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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-3849508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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