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NDT Advance Access originally published online on November 6, 2007
Nephrology Dialysis Transplantation 2008 23(4):1285-1290; doi:10.1093/ndt/gfm782
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© The Author [2007]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Inflammatory markers and the progression of IgA glomerulonephritis

Kati Kaartinen1, Jaana Syrjänen1,2, Ilkka Pörsti1,2, Mikko Hurme1, Aimo Harmoinen3, Amos Pasternack1, Heini Huhtala4 and Jukka Mustonen1,2

1 Medical School, University of Tampere 2 Department of Internal Medicine, Tampere University Hospital, Tampere 3 Department of Laboratory Medicine, Savonlinna Central Hospital, Savonlinna 4 School of Public Health, University of Tampere, Tampere, Finland

Kati Kaartinen, Kapteeninkatu 8-10 E 26, FIN-00140 Helsinki, Finland. Tel: +358-40-70-10-287; E-mail: kati.kaartinen{at}elisanet.fi



  Abstract

Background. IgA glomerulonephritis (IgAGN) composes a variable prognosis with 15–40% of the patients eventually progressing to end-stage renal failure. Known risk factors for progressive course of IgAGN include hypertension, proteinuria and renal insufficiency. Although markers of inflammation such as serum or urinary interleukin-6 (IL-6) and serum albumin have predicted progression in some studies, sensitive CRP (hs-CRP) has not been directly linked to the progression of IgAGN.

Methods. A total of 174 (70 females) patients were invited for two visits 11 and 16 years (medians) after IgAGN was diagnosed in renal biopsy. All patients had been diagnosed at least 5 years before the first visit. Progressive disease was defined as cystatin-C exceeding normal limits and showing over 20% elevation between the visits, or kidney transplantation or start of dialysis. Cystatin-C and creatinine clearance, serum hs-CRP, s-albumin, s-IL-6 and white blood cell count (WBC) were available for analysis from 118 patients.

Results. IgAGN was progressive in 19.5% of the patients on the second visit. Hs-CRP, s-albumin and WBC of the first visit were significantly associated with the progression of IgAGN (P = 0.014; P = 0.0001; P = 0.023, respectively). S-IL-6 was not associated with the progression. All inflammatory variables correlated significantly with the concurrent level of kidney function. Possible study limitations are the relatively low number of outcomes in the study groups, and the lack of generally accepted definitions for disease progression.

Conclusions. Our results suggest that inflammatory markers hs-CRP, s-albumin and WBC are associated with the progression of IgAGN.

Keywords: albumin; hs-CRP; IgA glomerulonephritis; interleukin-6; white blood cell count

Received for publication: 23. 3.07
Accepted in revised form: 8.10.07


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