alexa Increased Serum Macrophage Migration Inhibitory Factor (MIF)Concentrations as Potential Risk Factors in Steroid-Resistant Nephrotic Syndrome
ISSN: 2161-0959

Journal of Nephrology & Therapeutics
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Research Article

Increased Serum Macrophage Migration Inhibitory Factor (MIF)Concentrations as Potential Risk Factors in Steroid-Resistant Nephrotic Syndrome

Oke Rina Ramayani1*, Nanan Sekarwana2, Partini Pudjiastuti Trihono3, Ahmad Hamim Sadewa4, Aznan Lelo5 and Putri Chairani Eyanoer6

1Department of Pediatrics, Sumatera Utara University, Indonesia

2Department of Pediatrics, Padjajaran University, Indonesia

3Department of Pediatrics, Indonesia University, Indonesia

4Department of Biochemistry, Gadjah Mada University, Indonesia

5Department of Pharmacology and Therapeutics, Sumatera Utara University, Indonesia

6Department of Community Medicine, Sumatera Utara University, Indonesia

*Corresponding Author:
Oke Rina Ramayani
Department of Pediatrics
Sumatera Utara University, Indonesia
Tel: 061-8365663
E-mail: [email protected]

Received Date: October 20, 2013; Accepted Date: November 18, 2013; Published Date: November 22, 2013

Citation: Ramayani OR, Sekarwana N, Trihono PP, Sadewa AH, Lelo A, et al. (2013) Increased Serum Macrophage Migration Inhibitory Factor (MIF) Concentrations as Potential Risk Factors in Steroid-Resistant Nephrotic Syndrome. J Nephrol Ther 3:142. doi:10.4172/2161-0959.1000142

Copyright: © 2013 Ramayani OR, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Background: Patients with steroid-resistant nephrotic syndrome (SRNS) tend to progress to end-stage renal disease (ESRD). Although the risk of steroid resistance depends mainly on histopathology, other factors, such as cytokines, may contribute to this condition. Cytokine macrophage Migration Inhibitory Factor (MIF) acts to counterregulate glucocorticoids, which have become the main drug therapy for NS. The aim of this study was to evaluate whether raised serum MIF levels represent a potential risk factor for SRNS patients.
Methods: A prospective study was conducted in a multi-centre hospital and school in Medan, Sumatera, Indonesia. A total of 99 subjects were included in the study consisting well child (n=31) and NS patients (n=68). Serum macrophage migration inhibitory factor (MIF) was collected and measured. Patient’s data about demographics, blood pressure, threshold steroid dosage at inclusion, urinary albumin creatinine ratio, plasma angiotensin II and serum MIF were compared between groups.
Results: Majority of subjects showed MIF levels between 10.4 and 31.8 ng/ml. Group SRNS had  significantly higher serum MIF (median 31.9 (14.3-117.2) ng/mL) compared to the levels in group SSNS (median 21.8 (10.4-31.8) ng/mL) and well child (median 24.1 (11.4-31.1) ng/mL. Half of SRNS subjects (n=20) showed higher levels of MIF. In logistic regression analysis, diastolic blood pressure and plasma angiotensin II levels were found to be independently associated with higher serum MIF. There was a weak positive liniear correlation between concentration of MIF serum and angiotensin II plasma.
Conclusions: The serum MIF levels in group SRNS is higher than SSNS and well child. Diastolic blood pressure and plasma angiotensin II levels were found to be independently factors associated with higher MIF serum.

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