Literature DB >> 22541400

Using latent class growth analysis to identify childhood wheeze phenotypes in an urban birth cohort.

Qixuan Chen1, Allan C Just, Rachel L Miller, Matthew S Perzanowski, Inge F Goldstein, Frederica P Perera, Robin M Whyatt.   

Abstract

BACKGROUND: To advance asthma cohort research, we need a method that can use longitudinal data, including when collected at irregular intervals, to model multiple phenotypes of wheeze and identify both time-invariant (eg, sex) and time-varying (eg, environmental exposure) risk factors.
OBJECTIVE: To demonstrate the use of latent class growth analysis (LCGA) in defining phenotypes of wheeze and examining the effects of causative factors, using repeated questionnaires in an urban birth cohort study.
METHODS: We gathered repeat questionnaire data on wheeze from 689 children ages 3 through 108 months (n = 7,048 questionnaires) and used LCGA to identify wheeze phenotypes and model the effects of time-invariant (maternal asthma, ethnicity, prenatal environmental tobacco smoke, and child sex) and time-varying (cold/influenza [flu] season) risk factors on prevalence of wheeze in each phenotype.
RESULTS: LCGA identified four wheezing phenotypes: never/infrequent (47.1%), early-transient (37.5%), early-persistent (7.6%), and late-onset (7.8%). Compared with children in the never/infrequent phenotype, maternal asthma was a risk factor for the other 3 phenotypes; Dominican versus African American ethnicity was a risk factor for the early-transient phenotype; and male sex was a risk factor for the early-persistent phenotype. The prevalence of wheeze was higher during the cold/flu season than otherwise among children in the early-persistent phenotype (P = .08).
CONCLUSION: This is the first application of LCGA to identify wheeze phenotypes in asthma research. Unlike other methods, this modeling technique can accommodate questionnaire data collected at irregularly spaced age intervals and can simultaneously identify multiple trajectories of health outcomes and associations with time-invariant and time-varying causative factors.
Copyright © 2012 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22541400      PMCID: PMC3371648          DOI: 10.1016/j.anai.2012.02.016

Source DB:  PubMed          Journal:  Ann Allergy Asthma Immunol        ISSN: 1081-1206            Impact factor:   6.347


  18 in total

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Authors:  R L Miller; G L Chew; C A Bell; S A Biedermann; M Aggarwal; P L Kinney; W Y Tsai; R M Whyatt; F P Perera; J G Ford
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Review 4.  Impact of gender on asthma in childhood and adolescence: a GA2LEN review.

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Journal:  Allergy       Date:  2007-09-05       Impact factor: 13.146

5.  Characterization of wheezing phenotypes in the first 10 years of life.

Authors:  R J Kurukulaaratchy; M H Fenn; L M Waterhouse; S M Matthews; S T Holgate; S H Arshad
Journal:  Clin Exp Allergy       Date:  2003-05       Impact factor: 5.018

Review 6.  Recurrent wheezing illness in preschool-aged children: assessment and management in primary care practice.

Authors:  Gordon R Bloomberg
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7.  Cat ownership is a risk factor for the development of anti-cat IgE but not current wheeze at age 5 years in an inner-city cohort.

Authors:  Matthew S Perzanowski; Ginger L Chew; Adnan Divjan; Alina Johnson; Inge F Goldstein; Robin S Garfinkel; Lori A Hoepner; Thomas A E Platts-Mills; Frederica P Perera; Rachel L Miller
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Authors:  Rosalind L Smyth
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8.  Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood.

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10.  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.

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