CRP polymorphisms and chronic kidney disease in the third national health and nutrition examination survey
2011

CRP Gene Variants and Chronic Kidney Disease

Sample size: 5955 publication 10 minutes Evidence: moderate

Author Information

Author(s): Adriana M Hung, T Alp Ikizler, Marie R Griffin, Kimberly Glenn, Robert A Greevy, Carlos G Grijalva, Edward D Siew, Dana C Crawford

Primary Institution: Vanderbilt University

Hypothesis

CRP gene polymorphisms are associated with chronic kidney disease (CKD) progression.

Conclusion

The CRP gene variant rs2808630 is associated with CKD, particularly through its link to albuminuria in non-Hispanic blacks.

Supporting Evidence

  • CRP rs2808630 AG genotype was associated with CKD in non-Hispanic blacks.
  • The study included a large, ethnically diverse sample.
  • Adjusted odds ratios indicated a significant association between the AG genotype and CKD.
  • Findings support previous research linking CRP variants to kidney disease.
  • Albuminuria was identified as a key risk factor for CKD progression.
  • Statistical significance was maintained after Bonferroni correction.
  • Participants with CKD had higher prevalence of diabetes and hypertension.
  • Genetic predisposition to inflammation may influence CKD risk.

Takeaway

This study found that a specific gene variant is linked to kidney disease in some people, especially in African Americans.

Methodology

Data from 5955 participants in NHANES III was analyzed to assess the association between CRP polymorphisms and CKD.

Potential Biases

Potential bias due to the population-based sample design and exclusion of certain demographics.

Limitations

The study's cross-sectional design limits the ability to assess disease progression, and a single creatinine measurement may misclassify participants.

Participant Demographics

Participants included non-Hispanic blacks, non-Hispanic whites, and Mexican Americans, with a mean age of 42 years.

Statistical Information

P-Value

0.001

Confidence Interval

95% CI 1.65-5.8

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2350-12-65

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