
INTERLEUKIN-1β AND TUMOR NECROSIS FACTOR-α GENE POLYMORPHISMS IN SYSTEMIC SCLEROSIS Hakami M.A1, Alotaibi B.S1, Alkhalil S.S1, Das S2, Nasreen N3, Jeraiby M.A4, Jawed A5, Lohani M5, Dar S.A5* *Corresponding Author: *Corresponding Author: Sajad Ahmad Dar, Department of Nursing, College of Nursing and Health Sciences, Jazan University, Jazan – 45142, Saudi Arabia; Email: sdar@jazanu.edu.sa page: 59 download article in pdf format
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Abstract
The complex cytokine network plays an important
role in disease susceptibility and development, therefore
single-nucleotide polymorphisms (SNPs) in or near cyto-
kine genes may be relevant to development of systemic
sclerosis (SSc). We in this study investigated 22 SNPs in
13 cytokine genes of SSc patients, and their association
with disease susceptibility. Twenty-three clinically diag-
nosed SSc patients were enrolled for this purpose along
with 80 healthy volunteers for comparisons. Aseptically
collected 2ml of peripheral venous blood from each subject
was processed for DNA extraction. Cytokine genotyp-
ing was carried out using the extracted genomic DNA
by PCR employing sequence-specific primers and data
was analyzed for any association with SSc susceptibility.
Variations in allele, genotype, or haplotype distribution
between patients and healthy volunteers were observed
for the following SNPs: IL-1β –511 C/T (rs16944) and
+3962 T/C (rs1143634); IL-4Rα +1902 G/A (rs1801275);
IL-12 –1188 C/A (rs3212227); TGF-β1 codon 25 G/C
(rs1800471); TNF-α–308 G/A (rs1800629) and –238 G/A
(rs361525); IL-4 –1098 T/G (rs2243248) and –590 T/C
(rs2243250); IL-6 –174 G/C (rs1800795) and nt565 G/A
(rs1800797); and IL-10 –1082 G/A (rs1800896), –819
C/T (rs1800871) and –592 C/A (rs1800872). However,
only the SNPs in IL-1β –511 and +3962, and TNF-α –308
and –238 were found to be significantly associated with
SSc susceptibility. Our findings suggest that IL-1β and
TNF-α gene SNPs may play a role in development of SSc,
although large observational and experimental studies are
needed to substantiate these findings.
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