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Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample

BACKGROUND: Identifying children with childhood-onset neurodevelopmental problems (NDPs, defined here as autism spectrum disorders [ASDs], attention-deficit/hyperactivity disorder [AD/HD], tic disorders [TDs], learning disorders [LDs] and development coordination disorder), using easily administered...

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Autores principales: Larson, Tomas, Lundström, Sebastian, Nilsson, Thomas, Selinus, Eva Norén, Råstam, Maria, Lichtenstein, Paul, Gumpert, Clara Hellner, Anckarsäter, Henrik, Kerekes, Nóra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849508/
https://www.ncbi.nlm.nih.gov/pubmed/24066834
http://dx.doi.org/10.1186/1471-244X-13-233
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author Larson, Tomas
Lundström, Sebastian
Nilsson, Thomas
Selinus, Eva Norén
Råstam, Maria
Lichtenstein, Paul
Gumpert, Clara Hellner
Anckarsäter, Henrik
Kerekes, Nóra
author_facet Larson, Tomas
Lundström, Sebastian
Nilsson, Thomas
Selinus, Eva Norén
Råstam, Maria
Lichtenstein, Paul
Gumpert, Clara Hellner
Anckarsäter, Henrik
Kerekes, Nóra
author_sort Larson, Tomas
collection PubMed
description BACKGROUND: Identifying children with childhood-onset neurodevelopmental problems (NDPs, defined here as autism spectrum disorders [ASDs], attention-deficit/hyperactivity disorder [AD/HD], tic disorders [TDs], learning disorders [LDs] and development coordination disorder), using easily administered screening instruments, is a prerequisite for epidemiological research. Such instruments are also clinically useful to prioritize children for comprehensive assessments, to screen risk groups, and to follow controls. Autism–Tics, ADHD, and other Co-morbidities inventory (A-TAC) was developed to meet these requirements; here the A-TAC’s prospective and psychometric properties are examined, when used in a population-based, epidemiological setting. METHODS: Since 2004, parents of all Swedish twins have been asked to take part in an ongoing, nation-wide twin study (The Child and Adolescent Twin Study in Sweden). The study includes the A-TAC, carried out as a telephone interview with parents of twins aged 9 or 12. In the present study, screen-positive twins from three birth year cohorts (1993–1995) were invited to a comprehensive clinical follow-up (blinded for previous screening results) together with their co-twins and randomly selected, healthy controls at age 15 (Total N = 452). RESULTS: Sensitivity and specificity of A-TAC scores for predicting later clinical diagnoses were good to excellent overall, with values of the area under the receiver operating characteristics curves ranging from 0.77 (AD/HD) to 0.91 (ASDs). Among children who were screen-positive for an ASD, 48% received a clinical diagnosis of ASDs. For AD/HD, the corresponding figure was also 48%, for LDs 16%, and for TDs 60%. Between 4% and 35% of screen-positive children did not receive any diagnosis at the clinical follow-up three years later. Among screen-negative controls, prevalence of ASDs, AD/HD, LDs, and TDs was 0%, 7%, 4%, and 2%, respectively. CONCLUSIONS: The A–TAC appeared to be a valid instrument to assess NDPs in this population-based, longitudinal study. It has good-to-excellent psychometric properties, with an excellent ability to distinguish NDPs (mainly ASDs) from non-NDPs at least three years after the screening evaluations, although specific diagnoses did not correspond closely to actual clinical diagnoses.
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spelling pubmed-38495082013-12-05 Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample Larson, Tomas Lundström, Sebastian Nilsson, Thomas Selinus, Eva Norén Råstam, Maria Lichtenstein, Paul Gumpert, Clara Hellner Anckarsäter, Henrik Kerekes, Nóra BMC Psychiatry Research Article BACKGROUND: Identifying children with childhood-onset neurodevelopmental problems (NDPs, defined here as autism spectrum disorders [ASDs], attention-deficit/hyperactivity disorder [AD/HD], tic disorders [TDs], learning disorders [LDs] and development coordination disorder), using easily administered screening instruments, is a prerequisite for epidemiological research. Such instruments are also clinically useful to prioritize children for comprehensive assessments, to screen risk groups, and to follow controls. Autism–Tics, ADHD, and other Co-morbidities inventory (A-TAC) was developed to meet these requirements; here the A-TAC’s prospective and psychometric properties are examined, when used in a population-based, epidemiological setting. METHODS: Since 2004, parents of all Swedish twins have been asked to take part in an ongoing, nation-wide twin study (The Child and Adolescent Twin Study in Sweden). The study includes the A-TAC, carried out as a telephone interview with parents of twins aged 9 or 12. In the present study, screen-positive twins from three birth year cohorts (1993–1995) were invited to a comprehensive clinical follow-up (blinded for previous screening results) together with their co-twins and randomly selected, healthy controls at age 15 (Total N = 452). RESULTS: Sensitivity and specificity of A-TAC scores for predicting later clinical diagnoses were good to excellent overall, with values of the area under the receiver operating characteristics curves ranging from 0.77 (AD/HD) to 0.91 (ASDs). Among children who were screen-positive for an ASD, 48% received a clinical diagnosis of ASDs. For AD/HD, the corresponding figure was also 48%, for LDs 16%, and for TDs 60%. Between 4% and 35% of screen-positive children did not receive any diagnosis at the clinical follow-up three years later. Among screen-negative controls, prevalence of ASDs, AD/HD, LDs, and TDs was 0%, 7%, 4%, and 2%, respectively. CONCLUSIONS: The A–TAC appeared to be a valid instrument to assess NDPs in this population-based, longitudinal study. It has good-to-excellent psychometric properties, with an excellent ability to distinguish NDPs (mainly ASDs) from non-NDPs at least three years after the screening evaluations, although specific diagnoses did not correspond closely to actual clinical diagnoses. BioMed Central 2013-09-25 /pmc/articles/PMC3849508/ /pubmed/24066834 http://dx.doi.org/10.1186/1471-244X-13-233 Text en Copyright © 2013 Larson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Larson, Tomas
Lundström, Sebastian
Nilsson, Thomas
Selinus, Eva Norén
Råstam, Maria
Lichtenstein, Paul
Gumpert, Clara Hellner
Anckarsäter, Henrik
Kerekes, Nóra
Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title_full Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title_fullStr Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title_full_unstemmed Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title_short Predictive properties of the A-TAC inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
title_sort predictive properties of the a-tac inventory when screening for childhood-onset neurodevelopmental problems in a population-based sample
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849508/
https://www.ncbi.nlm.nih.gov/pubmed/24066834
http://dx.doi.org/10.1186/1471-244X-13-233
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