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

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          Abstract

          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.

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          Author and article information

          Journal
          Am J Respir Crit Care Med
          American journal of respiratory and critical care medicine
          American Thoracic Society
          1535-4970
          1073-449X
          Oct 15 2022
          : 206
          : 8
          Affiliations
          [1 ] National Heart and Lung Institute and.
          [2 ] Royal Aberdeen Children's Hospital National Health Service Grampian Aberdeen, Aberdeen, United Kingdom.
          [3 ] Child Health, University of Aberdeen, Aberdeen, United Kingdom.
          [4 ] Division of Immunology, Immunity to Infection and Respiratory Medicine, School of Biological Sciences, The University of Manchester, Manchester Academic Health Science Centre, and Manchester University National Health Service Foundation Trust, Manchester, United Kingdom.
          [5 ] Human Development and Health and.
          [6 ] National Institute for Health and Care Research Southampton Biomedical Research Centre, University Hospitals Southampton NHS Foundation Trust, Southampton, United Kingdom.
          [7 ] David Hide Asthma and Allergy Research Centre, Isle of Wight, United Kingdom; and.
          [8 ] Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
          [9 ] Faculty of Engineering, Department of Bioengineering, Imperial College London, London, United Kingdom.
          [10 ] MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
          Article
          10.1164/rccm.202110-2418OC
          35679320
          739676f7-e637-4c47-b8fe-f72e22e7d36e
          History

          wheeze,asthma,eczema,birth cohorts,atopic march
          wheeze, asthma, eczema, birth cohorts, atopic march

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