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The role of UA as a predictor of the progression rate of multiple non-motor symptoms was also proven in some clinical trials [92, 93]

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All participants had a diagnosis of ASD established with DSM-IV-TR or DSM-5 and validated with ADOS-2 and/or ADI-R, while individuals with neurological or psychiatric comorbidities, recent probiotic or oxytocin use, or unstable medications were excluded

By delaying the rate at which food leaves the stomach and enters the small intestine, GLP-1 effectively moderates the speed at which nutrients are exposed to digestive enzymes