Volume 33, Issue 1 737169 pp. 35-42
Article
Open Access

Relation between MicroRNA Expression in Peritoneal Dialysis Effluent and Peritoneal Transport Characteristics

Jin Chen

Jin Chen

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

Division of Nephrology Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital Chengdu Sichuan, China

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Philip Kam-Tao

Philip Kam-Tao

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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Bonnie Ching-Ha Kwan

Bonnie Ching-Ha Kwan

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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Kai-Ming Chow

Kai-Ming Chow

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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Ka-Bik Lai

Ka-Bik Lai

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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Cathy Choi-Wan Luk

Cathy Choi-Wan Luk

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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Cheuk-Chun Szeto

Corresponding Author

Cheuk-Chun Szeto

Department of Medicine and Therapeutics Prince of Wales Hospital The Chinese University of Hong Kong Shatin Hong Kong, China , cuhk.edu.hk

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First published: 23 May 2013
Citations: 2

Abstract

Background: The role of microRNAs (miRNAs) in peritoneal transport is uncertain.

Methods: We studied 82 new peritoneal dialysis (PD) patients, 22 prevalent patients without ultrafiltration problem, and 6 patients with documented ultrafiltration problem. Peritoneal transport was determined by standard peritoneal equilibration test (PET). RNA was extracted from the PD effluent after PET, and intra-peritoneal expression of miRNA targets were quantified.

Results: There were significant difference in the PDE expressions of miR-15a and miR-21. There were modest inverse correlations between ultrafiltration volume and PDE expression of miR-17 (r = −0.198, p = 0.041) and miR-377 (r = −0.201, p = 0.041). There was an inverse correlations between dialysate-to-plasma creatinine concentration at 4 hours and PDE expression of miR-192 (r = −0.199, p = 0.040); while mass transfer area coefficient of creatinine correlated with PDE expression of miR-192 (r = −0.191, p = 0.049) and miR-377 (r = 0.201, p = 0.041). Amongst 7 randomly selected patients who had repeat PET after one year, there was a significant correlation between baseline PDE expression of miR-377 and change in ultrafiltration volume (r = −0.852, p = 0.015).

Conclusion: The miRNA expression in PDE, including miR-15a, miR-17, miR-21, miR-30, miR-192, and miR-377, correlated with peritoneal transport characteristics. Our result suggests that miRNA may play a role in the regulation of peritoneal membrane function.

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