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Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis

OBJECTIVE: To compare the reported accuracy and sensitivity of the various modalities used to diagnose autism spectrum disorders (ASD) in efforts to help focus further biomarker research on the most promising methods for early diagnosis. METHODS: The Medline scientific literature database was search...

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Autores principales: Ansel, Ashley, Posen, Yehudit, Ellis, Ronald, Deutsch, Lisa, Zisman, Philip D., Gesundheit, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rambam Health Care Campus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824829/
https://www.ncbi.nlm.nih.gov/pubmed/31675302
http://dx.doi.org/10.5041/RMMJ.10375
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author Ansel, Ashley
Posen, Yehudit
Ellis, Ronald
Deutsch, Lisa
Zisman, Philip D.
Gesundheit, Benjamin
author_facet Ansel, Ashley
Posen, Yehudit
Ellis, Ronald
Deutsch, Lisa
Zisman, Philip D.
Gesundheit, Benjamin
author_sort Ansel, Ashley
collection PubMed
description OBJECTIVE: To compare the reported accuracy and sensitivity of the various modalities used to diagnose autism spectrum disorders (ASD) in efforts to help focus further biomarker research on the most promising methods for early diagnosis. METHODS: The Medline scientific literature database was searched to identify publications assessing potential clinical ASD biomarkers. Reports were categorized by the modality used to assess the putative markers, including protein, genetic, metabolic, or objective imaging methods. The reported sensitivity, specificity, area under the curve, and overall agreement were summarized and analyzed to determine weighted averages for each diagnostic modality. Heterogeneity was measured using the I(2) test. RESULTS: Of the 71 papers included in this analysis, each belonging to one of five modalities, protein-based followed by metabolite-based markers provided the highest diagnostic accuracy, each with a pooled overall agreement of 83.3% and respective weighted area under the curve (AUC) of 89.5% and 88.3%. Sensitivity provided by protein markers was highest (85.5%), while metabolic (85.9%) and protein markers (84.7%) had the highest specificity. Other modalities showed degrees of sensitivity, specificity, and overall agreements in the range of 73%–80%. CONCLUSIONS: Each modality provided for diagnostic accuracy and specificity similar or slightly higher than those reported for the gold-standard Autism Diagnostic Observation Schedule (ADOS) instrument. Further studies are required to identify the most predictive markers within each modality and to evaluate biological pathways or clustering with possible etiological relevance. Analyses will also be necessary to determine the potential of these novel biomarkers in diagnosing pediatric patients, thereby enabling early intervention.
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spelling pubmed-68248292019-11-21 Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis Ansel, Ashley Posen, Yehudit Ellis, Ronald Deutsch, Lisa Zisman, Philip D. Gesundheit, Benjamin Rambam Maimonides Med J Original Research OBJECTIVE: To compare the reported accuracy and sensitivity of the various modalities used to diagnose autism spectrum disorders (ASD) in efforts to help focus further biomarker research on the most promising methods for early diagnosis. METHODS: The Medline scientific literature database was searched to identify publications assessing potential clinical ASD biomarkers. Reports were categorized by the modality used to assess the putative markers, including protein, genetic, metabolic, or objective imaging methods. The reported sensitivity, specificity, area under the curve, and overall agreement were summarized and analyzed to determine weighted averages for each diagnostic modality. Heterogeneity was measured using the I(2) test. RESULTS: Of the 71 papers included in this analysis, each belonging to one of five modalities, protein-based followed by metabolite-based markers provided the highest diagnostic accuracy, each with a pooled overall agreement of 83.3% and respective weighted area under the curve (AUC) of 89.5% and 88.3%. Sensitivity provided by protein markers was highest (85.5%), while metabolic (85.9%) and protein markers (84.7%) had the highest specificity. Other modalities showed degrees of sensitivity, specificity, and overall agreements in the range of 73%–80%. CONCLUSIONS: Each modality provided for diagnostic accuracy and specificity similar or slightly higher than those reported for the gold-standard Autism Diagnostic Observation Schedule (ADOS) instrument. Further studies are required to identify the most predictive markers within each modality and to evaluate biological pathways or clustering with possible etiological relevance. Analyses will also be necessary to determine the potential of these novel biomarkers in diagnosing pediatric patients, thereby enabling early intervention. Rambam Health Care Campus 2019-10-29 /pmc/articles/PMC6824829/ /pubmed/31675302 http://dx.doi.org/10.5041/RMMJ.10375 Text en Copyright: © 2019 Ansel et al This is an open-access article. All its content, except where otherwise noted, is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Ansel, Ashley
Posen, Yehudit
Ellis, Ronald
Deutsch, Lisa
Zisman, Philip D.
Gesundheit, Benjamin
Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title_full Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title_fullStr Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title_full_unstemmed Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title_short Biomarkers for Autism Spectrum Disorders (ASD): A Meta-analysis
title_sort biomarkers for autism spectrum disorders (asd): a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824829/
https://www.ncbi.nlm.nih.gov/pubmed/31675302
http://dx.doi.org/10.5041/RMMJ.10375
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