全性概况。我们进行了基于频数的 NMA,并使用偏倚风险工具评估了偏倚风险。当前研究的主要结果将通过基于贝叶斯的 NMA 的敏感性测试再次确认:我们的分析包括 22 项 RCT,涉及 138,282 名参与者(平均年龄 64.8 岁,36.4% 为女性)。在所有研究药物中,与对照组相比,只有达帕格列净具有显著的预防效果,特别是在预防帕金森病方面(几率比=0.28,95%置信区间=0.09-0.93)。GLP-1受体激动剂和其他SGLT2抑制剂均未显示出对任何一种神经退行性疾病的显著预防效果。所有治疗方法的退出率相当:这项全面的NMA揭示了达帕格列净对帕金森病的新型特异性预防效果,代表了预防性神经病学的潜在突破。dapagliflozin对帕金森病的特异性保护作用可能依赖于其对SGLT2的高度选择性抑制。这些发现为今后的研究提供了重要方向,可为帕金森病高危人群的预防策略提供参考:ProCORD42021252381.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The pharmacodynamics-based prophylactic benefits of GLP-1 receptor agonists and SGLT2 inhibitors on neurodegenerative diseases: evidence from a network meta-analysis.

Background: Glucagon-like peptide-1 (GLP-1) receptor agonists and sodium-glucose cotransporter 2 (SGLT2) inhibitors represent a new generation of antihyperglycemic agents that operate through mechanisms distinct from conventional diabetes treatments. Beyond their metabolic effects, these medications have demonstrated neuroprotective properties in preclinical studies. While clinical trials have explored their therapeutic potential in established neurodegenerative conditions, their role in disease prevention remains unclear. We conducted a network meta-analysis (NMA) to comprehensively evaluate the prophylactic benefits of these agents across multiple neurodegenerative diseases and identify the most promising preventive strategies.

Methods: We systematically searched PubMed, Embase, ClinicalKey, Cochrane CENTRAL, ProQuest, ScienceDirect, Web of Science, and ClinicalTrials.gov through October 24th, 2024, for randomized controlled trials (RCTs) of GLP-1 receptor agonists or SGLT2 inhibitors. Our primary outcome was the incidence of seven major neurodegenerative diseases: Parkinson's disease, Alzheimer's disease, Lewy body dementia, multiple sclerosis, amyotrophic lateral sclerosis, frontotemporal dementia, and Huntington's disease. Secondary outcomes included safety profiles assessed through dropout rates. We performed a frequentist-based NMA and evaluated risk of bias with Risk of Bias tool. The main result of the primary outcome in the current study would be re-affirmed via sensitivity test with Bayesian-based NMA.

Results: Our analysis encompassed 22 RCTs involving 138,282 participants (mean age 64.8 years, 36.4% female). Among all investigated medications, only dapagliflozin demonstrated significant prophylactic benefits, specifically in preventing Parkinson's disease (odds ratio = 0.28, 95% confidence intervals = 0.09 to 0.93) compared to controls. Neither GLP-1 receptor agonists nor other SGLT2 inhibitors showed significant preventive effects for any of the investigated neurodegenerative conditions. Drop-out rates were comparable across all treatments.

Conclusions: This comprehensive NMA reveals a novel and specific prophylactic effect of dapagliflozin against Parkinson's disease, representing a potential breakthrough in preventive neurology. The specificity of dapagliflozin's protective effect to Parkinson's disease might rely on its highly selective inhibition to SGLT2. These findings provide important direction for future research and could inform preventive strategies for populations at risk of Parkinson's disease.

Trial registration: PROSPERO CRD42021252381.

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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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