二甲双胍对哮喘和代谢综合征呼吸和代谢结局的影响:一项双盲、随机、安慰剂对照的临床试验。

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-07-18 eCollection Date: 2025-08-01 DOI:10.1097/MS9.0000000000003552
Hossein Mehravaran, Adeleh Bahar, Fatemeh Hajimohammadi, Zahra Kashi, Masoud Aliyali, Fatemeh Varshoei, Reza Alizadeh-Navaei, Jamshid Yazdani Charati, Alireza Kashefizadeh, Mobina Gheibi, Erfan Ghadirzadeh
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引用次数: 0

摘要

代谢综合征(MetS)可能与哮喘控制恶化和更严重和频繁的哮喘发作有关。二甲双胍已被认为是MetS的潜在治疗方法,它可以降低气道反应性,改善哮喘控制,减少急诊就诊。然而,现有的数据主要集中在糖尿病患者。因此,在本研究中,我们旨在研究二甲双胍对并发哮喘和MetS患者的影响。方法:该试验在两组同时患有哮喘和MetS的患者(每组55人)中进行,每组接受盐酸二甲双胍或相同的安慰剂。3个月后对患者进行随访,评估临床结果、哮喘控制试验(act)、肺功能试验参数、c反应蛋白(CRP)水平、哮喘发作频率、ED就诊次数和住院率。结果:与安慰剂组相比,二甲双胍组在ACT评分、血氧饱和度、人体测量指标、血糖控制、CRP、血脂等指标均有统计学意义的改善(P < 0.05)。此外,在控制基线参数和性别混杂效应后的多因素分析中,二甲双胍组1 s内用力呼气量(FEV1) (P = 0.014,效应值= 5.6%)和用力肺活量(FVC) (P = 0.001,效应值= 9.2%)显著高于对照组。虽然二甲双胍组显示出严重哮喘发作、急诊科就诊或住院率降低的趋势,但效果无统计学意义(P < 0.05)。结论:我们的研究结果表明,同时患有哮喘和MetS的患者服用二甲双胍可以显著提高ACT评分、FEV1和FVC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metformin effects on respiratory and metabolic outcomes in asthma and metabolic syndrome: a double-blind, randomized, placebo-controlled clinical trial.

Metformin effects on respiratory and metabolic outcomes in asthma and metabolic syndrome: a double-blind, randomized, placebo-controlled clinical trial.

Metformin effects on respiratory and metabolic outcomes in asthma and metabolic syndrome: a double-blind, randomized, placebo-controlled clinical trial.

Introduction: Metabolic syndrome (MetS) could be associated with worsened asthma control and more severe and frequent asthma attacks. Metformin has been suggested as a potential treatment for MetS, which could decrease airway reactivity and lead to improved asthma control and reduced emergency department (ED) visits. However, the existing data have predominantly focused on diabetic patients only. Thus, in the present study, we aimed to investigate the effects of metformin in patients with concurrent asthma and MetS.

Methods: This trial was conducted on two groups of patients (55 in each group) with concurrent asthma and MetS, each receiving either metformin hydrochloride or an identical placebo. Patients were followed up after 3 months and assessed regarding clinical outcomes, asthma control tests (ACTs), pulmonary function test parameters, C-reactive protein (CRP) levels, frequency of asthma attacks, ED visits, and hospitalization rate.

Results: The metformin group showed statistically significant improvements in indices regarding ACT score, O2 saturation, anthropometric indices, blood sugar control, CRP, and lipid profile compared to the placebo group (all P < 0.05). Additionally, the metformin group showed significantly higher forced expiratory volume in 1 s (FEV1) (P = 0.014, and effect size = 5.6%) and forced vital capacity (FVC) (P = 0.001, and effect size = 9.2%) in the multivariate analysis after controlling for the confounding effects of baseline parameters and sex. Although the metformin group demonstrated a trend toward a reduction in severe asthma attacks, ED visits, or hospitalization rates, the effects were not statistically significant (P > 0.05).

Conclusion: Our findings demonstrate that metformin administration in patients with concurrent asthma and MetS could lead to substantial enhancements in ACT score, FEV1, and FVC.

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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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