Evaluation of HE4 and IGFBPs as Novel Biomarkers of Systemic Lupus Erythematosus with Lupus Nephritis
DOI:
https://doi.org/10.37506/ijfmt.v14i4.12287Keywords:
SLE, LN, HE4, IGFBP-2, CKDAbstract
Background: many organs of the body such as kidneys, skin, joints, nervous system, blood cells, blood
vessels and serous membranes can be affected by systemic lupus erythematosus (SLE). A wide range of
this disease effects may be attributed to its behavior as an autoimmune disease; this means, numerous
complications of SLE with many organs can be results. In this study, levels of serum human epdidymis
secretory protein4 (HE4) and insulin like growth factor binding protein-2 (IGFBP-2) for Iraqi patients in
SLE with and without lupus nephritis (LN) were investigated to knowledge their ability to be useful markers
for identification of kidney diseases, like lupus nephritis and chronic kidney disease in patients who suffering
from SLE.
Methods: one hundred twenty subjects from both sexes were enrolled in this study. They have been classified
into two patients groups together with the control group. Forty patients of SLE with LN (8male-32female)
with age range (19-44) years, represent the first patients group, the second patients group includes forty
patients suffer from SLE without LN at (16-45) years age range and the control group which consists of 40
healthy subjects with age range (19-62) years. HE4 and IGFBP were estimated by ELISA method.
Results: results show high level of HE4 and IGFBP in both patient groups with SLE in comparison with
control group. At the same time, results confirmed a high positive correlation between HE4 and IGFBP (r =
0.85, p<0.01), ROC analysis data revealed that HE4 is the best parameters for predicting development lupus
nephritis as a main complication of SLE disease.
Conclusion: both patient groups revealed a significantly increase in levels of HE4 and IGFBP compared
with control group. High positive correlation coefficient between HE4 and IGFBP is obtained. Data of ROC
analysis confirmed that HE4 represents a better biomarker for diagnosis of LN in patients with SLE disease.
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