Abstract

BackgroundThe prognostic values of baseline, longitudinal high-sensitivity C-reactive protein (hs-CRP) and its change over time on mortality in patients undergoing continuous ambulatory peritoneal dialysis (CAPD) remain uncertain.MethodsWe retrospectively studied 1228 consecutive CAPD patients from 2007 to 2012, and followed up through December 2014. Cox regression models were performed to assess the association of hs-CRP on outcomes using serum hs-CRP levels as: (1) stratified by tertile of baseline or longitudinal hs-CRP levels; (2) baseline or longitudinal hs-CRP levels as continuous variables; and (3) categorized by tertile of slopes of hs-CRP change per year for each subject.ResultsHigher baseline hs-CRP levels were not associated with clinical outcomes after adjustment for potential confounders. However, patients with the upper tertile of longitudinal hs-CRP had a nearly twice-fold increased risk of both all-cause and cardiovascular mortality [adjusted hazard ratio (HR) 1.77; (95% CI 1.16–2.70) and 2.08 (1.17–3.71), respectively], as compared with those with lower tertile. Results were similar when baseline or longitudinal hs-CRP was assessed as continuous variable. Additionally, the risk of all-cause and cardiovascular mortality in patients with increased trend in serum hs-CRP levels over time (tertile 3) was significantly higher [adjusted HR 2.48 (1.58–3.87) and 1.99 (1.11–3.56), respectively] when compared to those with relatively stable hs-CRP levels during follow-up period. These associations persisted after excluding subjects with less than 1-year follow up.ConclusionsHigher longitudinal serum hs-CRP levels and its elevated trend over time, but not baseline levels were predictive of worse prognosis among CAPD patients.

Highlights

  • The prognostic values of baseline, longitudinal high-sensitivity C-reactive protein and its change over time on mortality in patients undergoing continuous ambulatory peritoneal dialysis (CAPD) remain uncertain

  • When treating high-sensitivity C-reactive protein (hs-CRP) as a continuous variable after log transformation, baseline hs-CRP level was not associated with all-cause mortality [hazard ratio (HR) = 1.19; P = 0.246], but borderline significantly associated with cardiovascular disease (CVD) mortality [HR = 1.50; P = 0.048] (Table 2)

  • In the present study, we found that higher baseline serum hs-CRP levels were not associated with elevated risk of all-cause and CVD mortality in CAPD patients

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Summary

Introduction

The prognostic values of baseline, longitudinal high-sensitivity C-reactive protein (hs-CRP) and its change over time on mortality in patients undergoing continuous ambulatory peritoneal dialysis (CAPD) remain uncertain. Previous studies have demonstrated that an elevated serum hs-CRP level at a single time point is an important predictor of cardiovascular events both in general population [3, 4] and dialysis patients [5,6,7,8,9,10,11]. HD patients with persistently high CRP levels but not an elevated CRP level only at a signal time point was associated with increased mortality risk, compared with a persistently low CRP levels [17, 18]. Only a few small studies have assessed the consequences of longitudinal conventional CRP, but not hs-CRP, fluctuation on mortality among peritoneal dialysis (PD) patients [19, 20]

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