Suppr超能文献

生命历程中第一秒用力呼气容积/用力肺活量(FEV/FVC)轨迹与中年之前呼吸系统症状的关联:两项前瞻性队列研究数据分析

Associations between life-course FEV/FVC trajectories and respiratory symptoms up to middle age: analysis of data from two prospective cohort studies.

作者信息

Perret Jennifer L, Bui Dinh S, Pistenmaa Carrie, Vicendese Don, Khan Sadiya S, Han MeiLan K, San José Estépar Raul, Lowe Adrian J, Lodge Caroline J, Labaki Wassim W, Pham Jonathan V, Idrose Nur Sabrina, Senaratna Chamara V, Tan Daniel J, Hamilton Garun S, Thompson Bruce R, Munsif Maitri, Arynchyn Alexander, Jacobs David R, Abramson Michael J, Walters E Haydn, Washko George R, Kalhan Ravi, Dharmage Shyamali C

机构信息

Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Department of Respiratory and Sleep Medicine, Austin Hospital, Melbourne, VIC, Australia; Institute for Breathing and Sleep (IBAS), Melbourne, VIC, Australia.

Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia.

出版信息

Lancet Respir Med. 2025 Feb;13(2):130-140. doi: 10.1016/S2213-2600(24)00265-0. Epub 2024 Nov 29.

Abstract

BACKGROUND

Life-course lung function trajectories leading to airflow obstruction, as measured by impaired FEV/FVC (forced vital capacity), precede the onset of chronic obstructive pulmonary disease (COPD). We aimed to investigate whether individuals on impaired FEV/FVC trajectories have an increased burden of respiratory symptoms, including those who do not meet the spirometric criteria for COPD.

METHODS

We analysed serial life-course data from two population-based cohort studies separately, which included respiratory symptoms and spirometry: the Tasmanian Longitudinal Health Study (TAHS, Australia) cohort was recruited at age 6-7 years and followed up until middle age (mean age 53 years; range 51-55); and the Coronary Artery Risk Development in Young Adults (CARDIA, USA) cohort was recruited at a mean age of 25 years (range 18-30) and followed up to a mean age of 55 years (range 47-64). Participants' symptom profiles at ages 53 and 55 years were derived by latent class analysis. Symptom profiles were compared across pre-bronchodilator FEV/FVC trajectories derived by group-based modelling, then restricted to those without COPD defined by post-bronchodilator airflow obstruction (FEV/FVC <5th percentile) at ages 51-55 years and 47-64 years.

FINDINGS

Six FEV/FVC trajectories previously derived for TAHS were replicated in CARDIA. Optimal models identified five symptom profiles in TAHS (n=2421) and six in CARDIA (n=3153). For both cohorts, the most impaired FEV/FVC trajectory (early low, rapid decline in TAHS; low peak, rapid decline in CARDIA) was associated with predominant wheeze (multinomial odds ratio [mOR] 6·71 [95% CI 4·10-10·90] in TAHS and 9·90 [4·52-21·70] in CARDIA) and nearly all respiratory symptoms (4·95 [2·52-9·74] and 14·80 [5·97-36·60]) at age 51-55 years in TAHS and age 47-64 years in CARDIA, compared with the average trajectory. Among individuals belonging to the three most impaired trajectories, the associations with predominant wheeze increased with worsening FEV/FVC impairment and persisted when considering only those without spirometry-defined COPD. Additionally, for those belonging to the two rapid decline trajectories, both wheezing and usual phlegm or bronchitis were reported by 54 (20%) of 265 participants younger than 14 years in TAHS and by 31 (25%) of 123 participants aged 30 years or younger in CARDIA.

INTERPRETATION

In two independent cohorts that collected similar data, people on impaired FEV/FVC trajectories often had a longstanding history of both wheeze and phlegm or bronchitis, and wheeze was the predominant symptom in individuals aged 47-64 years among those who had not already progressed to COPD.

FUNDING

National Health and Medical Research Council (Australia); The University of Melbourne; Clifford Craig Medical Research Trust; Victorian, Queensland & Tasmanian Asthma Foundations; Royal Hobart Hospital Research Foundation; Helen MacPherson Smith Trust; GlaxoSmithKline; National Heart, Lung, and Blood Institute of the US National Institutes of Health.

摘要

背景

以FEV/FVC(用力肺活量)受损来衡量的、导致气流受限的终生肺功能轨迹先于慢性阻塞性肺疾病(COPD)的发病。我们旨在调查处于FEV/FVC轨迹受损状态的个体是否有更高的呼吸道症状负担,包括那些不符合COPD肺量计标准的个体。

方法

我们分别分析了两项基于人群的队列研究的系列终生数据,这些数据包括呼吸道症状和肺量计检查结果:塔斯马尼亚纵向健康研究(TAHS,澳大利亚)队列在6至7岁时招募,随访至中年(平均年龄53岁;范围51 - 55岁);青年成人冠状动脉风险发展研究(CARDIA,美国)队列平均年龄25岁(范围18 - 30岁)时招募,随访至平均年龄55岁(范围47 - 64岁)。通过潜在类别分析得出参与者在53岁和55岁时的症状特征。对基于群组建模得出的支气管扩张剂使用前FEV/FVC轨迹的症状特征进行比较,然后将范围限定为在51 - 55岁(TAHS)和47 - 64岁(CARDIA)时未被支气管扩张剂后气流受限(FEV/FVC<第5百分位数)定义为COPD的个体。

研究结果

先前在TAHS中得出的6条FEV/FVC轨迹在CARDIA中得到了重复。最佳模型在TAHS(n = 2421)中确定了5种症状特征,在CARDIA(n = 3153)中确定了6种。对于两个队列,FEV/FVC受损最严重的轨迹(TAHS中为早期低水平、快速下降;CARDIA中为低峰值、快速下降)与主要喘息相关(TAHS中多项比值比[mOR]为6.71[95%CI 4.10 - 10.90],CARDIA中为9.90[4.52 - 21.70]),并且与TAHS中51 - 55岁以及CARDIA中47 - 系中47 - 64岁时几乎所有呼吸道症状相关(分别为4.95[2.52 - 9.74]和14.80[5.97 - 36.60]),与平均轨迹相比。在属于受损最严重的三条轨迹的个体中,与主要喘息的关联随着FEV/FVC受损程度的加重而增加,并且在仅考虑那些没有肺量计定义的COPD的个体时仍然存在。此外,对于属于两条快速下降轨迹的个体,TAHS中265名14岁以下参与者中有54名(20%)报告有喘息和经常性咳痰或支气管炎,CARDIA中123名30岁及以下参与者中有31名(25%)报告有喘息和经常性咳痰或支气管炎。

解读

在两项收集了类似数据的独立队列研究中,处于FEV/FVC轨迹受损状态的人通常有长期的喘息和咳痰或支气管炎病史,并且在尚未发展为COPD的47 - 64岁个体中,喘息是主要症状。

资金来源

澳大利亚国家卫生与医学研究委员会;墨尔本大学;克利福德·克雷格医学研究信托基金;维多利亚州、昆士兰州和塔斯马尼亚州哮喘基金会;皇家霍巴特医院研究基金会;海伦·麦克弗森·史密斯信托基金;葛兰素史克公司;美国国立卫生研究院国家心肺血液研究所。

相似文献

6
Pulmonary rehabilitation for chronic obstructive pulmonary disease.慢性阻塞性肺疾病的肺康复治疗
Cochrane Database Syst Rev. 2015 Feb 23;2015(2):CD003793. doi: 10.1002/14651858.CD003793.pub3.

本文引用的文献

1
Implications of Race Adjustment in Lung-Function Equations.种族调整在肺功能方程中的影响。
N Engl J Med. 2024 Jun 13;390(22):2083-2097. doi: 10.1056/NEJMsa2311809. Epub 2024 May 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验