Author/Authors :
Abediazar, Sima Kidney Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Shekarchi, Morteza Kidney Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Zununi-Vahed, Sepideh Kidney Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Jafari-Nakhjavani, Mohammadreza Department of Rheumatology - Connective Tissue Diseases Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Ghorbanihaghjo, Amir Tabriz University of Medical Sciences - Tabriz, Iran
Abstract :
Kidney involvement is a hallmark of systemic lupus
erythematosus (SLE) and evaluation of its inflammatory response
is demanding. It was the aim of the present study to evaluate the
levels of CXCL10 and vitamin D in serum samples of cases with
active lupus nephritis (LN).
Methods. Fifty lupus patients were enrolled in our study, 25 patients
had lupus nephritis and 25 patients were without evidence of LN.
Thirty-nine healthy subjects were also participated as a control
group. Complete biochemical and serological parameters were
measured and their correlation with serum levels of vitamin D
and CXCL10 were assessed in the studied groups.
Results. Serum levels of CXCL10 were significantly elevated (P≤
0.020), while vitamin D were diminished in SLE group and active
LN as compared with healthy controls and SLE patients without
nephritis, respectively. CXCL10 correlated with SLE disease activity
index (SLEDAI) and renal activity (P < .05), while vitamin D
correlated with C3 and anti-dsDNA antibody (P < .05). Based on
the receiver operator characteristic (ROC) curve analysis, CXCL10
and vitamin D levels were not better than conventional biomarkers
for discriminating LN patients from non-nephritis SLE patients;
however, they could differentiate most of SLE cases from healthy
individuals with area under the curve (AUC) ≥ 0.703 (P < .05).
Conclusion. Results indicated the importance of elevated levels
of CXCL10 and deficiency of vitamin D on the pathogenesis of
active LN disease.