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Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures

Age at onset is the most important feature of schizophrenia that could indicate its origin. Minor physical anomalies (MPAs) characterize potential marker indices of disturbances in early neurodevelopment. However, the association between MPAs and age at onset of schizophrenia is still unclear. We ai...

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Autores principales: Tsai, I-Ning, Lin, Jin-Jia, Lu, Ming-Kun, Tan, Hung-Pin, Jang, Fong-Lin, Gan, Shu-Ting, Lin, Sheng-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265874/
https://www.ncbi.nlm.nih.gov/pubmed/27472737
http://dx.doi.org/10.1097/MD.0000000000004406
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author Tsai, I-Ning
Lin, Jin-Jia
Lu, Ming-Kun
Tan, Hung-Pin
Jang, Fong-Lin
Gan, Shu-Ting
Lin, Sheng-Hsiang
author_facet Tsai, I-Ning
Lin, Jin-Jia
Lu, Ming-Kun
Tan, Hung-Pin
Jang, Fong-Lin
Gan, Shu-Ting
Lin, Sheng-Hsiang
author_sort Tsai, I-Ning
collection PubMed
description Age at onset is the most important feature of schizophrenia that could indicate its origin. Minor physical anomalies (MPAs) characterize potential marker indices of disturbances in early neurodevelopment. However, the association between MPAs and age at onset of schizophrenia is still unclear. We aimed to compare risk assessment and familial aggregation in patients with early-onset schizophrenia (EOS) and adult-onset schizophrenia (AOS) with MPAs and craniofacial measures. We estimated the risk assessment of MPAs among patients with EOS (n = 68), patients with AOS (n = 183), nonpsychotic relatives (n = 147), and healthy controls (n = 241) using 3 data-mining algorithms. In addition, we assessed the magnitude of familial aggregation of MPAs with respect to the age at onset of schizophrenia. The performance of EOS was superior to that of AOS, with discrimination accuracies of 89% and 76%, respectively. Combined MPA scores as the risk assessment were significantly higher in all schizophrenia subgroups and the nonpsychotic relatives of EOS patients than in the healthy controls. The recurrence risk ratio for familial aggregation of the MPA scores of EOS families (odds ratio 9.27) was substantially higher than that of AOS families (odds ratio 2.47). The results highlight that EOS improves risk assessment and has a severe magnitude of familial aggregation of MPAs. These findings indicate that EOS might result from a stronger genetic susceptibility to neurodevelopmental deficits.
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spelling pubmed-52658742017-02-03 Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures Tsai, I-Ning Lin, Jin-Jia Lu, Ming-Kun Tan, Hung-Pin Jang, Fong-Lin Gan, Shu-Ting Lin, Sheng-Hsiang Medicine (Baltimore) 5000 Age at onset is the most important feature of schizophrenia that could indicate its origin. Minor physical anomalies (MPAs) characterize potential marker indices of disturbances in early neurodevelopment. However, the association between MPAs and age at onset of schizophrenia is still unclear. We aimed to compare risk assessment and familial aggregation in patients with early-onset schizophrenia (EOS) and adult-onset schizophrenia (AOS) with MPAs and craniofacial measures. We estimated the risk assessment of MPAs among patients with EOS (n = 68), patients with AOS (n = 183), nonpsychotic relatives (n = 147), and healthy controls (n = 241) using 3 data-mining algorithms. In addition, we assessed the magnitude of familial aggregation of MPAs with respect to the age at onset of schizophrenia. The performance of EOS was superior to that of AOS, with discrimination accuracies of 89% and 76%, respectively. Combined MPA scores as the risk assessment were significantly higher in all schizophrenia subgroups and the nonpsychotic relatives of EOS patients than in the healthy controls. The recurrence risk ratio for familial aggregation of the MPA scores of EOS families (odds ratio 9.27) was substantially higher than that of AOS families (odds ratio 2.47). The results highlight that EOS improves risk assessment and has a severe magnitude of familial aggregation of MPAs. These findings indicate that EOS might result from a stronger genetic susceptibility to neurodevelopmental deficits. Wolters Kluwer Health 2016-07-29 /pmc/articles/PMC5265874/ /pubmed/27472737 http://dx.doi.org/10.1097/MD.0000000000004406 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 5000
Tsai, I-Ning
Lin, Jin-Jia
Lu, Ming-Kun
Tan, Hung-Pin
Jang, Fong-Lin
Gan, Shu-Ting
Lin, Sheng-Hsiang
Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title_full Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title_fullStr Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title_full_unstemmed Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title_short Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
title_sort improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures
topic 5000
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265874/
https://www.ncbi.nlm.nih.gov/pubmed/27472737
http://dx.doi.org/10.1097/MD.0000000000004406
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