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Open AccessResearch article

Offspring of parents with Balkan Endemic Nephropathy have higher C-reactive protein levels suggestive of inflammatory processes: a longitudinal study

Wilfried Karmaus1 email, Plamen Dimitrov2 email, Valeri Simeonov3 email, Svetla Tsolova2 email and Vecihi Batuman4 email

Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, South Carolina, USA

National Center of Public Health Protection, Sofia, Bulgaria

Vratza District Hospital, Vratza, Bulgaria

Section of Nephrology-Hypertension, Tulane University Medical Center, New Orleans, USA

author email corresponding author email

BMC Nephrology 2009, 10:10doi:10.1186/1471-2369-10-10

Published: 28 April 2009

Abstract

Background

Despite the characteristic extensive tubulointerstitial fibrosis, Balkan Endemic Nephropathy (BEN) is usually considered a non-inflammatory disease.

Methods

We examined a marker of inflammation, C-reactive protein (CRP), in the offspring of patients with BEN, a population at risk for BEN, prior to development of established disease to determine if an inflammatory process could be identified in the early stages of the disease. In 2003/04, 102 adult offspring whose parents had BEN and a control group of 99 adult offspring of non-BEN patients were enrolled in this prospective study. This cohort was re-examined yearly for four consecutive years. Levels of serum CRP were measured in years 3 and 4 and compared between groups. The data were analyzed with mixed models.

Results

Compared to controls, offspring of BEN parents had statistically higher CRP levels in two consecutive years, suggestive of early inflammatory reactivity. Whenever the mother was affected by BEN (both parents, or mother only), serum CRP was significantly increased, but not if only the father had BEN. CRP was inversely related to kidney cortex width but not to markers or renal function.

Conclusion

Early stages of BEN may involve inflammatory processes. The observation of a maternal involvement supports the concept of fetal programming, which has been implicated in the pathogenesis of other chronic kidney diseases.


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