Literature DB >> 12757241

Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant.

Pasra Arnutti1, Oytip Nathalang, Suwanna Cowawintaweewat, Wichai Prayoonwiwat, Punbupa Choovichian.   

Abstract

Renal transplantation provides the best long-term treatment for chronic renal failure, but thrombosis of the transplanted renal artery or renal vein is one of the causes of kidney failure in the early postoperative period. Factor V Leiden (FVL) and prothrombin G20210A mutation are the most frequent genetic abnormalities associated with venous thrombosis. We investigated the prevalence of FVL and prothrombin G20210A by polymerase chain reaction with restriction fragment length polymorphism in 75 Thai patients awaiting renal transplant, and a control group of 106 healthy blood donors. Of those awaiting renal transplant, none was found to carry FVL or prothrombin G20210A mutations. Neither the heterozygous nor the homozygous FVL mutation nor the prothrombin G20210A mutation was detected in the 106 healthy volunteers. Although we failed to detect FVL and prothrombin G20210A mutation among those waiting for a kidney transplant, the population size was small. Further studies need to be performed in order to ascertain if these coagulation mutations are of relevance in predicting patients at risk of early transplant failure.

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Year:  2002        PMID: 12757241

Source DB:  PubMed          Journal:  Southeast Asian J Trop Med Public Health        ISSN: 0125-1562            Impact factor:   0.267


  1 in total

1.  Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs.

Authors:  Wassim Y Almawi; Sose H Keleshian; Lobna Borgi; Naglaa A Fawaz; Nisreen Abboud; Nabil Mtiraoui; Touhami Mahjoub
Journal:  J Thromb Thrombolysis       Date:  2005-12       Impact factor: 2.300

  1 in total

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