Movement Disorders Clinical Practice · 2023 · 13 citations · 31 references
MedicinePharmacologyPharmacotherapyClinical PharmacologyMeta-analysisPharmacovigilanceClinical TrialsDiabetes MellitusDrug Efficacy AssessmentGlucagon-like Peptide-1 Receptor AgonistsParkinson DiseasePharmacoepidemiologyDipeptidyl PeptidasesGlucagon-like Peptide 1 Receptor AgonismGlucose-lowering TherapyParkinson's Disease PharmacotherapyParkinson’s Disease PharmacotherapyParkinson’s Disease TreatmentPooled Odds RatiosRandomized Clinical Trials
Background: The association between newer classes of glucose-lowering drugs (GLDs) and the risk of Parkinson's disease (PD) remains unclear. Objective: The aim was to examine the effect of newer GLDs on the risk of PD through a meta-analysis of randomized outcome trials. Methods: The methods included randomized placebo-controlled outcome trials that reported PD events associated with three newer classes of GLDs (ie, dipeptidyl peptidase-4 inhibitors, glucagon-like peptide-1 receptor agonists, and sodium-glucose co-transporter-2 inhibitors) in participants with or without type 2 diabetes. The pooled odds ratio (OR) and 95% confidence interval (CI) were estimated using Peto's method. Results: The study included 24 trials involving 33 PD cases among 185,305 participants during a median follow-up of 2.2 years. Newer GLDs were significantly associated with a lower PD risk (OR: 0.50; 95% CI: 0.25-0.98) than placebo. Conclusion: Newer GLDs may possibly be associated with a decreased risk of PD; however, larger datasets are required to confirm or refute this notion.
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The Cochrane Collaboration's tool for assessing risk of bias in randomised trials
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