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Sökning: WFRF:(Zhou Kaixin) > (2023) > Association of mito...

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

Liu, Yang (författare)
Univ Chinese Acad Sci, Peoples R China
Pan, Ying (författare)
Jiangsu Univ, Peoples R China
Tian, Zijian (författare)
Chinese Acad Sci, Peoples R China
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Wang, Jing (författare)
Linköpings universitet,Avdelningen för cellbiologi,Medicinska fakulteten
Chen, Fei (författare)
Friendship Hosp, Peoples R China
Geng, Zhaoxu (författare)
Chinese Acad Sci, Peoples R China
Li, Qian (författare)
Univ Chinese Acad Sci, Peoples R China
Liu, Ziqing (författare)
Univ Chinese Acad Sci, Peoples R China
Zhou, Xiaozhou (författare)
Univ Chinese Acad Sci, Peoples R China
Zhou, Kaixin (författare)
Guangzhou Lab, Peoples R China
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 (creator_code:org_t)
BMC, 2023
2023
Engelska.
Ingår i: BMC Geriatrics. - : BMC. - 1471-2318. ; 23:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • 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.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Annan medicin och hälsovetenskap -- Gerontologi, medicinsk/hälsovetenskaplig inriktning (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Other Medical and Health Sciences -- Gerontology, specialising in Medical and Health Sciences (hsv//eng)

Nyckelord

Biomarker; Mitochondrial DNA copy number; Chronic kidney disease; Older adults

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