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Validation of novel wheeze phenotypes using longitudinal airway function and atopic sensitization data in the first 6 years of life: Evidence from the Southampton Women's survey
被引:37
作者:
Collins, Samuel A.
[1
,2
,3
]
Pike, Katharine C.
[1
,2
,3
]
Inskip, Hazel M.
[1
,4
]
Godfrey, Keith M.
[1
,2
,3
,4
]
Roberts, Graham
[1
,2
,3
]
Holloway, John W.
[1
]
Lucas, Jane S. A.
[1
,2
,3
]
机构:
[1] Univ Southampton, Fac Med, Southampton SO9 5NH, Hants, England
[2] Univ Southampton, NIHR Southampton Biomed Res Ctr, Southampton, Hants, England
[3] Univ Hosp Southampton NHS Fdn Trust, Southampton SO16 6YD, Hants, England
[4] Univ Southampton, Southampton Med Res Council, Lifecourse Epidemiol Unit, Southampton, Hants, England
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
wheeze;
asthma;
phenotype;
lung function;
cohort;
atopy;
LUNG-FUNCTION;
CHILDHOOD ASTHMA;
BIRTH;
RESPONSIVENESS;
POLYMORPHISMS;
SYMPTOMS;
GROWTH;
EXPOSURE;
CHILDREN;
INFANCY;
D O I:
10.1002/ppul.22766
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Background In 1995 the Tucson Children's Respiratory Study (TCRS) identified clinically distinct phenotypes amongst early wheezers; the Avon Longitudinal Study of Parents And Children (ALSPAC) has recently re-examined these. Objectives To validate statistically derived ALSPAC phenotypes in the Southampton Women's Survey (SWS) using infant and 6-year lung function, and allergic sensitization at 1, 3, and 6 years, comparing these with TCRS phenotypes. Methods Complete 6-year follow-up data were available for 926 children, selected from 1,973 infants born to 12,579 women characterized pre-conception. Ninety-five children had V'maxFRC and FEV0.4 measured age 5-14 weeks using rapid compression/raised volume techniques. At 6 years we performed spirometry (n=791), fractional exhaled nitric oxide (FeNO, n=589) and methacholine challenge (n=234). Skin prick testing was performed at 12m, 3 and 6 years (n=1,494, 1,255, 699, respectively). Using wheeze status questionnaire data at 6m, 12m, 2, 3 and 6 years we classified children into TCRS (never, transient early, persistent, late-onset) and ALSPAC based groups (never, early, transient, intermediate-onset, late-onset, persistent). Results Amongst ALSPAC groups, persistent and late-onset wheeze were associated with atopy at 3 and 6 years, whilst intermediate-onset wheeze showed earlier atopic association at 1 year; all three were associated with FeNO at 6 years. Persistent wheezers had lower infant (V'maxFRC P<0.05) and 6-year lung function (FEV1, FEV1/FVC, and FEF25-75, P<0.05), whilst late and intermediate-onset wheezers showed no lung function deficits. Transient wheezers were non-atopic but showed persistent lung function deficits (V'maxFRC in infancy, FEV1 and FEF25-75 at 6 years, all P<0.05). Those who wheezed only in the first year (early phenotype) showed no lung function deficits. No associations were seen with 6 years bronchial hyper-responsiveness or infancy FEV0.4. Conclusion SWS cohort data validates the statistically derived ALSPAC six-class model. In particular, lung function and atopy successfully differentiate persistent, late-onset and intermediate-onset wheeze, whilst the Tucson transient early wheeze phenotype can be sub-classified into groups that reflect early lung function. Since the 4-class model fails to adequately differentiate phenotypes based on lung function and atopy, we propose that strong consideration be given to using the 6-class paradigm for longitudinal outcome work in wheezing with onset in early life. Pediatr Pulmonol. 2013; 48:683-692. (c) 2013 Wiley Periodicals, Inc.
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页码:683 / 692
页数:10
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