The association of fractalkine receptor (T280m) polymorphism in the pathogenesis of acute coronary syndrome in the Egyptian population

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dc.contributor.author Hassan D.S.
dc.contributor.author Hashad I.M.
dc.contributor.author Rahman M.F.A.
dc.contributor.author Abdel-Maksoud S.M.
dc.contributor.other Clinical Biochemistry Unit
dc.contributor.other Faculty of Pharmacy and Biotechnology
dc.contributor.other German University in Cairo
dc.contributor.other Cairo
dc.contributor.other Egypt; Biochemistry Department
dc.contributor.other Faculty of Pharmacy
dc.contributor.other October University for Modern Science and Arts
dc.contributor.other Giza
dc.contributor.other Egypt
dc.date.accessioned 2020-01-09T20:40:43Z
dc.date.available 2020-01-09T20:40:43Z
dc.date.issued 2019
dc.identifier.issn 13892010
dc.identifier.other https://doi.org/10.2174/1389201019666181031163748
dc.identifier.other PubMed ID 30381070
dc.identifier.uri https://t.ly/xRmwp
dc.description Scopus
dc.description.abstract Fractalkine (FKN) in its free and membrane bound-forms and its receptor CX3CR1are reported to have an atherosclerotic effect. The relationship of Single Nucleotide Polymorphisms (SNPs) in FKN and CX3CR1genes with the Coronary Artery Disease (CAD) risk showed conflicting results in different populations. The aim of this study was to investigate the influence of CX3CR1 threonine 280 methionine (T280M) polymorphism in the predisposition of Acute Coronary Syndrome (ACS) in Egyptians. Methods: 200 Egyptian subjects were recruited for the study. They were divided into 100 ACS patients and 100 healthy controls. Genotyping of CX3CR1 T280M was performed using a Polymerase Chain Reaction-restriction Fragment Length Polymorphism (PCR-RFLP). Serum FKN was assayed by Enzyme - Linked - Immuno- Sorbent-Assay (ELISA). Results: T and M allele frequencies for CX3CR1gene were not significantly different between ACS and Controls (p=0.76). Moreover, none of the genotypes had an atheroprotective effect. Serum analysis showed higher levels of FKN in ACS patients (p=0.041). FKN levels were not significantly different among genotypes of control and ACS groups (p=0.34) and (p=0.38) respectively. Conclusion: This study shows that CX3CR1 T280M polymorphism does not affect the incidence of ACS the Egyptian population. Moreover, none of the genotypes were associated with higher FKN levels. � 2018 Bentham Science Publishers. en_US
dc.description.uri https://www.scimagojr.com/journalsearch.php?q=15581&tip=sid&clean=0
dc.language.iso English en_US
dc.publisher Bentham Science Publishers B.V. en_US
dc.relation.ispartofseries Current Pharmaceutical Biotechnology
dc.relation.ispartofseries 19
dc.subject October University for Modern Sciences and Arts
dc.subject University for Modern Sciences and Arts
dc.subject MSA University
dc.subject جامعة أكتوبر للعلوم الحديثة والآداب
dc.subject October University for Modern Sciences and Arts
dc.subject University for Modern Sciences and Arts
dc.subject MSA University
dc.subject جامعة أكتوبر للعلوم الحديثة والآداب
dc.subject Acute coronary syndrome en_US
dc.subject CX3CR1 en_US
dc.subject Egyptians en_US
dc.subject Fractalkine receptor en_US
dc.subject Inflammation en_US
dc.subject T280M polymorphism en_US
dc.subject biochemical marker en_US
dc.subject chemokine receptor CX3CR1 en_US
dc.subject triacylglycerol en_US
dc.subject chemokine receptor CX3CR1 en_US
dc.subject CX3CL1 protein, human en_US
dc.subject CX3CR1 protein, human en_US
dc.subject fractalkine en_US
dc.subject acute coronary syndrome en_US
dc.subject adult en_US
dc.subject Article en_US
dc.subject autosomal dominant inheritance en_US
dc.subject autosomal recessive inheritance en_US
dc.subject cholesterol blood level en_US
dc.subject comparative study en_US
dc.subject controlled study en_US
dc.subject coronary artery atherosclerosis en_US
dc.subject disease predisposition en_US
dc.subject Egyptian en_US
dc.subject enzyme linked immunosorbent assay en_US
dc.subject female en_US
dc.subject gene frequency en_US
dc.subject genetic association en_US
dc.subject genetic polymorphism en_US
dc.subject genetic variability en_US
dc.subject genotype en_US
dc.subject human en_US
dc.subject major clinical study en_US
dc.subject male en_US
dc.subject middle aged en_US
dc.subject non ST segment elevation myocardial infarction en_US
dc.subject pathogenesis en_US
dc.subject polymerase chain reaction en_US
dc.subject prevalence en_US
dc.subject restriction fragment length polymorphism en_US
dc.subject ST segment elevation myocardial infarction en_US
dc.subject unstable angina pectoris en_US
dc.subject acute coronary syndrome en_US
dc.subject Egypt en_US
dc.subject genetic predisposition en_US
dc.subject genetics en_US
dc.subject incidence en_US
dc.subject metabolism en_US
dc.subject single nucleotide polymorphism en_US
dc.subject Acute Coronary Syndrome en_US
dc.subject Chemokine CX3CL1 en_US
dc.subject CX3C Chemokine Receptor 1 en_US
dc.subject Egypt en_US
dc.subject Female en_US
dc.subject Gene Frequency en_US
dc.subject Genetic Predisposition to Disease en_US
dc.subject Genotype en_US
dc.subject Humans en_US
dc.subject Incidence en_US
dc.subject Male en_US
dc.subject Middle Aged en_US
dc.subject Polymorphism, Single Nucleotide en_US
dc.title The association of fractalkine receptor (T280m) polymorphism in the pathogenesis of acute coronary syndrome in the Egyptian population en_US
dc.type Article en_US
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dcterms.source Scopus
dc.identifier.doi https://doi.org/10.2174/1389201019666181031163748
dc.identifier.doi PubMed ID 30381070
dc.Affiliation October University for modern sciences and Arts (MSA)


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