Abstract

Abstract Objectives The systemic immune inflammation index (SII) is a novel biomarker based on platelet, neutrophil and lymphocyte counts. SII serum levels have diagnostic, prognostic degrees and correlations with various immune, inflammatory diseases. Celiac disease (CD) is an immune-mediated chronic enteropathy with inflammatory situations. Here we aimed to evaluate clinical significance of SII and to compare SII with other inflammatory markers in CD. Methods 161 pathologically confirmed CD and 75 dyspeptic patients were enrolled. Hemogram, biochemical markers, SII, platelet-to-lymphocyte ratio (PLR), neutrophil-to-lymphocyte ratio (NLR), mean platelet volume-to-platelet ratio (MPR) and monocyte-to-high density lipoprotein cholesterol ratio (MHR) were evaluated. Results There was a statistically significant difference between groups for SII (p<0.001). SII was statistically correlated with and superior to inflammatory markers in relation with CD. There were also statistically significant differences between groups for hsCRP, PLR, NLR, MPR, haemoglobin, platelet count, platelet volume distribution width, plateletcrit, ferritin, total cholesterol and HDL cholesterol (p=0.034; 0.015; 0.032; <0.001; <0.001; <0.001; 0.030; 0.001; <0.001; <0.001; 0.048, respectively). Correlations between SII and NLR, PLR, MHR, hsCRP were statistically significant (p≤0.001; <0.001; 0.033; 0.030, respectively). ROC analysis was used to determine the optimal cut-off value for CD by SII. A baseline SII level >560.0 was associated with CD with 64% specificity, 78% sensitivity (p<0.001). Conclusions To the best of our knowledge, this is the first study analyzed the diagnostic value of SII in CD. SII may serve as a beneficial marker for the diagnosis of inflammatory state superior to that of hsCRP, PLR, NLR, MHR, MPR and WBC.

Highlights

  • Celiac disease (CD) is a frequently seen immune mediated genetic disease

  • Statistically significant differences were found between two study groups for Hb, PLT, platelet volume distribution width (PDW), PCT, ferritin, total cholesterol (TC), high density lipoprotein cholesterol (HDL-c), systemic immune inflammation index (SII), high sensitive C-reactive protein (hsCRP), platelet-to-lymphocyte ratio (PLR) and mean platelet volume-to-platelet ratio (MPR) levels (Table 2)

  • In inflammatory processes neutrophils are rapidly recruited from the blood stream into inflamed tissues

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Summary

Introduction

Until the last decades the most believed opinion was that CD was a disease of children, but today lots of studies demonstrate a remarkable increase of CD prevalance in adults [1]. The precise and the gold standard diagnosis of CD is the biopsy of small bowel and CD can be presented by demonstrating villous atrophies in intestinal biopsies [2, 3]. Chronic inflammation caused by dietary gluten peptides of wheat or rye and barley reveals the disease in susceptible people [4]. These peptides are responsible for small intestinal epithelial inflammation, villous atrophy and mucosal damage so symptoms of malabsorption occur [5]. Patients with CD have some complications such as bone fractures, lung infections, hyposplenism, intestinal ulcers, collagenous enteritis and intestinal carcinoma [7]

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