Abstract

BackgroundSarcoidosis is a systemic inflammatory disease of unknown etiology. Osteopontin (SPP1, OPN) is an extra cellular matrix glycoprotein and cytokine with a known role in granuloma formation and in autoimmune and inflammatory diseases.ObjectiveTo determine whether plasma OPN levels are elevated in patients with sarcoidosis and compare the frequency of four single nucleotide polymorphism (SNPs) variants in the OPN gene in sarcoidosis patients compared to healthy controls.MethodsDemographic and clinical information, radiological studies and pulmonary function tests were evaluated in 113 patients with sarcoidosis and in 79 healthy controls. Blood samples were analyzed for SNPs of the OPN gene and for plasma OPN and CRP levels. Association between clinical features of disease and OPN levels as well as SNP frequencies was determined.ResultsPlasma OPN levels were higher in sarcoidosis patients than in healthy subjects, (median: 217 vs 122ng/ml, p<0.001). Area under the curve for receiver operator curves (ROC) was 0.798 (0.686–0.909 95% CI.) No differences were observed between sarcoidosis patients and controls in the frequency of any of the SNPs evaluated. Presence of lung parenchymal involvement was associated with SNP distribution at rs1126772 (p = 0.02). We found no correlation between SNPs distribution and plasma OPN levels.ConclusionsOsteopontin protein levels are elevated in sarcoidosis. We found no evidence for an association between SNPs on the osteopontin gene and plasma OPN levels or the presence of sarcoidosis, however, an association between genotype and several phenotypic clinical parameters of disease was observed.

Highlights

  • Sarcoidosis is a systemic inflammatory disease of unknown etiology, characterised by noncaseating granuloma formation in various organs, with several recognized genetic and environmental risk factors

  • Area under the curve for receiver operator curves (ROC) was 0.798 (0.686–0.909 95% CI.) No differences were observed between sarcoidosis patients and controls in the frequency of any of the single nucleotide polymorphism (SNPs) evaluated

  • We found no correlation between SNPs distribution and plasma OPN levels

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Summary

Introduction

Sarcoidosis is a systemic inflammatory disease of unknown etiology, characterised by noncaseating granuloma formation in various organs, with several recognized genetic and environmental risk factors. Genetic susceptibility to sarcoidosis has been found to be related to specific genes such as Butyrophilin-like protein 2 (BTNL2), which Belongs to the immunoglobulin superfamily [6], Annexin A11 (ANAXA11), which gives rise to auto-antibodies in several inflammatory diseases, including rheumatoid arthritis, systemic lupus erythematosus and Sjogren syndrome [7], Solute carrier family 11 (Proton-coupled divalent metal ion transporter), member 1 (SLC11A1), which is associated with risk of intracellular pathogens such as tuberculosis, and with autoimmune diseases such as rheumatoid arthritis, crohn’s disease, type 1 diabetes, and primary biliary cirrhosis [8]; and to Interferon alpha (IFNA) genes polymorphisms [9], known for its involvement in Th1 diseases.

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