Auth Roger, Dougherty Brian, Putnam Melissa, Scully Kevin
Department of Medicine, Division of Pulmonary Critical Care and Sleep, Alpert Medical School of Brown University, Providence, Rhode Island.
Division of Endocrinology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
AACE Endocrinol Diabetes. 2025 Apr 11;12(2):67-70. doi: 10.1016/j.aed.2025.03.011. eCollection 2025 Jul-Aug.
BACKGROUND/OBJECTIVE: Cystic fibrosis (CF)-related diabetes (CFRD) is a common extrapulmonary complication of CF, with increasing prevalence. As individuals with CF live longer, obesity rates are increasing, leading to an emerging phenotype called CFRD with metabolic syndrome. The objective of this report is to describe the use of semaglutide in an adult with CFRD, obesity, and clinical insulin resistance.
A 32-year-old man with CF, pancreatic insufficiency, obesity, and poorly controlled CFRD presented with worsening blood sugar control, increasing insulin requirements, and a strong family history of metabolic syndrome. His body mass index was 38.5 kg/m, and his hemoglobin A1c level ranged from 9.4% to 11.4%. He reported difficulty adhering to insulin therapy and concerns regarding weight and body image. A continuous glucose monitor was initiated; however, it did not significantly improve glycemic control. Given his metabolic profile and desire to lose weight, semaglutide was introduced and gradually increased over 5 months. This improved the hemoglobin A1c level by 5.7%, lowered the mean glucose levels, reduced the body mass index to 33.4 kg/m, and decreased insulin requirements without adverse effects.
Although insulin is the primary treatment for CFRD, glucagon-like peptide 1 receptor agonists may provide additional benefits in carefully selected patients.
This case highlights the potential benefits of glucagon-like peptide 1 receptor agonists in CFRD with metabolic syndrome and emphasizes the need for further investigation.
背景/目的:囊性纤维化(CF)相关糖尿病(CFRD)是CF常见的肺外并发症,其患病率呈上升趋势。随着CF患者寿命延长,肥胖率不断增加,导致一种称为合并代谢综合征的CFRD新表型出现。本报告的目的是描述司美格鲁肽在一名患有CFRD、肥胖和临床胰岛素抵抗的成年人中的应用情况。
一名32岁男性,患有CF、胰腺功能不全、肥胖且CFRD控制不佳,出现血糖控制恶化、胰岛素需求量增加以及代谢综合征家族史明显。他的体重指数为38.5kg/m²,糖化血红蛋白水平在9.4%至11.4%之间。他表示难以坚持胰岛素治疗,并对体重和体型感到担忧。开始使用持续葡萄糖监测仪;然而,血糖控制并未得到显著改善。鉴于他的代谢状况以及减肥意愿,开始使用司美格鲁肽,并在5个月内逐渐增加剂量。这使糖化血红蛋白水平降低了5.7%,平均血糖水平下降,体重指数降至33.4kg/m²,胰岛素需求量减少,且无不良反应。
尽管胰岛素是CFRD的主要治疗方法,但胰高血糖素样肽1受体激动剂在精心挑选的患者中可能会带来额外益处。
本病例突出了胰高血糖素样肽1受体激动剂在合并代谢综合征的CFRD中的潜在益处,并强调了进一步研究的必要性。