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Accordingly, preclinical AD and PD models suggest that dual and triple agonists may enhance neurotrophic and neuroprotective actions, while reducing A and -synuclein pathology, oxidative stress, and inflammation (49, 208, 209)

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Clinical trial criteria excluded a significant number of adults without diabetes eligible for GLP-1 receptor agonist treatment from studies assessing the drugs safety and efficacy, results of a research letter showed

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