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Residual Associations of Inflammatory Markers with eGFR after Accounting for Measured GFR in a Community-Based Cohort without CKD
Author(s) -
Jørgen Schei,
Vidar T.N. Stefansson,
Ulla Dorte Mathisen,
Bjørn O. Eriksen,
Marit D. Solbu,
Trond Jenssen,
Toralf Melsom
Publication year - 2015
Publication title -
clinical journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.755
H-Index - 151
eISSN - 1555-905X
pISSN - 1555-9041
DOI - 10.2215/cjn.07360715
Subject(s) - medicine , cystatin c , renal function , creatinine , confounding , kidney disease , confidence interval , fibrinogen , diabetes mellitus , urology , iohexol , endocrinology
eGFR on the basis of creatinine (eGFRcre) associates differently with cardiovascular disease and mortality than eGFR on the basis of cystatin C (eGFRcys). This may be related to risk factors affecting the level of creatinine and cystatin C along non-GFR pathways, which may confound the association between eGFR and outcome. Nontraditional risk factors are usually not measured in epidemiologic studies of eGFR and cannot be adjusted for to reduce confounding. We examined whether the inflammatory markers soluble TNF receptor type 2 (sTNFR2), C-reactive protein (CRP), and fibrinogen associated differently with eGFR than with measured GFR (mGFR).

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