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Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences
BACKGROUND: Gender and sex differences in the development of children and adolescents are commonly found in the psychiatric examination. Family and developmental history is an important part of the clinical diagnostic interview, the basic examination technique. Attention-deficit/hyperactivity disord...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390694/ https://www.ncbi.nlm.nih.gov/pubmed/37533883 http://dx.doi.org/10.3389/fpsyt.2023.1072735 |
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author | Waltereit, Johanna Zimmer, Jonas Roessner, Veit Waltereit, Robert |
author_facet | Waltereit, Johanna Zimmer, Jonas Roessner, Veit Waltereit, Robert |
author_sort | Waltereit, Johanna |
collection | PubMed |
description | BACKGROUND: Gender and sex differences in the development of children and adolescents are commonly found in the psychiatric examination. Family and developmental history is an important part of the clinical diagnostic interview, the basic examination technique. Attention-deficit/hyperactivity disorder (ADHD) is associated with diagnosis-specific markers in family and development history. However, it is unclear to what extent ADHD-specific signs and narratives differ between females and males. The aim of this study was to assess and to compare the family and developmental history profiles of female versus male adolescents with ADHD. METHODS: Data were collected using the clinical diagnostic interview technique from parents of female and male patients diagnosed with ADHD (ICD-10 F90.0, F90.1 and F98.8) between the ages of 12 and 17 years (n = 92). The two groups were matched in pairs for sex, IQ and ICD-10 diagnosis (F90.0, F90.1 and F98.8). Interview data were operationalized in three categories: 0 - physiological marker, 1 - subclinical marker, 2 - clinical marker. The two groups were compared with two-way ANOVA. RESULTS: Information about female in comparison to male adolescents were reported in the parental interview with few differences. CONCLUSION: Our study suggests that family and developmental history of the neurodevelopmental disorder ADHD is only poorly influenced by gender or sex. |
format | Online Article Text |
id | pubmed-10390694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103906942023-08-02 Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences Waltereit, Johanna Zimmer, Jonas Roessner, Veit Waltereit, Robert Front Psychiatry Psychiatry BACKGROUND: Gender and sex differences in the development of children and adolescents are commonly found in the psychiatric examination. Family and developmental history is an important part of the clinical diagnostic interview, the basic examination technique. Attention-deficit/hyperactivity disorder (ADHD) is associated with diagnosis-specific markers in family and development history. However, it is unclear to what extent ADHD-specific signs and narratives differ between females and males. The aim of this study was to assess and to compare the family and developmental history profiles of female versus male adolescents with ADHD. METHODS: Data were collected using the clinical diagnostic interview technique from parents of female and male patients diagnosed with ADHD (ICD-10 F90.0, F90.1 and F98.8) between the ages of 12 and 17 years (n = 92). The two groups were matched in pairs for sex, IQ and ICD-10 diagnosis (F90.0, F90.1 and F98.8). Interview data were operationalized in three categories: 0 - physiological marker, 1 - subclinical marker, 2 - clinical marker. The two groups were compared with two-way ANOVA. RESULTS: Information about female in comparison to male adolescents were reported in the parental interview with few differences. CONCLUSION: Our study suggests that family and developmental history of the neurodevelopmental disorder ADHD is only poorly influenced by gender or sex. Frontiers Media S.A. 2023-07-17 /pmc/articles/PMC10390694/ /pubmed/37533883 http://dx.doi.org/10.3389/fpsyt.2023.1072735 Text en Copyright © 2023 Waltereit, Zimmer, Roessner and Waltereit. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Waltereit, Johanna Zimmer, Jonas Roessner, Veit Waltereit, Robert Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title | Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title_full | Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title_fullStr | Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title_full_unstemmed | Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title_short | Family and developmental history of female versus male adolescents with ADHD: diagnosis-specific overlap, few gender/sex differences |
title_sort | family and developmental history of female versus male adolescents with adhd: diagnosis-specific overlap, few gender/sex differences |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390694/ https://www.ncbi.nlm.nih.gov/pubmed/37533883 http://dx.doi.org/10.3389/fpsyt.2023.1072735 |
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