Association of miR-146 rs2910164, miR-196a rs11614913, miR-221 rs113054794 and miR-224 rs188519172 polymorphisms with anti-TNF treatment response in a Greek population with Crohn's disease
- PMID: 29152405
- PMCID: PMC5680166
- DOI: 10.4292/wjgpt.v8.i4.193
Association of miR-146 rs2910164, miR-196a rs11614913, miR-221 rs113054794 and miR-224 rs188519172 polymorphisms with anti-TNF treatment response in a Greek population with Crohn's disease
Abstract
Aim: To investigate the correlation between rs2910164, rs11 614913, rs113054794, and rs188519172 polymorphisms and response to anti-TNF treatment in patients with Crohn's disease (CD).
Methods: One hundred seven patients with CD based on standard clinical, endoscopic, radiological, and pathological criteria were included in the study. They all received infliximab or adalimumab intravenously or subcutaneously at standard induction doses as per international guidelines. Clinical and biochemical response was assessed using the Harvey-Bradshaw index and CRP levels respectively. Endoscopic response was evaluated by ileocolonoscopy at week 12-20 of therapy. The changes in endoscopic appearance compared to baseline were classified into four categories, and patients were classified as responders and non-responders. Whole peripheral blood was extracted and genotyping was performed by PCR.
Results: One hundred and seven patients were included in the study. Seventy two (67.3%) patients were classified as complete responders, 22 (20.5%) as partial while 13 (12.1%) were primary non-responders. No correlation was detected between response to anti-TNF agents and patients' characteristics such as gender, age and disease duration while clinical and biochemical indexes used were associated with endoscopic response. Concerning prevalence of rs2910164, rs11614913, and rs188519172 polymorphisms of miR-146, miR-196a and miR-224 respectively no statistically important difference was found between complete, partial, and non-responders to anti-TNF treatment. Actually CC genotype of rs2910164 was not detected in any patient. Regarding rs113054794 of miR-221, normal CC genotype was the only one detected in all studied patients, suggesting this polymorphism is highly rare in the studied population.
Conclusion: No correlation is detected between studied polymorphisms and patients' response to anti-TNF treatment. Polymorphism rs113054794 is not detected in our population.
Keywords: Anti-TNF; Biomarkers; Crohn’s disease; MicroRNA; Polymorphisms.
Conflict of interest statement
Conflict-of-interest statement: None to declare.
Similar articles
-
Association of rs1568885, rs1813443 and rs4411591 polymorphisms with anti-TNF medication response in Greek patients with Crohn's disease.World J Gastroenterol. 2014 Apr 7;20(13):3609-14. doi: 10.3748/wjg.v20.i13.3609. World J Gastroenterol. 2014. PMID: 24707144 Free PMC article.
-
Magnetic resonance enterography changes after antibody to tumor necrosis factor (anti-TNF) alpha therapy in Crohn's disease: correlation with SES-CD and clinical-biological markers.BMC Med Imaging. 2016 May 5;16(1):37. doi: 10.1186/s12880-016-0139-7. BMC Med Imaging. 2016. PMID: 27149857 Free PMC article.
-
Genetic polymorphisms predict response to anti-tumor necrosis factor treatment in Crohn's disease.World J Gastroenterol. 2017 Jul 21;23(27):4958-4967. doi: 10.3748/wjg.v23.i27.4958. World J Gastroenterol. 2017. PMID: 28785150 Free PMC article.
-
[Anti-TNF therapy in treatment of luminal Crohn's disease].Acta Med Croatica. 2013 Apr;67(2):179-89. Acta Med Croatica. 2013. PMID: 24471301 Review. Croatian.
-
Tumor necrosis factor-alpha antibody for maintenance of remission in Crohn's disease.Cochrane Database Syst Rev. 2008 Jan 23;(1):CD006893. doi: 10.1002/14651858.CD006893. Cochrane Database Syst Rev. 2008. PMID: 18254120 Review.
Cited by
-
Circulating microRNAs as biomarkers for diabetic neuropathy: A novel approach.World J Exp Med. 2018 Nov 30;8(3):18-23. doi: 10.5493/wjem.v8.i3.18. eCollection 2018 Nov 30. World J Exp Med. 2018. PMID: 30596030 Free PMC article. Review.
-
Micro-RNA-21 rs1292037 A>G polymorphism can predict hepatocellular carcinoma prognosis (HCC), and plays a key role in cell proliferation and ischemia-reperfusion injury (IRI) in HCC cell model of IRI.Saudi Med J. 2020 Apr;41(4):383-392. doi: 10.15537/smj.2020.4.24994. Saudi Med J. 2020. PMID: 32291425 Free PMC article.
-
Patient sex does not affect endoscopic outcomes of biologicals in inflammatory bowel disease but is associated with adverse events.Int J Colorectal Dis. 2020 Aug;35(8):1489-1500. doi: 10.1007/s00384-020-03663-2. Epub 2020 Jun 26. Int J Colorectal Dis. 2020. PMID: 32592091 Free PMC article. Review.
-
Inflammation and Pancreatic Cancer: Focus on Metabolism, Cytokines, and Immunity.Int J Mol Sci. 2019 Feb 5;20(3):676. doi: 10.3390/ijms20030676. Int J Mol Sci. 2019. PMID: 30764482 Free PMC article. Review.
-
Analysis of molecular and clinical parameters of 4-year adalimumab therapy in psoriatic patients.Postepy Dermatol Alergol. 2020 Oct;37(5):736-745. doi: 10.5114/ada.2020.100484. Epub 2020 Nov 7. Postepy Dermatol Alergol. 2020. PMID: 33240014 Free PMC article.
References
-
- Rutgeerts P, Vermeire S, Van Assche G. Biological therapies for inflammatory bowel diseases. Gastroenterology. 2009;136:1182–1197. - PubMed
-
- Ding NS, Hart A, De Cruz P. Systematic review: predicting and optimising response to anti-TNF therapy in Crohn’s disease - algorithm for practical management. Aliment Pharmacol Ther. 2016;43:30–51. - PubMed
-
- Billiet T, Ferrante M, Van Assche G. The use of prognostic factors in inflammatory bowel diseases. Curr Gastroenterol Rep. 2014;16:416. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous