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During follow-up, 12 patients in the oral semaglutide (10.4%) and 11 patients in the subcutaneous semaglutide (6.2%%) group discontinued treatment due to side effects, without significant differences between the two formulations ( p = 0.27) (Supplementry Figure S2o)
p = 0.002) levels, along with decreased TSH levels (SMD = 2.00
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Both medications require gradual dose titration to mitigate gastrointestinal (GI) symptoms and improve adherence
Exploring the interactions between ER stress and inflammation
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