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A small number of abnormal brain connections predicts adult autism spectrum disorder

Although autism spectrum disorder (ASD) is a serious lifelong condition, its underlying neural mechanism remains unclear. Recently, neuroimaging-based classifiers for ASD and typically developed (TD) individuals were developed to identify the abnormality of functional connections (FCs). Due to over-...

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Detalles Bibliográficos
Autores principales: Yahata, Noriaki, Morimoto, Jun, Hashimoto, Ryuichiro, Lisi, Giuseppe, Shibata, Kazuhisa, Kawakubo, Yuki, Kuwabara, Hitoshi, Kuroda, Miho, Yamada, Takashi, Megumi, Fukuda, Imamizu, Hiroshi, Náñez Sr, José E., Takahashi, Hidehiko, Okamoto, Yasumasa, Kasai, Kiyoto, Kato, Nobumasa, Sasaki, Yuka, Watanabe, Takeo, Kawato, Mitsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834637/
https://www.ncbi.nlm.nih.gov/pubmed/27075704
http://dx.doi.org/10.1038/ncomms11254
Descripción
Sumario:Although autism spectrum disorder (ASD) is a serious lifelong condition, its underlying neural mechanism remains unclear. Recently, neuroimaging-based classifiers for ASD and typically developed (TD) individuals were developed to identify the abnormality of functional connections (FCs). Due to over-fitting and interferential effects of varying measurement conditions and demographic distributions, no classifiers have been strictly validated for independent cohorts. Here we overcome these difficulties by developing a novel machine-learning algorithm that identifies a small number of FCs that separates ASD versus TD. The classifier achieves high accuracy for a Japanese discovery cohort and demonstrates a remarkable degree of generalization for two independent validation cohorts in the USA and Japan. The developed ASD classifier does not distinguish individuals with major depressive disorder and attention-deficit hyperactivity disorder from their controls but moderately distinguishes patients with schizophrenia from their controls. The results leave open the viable possibility of exploring neuroimaging-based dimensions quantifying the multiple-disorder spectrum.