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Updated: Jun 13, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Association between baseline kidney function and change in CRP: an analysis of the cardiovascular health study
Dena E Rifkin1, Ronit Katz, Linda F Fried
1Division of Nephrology, University of California, San Diego and Veterans' Affair Hospital, San Diego, CA 92093-9111, USA. drifkin@ucsd.edu
Insights
This study found no link between kidney function and changes in C-reactive protein (CRP) over time. While cross-sectional studies show an inverse relationship, this longitudinal analysis in older adults did not confirm it, suggesting other factors may be involved.
Area of Science:
- Nephrology
- Cardiovascular Health
- Inflammation Markers
Background:
- Cross-sectional studies indicate an inverse relationship between C-reactive protein (CRP) levels and kidney function.
- The longitudinal association between kidney function and subsequent changes in CRP remains unclear.
Purpose of the Study:
- To investigate the relationship between estimated glomerular filtration rate (eGFR) and changes in CRP over time in a cohort of older adults.
Main Methods:
- Analysis of 4,364 individuals from the Cardiovascular Health Study.
- Baseline eGFR estimated using cystatin C (eGFRcys).
- CRP measured at baseline and over 7 years; change in CRP calculated.
Main Results:
- Mean age was 72 years, mean eGFRcys was 78.9 ml/min/1.73 m(2).
- No significant association was found between baseline eGFR and yearly changes in CRP after adjustments.
- A lower baseline eGFR was associated with a non-significant increase in CRP (0.032 mg/l/year).
Conclusions:
- No relationship was observed between kidney function (eGFR) and subsequent changes in CRP in this cohort.
- The cross-sectional association may be confounded by atherosclerosis or masked by comorbidity and mortality in older adults.
- Further research in younger populations is needed to clarify the longitudinal impact of kidney function on inflammation.
Background:
In cross-sectional analyses, C-reactive protein (CRP) levels are inversely related to levels of kidney function. The relationship between kidney function and subsequent changes in CRP is unknown.
Methods:
We studied 4,364 individuals from the Cardiovascular Health Study, a longitudinal cohort of community-dwelling older adults. Baseline eGFRcys was estimated using cystatin C. CRP was measured at baseline and after 3 and 7 years of follow-up; slopes of change in CRP were calculated.
Results:
The mean (SD) age of the cohort was 72 (5.2) years; mean (SD) eGFRcys was 78.9 (18.4) ml/min/1.73 m(2). The median (interquartile range IQR) baseline CRP was 2.39 (1.22, 4.33) mg/l; the median (IQR) yearly change in CRP was -0.0051 (-0.020 to 0.27) mg/l/year. After adjustment for demographic characteristics and the initial level of CRP, each standard deviation lower baseline eGFR was associated with a small and non-significant yearly increase in CRP (0.032 mg/l/year; 95% CI: -0.005 to 0.070, p = 0.094).
Conclusions:
We did not find a relationship between eGFR and subsequent changes in CRP. The association between kidney function and CRP in cross-sectional analyses may reflect unmeasured confounding by atherosclerosis; alternatively, the burden of comorbidity and interval mortality in this population may have masked a stronger longitudinal association between kidney function and change in CRP. Further study in younger populations may clarify whether impaired kidney function leads to change in inflammation over time.
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