Humeyra Rekali Sahin, Serdar Sahin, Betul Sarac, Cem Sulu, Pinar Kadioglu, Hande Mefkure Ozkaya
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引用次数: 0
Abstract
background: The increase in portal insulin levels has been shown to upregulate growth hormone receptor expression in the liver, leading to increased insulin-like growth hormone-1 levels. Metformin inhibits hepatic gluconeogenesis and reduces fasting insulin. objective: We evaluated the effect of metformin treatment in patients with acromegaly on growth hormone, insulin-like growth hormone-1, and pituitary adenoma size. method: Patients who were followed up with the diagnosis of acromegaly in Istanbul University-Cerrahpaşa, Cerrahpaşa Medical Faculty were evaluated. The patients were divided into three groups after pituitary adenectomy as those who received somatostatin receptor ligand and metformin treatment (group A), somatostatin receptor ligand treatment only (group B), and those who received metformin treatment only (group C). Groups A and B were compared with each other, and patients in group C were compared among themselves. result: Insulin-like growth factor-1 levels were significantly lower in group A than in group B (p=0.020). There was no significant difference in post-treatment growth hormone levels and residual adenoma sizes between groups A and B (p>0.005). In group C, there was no significant difference in growth hormone values pre-and post-metformin treatment (p=0.078); however, post-metformin treatment insulin-like growth factor-1 values were significantly lower than pre-treatment insulin-like growth factor-1 values (p=0.027). conclusion: Due to the effect of metformin treatment on insulin-like growth factor-1 values in patients with acromegaly, it can be used in disease control, as well as a diabetes treatment
期刊介绍:
Aims & Scope
This journal is devoted to timely reviews and original articles of experimental and clinical studies in the field of endocrine, metabolic, and immune disorders. Specific emphasis is placed on humoral and cellular targets for natural, synthetic, and genetically engineered drugs that enhance or impair endocrine, metabolic, and immune parameters and functions. Moreover, the topics related to effects of food components and/or nutraceuticals on the endocrine-metabolic-immune axis and on microbioma composition are welcome.