دورية أكاديمية

Gene co-expression architecture in peripheral blood in a cohort of remitted first-episode schizophrenia patients

التفاصيل البيبلوغرافية
العنوان: Gene co-expression architecture in peripheral blood in a cohort of remitted first-episode schizophrenia patients
المؤلفون: Rodríguez, Natalia, Gassó, P., Martínez-Pinteño, A., González Segura, Álex, Mezquida, G., Moreno-Izco, Lucia, González-Peñas, J., Zorrilla, Iñaki, Martin, Marta, Rodriguez-Jimenez, R., Corripio, I., Sarró, S., Ibáñez, A., Butjosa, Anna, Contreras, Fernando, Bioque, Miquel, Cuesta, Manuel Jesús, Parellada, M., González-Pinto, A., Berrocoso Domínguez, Esther María, Bernardo, Miquel, Mas, Sergi, 2EPS group
المساهمون: Psicología
المصدر: Schizophrenia, Vol. 8, Núm. 1
بيانات النشر: NATURE PORTFOLIO
سنة النشر: 2023
المجموعة: RODIN - Repositorio de Objetos de Docencia e Investigación de la Universidad de Cádiz
الوصف: A better understanding of schizophrenia subtypes is necessary to stratify the patients according to clinical attributes. To explore the genomic architecture of schizophrenia symptomatology, we analyzed blood co-expression modules and their association with clinical data from patients in remission after a first episode of schizophrenia. In total, 91 participants of the 2EPS project were included. Gene expression was assessed using the Clariom S Human Array. Weighted-gene co-expression network analysis (WGCNA) was applied to identify modules of co-expressed genes and to test its correlation with global functioning, clinical symptomatology, and premorbid adjustment. Among the 25 modules identified, six modules were significantly correlated with clinical data. These modules could be clustered in two groups according to their correlation with clinical data. Hub genes in each group showing overlap with risk genes for schizophrenia were enriched in biological processes related to metabolic processes, regulation of gene expression, cellular localization and protein transport, immune processes, and neurotrophin pathways. Our results indicate that modules with significant associations with clinical data showed overlap with gene sets previously identified in differential gene-expression analysis in brain, indicating that peripheral tissues could reveal pathogenic mechanisms. Hub genes involved in these modules revealed multiple signaling pathways previously related to schizophrenia, which may represent the complex interplay in the pathological mechanisms behind the disease. These genes could represent potential targets for the development of peripheral biomarkers underlying illness traits in clinical remission stages after a first episode of schizophrenia.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: info:eu-repo/grantAgreement/ES/ISCIII/PI08-0208; info:eu-repo/grantAgreement/ES/MINECO-ISCIII-FEDER/PI11-00325; info:eu-repo/grantAgreement/ES/MINECO-ISCIII-FEDER/PI14-00612; http://hdl.handle.net/10498/27853Test
DOI: 10.1038/s41537-022-00215-1
الإتاحة: https://doi.org/10.1038/s41537-022-00215-1Test
http://hdl.handle.net/10498/27853Test
حقوق: Atribución 4.0 Internacional ; http://creativecommons.org/licenses/by/4.0Test/ ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.F8C68540
قاعدة البيانات: BASE