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Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population
BACKGROUND: Circulating cell-free mitochondrial DNA (cf-mtDNA) fragments in blood plasma have been reported in patients with schizophrenia (SZ). Although the relationship of cf-mtDNA to the cognitive status of patients with SZ has not yet been explored, it is known that cognitive impairment in SZ co...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607197/ https://www.ncbi.nlm.nih.gov/pubmed/31388301 http://dx.doi.org/10.2147/NDT.S208587 |
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author | García-de la Cruz, Dulce Dajheanne Juárez-Rojop, Isela Esther Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime Genis-Mendoza, Alma Delia Nicolini, Humberto González-Castro, Thelma Beatriz Guzmán-Priego, Crystell Guadalupe López-Martínez, Nancy Adanelly Hernández-Cisneros, Javier Antonio Caballero-Prado, Francisco |
author_facet | García-de la Cruz, Dulce Dajheanne Juárez-Rojop, Isela Esther Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime Genis-Mendoza, Alma Delia Nicolini, Humberto González-Castro, Thelma Beatriz Guzmán-Priego, Crystell Guadalupe López-Martínez, Nancy Adanelly Hernández-Cisneros, Javier Antonio Caballero-Prado, Francisco |
author_sort | García-de la Cruz, Dulce Dajheanne |
collection | PubMed |
description | BACKGROUND: Circulating cell-free mitochondrial DNA (cf-mtDNA) fragments in blood plasma have been reported in patients with schizophrenia (SZ). Although the relationship of cf-mtDNA to the cognitive status of patients with SZ has not yet been explored, it is known that cognitive impairment in SZ compromises the functional and social capacity of these patients and diminishes their quality of life. In this sense, the assessment of the severity of cognitive impairment in a Mexican population with SZ and its association with cf-mtDNA levels in blood plasma may provide the possibility of using cf-mtDNA as a biomarker to determine the status of the disease and the possible ensuing changes over time. METHODS: Subjects for a case–control study will be recruited. cf-mtDNA obtained from blood plasma will be quantified by real-time polymerase chain reaction, using melting curve technology with SYBR green as amplification marker. Patients with SZ will be grouped into those with severe, mild, and no cognitive impairment according to Montreal Cognitive Assessment scale scores, to determine differences between cognitive performance and cf-mtDNA levels in blood plasma. ETHICS AND COMMUNICATION: This study has been approved by the ethics and investigation committees of the High Specialty Regional Hospital of Mental Health (Hospital Regional de Alta Especialidad de Salud Mental); project No. HRAESM/DG/RP/1128/2018. We plan to communicate our research findings in scientific conferences and in peer-reviewed journals. CONCLUSION: It is known that cognitive dysfunction provokes negative effects in an SZ patient´s life. This project aims to provide better knowledge about the role of cf-mtDNA in the pathogenesis of cognitive impairment in SZ, as an attempt to achieve improvements to the existing treatments, thereby helping to prevent major cognitive deterioration. |
format | Online Article Text |
id | pubmed-6607197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66071972019-08-06 Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population García-de la Cruz, Dulce Dajheanne Juárez-Rojop, Isela Esther Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime Genis-Mendoza, Alma Delia Nicolini, Humberto González-Castro, Thelma Beatriz Guzmán-Priego, Crystell Guadalupe López-Martínez, Nancy Adanelly Hernández-Cisneros, Javier Antonio Caballero-Prado, Francisco Neuropsychiatr Dis Treat Study Protocol BACKGROUND: Circulating cell-free mitochondrial DNA (cf-mtDNA) fragments in blood plasma have been reported in patients with schizophrenia (SZ). Although the relationship of cf-mtDNA to the cognitive status of patients with SZ has not yet been explored, it is known that cognitive impairment in SZ compromises the functional and social capacity of these patients and diminishes their quality of life. In this sense, the assessment of the severity of cognitive impairment in a Mexican population with SZ and its association with cf-mtDNA levels in blood plasma may provide the possibility of using cf-mtDNA as a biomarker to determine the status of the disease and the possible ensuing changes over time. METHODS: Subjects for a case–control study will be recruited. cf-mtDNA obtained from blood plasma will be quantified by real-time polymerase chain reaction, using melting curve technology with SYBR green as amplification marker. Patients with SZ will be grouped into those with severe, mild, and no cognitive impairment according to Montreal Cognitive Assessment scale scores, to determine differences between cognitive performance and cf-mtDNA levels in blood plasma. ETHICS AND COMMUNICATION: This study has been approved by the ethics and investigation committees of the High Specialty Regional Hospital of Mental Health (Hospital Regional de Alta Especialidad de Salud Mental); project No. HRAESM/DG/RP/1128/2018. We plan to communicate our research findings in scientific conferences and in peer-reviewed journals. CONCLUSION: It is known that cognitive dysfunction provokes negative effects in an SZ patient´s life. This project aims to provide better knowledge about the role of cf-mtDNA in the pathogenesis of cognitive impairment in SZ, as an attempt to achieve improvements to the existing treatments, thereby helping to prevent major cognitive deterioration. Dove 2019-06-28 /pmc/articles/PMC6607197/ /pubmed/31388301 http://dx.doi.org/10.2147/NDT.S208587 Text en © 2019 García-de la Cruz et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Study Protocol García-de la Cruz, Dulce Dajheanne Juárez-Rojop, Isela Esther Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime Genis-Mendoza, Alma Delia Nicolini, Humberto González-Castro, Thelma Beatriz Guzmán-Priego, Crystell Guadalupe López-Martínez, Nancy Adanelly Hernández-Cisneros, Javier Antonio Caballero-Prado, Francisco Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title | Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title_full | Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title_fullStr | Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title_full_unstemmed | Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title_short | Association between mitochondrial DNA and cognitive impairment in schizophrenia: study protocol for a Mexican population |
title_sort | association between mitochondrial dna and cognitive impairment in schizophrenia: study protocol for a mexican population |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607197/ https://www.ncbi.nlm.nih.gov/pubmed/31388301 http://dx.doi.org/10.2147/NDT.S208587 |
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