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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.
Afiliación
  • Liu Y; College of Life Sciences, University of Chinese Academy of Sciences, 100049, Beijing, China.
  • Pan Y; Department of Endocrinology, Kunshan Hospital Affiliated to Jiangsu University, 215300, Suzhou, China.
  • Tian Z; Institute of Biophysics, Chinese Academy of Sciences, 100101, Beijing, China.
  • Wang J; Science for Life Laboratory, Department of Biomedical and Clinical Sciences (BKV), Linköping University, Linköping, 58183, Sweden.
  • Chen F; Department of Endocrinology, Friendship Hospital, Beijing, 100029, China.
  • Geng Z; Institute of Biophysics, Chinese Academy of Sciences, 100101, Beijing, China.
  • Li Q; College of Life Sciences, University of Chinese Academy of Sciences, 100049, Beijing, China.
  • Liu Z; College of Life Sciences, University of Chinese Academy of Sciences, 100049, Beijing, China.
  • Zhou X; College of Life Sciences, University of Chinese Academy of Sciences, 100049, Beijing, China.
  • Zhou K; Guangzhou Laboratory, 510000, Guangzhou, China. zhoukx@ucas.ac.cn.
BMC Geriatr ; 23(1): 514, 2023 08 24.
Article en En | MEDLINE | ID: mdl-37620817
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 m2 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Insuficiencia Renal Crónica Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: BMC Geriatr Asunto de la revista: GERIATRIA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Insuficiencia Renal Crónica Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: BMC Geriatr Asunto de la revista: GERIATRIA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido