4.6 Article

Peritoneal inflammation precedes encapsulating peritoneal sclerosis: results from the GLOBAL Fluid Study

期刊

NEPHROLOGY DIALYSIS TRANSPLANTATION
卷 31, 期 3, 页码 480-486

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfv440

关键词

chronic inflammation; encapsulating peritoneal sclerosis; peritoneal dialysis; peritoneal membrane

资金

  1. Baxter Healthcare Renal Division
  2. International Society for Peritoneal Dialysis
  3. National Institutes of Health Research (NIHR) [PB-PG-0610-22456] Funding Source: National Institutes of Health Research (NIHR)
  4. National Institute for Health Research [PB-PG-0610-22456] Funding Source: researchfish

向作者/读者索取更多资源

Encapsulating peritoneal sclerosis (EPS) is an uncommon condition, strongly associated with a long duration of peritoneal dialysis (PD), which is itself associated with increased fibrosis in the peritoneal membrane. The peritoneal membrane is inflamed during PD and inflammation is often associated with fibrosis. We hypothesized that patients who subsequently develop EPS might have a more inflamed peritoneal membrane during PD. We performed a nested, case-control study identifying all EPS cases in the UK arm of the GLOBAL Fluid Study and matching them by centre and duration of PD with two to three controls. Dialysate and plasma samples were taken during repeated peritoneal equilibration tests prior to cessation of PD from cases and controls. Samples were assayed by electrochemiluminescence immunoassay for interleukin-1 beta (IL-1 beta), tumour necrosis factor alpha (TNF-alpha), interferon-gamma (IFN-gamma) and IL-6. Results were analysed by linear mixed models adjusted for age and time on PD. Eleven EPS cases were matched with 26 controls. Dialysate TNF-alpha {0.64 [95% confidence interval (CI) 0.23, 1.05]} and IL-6 [0.79 (95% CI 0.03, 1.56)] were significantly higher in EPS cases, while IL-1 beta [1.06 (95% CI -0.11, 2.23)] and IFN-gamma [0.62 (95% CI -0.06, 1.29)] showed a similar trend. Only IL-6 was significantly higher in the plasma [0.42 (95% CI 0.07, 0.78)]. Solute transport was not significantly different between cases and controls but did increase in both groups with the duration of PD. The peritoneal cavity has higher levels of inflammatory cytokines during PD in patients who subsequently develop EPS, but neither inflammatory cytokines nor peritoneal solute transport clearly discriminates EPS cases. Increased systemic inflammation is also evident and is probably driven by increased peritoneal inflammation.

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