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      Comorbidities in childhood atopic dermatitis: A population‐based study

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          Abstract

          Background

          Atopic dermatitis (AD) is a chronic inflammatory skin disease that is associated with allergic comorbidities. However, studies examining comorbidities in childhood AD are incomplete, which may contribute to suboptimal care.

          Objective

          The objective was to compare the risk of developing different allergic and non‐allergic comorbidities among children with AD to that of a matched non‐AD reference cohort in Sweden.

          Methods

          This was a nationwide population‐based cohort study using longitudinal data from primary and specialist care registers. Patients with AD were identified by confirmed diagnosis in primary or specialist care. The non‐AD reference cohort was randomly drawn from the general population and matched 1:1 with the AD patients. The risk of developing the following conditions was evaluated: hypersensitivity and allergic disorders, neurological disorders, psychiatric disorders, infections, immunological and inflammatory disorders, Type 1 diabetes (T1D), endocrine and metabolic disorders, skeletal disorders, ocular disorders and malignancies.

          Results

          This study included 165,145 patients with AD (mild‐to‐moderate [ n = 126,681] and severe [ n = 38,464]) and an equally sized reference cohort. Patients with AD displayed a higher risk of developing comorbid conditions for all investigated categories, except for T1D and skeletal disorders, compared with the reference cohort. The highest risk compared with the reference cohort was observed for hypersensitivity and allergic disorders (hazard ratio [HR]: 3.87), followed by malignancies (HR: 2.53) and immunological and inflammatory disorders (HR: 2.36). Patients with AD also had higher risk of developing multiple comorbidities (≥2). The risk of comorbidity onset increased alongside AD severity and patients with active AD were associated with increased risk of comorbidity onset compared with patients in remission.

          Conclusions

          The clinical burden of AD is substantial for children with AD and patients are at an increased risk of developing several comorbid conditions extending beyond the atopic march. Our results also showed a positive association between worsening severity of AD and an increased risk of comorbidity onset.

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          The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.

          Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalizability. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included in an accurate and complete report of an observational study. We defined the scope of the recommendations to cover three main study designs: cohort, case-control and cross-sectional studies. We convened a two-day workshop, in September 2004, with methodologists, researchers and journal editors to draft a checklist of items. This list was subsequently revised during several meetings of the coordinating group and in e-mail discussions with the larger group of STROBE contributors, taking into account empirical evidence and methodological considerations. The workshop and the subsequent iterative process of consultation and revision resulted in a checklist of 22 items (the STROBE Statement) that relate to the title, abstract, introduction, methods, results and discussion sections of articles. Eighteen items are common to all three study designs and four are specific for cohort, case-control, or cross-sectional studies. A detailed Explanation and Elaboration document is published separately and is freely available on the web sites of PLoS Medicine, Annals of Internal Medicine and Epidemiology. We hope that the STROBE Statement will contribute to improving the quality of reporting of observational studies.
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            The Environment and Disease: Association or Causation?

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              Filaggrin mutations associated with skin and allergic diseases.

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                Author and article information

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                Journal
                Journal of the European Academy of Dermatology and Venereology
                Acad Dermatol Venereol
                Wiley
                0926-9959
                1468-3083
                February 2024
                October 22 2023
                February 2024
                : 38
                : 2
                : 354-364
                Affiliations
                [1 ] Department of Occupational and Environmental Dermatology Skåne University Hospital, Lund University Lund Sweden
                [2 ] Inflammation and Immunology Pfizer AB Stockholm Sweden
                [3 ] Department of Medical Sciences Uppsala University Uppsala Sweden
                [4 ] Institute of Environmental Medicine Karolinska Institutet Stockholm Sweden
                [5 ] Department of Dermatology and Sexual Health Södersjukhuset Stockholm Sweden
                [6 ] Department of Clinical Science and Education Södersjukhuset, Karolinska Institutet Stockholm Sweden
                [7 ] Inflammation and Immunology Pfizer Inc. Collegeville Pennsylvania USA
                [8 ] Quantify Research AB Stockholm Sweden
                [9 ] Dermatology and Venereology, Department of Public Health and Clinical Medicine Umeå University Umeå Sweden
                [10 ] Department of Dermatology Skåne University Hospital Malmö Sweden
                [11 ] Inflammation and Immunology Pfizer Inc. New York New York USA
                [12 ] Global Biometrics and Data Management (Statistics) Pfizer Inc. Groton Connecticut USA
                [13 ] Department of Dermatology and Venereology Bispebjerg Hospital, University of Copenhagen Copenhagen Denmark
                Article
                10.1111/jdv.19569
                37824103
                6a4fd76c-ae10-4d85-88ed-28fe1b67e475
                © 2024

                http://creativecommons.org/licenses/by-nc/4.0/

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