A 1-Year Weight Management Program for Difficult-to-Treat Asthma With Obesity: A Randomized Controlled Study.

IF 9.5 1区 医学 Q1 CRITICAL CARE MEDICINE
Chest Pub Date : 2025-01-01 Epub Date: 2024-10-18 DOI:10.1016/j.chest.2024.09.042
Varun Sharma, Helen Clare Ricketts, Louise McCombie, Naomi Brosnahan, Luisa Crawford, Lesley Slaughter, Anna Goodfellow, Femke Steffensen, Rekha Chaudhuri, Michael E J Lean, Douglas C Cowan
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引用次数: 0

Abstract

Background: Obesity-associated asthma results in increased morbidity and mortality. We report 1-year asthma outcomes with a weight management regimen, the Counterweight-Plus Programme (CWP), compared with usual care (UC) in a single-center, randomized controlled trial in patients with difficult-to-treat asthma and obesity.

Research question: Can use of the CWP result in improved asthma control and quality of life compared with UC at 1 year in patients with difficult-to-treat asthma and obesity?

Study design and methods: Adults with difficult-to-treat asthma and BMI ≥ 30 kg/m2 were randomized (1:1 CWP:UC) to treatment. The CWP, with dietitian support, included a 12-week total diet replacement phase (850 kcal/d low-energy formula), and then subsequent food reintroduction and maintenance phases up to 1 year. Outcomes include results of the six-item Asthma Control Questionnaire (ACQ-6) and Asthma Quality of Life Questionnaire (AQLQ), as well as health care usage. A minimal clinically important difference (MCID) is 0.5 for ACQ-6 and AQLQ.

Results: Of 36 patients recruited, 29 attended visits at 52 weeks (13 CWP and 16 UC). The CWP resulted in greater weight change (median, -14 kg [interquartile range (IQR), -15 to -9 kg]) compared with UC (median, 2 kg [IQR, -7 to 8 kg]; P = .015) at 52 weeks. A greater proportion achieved MCID with the CWP vs UC in AQLQ (71% vs 6%, respectively; P < .001). No between-group differences were observed in ACQ-6. Median exacerbation frequency was reduced over 52 weeks with the CWP from 4 (IQR, 2 to 5) to 0 (IQR, 0 to 2) (P < .001), although no between-group difference was observed. Seventy percent of the CWP group lost ≥ 10% body weight and had improvement in ACQ-6 (mean difference, -1.1; 95% CI, -1.9 to -0.3; P = .018) and AQLQ (mean difference, 1.2; 95% CI, 0.4, 2.1; P = .011) across 52 weeks.

Interpretation: In this study, the use of a dietitian-supported weight management program resulted in sustained weight loss and is a potential treatment for obesity in asthma. The CWP resulted in a higher proportion achieving MCID improvements in AQLQ compared with UC. Within-group differences in AQLQ and exacerbation frequency suggest potential with the CWP. These encouraging signals justify a larger sample study to further assess asthma-related outcomes.

针对难治性肥胖哮喘的为期一年的体重管理计划:随机对照研究。
背景:肥胖引起的哮喘会增加发病率和死亡率。我们报告了在一项单中心随机对照试验中,Counterweight-Plus 体重管理计划(CWP)与常规护理(UC)相比,对难以治疗的哮喘和肥胖患者一年的哮喘治疗结果:研究问题:对于难以治疗的哮喘和肥胖症患者,使用 CWP 一年后,其哮喘控制率和生活质量能否比常规护理有所提高?我们对哮喘难以治愈且体重指数≥30kg/m2的成人患者进行了随机分组(1:1 CWP:UC)。有营养师支持的 CWP:为期 12 周的全面饮食替代阶段(850 千卡/天的低能量配方);食物再引入和维持阶段,最长一年。结果包括哮喘控制问卷(ACQ-6)、哮喘生活质量问卷(AQLQ)和医疗保健使用情况。ACQ-6 和 AQLQ 的最小临床重要差异(MCID)为 0.5:在招募的 36 人中,29 人参加了 52 周的治疗:13 人参加了 CWP,16 人参加了 UC。在 52 周时,CWP 与 UC(2 千克 [-7, 8];P=0.015)相比,体重变化更大(中位数 -14 千克 [IQR -15, -9])。CWP与UC相比,在AQLQ方面达到MCID的比例更高(分别为71%对6%;P解释:使用营养师支持的体重管理计划可持续减轻体重,是治疗哮喘患者肥胖症的一种潜在方法。与 UC 相比,CWP 可使更高比例的患者在 AQLQ 方面获得 MCID 改善。AQLQ和恶化频率的组内差异表明,CWP具有潜力。这些令人鼓舞的信号表明,有必要进行更大规模的样本研究,以进一步评估与哮喘相关的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chest
Chest 医学-呼吸系统
CiteScore
13.70
自引率
3.10%
发文量
3369
审稿时长
15 days
期刊介绍: At CHEST, our mission is to revolutionize patient care through the collaboration of multidisciplinary clinicians in the fields of pulmonary, critical care, and sleep medicine. We achieve this by publishing cutting-edge clinical research that addresses current challenges and brings forth future advancements. To enhance understanding in a rapidly evolving field, CHEST also features review articles, commentaries, and facilitates discussions on emerging controversies. We place great emphasis on scientific rigor, employing a rigorous peer review process, and ensuring all accepted content is published online within two weeks.
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