De Fano Michelantonio, Falorni Alberto, Malara Massimo, Porcellati Francesca, Fanelli Carmine Giuseppe
Department of Medicine and Surgery, Endocrine and Metabolic Sciences Section, University of Perugia, Perugia, Italy.
Diabetes Metab Syndr Obes. 2024 Jul 23;17:2761-2774. doi: 10.2147/DMSO.S466328. eCollection 2024.
Patients suffering from acromegaly and Cushing's Disease (CD) face the risk of several clinical complications. The onset of diabetes mellitus (DM) is among the most important: exposure to elevated growth hormone or cortisol levels is associated with insulin resistance (IR). DM contributes to increasing cardiovascular risk for these subjects, which is higher compared to healthy individuals. Hyperglycemia may also be caused by pasireotide, a second-generation somatostatin receptor ligand (SRLs), currently used for the treatment of these diseases. Accordingly, with 2014 medical expert recommendations, the management of hyperglycemia in patients with CD and treated with pasireotide is based on lifestyle changes, metformin, DPP-4 inhibitors (DPP-4i) and, subsequently, GLP-1 Receptor Agonists (GLP-1 RAs). There is no position for SGLT2-inhibitors (SGLT2-i). However, a very recent experts' consensus regarding the management of pasireotide-induced hyperglycemia in patients with acromegaly suggests the use of GLP-1 RAs as first line treatment (in suitable patients) and the use of SGLT2-i as second line treatment in patients with high cardiovascular risk or renal disease. As a matter of fact, beyond the hypoglycemic effect of GLP1-RAs and SGLT2-i, there is increasing evidence regarding their role in the reduction of cardiovascular risk, commonly very high in acromegaly and CD and often tough to improve despite biochemical remission. So, an increasing use of GLP1-RAs and SGLT2-i to control hyperglycemia is desirable in these diseases. Obviously, all of that must be done with due attention in order to minimize the occurrence of adverse events. For this reason, large studies are needed to analyze the presence of potential limitations.
患有肢端肥大症和库欣病(CD)的患者面临多种临床并发症的风险。糖尿病(DM)的发生是其中最重要的:生长激素或皮质醇水平升高与胰岛素抵抗(IR)相关。DM会增加这些患者的心血管风险,与健康个体相比更高。高血糖也可能由帕西瑞肽引起,帕西瑞肽是一种第二代生长抑素受体配体(SRLs),目前用于治疗这些疾病。因此,根据2014年医学专家建议,接受帕西瑞肽治疗的CD患者高血糖的管理基于生活方式改变、二甲双胍、二肽基肽酶-4抑制剂(DPP-4i),随后是胰高血糖素样肽-1受体激动剂(GLP-1 RAs)。不推荐使用钠-葡萄糖协同转运蛋白2抑制剂(SGLT2-i)。然而,最近一项关于肢端肥大症患者帕西瑞肽诱导的高血糖管理的专家共识建议,将GLP-1 RAs作为一线治疗(适用于合适的患者),将SGLT2-i作为心血管风险高或患有肾脏疾病患者的二线治疗。事实上,除了GLP1-RAs和SGLT2-i的降血糖作用外,越来越多的证据表明它们在降低心血管风险方面的作用,在肢端肥大症和CD中,心血管风险通常非常高,尽管生化缓解,但往往难以改善。因此,在这些疾病中越来越多地使用GLP1-RAs和SGLT2-i来控制高血糖是可取的。显然,所有这些都必须在充分关注的情况下进行,以尽量减少不良事件的发生。因此,需要进行大型研究来分析潜在局限性的存在情况。