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Is C-reactive protein a useful predictor of outcome in peritoneal dialysis patients?
Karen Ann Herzig1, David Michael Purdie2, Wendy Chang1
1Department of Renal Medicine, Princess Alexandra Hospital, Brisbane, Australia.
Insights
Elevated C-reactive protein (CRP) in peritoneal dialysis (PD) patients predicts myocardial infarction. This finding suggests closer cardiovascular monitoring for PD patients with high CRP levels.
Area of Science:
- Nephrology
- Cardiology
- Biomarkers
Background:
- Elevated C-reactive protein (CRP) predicts mortality in hemodialysis patients.
- The predictive value of CRP in peritoneal dialysis (PD) patients remains unassessed.
Purpose of the Study:
- To assess the predictive value of CRP in PD patients.
- To determine if CRP predicts cardiovascular events or mortality in PD patients.
Main Methods:
- Prospective cohort study of 50 PD patients over 3 years.
- Baseline CRP levels were determined and correlated with clinical parameters.
- Multivariate Cox proportional hazards model used to adjust for confounding factors.
Main Results:
- Elevated CRP (>6 mg/L) was associated with lower prealbumin, decreased creatinine clearance, and increased left ventricular thickness.
- Elevated CRP independently predicted myocardial infarction (HR 4.8, P=0.048).
- CRP showed a trend towards predicting fatal myocardial infarction (HR 6.0, P=0.07) but not all-cause mortality (HR 2.1, P=0.15).
Conclusions:
- Elevated CRP is common in PD patients and independently predicts future myocardial infarction.
- PD patients with elevated CRP may require enhanced cardiovascular risk factor management and monitoring.
- CRP serves as a potential biomarker for cardiovascular risk in the PD population.
Abstract:
An elevated C-reactive protein (CRP) has recently been shown to be strongly predictive of mortality in hemodialysis patients. However, its predictive value in peritoneal dialysis (PD) patients has not been assessed. A cohort of 50 PD patients was followed prospectively for a 3-yr period, after initial determination of CRP. Patients with an elevated CRP (>6 mg/L; n = 29) had significantly reduced plasma prealbumin (0.36 +/- 0.02 versus 0.44 +/- 0.03 g/L; P: < 0.05), decreased total weekly creatinine clearance (C(Cr); 52.5 +/- 2.3 versus 63.1 +/- 3.2 L/1.73 m(2); P: < 0.01), and increased left ventricular thickness (1.24 +/- 0.05 versus 1.08 +/- 0.06 cm; P: < 0.05) at baseline compared with those who had a normal CRP (< or =6 mg/L; n = 21). Baseline CRP (log-transformed) correlated weakly with baseline Kt/V, C(Cr), and pre-albumin. With the use of a multivariate Cox's proportional hazards model to adjust for potential confounding factors, an elevated CRP was predictive of myocardial infarction (adjusted hazard ratio, 4.8; 95% confidence interval [CI], 1.0 to 23; P: = 0.048) and tended to be predictive of fatal myocardial infarction (adjusted hazard ratio, 6.0; 95% CI, 0.8 to 43; P: = 0.07). However, CRP was not significantly associated with all-cause mortality (adjusted hazard ratio, 2.1; 95% CI,0.8 to 5.4; P: = 0.15). In conclusion, CRP elevation occurs in a substantial proportion of PD patients and is independently predictive of future myocardial infarction. Such patients may warrant closer monitoring and attention to modifiable cardiovascular risk factors.
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