Prediction of adult asthma risk in early childhood using novel adult asthma predictive risk scores

被引:5
|
作者
Farhan, Abdal J. [1 ,2 ]
Kothalawala, Dilini M. [3 ,4 ]
Kurukulaaratchy, Ramesh J. [1 ,2 ,3 ]
Granell, Raquel [5 ]
Simpson, Angela [6 ,7 ]
Murray, Clare
Custovic, Adnan [8 ]
Roberts, Graham [1 ,2 ,3 ]
Zhang, Hongmei [9 ]
Arshad, S. Hasan [1 ,2 ,3 ]
机构
[1] St Marys Hosp, David Hide Asthma & Allergy Res Ctr, Isle of Wight, England
[2] Univ Southampton, Clin & Expt Sci, Fac Med, Southampton, Hants, England
[3] Univ Hosp Southampton, NIHR Biomed Res Ctr, Southampton, Hants, England
[4] Univ Southampton, Human Dev & Hlth, Fac Med, Southampton, Hants, England
[5] Univ Bristol, Bristol Med Sch, MRC Integrat Epidemiol Unit, Populat Hlth Sci, Bristol, Avon, England
[6] Univ Manchester, Manchester Acad Hlth Sci Ctr, Sch Biol Sci, Div Infect Immun & Resp Med, Manchester, Lancs, England
[7] Manchester Univ NHS Fdn Trust, Manchester, Lancs, England
[8] Imperial Coll London, Natl Heart & Lung Inst, London, England
[9] Univ Memphis, Sch Publ Hlth, Div Epidemiol Biostat & Environm Hlth, Memphis, TN USA
基金
英国惠康基金; 美国国家卫生研究院; 英国医学研究理事会;
关键词
allergic sensitisation; asthma; prediction; risk scores; wheeze; HOUSE-DUST MITE; ALLERGEN-SPECIFIC IMMUNOTHERAPY; TERM SUBLINGUAL IMMUNOTHERAPY; QUALITY-OF-LIFE; DOUBLE-BLIND; PERSISTENT ASTHMA; CLINICAL-EFFICACY; PRESCHOOL-CHILDREN; END-POINTS; RHINITIS;
D O I
10.1111/all.15876
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Numerous risk scores have been developed to predict childhood asthma. However, they may not predict asthma beyond childhood. We aim to create childhood risk scores that predict development and persistence of asthma up to young adult life. Methods: The Isle of Wight Birth Cohort (n = 1456) was prospectively assessed up to 26 years of age. Asthma predictive scores were developed based on factors during the first 4 years, using logistic regression and tested for sensitivity, specificity and area under the curve (AUC) for prediction of asthma at (i) 18 and (ii) 26 years, and persistent asthma (PA) (iii) at 10 and 18 years, and (iv) at 10, 18 and 26 years. Models were internally and externally validated. Results: Four models were generated for prediction of each asthma outcome. ASthma PredIctive Risk scorE ( ASPIRE)-1: a 2-factor model (recurrent wheeze [RW] and positive skin prick test [+SPT] at 4 years) for asthma at 18 years (sensitivity: 0.49, specificity: 0.80, AUC: 0.65). ASPIRE-2: a 3-factor model (RW, +SPT and maternal rhinitis) for asthma at 26 years (sensitivity: 0.60, specificity: 0.79, AUC: 0.73). ASPIRE-3: a 3-factor model (RW, +SPT and eczema at 4 years) for PA-18 (sensitivity: 0.63, specificity: 0.87, AUC: 0.77). ASPIRE-4: a 3-factor model (RW, +SPT at 4 years and recurrent chest infection at 2 years) for PA-26 (sensitivity: 0.68, specificity: 0.87, AUC: 0.80). ASPIRE-1 and ASPIRE-3 scores were replicated externally. Further assessments indicated that ASPIRE-1 can be used in place of ASPIRE-2- 4 with same predictive accuracy. Conclusion: ASPIRE predicts persistent asthma up to young adult life.
引用
收藏
页码:2969 / 2979
页数:11
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