MBL2 and MIF gene polymorphisms in cardiovascular patients with atherosclerotic lesions undergoing heart valve replacement
Autor: | Sibel Oguzkan-Balci, Mustafa Bilge Erdoğan, Sacide Pehlivan, Ayşen Bayram, Mustafa Pehlivan, Fahriye Ekşi, Birol Yamak |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
gene polymorphisms medicine.medical_specialty medicine.medical_treatment lcsh:Biotechnology mannose binding lectin-2 030204 cardiovascular system & hematology Biology Gastroenterology 03 medical and health sciences 0302 clinical medicine Valve replacement Internal medicine lcsh:TP248.13-248.65 Genotype Coronary bypass surgery medicine Allele Mannose binding Mitral valve replacement 030104 developmental biology Bypass surgery Macrophage migration inhibitory factor migration inhibitory factor Restriction fragment length polymorphism valve replacement Biotechnology |
Zdroj: | Biotechnology & Biotechnological Equipment, Vol 31, Iss 6, Pp 1173-1177 (2017) |
ISSN: | 1314-3530 1310-2818 |
Popis: | The basic underlying factor for cardiovascular diseases is atherosclerosis, which is a multifactorial disease driven by environmental and genetic factors. We aimed to study the genetic polymorphism in mannose binding lectin-2 (MBL2) and macrophage migration inhibitory factor (MIF) in the arteries of patients with atherosclerotic lesions who underwent cardiac valve replacement for cardiac valve stenosis. Thirty-five patients (38.9 %) operated with coronary bypass surgery (coronary group, CG), 55 (61.1 %) patients operated with aortic or mitral valve replacement (valve group, VG) and 100 healthy controls were analyzed for codon 54 A/B polymorphism in the MBL2 gene and –173 G/C polymorphism in the MIF gene by using the method of polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). The comparison of the healthy control group with CG and VG in terms of the MBL2 genotypes revealed significantly lower AA genotype and A allele ratios. The comparison of the healthy control group with CG and VG in terms of the MIF genotypes showed significantly lower GG genotype and G allele ratios. We suggest that the lower frequency of the GG genotype/G allele of the MIF gene and of the AA genotype/A allele of the MBL2 gene may be associated with the ethiopathogenesis of CG and VG patients. |
Databáze: | OpenAIRE |
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