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Plasma Mitochondrial DNA Level is a Prognostic Marker in Peritoneal Dialysis Patients

Overview
Publisher Karger
Specialty Nephrology
Date 2016 Jun 30
PMID 27355627
Citations 4
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Abstract

Background/aims: Circulating bacterial DNA fragment is related to systemic inflammatory state in peritoneal dialysis (PD) patients. We hypothesize that circulating mitochondrial DNA, which has a similar structure with bacterial DNA, correlates with systemic inflammatory state and predicts cardiovascular event in new PD patients.

Methods: We measured plasma mitochondrial DNA level by quantitative polymerase chain reaction (PCR) in 197 new PD patients and 150 patients with chronic kidney disease. PD patients were followed for 24 months for the development of cardiovascular event, hospitalization, and patient survival.

Results: There was a stepwise increase in plasma mitochondrial DNA level with worsening renal function. The average plasma mitochondrial DNA level was 18.0 ± 1.2 PCR cycles. Plasma mitochondrial DNA level correlated with serum CRP level (r = -0.538, p < 0.0001). At 24 months, the event-free survival was 67.4%, 66.4%, 63.4% and 44.2% for plasma mitochondrial DNA level quartiles I, II, III and IV, respectively (p = 0.049). After adjusting for confounders, plasma mitochondrial DNA level, malnutrition-inflammation score, and baseline arterial pulse wave velocity were independent predictors of composite cardiovascular end-point; each doubling in plasma mitochondrial DNA level confers 16.0% (95% confidence interval, 2.5 - 31.3%, p = 0.001) excess in risk. Plasma mitochondrial DNA also correlated with the number of hospital admission (r = -0.218, p = 0.002) and duration of hospitalization for cardiovascular reasons (r = -0.232, p = 0.001).

Conclusion: Plasma mitochondrial DNA level significantly correlates with systemic inflammatory state, and is a strong predictor of cardiovascular event as well as the need of hospitalization in new PD patients.

Citing Articles

Roles of Mitochondrial DNA Damage in Kidney Diseases: A New Biomarker.

Feng J, Chen Z, Liang W, Wei Z, Ding G Int J Mol Sci. 2022; 23(23).

PMID: 36499488 PMC: 9735745. DOI: 10.3390/ijms232315166.


Mitochondrial Dysfunction Plays a Relevant Role in Pathophysiology of Peritoneal Membrane Damage Induced by Peritoneal Dialysis.

Ramil-Gomez O, Rodriguez-Carmona A, Fernandez-Rodriguez J, Perez-Fontan M, Ferreiro-Hermida T, Lopez-Pardo M Antioxidants (Basel). 2021; 10(3).

PMID: 33805753 PMC: 7998819. DOI: 10.3390/antiox10030447.


Depression does not predict clinical outcome of Chinese peritoneal Dialysis patients after adjusting for the degree of frailty.

Chan G, Ng J, Chow K, Kwan B, Kwong V, Pang W BMC Nephrol. 2020; 21(1):329.

PMID: 32758180 PMC: 7405374. DOI: 10.1186/s12882-020-01994-4.


Dialysate cell-free mitochondrial DNA fragments as a marker of intraperitoneal inflammation and peritoneal solute transport rate in peritoneal dialysis.

Xie X, Wang J, Xiang S, Chen Z, Zhang X, Chen J BMC Nephrol. 2019; 20(1):128.

PMID: 30975091 PMC: 6458606. DOI: 10.1186/s12882-019-1284-3.