Division of Endocrinology, Metabolism, & Lipid Research, Department of Medicine, Washington University, St. Louis, Missouri, USA.
Nutrition Support Service, Barnes-Jewish Hospital, St. Louis, Missouri, USA.
J Cyst Fibros. 2022 Mar;21(2):265-271. doi: 10.1016/j.jcf.2021.11.012. Epub 2021 Dec 1.
Though weight gain has been reported in some clinical trials of CFTR modulators, the effect of elexacaftor-tezacaftor-ivacaftor on body weight, body mass index (BMI), blood pressure, lipids and glycemic control in the real-world setting remains incompletely described.
We performed a single-center, retrospective, observational analysis of the effect of elexacaftor-tezacaftor-ivacaftor on body weight and cardiometabolic parameters in 134 adult CF patients of the Washington University Adult Cystic Fibrosis Center. Body weight, BMI, and blood pressure were extracted from outpatient clinic visits for the year preceding and the period following the initiation of elexacaftor-tezacaftor-ivacaftor. Other metabolic parameters were extracted at baseline and at latest available follow-up.
A mean of 12.2 months of follow-up data was available for analysis. The mean rate of change in BMI was 1.47 kg/m/yr (95% CI, 1.08 to 1.87) greater after initiation of elexacaftor-tezacaftor-ivacaftor. Significant increases in blood pressure were observed. In those without CFRD, random blood glucose and hemoglobin A1c were decreased after elexacaftor-tezacaftor-ivacaftor initiation. In those with CFRD, elexacaftor-tezacaftor-ivacaftor increased serum total cholesterol, HDL-cholesterol, and LDL-cholesterol.
In this single-center, retrospective, observational study of 134 adults with CF, initiation of elexacaftor-tezacaftor-ivacaftor was associated with increases in BMI at a mean follow up of 12.2 months. Changes in other cardiometabolic risk factors were also observed. Widespread use of elexacaftor-tezacaftor-ivacaftor may be expected to increase the incidence of overnutrition in the CF population.
尽管在一些 CFTR 调节剂的临床试验中报告了体重增加,但在真实环境中,依伐卡托与泰比卡托和艾美拉唑联合使用对体重、体重指数(BMI)、血压、血脂和血糖控制的影响仍不完全清楚。
我们对华盛顿大学成人囊性纤维化中心的 134 名成年 CF 患者进行了一项单中心、回顾性、观察性分析,以评估依伐卡托与泰比卡托和艾美拉唑联合使用对体重和心血管代谢参数的影响。在开始使用依伐卡托与泰比卡托和艾美拉唑之前的一年和之后的门诊就诊中提取体重、BMI 和血压数据。在基线和最新的随访中提取其他代谢参数。
可分析的平均随访数据为 12.2 个月。开始使用依伐卡托与泰比卡托和艾美拉唑后,BMI 的平均变化率增加了 1.47kg/m/yr(95%CI,1.08 至 1.87)。血压显著升高。在没有 CFRD 的患者中,依伐卡托与泰比卡托和艾美拉唑治疗后随机血糖和糖化血红蛋白降低。在有 CFRD 的患者中,依伐卡托与泰比卡托和艾美拉唑治疗后血清总胆固醇、HDL-胆固醇和 LDL-胆固醇升高。
在这项对 134 名 CF 成年患者的单中心、回顾性、观察性研究中,在平均 12.2 个月的随访中,开始使用依伐卡托与泰比卡托和艾美拉唑与 BMI 增加相关。还观察到其他心血管代谢危险因素的变化。预计依伐卡托与泰比卡托和艾美拉唑的广泛使用将增加 CF 人群中营养过剩的发生率。