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Nos centraremos en las acciones de los AR-GLP-1, los cuales se dividen en dos grupos segn su origen: derivados de exendinas (exenatida, lixisenatida y efpeglenatida) y anlogos del GLP-1 humano (liraglutida, albiglutida, dulaglutida, se maglutida) (Figura 2)
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Menopause has also been suggested as a factor that increases the probability of maintaining normoprolactinemia after dopamine agonist therapy is stopped.18 Unless there is evidence of growth of a prolactinoma or related symptoms, such as headache, there is no indication to continue dopamine agonist therapy after menopause.18 There are no significant differences in age, sex, initial dopamine agonist dose or length of treatment between those with continued normoprolactinemia and those with recurrence of hyperprolactinemia.18 We suggest that the dopamine agonist dose be decreased after 2 or 3 years of normal prolactin levels and that therapy be stopped if the prolactin levels remain unchanged after 1 year at the reduced dose
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Evolving utilization of bariatric surgery since the rise of semaglutide and tirzepatide
