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The prognosis and risk factors of baseline high peritoneal transporters on patients with peritoneal dialysis
Author(s) -
Huang Guansen,
Wang Yi,
Shi Yingfeng,
Ma Xiaoyan,
Tao Min,
Zang Xiujuan,
Qi Yinghui,
Qiao Cheng,
Du Lin,
Sheng Lili,
Zhuang Shougang,
Liu Na
Publication year - 2021
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/jcmm.16819
Subject(s) - peritoneal dialysis , hyperuricemia , medicine , uric acid , gastroenterology , logistic regression , proportional hazards model , peritoneum , dialysis , urology , surgery
The relationship between baseline high peritoneal solute transport rate (PSTR) and the prognosis of peritoneal dialysis (PD) patients remains unclear. The present study combined clinical data and basic experiments to investigate the impact of baseline PSTR and the underlying molecular mechanisms. A total of 204 incident CAPD patients from four PD centres in Shanghai between 1 January 2014 and 30 September 2020 were grouped based on a peritoneal equilibration test after the first month of dialysis. Analysed with multivariate Cox and logistic regression models, baseline high PSTR was a significant risk factor for technique failure (AHR 5.70; 95% CI 1.581 to 20.548 p  = 0.008). Baseline hyperuricemia was an independent predictor of mortality (AHR 1.006 95%CI 1.003 to 1.008, p  < 0.001) and baseline high PSTR (AOR 1.007; 95%CI 1.003 to 1.012; p  = 0.020). Since uric acid was closely related to high PSTR and adverse prognosis, the in vitro experiments were performed to explore the underlying mechanisms of which uric acid affected peritoneum. We found hyperuricemia induced epithelial‐to‐mesenchymal transition (EMT) of cultured human peritoneal mesothelial cells by activating TGF‐β1/Smad3 signalling pathway and nuclear transcription factors. Conclusively, high baseline PSTR induced by hyperuricaemia through EMT was an important reason of poor outcomes in CAPD patients.

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