Thrombosis is a major cause of morbidity and mortality worldwide. Genetic factors are one component of thrombosis. We studied the prevalence of two mutations that are known risk factors in the pathogenesis of arterial and venous thrombosis in the genetically isolated Circassian population in Jordan. Factor II G20210A and Factor V Leiden single nucleotide polymorphisms were analysed by polymerase chain reaction and restriction fragment length polymorphism method in 104 random unrelated subjects from the Circassian population in Jordan. The prevalence rates among the Circassian population in Jordan for Factor II G20210A was 12.2% and for Factor V Leiden was 7.7%. We have shown that the population is in Hardy-Weinberg equilibrium and that the prevalences of both mutations are within the range of other ethnic groups. This is the first study to describe Circassian health related genetic characteristics in Jordan. Such population-based studies will contribute to understanding the interaction between genetic and environmental risk factors. It will remain to be seen whether carriers of Factor II G20210A and Factor V Leiden are more likely to develop thrombosis. This issue should be studied in the future to determine the need for screening of these mutations particularly in thrombophilia patients.
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http://dx.doi.org/10.1007/s11239-012-0772-0 | DOI Listing |
J Community Genet
December 2023
Department of Biology and Biotechnology, The Hashemite University, Zarqa, 591504, Jordan.
Circassians and Chechens in Jordan, both with Caucasian ancestry, are genetically isolated due to high rate of endogamous marriages. Recent interest in these populations has led to studies on their genetic similarities, differences, and epidemiological differences in various diseases. Research has explored their predisposition to conditions like diabetes, hypertension, and cancer.
View Article and Find Full Text PDFFront Genet
October 2022
Institute of Archaeogenomics, Research Centre for the Humanities, Budapest, Hungary.
One hundred and six Rétköz and 48 Váh valley samples were collected from the contact zones of Hungarian-Slovakian territories and were genotyped for Y-chromosomal haplotypes and haplogroups. The results were compared with contemporary and archaic data from published sources. The genetic composition of the Rétköz population from Hungary and the Váh valley population from Slovakia indicates different histories.
View Article and Find Full Text PDFJ Immigr Minor Health
October 2022
Department of Biology and Biotechnology, Hashemite University, Zarqa, Jordan.
CYP2C8 is a member of Cytochrome P450 enzymes system. It plays an important role in metabolizing a wide range of exogenous and endogenous compounds. CYP2C8 is involved in the metabolism of more than 100 drugs, typical substrates include: anticancer agents, antidiabetic agents, antimalarial agents, lipid lowering drugs and many others that constitute 20% of clinically prescribed drugs.
View Article and Find Full Text PDFCystic fibrosis (CF) is a common monogenic disease caused by pathogenic variants in the gene. The distribution and frequency of variants vary in different countries and ethnic groups. The spectrum of pathogenic variants of the gene was previously studied in more than 1,500 CF patients from different regions of the European and North Caucasian region of Russia and the spectrum of the most frequent pathogenic variants of the gene and ethnic features of their distribution were determined.
View Article and Find Full Text PDFCurr Drug Metab
May 2021
Department of Biology and Biotechnology, Hashemite University, Zarqa 13133, Jordan.
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