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Mental and Somatic Conditions in Children With the Broad Avoidant Restrictive Food Intake Disorder Phenotype
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden; Neuroendocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; Translational Developmental Neuroscience Section, Division of Psychological and Social Medicine and Developmental Neurosciences, Faculty of Medicine, TU Dresden, Dresden, Germany.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
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2025 (English)In: JAMA pediatrics, ISSN 2168-6203, E-ISSN 2168-6211, Vol. 79, no 4, p. 428-437Article in journal (Refereed) Published
Abstract [en]

IMPORTANCE: Avoidant restrictive food intake disorder (ARFID) is a feeding and eating disorder characterized by limited variety and/or quantity of food intake impacting physical health and psychosocial functioning. Children with ARFID often present with diverse psychiatric and somatic symptoms and therefore consult various pediatric subspecialties. Large-scale studies mapping coexisting conditions are, however, lacking.

OBJECTIVE: To characterize the health care needs of youth with ARFID.

DESIGN, SETTING, AND PARTICIPANTS: This cohort study used the Child and Adolescent Twin Study in Sweden (CATSS), in combination with inpatient and specialized outpatient clinical diagnoses from the Swedish National Patient Register. Data were collected from July 2004 to April 2020, and data were analyzed from September 2022 to February 2024.

EXPOSURE: Using a composite measure derived from parent or guardian reports and register data, children with the broad ARFID phenotype occurring between the ages of 6 to 12 years were identified, as well as children without ARFID. MAIN OUTCOMES AND MEASURES: From more than 1000 diagnostic International Classification of Diseases (ICD) codes, mental and somatic conditions within or across ICD chapters, the number of distinct per-person diagnoses, and inpatient treatment days between participants' birth and 18th birthdays were specified (90 outcomes). Hazard ratios (HRs) and incidence rate ratios (IRRs) were calculated.

RESULTS: Of 30 795 CATSS participants, a total of 616 children (2.0%) with the broad ARFID phenotype occurring between the ages of 6 to 12 years were identified, and 30 179 children without ARFID were identified. Of 616 children with ARFID, 241 children were female (39.1%). Relative risks of neurodevelopmental, gastrointestinal, endocrine or metabolic, respiratory, neurological, and allergic disorders were substantially increased in children with ARFID (eg, autism: HR, 9.7; 95% CI, 7.5-12.5; intellectual disability: HR, 10.3; 95% CI, 7.6-13.9; gastroesophageal reflux disease: HR, 6.7; 95% CI, 4.6-9.9; pituitary conditions: HR, 5.6; 95% CI, 2.7-11.3; chronic lower respiratory diseases: HR, 4.9; 95% CI, 2.4-10.1; and epilepsy: HR, 5.8; 95% CI, 4.1-8.2). ARFID was not associated with elevated risks of autoimmune illnesses and obsessive-compulsive disorder. Children with ARFID had significantly more distinct mental diagnoses (IRR, 4.7; 95% CI, 4.0-5.4) and longer hospital stays (IRR, 5.5; 95% CI, 1.7-17.6) compared with children without ARFID. Children with ARFID were diagnosed with a mental condition earlier than children without ARFID. No sex-specific differences emerged.

CONCLUSIONS AND RELEVANCE: This cohort study yields the broadest and most detailed evidence of coexisting mental and somatic conditions in the largest sample of children with ARFID to date. Findings suggest a complex pattern of health needs in youth with ARFID, underscoring the critical importance of attention to the illness across all pediatric specialties.

Place, publisher, year, edition, pages
American Medical Association (AMA), 2025. Vol. 79, no 4, p. 428-437
National Category
Psychiatry
Identifiers
URN: urn:nbn:se:oru:diva-119324DOI: 10.1001/jamapediatrics.2024.6065ISI: 001428016900001PubMedID: 39960738Scopus ID: 2-s2.0-105003099920OAI: oai:DiVA.org:oru-119324DiVA, id: diva2:1938300
Funder
Swedish Research Council, 538-2013-8864Swedish Society for Medical Research (SSMF), PG-22-0478Swedish Psychiatric FoundationFredrik och Ingrid Thurings Stiftelse, 2021-00660
Note

Funding Agencies:

Dr Wronski was supported by the Endocrine Society (Research Experiences for Graduate and Medical Students program), the Else Kröner-Fresenius Foundation (structured doctoral program), and the German National Academic Scholarship Foundation. Dr Bulik was supported by the US National Institute of Mental Health (R56MH129437, R01MH120170, R01MH124871, R01MH119084, R01MH118278, and R01MH124871), the Swedish Research Council (Vetenskapsrådet, award 538-2013-8864), and the Lundbeck Foundation (R276-2018-4581). Dr Dinkler was supported by the Swedish Society for Medical Research (SSMF, PG-22-0478), the Swedish Mental Health Foundation (Fonden för Psykisk Hälsa, 2022 and 2023), and the Fredrik and Ingrid Thurings Foundation (2021-00660).

Available from: 2025-02-18 Created: 2025-02-18 Last updated: 2026-01-23Bibliographically approved

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