2021-12-292021-12-292011Sarıcaoğlu, H. vd. (2011). "Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease". Genetics and Molecular Research, 10(1), 1-6.1676-5680https://doi.org/10.4238/vol10-1gmr824http://www.funpecrp.com.br/gmr/year2011/vol10-1/pdf/gmr824.pdfhttp://hdl.handle.net/11452/23737Colchicine is commonly used in the treatment of Behcet's disease. However, some patients are unresponsive to colchicine treatment. Adenosine triphosphate-binding cassette subfamily B member 1 (ABCB1) transports colchicine out of cells. We investigated a possible association of C3435T polymorphism of the ABCB1 (MDR1) gene with colchicine response in patients with Behcet's disease. We randomly selected 97 patients with Behcet's disease, examined ABCB1 (MDR1) gene C3435T polymorphisms, and evaluated patient responses to colchicine. Forty-three patients were colchicine responsive, while the remaining 54 patients were unresponsive. No significant difference was found between genotypic and allelic frequencies of the ABCB1 C3435T polymorphisms in patients with Behcet's disease and healthy volunteers. Also, there was no significant difference among responsive and nonresponsive patients. We concluded that ABCB1 C3435T polymorphism is not associated with a colchicine response in patients with Behcet's disease.eninfo:eu-repo/semantics/openAccessBiochemistry & molecular biologyGenetics & heredityBehcet's diseaseColchicineABCB1 genePolymorphismFamilial mediterranean feverMultidrug-resistance geneP-glycoproteinClinical-relevanceMdr1AssociationEfficacyAdultBehcet syndromeCase control studiesColchicineFemaleGene frequencyGenotypeHumansMaleMiddle agedP-glycoproteinPolymorphism, single nucleotideArticle0002865273000012-s2.0-792515157711610121218380Biochemistry & molecular biologyGenetics & heredityMDR Gene; Multidrug Resistance Protein 1; Restriction Fragment Length PolymorphismsColchicineMultidrug resistance protein 1AdultArticleBehcet diseaseDiarrheaDrug withdrawalFemaleGene frequencyGenetic associationGenetic polymorphismGenotypeHumanLeukopeniaLiver dysfunctionMajor clinical studyMaleRandomized controlled trialSide effectStomach diseaseTreatment response