Evolution of Eczema, Wheeze, and Rhinitis from Infancy to Early Adulthood Four Birth Cohort Studies

被引:26
|
作者
Haider, Sadia [1 ]
Fontanella, Sara [1 ]
Ullah, Anhar [1 ]
Tumer, Stephen [3 ,4 ]
Simpson, Angela [5 ,6 ]
Roberts, Graham [7 ,9 ,10 ]
Murray, Clare S. [5 ,6 ]
Holloway, John W. [7 ,9 ]
Curtin, John A. [5 ,6 ]
Cullinan, Paul [1 ]
Arshad, Syed Hasan [8 ,9 ,10 ]
Hurault, Guillem [2 ]
Granell, Raquel [11 ]
Custovic, Adnan [1 ]
机构
[1] Natl Heart & Lung Inst, London, England
[2] Imperial Coll London, Fac Engn, Dept Bioengn, London, England
[3] Royal Aberdeen Childrens Hosp Natl Hlth Serv Gram, Aberdeen, Scotland
[4] Univ Aberdeen, Child Hlth, Aberdeen, Scotland
[5] Univ Manchester, Div Immunol Immun Infect & Resp Med, Manchester Acad Hlth Sci Ctr, Sch Biol Sci, Manchester, Lancs, England
[6] Manchester Univ Natl Hlth Serv Fdn Trust, Manchester, Lancs, England
[7] Univ Southampton, Fac Med, Human Dev & Hlth, Southampton, Hants, England
[8] Univ Southampton, Fac Med, Clin & Expt Sci, Southampton, Hants, England
[9] Univ Hosp Southampton NHS Fdn Trust, Natl Inst Hlth & Care Res, Southampton Biomed Res Ctr, Southampton, Hants, England
[10] David Hide Asthma & Allergy Res Ctr, Isle Of Wight, England
[11] Univ Bristol, Bristol Med Sch, MRC Integrat Epidemiol Unit, Populat Hlth Sci, Bristol, Avon, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
asthma; wheeze; eczema; atopic march; birth cohorts; ATOPIC-DERMATITIS; ASTHMA; CHILDREN; PHENOTYPES; COMORBIDITY; FILAGGRIN; EXPOSURE; ALLERGY; ONSET;
D O I
10.1164/rccm.202110-2418OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: The relationship between eczema, wheeze or asthma, and rhinitis is complex, and epidemiology and mechanisms of their comorbidities is unclear. Objectives: To investigate within-individual patterns of morbidity of eczema, wheeze, and rhinitis from birth to adolescence/early adulthood. Methods: We investigated onset, progression, and resolution of eczema, wheeze, and rhinitis using descriptive statistics, sequence mining, and latent Markov modeling in four population-based birth cohorts. We used logistic regression to ascertain if early-life eczema or wheeze, or genetic factors (filaggrin [FLG] mutations and 17q21 variants), increase the risk of multimorbidity. Measurements and Main Results: Single conditions, although the most prevalent, were observed significantly less frequently than by chance. There was considerable variation in the timing of onset/remission/persistence/intermittence. Multimorbidity of eczema+wheeze+rhinitis was rare but significantly overrepresented (three to six times more often than by chance). Although infantile eczema was associated with subsequent multimorbidity, most children with eczema (75.4%) did not progress to any multimorbidity pattern. FLG mutations and rs7216389 were not associated with persistence of eczema/wheeze as single conditions, but both increased the risk of multimorbidity (FLG by 2- to 3-fold, rs7216389 risk variant by 1.4- to 1.7-fold). Latent Markov modeling revealed five latent states (no disease/low risk, mainly eczema, mainly wheeze, mainly rhinitis, multimorbidity). The most likely transition to multimorbidity was from eczema state (0.21). However, although this was one of the highest transition probabilities, only one-fifth of those with eczema transitioned to multimorbidity. Conclusions: Atopic diseases fit a multimorbidity framework, with no evidence for sequential atopic march progression. The highest transition to multimorbidity was from eczema, but most children with eczema (more than three-quarters) had no comorbidities.
引用
收藏
页码:950 / 960
页数:11
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