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Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients

OBJECTIVE: Schizophrenia is a serious mental disorder. Mutations in mitochondrial genes can change energy metabolism. Telomere is a tandem sequence at the end of chromosomes. Shorter telomere length has been shown in schizophrenia. The aim of this study was to determine the relationship between ATPa...

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Autores principales: Uzuncakmak, Sevgi Karabulut, Dirican, Ebubekir, Ozcan, Halil, Takim, Ugur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889911/
https://www.ncbi.nlm.nih.gov/pubmed/36700322
http://dx.doi.org/10.9758/cpn.2023.21.1.162
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author Uzuncakmak, Sevgi Karabulut
Dirican, Ebubekir
Ozcan, Halil
Takim, Ugur
author_facet Uzuncakmak, Sevgi Karabulut
Dirican, Ebubekir
Ozcan, Halil
Takim, Ugur
author_sort Uzuncakmak, Sevgi Karabulut
collection PubMed
description OBJECTIVE: Schizophrenia is a serious mental disorder. Mutations in mitochondrial genes can change energy metabolism. Telomere is a tandem sequence at the end of chromosomes. Shorter telomere length has been shown in schizophrenia. The aim of this study was to determine the relationship between ATPase6 gene mutations and telomere length in schizophrenia patients. METHODS: Blood samples of 34 patients and 34 healthy controls were used. In this study conventional PCR, Sanger sequencing technic and real-time PCR were utilized. RESULTS: Five different mutations (A8860G, A8836, G8697A, C8676T, and A8701G) in the ATPase6 gene were identified in schizophrenia patients. The most seen mutation was A8860G (94%). Telomere length analysis indicated the relation of ATPase6 gene mutations and telomere length variations (p = 0.001). Patients carrying the A8860G mutation had shorter telomere lengths than patients carrying other mutations. Comparing telomere length between schizophrenia patients and healthy controls revealed that the mean telomere length of schizophrenia patients was shorter than healthy controls (p = 0.006). The demographic analysis demonstrated a significant relationship between marital status and telomere length (p = 0.011). Besides that, the duration of the illness is another factor that impacts telomere length (p = 0.044). There is no significant relation between telomere length and other clinical and demographic characteristics including education status, age, gender, etc. CONCLUSION: In conclusion, telomere length and ATPase6 gene mutations have a significant relation. Studies with larger patient populations and investigation of other mitochondrial gene mutations will make the clearer link between telomere length and mitochondrial mutations.
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spelling pubmed-98899112023-02-28 Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients Uzuncakmak, Sevgi Karabulut Dirican, Ebubekir Ozcan, Halil Takim, Ugur Clin Psychopharmacol Neurosci Original Article OBJECTIVE: Schizophrenia is a serious mental disorder. Mutations in mitochondrial genes can change energy metabolism. Telomere is a tandem sequence at the end of chromosomes. Shorter telomere length has been shown in schizophrenia. The aim of this study was to determine the relationship between ATPase6 gene mutations and telomere length in schizophrenia patients. METHODS: Blood samples of 34 patients and 34 healthy controls were used. In this study conventional PCR, Sanger sequencing technic and real-time PCR were utilized. RESULTS: Five different mutations (A8860G, A8836, G8697A, C8676T, and A8701G) in the ATPase6 gene were identified in schizophrenia patients. The most seen mutation was A8860G (94%). Telomere length analysis indicated the relation of ATPase6 gene mutations and telomere length variations (p = 0.001). Patients carrying the A8860G mutation had shorter telomere lengths than patients carrying other mutations. Comparing telomere length between schizophrenia patients and healthy controls revealed that the mean telomere length of schizophrenia patients was shorter than healthy controls (p = 0.006). The demographic analysis demonstrated a significant relationship between marital status and telomere length (p = 0.011). Besides that, the duration of the illness is another factor that impacts telomere length (p = 0.044). There is no significant relation between telomere length and other clinical and demographic characteristics including education status, age, gender, etc. CONCLUSION: In conclusion, telomere length and ATPase6 gene mutations have a significant relation. Studies with larger patient populations and investigation of other mitochondrial gene mutations will make the clearer link between telomere length and mitochondrial mutations. Korean College of Neuropsychopharmacology 2023-02-28 2023-02-28 /pmc/articles/PMC9889911/ /pubmed/36700322 http://dx.doi.org/10.9758/cpn.2023.21.1.162 Text en Copyright© 2023, Korean College of Neuropsychopharmacology https://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 (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Uzuncakmak, Sevgi Karabulut
Dirican, Ebubekir
Ozcan, Halil
Takim, Ugur
Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title_full Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title_fullStr Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title_full_unstemmed Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title_short Relation of ATPase6 Mutations and Telomere Length in Schizophrenia Patients
title_sort relation of atpase6 mutations and telomere length in schizophrenia patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889911/
https://www.ncbi.nlm.nih.gov/pubmed/36700322
http://dx.doi.org/10.9758/cpn.2023.21.1.162
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