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The pharmacodynamics-based prophylactic benefits of GLP-1 receptor agonists and SGLT2 inhibitors on neurodegenerative diseases: evidence from a network meta-analysis

  • 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*
  • *Corresponding author for this work
  • National Sun Yat-sen University
  • Prospect Clinic for Otorhinolaryngology & Neurology
  • I-Shou University
  • Deakin University
  • King's College London
  • University of Vienna
  • Triservice General Hospital Taiwan
  • National Yang Ming Chiao Tung University
  • Hsinchu Municipal MacKay Children’s Hospital
  • Chang Gung University
  • China Medical University Taichung
  • National Defense Medical University

Research output: Contribution to journalJournal Article peer-review

23 Scopus citations

Abstract

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.

Original languageEnglish
Article number197
Pages (from-to)197
JournalBMC Medicine
Volume23
Issue number1
DOIs
StatePublished - 07 04 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • GLP-1 receptor agonist
  • Network meta-analysis
  • Neurodegenerative disease
  • Parkinson’s disease
  • SGLT2 inhibitor

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