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hs-CRP Is Associated With Incident Diabetic Nephropathy: Findings From the Jackson Heart Study
Satyesh K Sinha1,2, Susanne B Nicholas3, Jung Hye Sung4
1Department of Internal Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA satyeshsinha@cdrewu.edu sunicholas@mednet.ucla.edu.
Insights
High levels of high-sensitivity C-reactive protein (hs-CRP) may increase the risk of developing diabetic nephropathy (DN) in African Americans. This inflammation marker is linked to a higher incidence of DN in this population.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Endocrinology
Background:
- Diabetic nephropathy (DN) disproportionately affects African Americans (AA).
- High-sensitivity C-reactive protein (hs-CRP) is linked to prevalent DN, but its role in incident DN among AA is not well understood.
Purpose of the Study:
- To investigate the association between hs-CRP levels and the incidence of DN in African Americans.
Main Methods:
- Longitudinal analysis of 4,043 Jackson Heart Study participants over a median follow-up of 7.8 years.
- Incident DN defined by urinary albumin-to-creatinine ratio (ACR) or dialysis/transplantation in participants with type 2 diabetes.
- Cox proportional hazards regression used to analyze hs-CRP tertiles and DN incidence, adjusting for covariates.
Main Results:
- Participants who developed DN had higher baseline hs-CRP, age, glucose, triglycerides, ACR, blood pressure, waist circumference, and diabetes duration.
- The incidence rate of DN was 7.9% over the follow-up period.
- High hs-CRP levels (highest tertile) were associated with a 2.34-fold increased hazard of incident DN compared to the lowest tertile.
Conclusions:
- Inflammation, indicated by hs-CRP, may be associated with incident DN in African Americans.
- Further research is needed to confirm this association and understand its underlying mechanisms.
Objective:
African Americans (AA) suffer disproportionately from diabetic nephropathy (DN). C-reactive protein (CRP) has been associated with prevalent DN, but its association with incident DN in AA is unknown. We examined hs-CRP and incident DN in AA.
Research Design And Methods:
We conducted a longitudinal analysis of data from exams 1, 2, and 3 in 4,043 eligible Jackson Heart Study (JHS) participants. Participants with DN or without hs-CRP at exam 1 were excluded. Incident DN was defined as urinary albumin-to-creatinine ratio (ACR) >30 mg/g or self-reported dialysis/transplantation and type 2 diabetes mellitus (DM) or HbA1c >6.5% by exam 2 or 3 among participants free of DN at exam 1. Kaplan-Meier curves examined DN event-free survival probability by hs-CRP. With Cox proportional hazards regression we estimated hazard ratios (HRs) and 95% CI for DN by hs-CRP tertiles, adjusting for demographics and clinical and laboratory data.
Results:
During 7.8 years of median follow-up time, participants who developed DN had significantly higher baseline hs-CRP, age, fasting glucose, triglycerides, ACR, systolic blood pressure, waist circumference, and duration of DM (P < 0.05). The overall incident rate of DN was 7.9%. The mean time to incident DN was shorter for participants with hs-CRP in the high tertile (>4.24 mg/L) than in the low tertile (<1.46 mg/L); P < 0.001. Participants with high hs-CRP had higher incidence of DN (HR 2.34, 95% CI 1.04-5.24) versus the reference group.
Conclusions:
Inflammation, as measured by hs-CRP levels, may be associated with incident DN in AA. Further studies are warranted to replicate and elucidate the basis for this association.
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