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Association of mitochondrial DNA copy number with chronic kidney disease in older adults

BACKGROUND: Mitochondrial dysfunction in kidney cells has been implicated in the pathogenesis of chronic kidney disease (CKD). Estimation of mitochondrial DNA copy number (mtDNA-CN) is considered a convenient method for representing mitochondrial function in large samples. However, no study has inve...

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Autores principales: Liu, Yang, Pan, Ying, Tian, Zijian, Wang, Jing, Chen, Fei, Geng, Zhaoxu, Li, Qian, Liu, Ziqing, Zhou, Xiaozhou, Zhou, Kaixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463711/
https://www.ncbi.nlm.nih.gov/pubmed/37620817
http://dx.doi.org/10.1186/s12877-023-04203-7
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author Liu, Yang
Pan, Ying
Tian, Zijian
Wang, Jing
Chen, Fei
Geng, Zhaoxu
Li, Qian
Liu, Ziqing
Zhou, Xiaozhou
Zhou, Kaixin
author_facet Liu, Yang
Pan, Ying
Tian, Zijian
Wang, Jing
Chen, Fei
Geng, Zhaoxu
Li, Qian
Liu, Ziqing
Zhou, Xiaozhou
Zhou, Kaixin
author_sort Liu, Yang
collection PubMed
description BACKGROUND: Mitochondrial dysfunction in kidney cells has been implicated in the pathogenesis of chronic kidney disease (CKD). Estimation of mitochondrial DNA copy number (mtDNA-CN) is considered a convenient method for representing mitochondrial function in large samples. However, no study has investigated the association between mtDNA-CN and CKD in older adults with the highest prevalence. The objective is to examine cross-sectional and prospective associations between mtDNA-CN values and CKD risk in older adults to determine whether mtDNA-CN represents a novel potential biomarker for the recognition of CKD risk. PATIENTS AND METHODS: In a Chinese community-based cohort of over 65-year-olds, we included 14,467 participants (52.6% females). CKD was defined by eGFR < 60 mL/min/1.73 m(2) or ICD-10 codes (patients = 3831 (26.5%)). Participants had peripheral blood levels of mtDNA-CN calculated from probe intensities of the Axiom CAS Array. RESULTS: The risk of CKD prevalence decreased with mtDNA-CN per 1-SD increment, independent of established risk factors for older CKD (odds ratio [OR] per SD 0.90, 95% confidence interval [CI] 0.86, 0.93, P < 0.001), and has comparable strength of association with these established risk factors. Furthermore, the progression of kidney function was stratified according to the worsening of eGFR categories. The risk of kidney function progression to a more severe stage gradually decreased as the mtDNA-CN increased (P trend < 0.001). Non-CKD participants in the highest quartile of mtDNA-CN had a lower risk of developing CKD compared to the lowest quartile within 2 years of follow-up, reducing the risk of CKD by 36% (95% CI 0.42, 0.97; P = 0.037). CONCLUSIONS: Based on the analysis of the largest sample to date investigating the association between mtDNA-CN and CKD in older adults, higher levels of mtDNA-CN were found to be associated with a lower risk of CKD, suggesting that a reduced level of mtDNA-CN is a potential risk factor for CKD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-023-04203-7.
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spelling pubmed-104637112023-08-30 Association of mitochondrial DNA copy number with chronic kidney disease in older adults Liu, Yang Pan, Ying Tian, Zijian Wang, Jing Chen, Fei Geng, Zhaoxu Li, Qian Liu, Ziqing Zhou, Xiaozhou Zhou, Kaixin BMC Geriatr Research BACKGROUND: Mitochondrial dysfunction in kidney cells has been implicated in the pathogenesis of chronic kidney disease (CKD). Estimation of mitochondrial DNA copy number (mtDNA-CN) is considered a convenient method for representing mitochondrial function in large samples. However, no study has investigated the association between mtDNA-CN and CKD in older adults with the highest prevalence. The objective is to examine cross-sectional and prospective associations between mtDNA-CN values and CKD risk in older adults to determine whether mtDNA-CN represents a novel potential biomarker for the recognition of CKD risk. PATIENTS AND METHODS: In a Chinese community-based cohort of over 65-year-olds, we included 14,467 participants (52.6% females). CKD was defined by eGFR < 60 mL/min/1.73 m(2) or ICD-10 codes (patients = 3831 (26.5%)). Participants had peripheral blood levels of mtDNA-CN calculated from probe intensities of the Axiom CAS Array. RESULTS: The risk of CKD prevalence decreased with mtDNA-CN per 1-SD increment, independent of established risk factors for older CKD (odds ratio [OR] per SD 0.90, 95% confidence interval [CI] 0.86, 0.93, P < 0.001), and has comparable strength of association with these established risk factors. Furthermore, the progression of kidney function was stratified according to the worsening of eGFR categories. The risk of kidney function progression to a more severe stage gradually decreased as the mtDNA-CN increased (P trend < 0.001). Non-CKD participants in the highest quartile of mtDNA-CN had a lower risk of developing CKD compared to the lowest quartile within 2 years of follow-up, reducing the risk of CKD by 36% (95% CI 0.42, 0.97; P = 0.037). CONCLUSIONS: Based on the analysis of the largest sample to date investigating the association between mtDNA-CN and CKD in older adults, higher levels of mtDNA-CN were found to be associated with a lower risk of CKD, suggesting that a reduced level of mtDNA-CN is a potential risk factor for CKD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-023-04203-7. BioMed Central 2023-08-24 /pmc/articles/PMC10463711/ /pubmed/37620817 http://dx.doi.org/10.1186/s12877-023-04203-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Yang
Pan, Ying
Tian, Zijian
Wang, Jing
Chen, Fei
Geng, Zhaoxu
Li, Qian
Liu, Ziqing
Zhou, Xiaozhou
Zhou, Kaixin
Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title_full Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title_fullStr Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title_full_unstemmed Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title_short Association of mitochondrial DNA copy number with chronic kidney disease in older adults
title_sort association of mitochondrial dna copy number with chronic kidney disease in older adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463711/
https://www.ncbi.nlm.nih.gov/pubmed/37620817
http://dx.doi.org/10.1186/s12877-023-04203-7
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