Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Diabetes Unit, Milan, Italy.
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Respiratory Unit and Cystic, Fibrosis Adult Center, Milan, Italy; University of Milan, Department of Pathophysiology and Transplantation, Milan, Italy.
Diabetes Metab. 2023 Sep;49(5):101466. doi: 10.1016/j.diabet.2023.101466. Epub 2023 Aug 1.
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators are a group of new drugs for the treatment of cystic fibrosis (CF) and elexacaftor + tezacaftor + ivacaftor (ETI) triple combination therapy has been approved as first choice therapy in the treatment of patients with at least 1 copy of F508del variation. Data on the effects of CFTR modulators on glucose metabolism are limited to small studies with conflicting results. We conducted a prospective observational study on 24 CF patients with CF-related diabetes requiring insulin therapy, with the aim to evaluate the effectiveness of ETI on glucose metabolism, glucose variability and body composition. After six months of treatment, HbA1c and coefficient of variation, measured through flash or continuous glucose monitoring, significantly decreased (median changes: -0.5, P = 0.029 and -6.3, P = 0.008, respectively), despite unchanged insulin requirements. Over the treatment period, percent of fat mass increased by a median value of 3% (p = 0.029).
囊性纤维化跨膜电导调节因子(CFTR)调节剂是一组用于治疗囊性纤维化(CF)的新药,艾美赛肽+特立氟胺+依伐卡托(ETI)三联组合疗法已被批准为治疗至少携带 1 个 F508del 变异的患者的首选疗法。关于 CFTR 调节剂对葡萄糖代谢影响的数据仅限于结果相互矛盾的小型研究。我们对 24 例需要胰岛素治疗的伴有 CF 相关糖尿病的 CF 患者进行了一项前瞻性观察性研究,旨在评估 ETI 对葡萄糖代谢、血糖变异性和身体成分的有效性。治疗 6 个月后,通过瞬感或连续血糖监测测量的糖化血红蛋白(HbA1c)和变异系数显著降低(中位数变化分别为 -0.5,P = 0.029 和 -6.3,P = 0.008),尽管胰岛素需求没有变化。在治疗期间,体脂百分比中位数增加了 3%(p = 0.029)。