Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center

Underlying medical causes of obesity (endocrine disorders, genetic obesity disorders, cerebral or medication-induced obesities) are thought to be rare. Even in specialized pediatric endocrinology clinics, low diagnostic yield is reported, but evidence is limited. Identifying these causes is vital fo...

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Veröffentlicht in:PloS one 2020-05, Vol.15 (5), p.e0232990
Hauptverfasser: Kleinendorst, Lotte, Abawi, Ozair, van der Voorn, Bibian, Jongejan, Mieke H T M, Brandsma, Annelies E, Visser, Jenny A, van Rossum, Elisabeth F C, van der Zwaag, Bert, Alders, Mariëlle, Boon, Elles M J, van Haelst, Mieke M, van den Akker, Erica L T
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container_issue 5
container_start_page e0232990
container_title PloS one
container_volume 15
creator Kleinendorst, Lotte
Abawi, Ozair
van der Voorn, Bibian
Jongejan, Mieke H T M
Brandsma, Annelies E
Visser, Jenny A
van Rossum, Elisabeth F C
van der Zwaag, Bert
Alders, Mariëlle
Boon, Elles M J
van Haelst, Mieke M
van den Akker, Erica L T
description Underlying medical causes of obesity (endocrine disorders, genetic obesity disorders, cerebral or medication-induced obesities) are thought to be rare. Even in specialized pediatric endocrinology clinics, low diagnostic yield is reported, but evidence is limited. Identifying these causes is vital for patient-tailored treatment. To present the results of a systematic diagnostic workup in children and adolescents referred to a specialized pediatric obesity center. This is a prospective observational study. Prevalence of underlying medical causes was determined after a multidisciplinary, systematic diagnostic workup including growth charts analysis, extensive biochemical and hormonal assessment and genetic testing in all patients. The diagnostic workup was completed in n = 282 patients. Median age was 10.8 years (IQR 7.7-14.1); median BMI +3.7SDS (IQR +3.3-+4.3). In 54 (19%) patients, a singular underlying medical cause was identified: in 37 patients genetic obesity, in 8 patients cerebral and in 9 patients medication-induced obesities. In total, thirteen different genetic obesity disorders were diagnosed. Obesity onset
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Even in specialized pediatric endocrinology clinics, low diagnostic yield is reported, but evidence is limited. Identifying these causes is vital for patient-tailored treatment. To present the results of a systematic diagnostic workup in children and adolescents referred to a specialized pediatric obesity center. This is a prospective observational study. Prevalence of underlying medical causes was determined after a multidisciplinary, systematic diagnostic workup including growth charts analysis, extensive biochemical and hormonal assessment and genetic testing in all patients. The diagnostic workup was completed in n = 282 patients. Median age was 10.8 years (IQR 7.7-14.1); median BMI +3.7SDS (IQR +3.3-+4.3). In 54 (19%) patients, a singular underlying medical cause was identified: in 37 patients genetic obesity, in 8 patients cerebral and in 9 patients medication-induced obesities. In total, thirteen different genetic obesity disorders were diagnosed. Obesity onset &lt;5 years (p = 0.04) and hyperphagia (p = 0.001) were indicators of underlying genetic causes, but only in patients without intellectual disability (ID). Patients with genetic obesity with ID more often had a history of neonatal feeding problems (p = 0.003) and short stature (p = 0.005). BMI-SDS was not higher in patients with genetic obesity disorders (p = 0.52). Patients with cerebral and medication-induced obesities had lower height-SDS than the rest of the cohort. To our knowledge, this is the first study to report the results of a systematic diagnostic workup aimed at identifying endocrine, genetic, cerebral or medication-induced causes of pediatric obesity. We found that a variety of singular underlying causes were identified in 19% of the patients with severe childhood obesity. 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This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Even in specialized pediatric endocrinology clinics, low diagnostic yield is reported, but evidence is limited. Identifying these causes is vital for patient-tailored treatment. To present the results of a systematic diagnostic workup in children and adolescents referred to a specialized pediatric obesity center. This is a prospective observational study. Prevalence of underlying medical causes was determined after a multidisciplinary, systematic diagnostic workup including growth charts analysis, extensive biochemical and hormonal assessment and genetic testing in all patients. The diagnostic workup was completed in n = 282 patients. Median age was 10.8 years (IQR 7.7-14.1); median BMI +3.7SDS (IQR +3.3-+4.3). In 54 (19%) patients, a singular underlying medical cause was identified: in 37 patients genetic obesity, in 8 patients cerebral and in 9 patients medication-induced obesities. In total, thirteen different genetic obesity disorders were diagnosed. Obesity onset &lt;5 years (p = 0.04) and hyperphagia (p = 0.001) were indicators of underlying genetic causes, but only in patients without intellectual disability (ID). Patients with genetic obesity with ID more often had a history of neonatal feeding problems (p = 0.003) and short stature (p = 0.005). BMI-SDS was not higher in patients with genetic obesity disorders (p = 0.52). Patients with cerebral and medication-induced obesities had lower height-SDS than the rest of the cohort. To our knowledge, this is the first study to report the results of a systematic diagnostic workup aimed at identifying endocrine, genetic, cerebral or medication-induced causes of pediatric obesity. We found that a variety of singular underlying causes were identified in 19% of the patients with severe childhood obesity. Because of this heterogeneity, an extensive diagnostic approach is needed to establish the underlying medical causes and to facilitate disease-specific, patient-tailored treatment.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32384097</pmid><doi>10.1371/journal.pone.0232990</doi><tpages>e0232990</tpages><orcidid>https://orcid.org/0000-0002-1343-6562</orcidid><orcidid>https://orcid.org/0000-0001-5352-9328</orcidid><orcidid>https://orcid.org/0000-0001-7182-3571</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Adolescent
Ambulatory Care Facilities
Biochemistry
Biology and Life Sciences
Brain Diseases - complications
Causes of
Child
Child health
Child, Preschool
Childhood
Childhood obesity
Children
Diagnosis
Diagnostic systems
Disabilities
Diseases
Disorders
Drug-Related Side Effects and Adverse Reactions - diagnosis
Drug-Related Side Effects and Adverse Reactions - etiology
Drugs
Endocrine disorders
Endocrine System Diseases - complications
Endocrinology
Female
Genetic research
Genetic screening
Genetic Testing
Genetics
Health services
Heterogeneity
Hospitals
Humans
Hyperphagia
Infant
Infant, Newborn
Intellectual disabilities
Intellectual Disability - complications
Internal medicine
Male
Medical diagnosis
Medical treatment
Medicine
Medicine and Health Sciences
Neonates
Netherlands
Newborn infants
Obesity
Outpatient care facilities
Patients
Pediatric Obesity - diagnosis
Pediatric Obesity - etiology
Pediatric Obesity - genetics
Pediatric research
Pediatrics
Phenotype
Prospective Studies
Short stature
Teenagers
Youth
title Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center
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