囊性纤维化患者接受 Elexacaftor/Tezacaftor/Ivacaftor 治疗一年后运动能力的变化 - 丹麦前瞻性队列。

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM Journal of Cystic Fibrosis Pub Date : 2024-11-01 DOI:10.1016/j.jcf.2024.04.010
Lue Katrine Drasbæk Philipsen , Hanne Vebert Olesen , Janne Hastrup Jensen , Mette Frahm Olsen , Daniel Faurholt-Jepsen , Frederik Buchvald , Kim Gjerum Nielsen , Marianne Skov , Tacjana Pressler
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引用次数: 0

摘要

背景:囊性纤维化(CF)是一种遗传性多器官疾病,会导致肺部损伤和早期死亡。与普通人相比,囊性纤维化患者(pwCF)的运动能力较弱。这是由于反复肺部感染、肺功能下降和营养不良导致肺功能加速衰退。自 2020 年起,CFTR 调节剂 Elexacaftor/Tezacaftor/Ivacaftor (ETI) 在丹麦获准用于 12 岁及以上的肺结核患者。该药物的初步治疗效果良好,包括肺功能改善和病情稳定。迄今为止,只有少数研究评估了 CFTR 调节剂对 pwCF 运动能力的影响:本研究旨在评估在不采取任何进一步干预措施的情况下,接受一年 ETI 治疗对通过心肺运动测试(CPET)测量的 12 岁及以上 pwCF 运动能力的影响:丹麦前瞻性登记队列研究,包括哥本哈根大学医院哥本哈根 CF 中心和奥胡斯大学医院奥胡斯 CF 中心的患病儿童。参与者在开始 ETI 之前和一年后的随访中接受了 CPET。主要结果为VO₂峰值(毫升/千克/分钟),次要结果为VO2峰值(毫升/分钟)、VO2峰值(预测值%)、最大功率、最大心率和最大饱和度。采用配对样本 t 检验法评估基线和随访之间的差异,并对相关结果进行回归分析:我们在分析中纳入了 229 名慢性阻塞性肺疾病患者。从基线到随访期间,我们观察到摄氧量、VO₂ 峰值(毫升/千克/分钟)的增加;0.6,95% CI [0.06; 1.09] p = 0.03。此外,所有其他 CPET 结果均有明显增加。回归分析显示,FEV₁% pred 和 BMI 的变化可解释部分差异,分别为 0.05 ml/kg/min,95% CI [0.01, 0.1] p = 0.02 和 -0.5 ml/kg/min,95% CI [-0.8, -0.2] p = 0.002:我们发现,在丹麦的慢性阻塞性肺病患者中,经过一年的 ETI 治疗后,摄氧量有了显著增加,但与临床无关。
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Changes in exercise capacity in people with Cystic Fibrosis after one year of Elexacaftor/Tezacaftor/Ivacaftor treatment – A Danish prospective cohort

Background

Cystic Fibrosis (CF) is an inherited multiorgan disease that causes lung damage and early death. People with CF (pwCF) experience diminished exercise capacity compared to the general population. This is due to an accelerated decline in lung function resulting from recurrent lung infections, declining lung function and nutritional challenges. Since 2020 the CFTR-modulator Elexacaftor/Tezacaftor/Ivacaftor (ETI) has been approved for pwCF aged 12 and above in Denmark. Initial experiences with the medication have shown promising results, including improved lung function and disease stability. To date a limited number of studies have evaluated the impact of CFTR-modulators on exercise capacity in pwCF.

Objective

The study aims to assess the impact of one year of ETI treatment, without any further intervention, on exercise capacity measured through cardiopulmonary exercise test (CPET) in pwCF aged 12 years and above.

Methods

A Danish prospective registry cohort study including pwCF from CF-Center Copenhagen, Copenhagen University Hospital and CF-Center Aarhus, Aarhus University Hospital. Participants underwent CPET before initiating ETI and at follow up one year later. Primary outcomes were VO₂ peak (ml/kg/min), secondary outcomes were VO2 peak (ml/min), VO2 peak (% pred), watt-max, HR-max and saturation at max. The difference between baseline and follow-up was assessed using a paired-sample t-test and regression analyses were applied to relevant outcomes.

Results

We included 229 pwCF in the analyses. An increase in oxygen uptake, VO₂ peak (ml/kg/min) from baseline to follow-up was observed; 0.6, 95% CI [0.06; 1.09] p = 0.03. Moreover, significant increase was noted for all other CPET outcomes. Regression analysis showed that changes in FEV₁% pred and BMI could explain some of the differences, 0.05 ml/kg/min, 95% CI [0.01, 0.1] p = 0.02 and -0.5 ml/kg/min, 95% CI [-0.8, -0.2] p = 0.002 respectively.

Conclusion

Among Danish pwCF we found a significant, but not clinically relevant, increase in oxygen uptake, after one year of ETI treatment.
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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
期刊最新文献
Real-world association between ivacaftor initiation and lung function variability: A registry study. Mycobacterium abscessus biofilm cleared from murine lung by monoclonal antibody against bacterial DNABII proteins. Personalized therapy with CFTR modulators: Response of p.Ile148Asn variant. Real-world outcomes of generic elexacaftor/tezacaftor/ivacaftor (gETI) in South Africans (SA) with CF using standard versus clarithromycin-boosted gETI, modulator-sparing strategies to reduce cost. Impact of CFTR modulator therapy on basic life needs and financial concerns in people with cystic fibrosis: Data from the Well-ME survey.
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