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Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Elevated High Sensitivity C-Reactive Protein Increases the Risk of Microalbuminuria in Subjects With Cardiovascular
Shi-Kun Yang1, Jun Liu1, Bin Yi1
1Department of Nephrology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Insights
High-sensitivity C-reactive protein (hs-CRP) is linked to microalbuminuria, an early sign of kidney damage, in adults with cardiovascular disease risk factors. Elevated hs-CRP amplifies kidney deterioration, highlighting chronic inflammation's role.
Area of Science:
- Nephrology
- Cardiology
- Clinical Chemistry
Background:
- Microalbuminuria is a crucial early indicator of kidney injury.
- Cardiovascular disease (CVD) risk factors are prevalent and associated with kidney damage.
- The role of chronic inflammation, as indicated by high-sensitivity C-reactive protein (hs-CRP), in microalbuminuria among individuals with CVD risk factors requires further investigation.
Purpose of the Study:
- To investigate the association between hs-CRP levels and the presence of microalbuminuria in adults with CVD risk factors.
- To determine if hs-CRP can independently predict microalbuminuria.
- To assess the impact of elevated hs-CRP on microalbuminuria risk in the context of established CVD risk factors.
Main Methods:
- A cross-sectional study involving 5667 adult subjects attending annual health screenings.
- Logistic regression analysis was employed to assess the association between hs-CRP, CVD risk factors, and microalbuminuria.
- Receiver Operating Characteristic (ROC) curve analysis was used to identify an optimal hs-CRP cut-off value for screening microalbuminuria.
Main Results:
- Elevated hs-CRP was significantly associated with microalbuminuria, independent of traditional CVD risk factors.
- Multivariate analysis confirmed that high hs-CRP (≥0.85 mg/L) independently predicted microalbuminuria (OR 1.41).
- In subjects with CVD risk factors, elevated hs-CRP further increased the risk of microalbuminuria (e.g., OR 1.71 in hypertension).
Conclusions:
- Elevated hs-CRP is an independent predictor of microalbuminuria in adults with CVD risk factors.
- Chronic inflammation, indicated by hs-CRP, may exacerbate kidney damage in individuals with existing CVD risk factors.
- hs-CRP holds potential as a screening biomarker for early kidney injury in at-risk populations.
Abstract:
Microalbuminuria is an early biomarker of kidney injury, the aim of this study was to investigate the impact of high sensitivity C-reactive protein (hs-CRP) on microalbuminuria in adults with cardiovascular disease (CVD) risk factors. A total of 5667 subjects who voluntarily attended annual health screenings in the Third Xiangya Hospital of Central South University were included in the study. Logistic regression was used to determine the validity of hs-CRP to predict the presence of microalbuminuria. In the unadjusted regression analysis, male gender (OR 2.23), age (OR 1.71), smoking status (OR 1.48), obesity (OR 2.41), hypertension(OR 4.03), diabetes (OR 4.61), hyperuricemia (OR 1.83), and high hs-CRP(OR 1.61) were associated with microalbuminuria. Multivariate logistic regression analysis showed that the adjusted odds ratios (OR) of diabetes, hypertension, male, abdominal obesity, and high hs-CRP for microalbuminuria were 2.71, 2.57, 1.51, 1.28 and 1.41 in all subjects, respectively (P < 0.01). ROC analysis indicated that the cut-off for hs-CRP with better properties for screening of microalbuminuria was identified as ≥0.85 mg/L. The ORs of microalbuminuria were 1.97, 1.49, 1.32 and 1.71 times in male, abdominal obesity, diabetes and hypertension subjects with hs-CRP ≥ 0.85 mg/L, respectively, compared with those without elevated hs-CRP (P < 0.01). Elevated hs-CRP level was associated with microalbuminuria independent of cardiovascular risk factors. In addition, elevated hs-CRP increased the risk of developing microalbuminuria in subjects with CVD risk factors, indicating that chronic inflammation could amplify the deterioration of kidney by effect of CVD risk factors.
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