Treatment of acromegaly-induced diabetes: an updated proposal.

IF 3.3 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Pituitary Pub Date : 2024-12-30 DOI:10.1007/s11102-024-01477-x
Betina Biagetti, Marta Araujo-Castro, Mónica Marazuela, Manel Puig-Domingo
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Abstract

Acromegaly-induced diabetes presents unique features due to the direct effects of excess growth hormone (GH) and insulin-like growth factor 1 (IGF-) on glucose metabolism, especially insulin resistance in association to low body fat content and water retention. Increased cardiovascular risk is much higher when acromegaly is complicated with diabetes, thus requiring a holistic management that addresses also these specific characteristics which differ from those of classical type 2 diabetes.The optimal management of diabetes in acromegaly requires not only an effective control of carbohydrate disturbances per se, but also the concurrent control of GH hypersecretion as it will directly impact on glucose control. If surgical treatment is not effective to normalize GH and IGF-1 levels, pharmacologic therapy for acromegaly must consider the metabolic effects that the different drugs may induce, as some of them may worsen carbohydrate metabolism. When treating acromegaly-induced diabetes, a comprehensive approach is essential, incorporating medications that may also protect against acromegaly associated comorbidities. Metformin remains the first-line therapy due to its ability to reduce hepatic glucose production enhance insulin sensitivity and its cost effectiveness. The newer drug classes, such as glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 inhibitors, offer benefits similar to those seen in type 2 diabetes, but the unique metabolic profile of acromegaly-including an enhanced ketogenic state and the effects of incretins on GH secretion-have to be considered as it may influence outcomes. Understanding the distinct pathophysiology of acromegaly-induced diabetes and the benefits of these newer drug classes for the patient with acromegaly is crucial for optimizing treatment outcomes and improving the quality of life.

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肢端肥大症诱导糖尿病的治疗:一项最新建议。
肢端肥大症诱导的糖尿病表现出独特的特征,因为过量的生长激素(GH)和胰岛素样生长因子1 (IGF-)对葡萄糖代谢的直接影响,特别是与低体脂含量和水潴持相关的胰岛素抵抗。当肢端肥大症合并糖尿病时,心血管风险增加,因此需要一个全面的管理,解决这些不同于典型2型糖尿病的具体特征。肢端肥大症糖尿病的最佳管理不仅需要有效控制碳水化合物本身的紊乱,还需要同时控制生长激素的高分泌,因为它将直接影响血糖的控制。如果手术治疗不能使GH和IGF-1水平正常化,肢端肥大症的药物治疗必须考虑不同药物可能引起的代谢影响,因为其中一些药物可能会使碳水化合物代谢恶化。当治疗肢端肥大症引起的糖尿病时,一个综合的方法是必不可少的,结合药物也可以防止肢端肥大症相关的合并症。二甲双胍仍然是一线治疗,因为它能够减少肝脏葡萄糖的产生,增强胰岛素敏感性和成本效益。较新的药物类别,如胰高血糖素样肽-1受体激动剂和钠-葡萄糖共转运蛋白-2抑制剂,提供与2型糖尿病相似的益处,但肢端肥大症的独特代谢特征——包括增强的生酮状态和肠促胰岛素对生长激素分泌的影响——必须考虑,因为它可能影响结果。了解肢端肥大症引起的糖尿病的独特病理生理学以及这些新型药物对肢端肥大症患者的益处对于优化治疗结果和改善生活质量至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pituitary
Pituitary 医学-内分泌学与代谢
CiteScore
7.10
自引率
7.90%
发文量
90
审稿时长
6 months
期刊介绍: Pituitary is an international publication devoted to basic and clinical aspects of the pituitary gland. It is designed to publish original, high quality research in both basic and pituitary function as well as clinical pituitary disease. The journal considers: Biology of Pituitary Tumors Mechanisms of Pituitary Hormone Secretion Regulation of Pituitary Function Prospective Clinical Studies of Pituitary Disease Critical Basic and Clinical Reviews Pituitary is directed at basic investigators, physiologists, clinical adult and pediatric endocrinologists, neurosurgeons and reproductive endocrinologists interested in the broad field of the pituitary and its disorders. The Editorial Board has been drawn from international experts in basic and clinical endocrinology. The journal offers a rapid turnaround time for review of manuscripts, and the high standard of the journal is maintained by a selective peer-review process which aims to publish only the highest quality manuscripts. Pituitary will foster the publication of creative scholarship as it pertains to the pituitary and will provide a forum for basic scientists and clinicians to publish their high quality pituitary-related work.
期刊最新文献
Correlates of prolonged length of stay after endoscopic transsphenoidal surgery for pituitary adenomas: varying definitions and non-clinical factors. Relationship between plasma urea and copeptin in response to arginine stimulation in healthy adults, patients with vasopressin deficiency and primary polydipsia. Selective resection of the medial wall of the cavernous sinus in pituitary surgery: results of a prospective single center analysis. Sheehan syndrome: a current approach to a dormant disease. The impact of non-clinical factors in pituitary surgery.
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