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Miler, Marijana; Nikolac Gabaj, Nora; Ćelap, Ivana; Grazio, Simeon; Tomašić, Vedran; Bišćanin, Alen; Mitrović, Joško; Đerek, Lovorka; Morović-Vergles, Jadranka; Vrkić, Nada; Štefanović, Mario
Rheumatology international, 12/2021, Letnik: 41, Številka: 12Journal Article
The hypothesis of the study was that polymorphisms in promoter regions -238 and -308 of TNF-α could be associated with different clinical outcomes in inflammatory bowel diseases (IBD) and immune-mediated rheumatic diseases (IMRD). The aim was to examine the possible association of both polymorphisms with concentration of C-reactive protein (CRP) and fecal calprotectin (fCAL), onset of the remission and development of the ADA in patients on therapy with anti-TNF inhibitors. The prospective study was done in patients with IBD and IMRD on infliximab (IFX) or adalimumab (ADM). Patients were genotyped for TNF-α -238 and -308 polymorphisms. The concentration of CRP, fCAL, IFX or ADM and antibodies to drugs were measured according to manufacturer’s instructions and followed-up for 6 or 12 months. Out of all patients ( N = 112), number of patients in remission did not differ according to genotypes (for IBD patients P = 0.509 vs 0.223; for IMRD patients P = 0.541 vs 0.132 for TNF-α -238 and -308, respectively). Initial CRP concentration was higher in IBD patients with TNF-α -308 GG than GA/AA genotypes in patients who failed to achieve remission 11.8 (4.4–39.6) vs 3.1 (1.5–6.5), P = 0.033. In IBD patients with remission, fCAL concentration after at least 6 months of therapy was higher in TNF-α -308 GG than in GA genotype 52 (25–552) vs 20 (20–20) µg/g, P = 0.041. Our results showed the association of TNF-α -308 GG genotype with a higher concentration of CRP and fecal calprotectin in patients with inflammatory bowel diseases on IFX or ADM therapy. Clinical remission and development of antibodies to anti-TNF drugs were not associated with TNF-α -238 and -308 polymorphisms.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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