Reduced airway function in early adulthood among subjects with wheezing disorder before two years of age

被引:29
作者
Goksor, Emma [1 ]
Gustafsson, Per M. [2 ]
Alm, Bernt [1 ]
Amark, Mainor [1 ]
Wennergren, Goeran [1 ]
机构
[1] Univ Gothenburg, Queen Silvia Childrens Hosp, Dept Paediat, SE-41685 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Paediat Clin Physiol, Quen Silvia Childrens Hosp, Gothenburg, Sweden
关键词
asthma; female gender; lung function; outcome; wheezing;
D O I
10.1002/ppul.20798
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim: To compare airway function in early adulthood in subjects with wheezing in infancy with age-matched controls and to analyze what accounts for a possible difference. Methods: Asthma development has been prospectively studied in 101 children hospitalized due to wheezing before the age of two. The cohort was re-investigated at age 17-20 years and tested with spirometry and for bronchial hyper-responsiveness and allergic sensitization. An age-matched population (n = 294) was used for comparison. Results: The cohort had a significantly lower FEV1/FVC ratio and MEF50, both pre- and post-bronchodilation, compared with the controls, P < 0.01. The reduction in airway function was most evident in current asthmatic female subjects, but a reduced pre-bronchodilation FEV1/FVC ratio was also seen in symptom-free cohort subjects, P = 0.03. In the multivariate analysis, female gender was the most prominent independent risk factor for reduced airway function in early adulthood, pre-bronchodilation OR 4.0 (1.4-11.3) and post-bronchodilation OR 8.8 (1.8-42.0). In addition, a history of early wheezing, that is, belonging to the cohort, was an independent risk factor for reduced airway function pre-bronchodilation, OR 3.3 (1.3-8.7). Furthermore, there was an association between current bronchial hyper-responsiveness and an increased risk of reduced airway function post-bronchodilation, OR 7.3 (2.0-26.6). Conclusion: Reduced airway function in early adulthood was found in subjects with wheezing early in life, compared with age-matched controls. The reduction was most prominent in females with current asthma.
引用
收藏
页码:396 / 403
页数:8
相关论文
共 35 条
[11]   Effect of sex hormones on eosinophilic inflammation in nasal mucosa [J].
Hamano, N ;
Terada, N ;
Maesako, K ;
Numata, T ;
Konno, A .
ALLERGY AND ASTHMA PROCEEDINGS, 1998, 19 (05) :263-269
[12]   THE EFFECT OF MATERNAL SMOKING DURING PREGNANCY ON EARLY INFANT LUNG-FUNCTION [J].
HANRAHAN, JP ;
TAGER, IB ;
SEGAL, MR ;
TOSTESON, TD ;
CASTILE, RG ;
VANVUNAKIS, H ;
WEISS, ST ;
SPEIZER, FE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (05) :1129-1135
[13]   REFERENCE VALUES FOR LUNG-FUNCTION TESTS IN MEN - REGRESSION EQUATIONS WITH SMOKING VARIABLES [J].
HEDENSTROM, H ;
MALMBERG, P ;
FRIDRIKSSON, HV .
UPSALA JOURNAL OF MEDICAL SCIENCES, 1986, 91 (03) :299-310
[14]  
HEDENSTROM H, 1985, B EUR PHYSIOPATH RES, V21, P551
[15]   GENDER DIFFERENCES IN LUNG GROWTH [J].
HIBBERT, M ;
LANNIGAN, A ;
RAVEN, J ;
LANDAU, L ;
PHELAN, P .
PEDIATRIC PULMONOLOGY, 1995, 19 (02) :129-134
[16]   FACTORS IN CHILDHOOD AS PREDICTORS OF ASTHMA IN ADULT LIFE [J].
JENKINS, MA ;
HOPPER, JL ;
BOWES, G ;
CARLIN, JB ;
FLANDER, LB ;
GILES, GG .
BRITISH MEDICAL JOURNAL, 1994, 309 (6947) :90-93
[17]   CHILDHOOD ASTHMA AND ADULT LUNG-FUNCTION [J].
KELLY, WJW ;
HUDSON, I ;
RAVEN, J ;
PHELAN, PD ;
PAIN, MCF ;
OLINSKY, A .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 138 (01) :26-30
[18]   Asthma and airway hyper-responsiveness in adults who required hospital admission for bronchiolitis in early childhood [J].
Larouche, V ;
Rivard, G ;
Deschesnes, F ;
Goulet, R ;
Turcotte, H ;
Boulet, LP .
RESPIRATORY MEDICINE, 2000, 94 (03) :288-294
[19]   GROWTH OF AIRWAYS AND AIR SPACES IN TEENAGERS IS RELATED TO SEX BUT NOT TO SYMPTOMS [J].
MERKUS, PJFM ;
BORSBOOM, GJJM ;
VANPELT, W ;
SCHRADER, PC ;
VANHOUWELINGEN, HC ;
KERREBIJN, KF ;
QUANJER, PH .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 75 (05) :2045-2053
[20]   Therapeutic implications of sex differences in asthma and atopy [J].
Osman, M .
ARCHIVES OF DISEASE IN CHILDHOOD, 2003, 88 (07) :587-590