Pregledni rad

https://doi.org/10.11613/BM.2014.018

A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient

Silvia Izquierdo Álvarez Izquierdo Álvarez orcid.org/0000-0002-7615-2399 ; Sección de Genética, Servicio de Bioquímica Clínica, Hospital Universitario Miguel Servet, Zaragoza, Spain
Eva Barrio Ollero ; Sección de Genética, Servicio de Bioquímica Clínica, Hospital Universitario Miguel Servet, Zaragoza, Spain; Facultad de Medicina. Universidad de Zaragoza, Spain
Francisco Miguel Llinares Sanjuan Llinares Sanjuan ; Departamento deHematología, Hospital de Barbastro, Huesca, Spain
Fabiola Lorente Martínez ; Sección de Genética, Servicio de Bioquímica Clínica, Hospital Universitario Miguel Servet, Zaragoza, Spain
María Teresa Calvo Martín ; Sección de Genética, Servicio de Bioquímica Clínica, Hospital Universitario Miguel Servet, Zaragoza, Spain

Sažetak

Introduction: Additional nucleotide substitutions in the 3´-untranslated region of prothrombin gene could explain some thrombotic events and also adverse pregnancy outcomes. We describe the first case of a homozygous 20209C>T mutation as the cause of deep vein thrombosis in a Spanish patient.
Case and methods: The 56-year-old male patient with a partial tear of the Achilles tendon developed calf (tibial) deep vein thrombosis after immobilization and was treated with an anticoagulant. To determine if the deep vein thrombosis was of genetic origin, a peripheral blood DNA sample was analysed for the presence of the three most frequent mutations associated with thrombotic events: factor V Leiden (1691G>A), prothrombin (20210G>A) and methylene tetrahydrofolate reductase (677C>T). The presence or absence of the normal allele of prothrombin could not be determined using the PTH-FV-MTHFR StripAssay (Vienna Lab).
Results: Comprehensive analysis showed that the patient had a variant interfering with the polymerase chain reaction product, we sequenced the entire prothrombin gene and found that the patient had a homozygous C>T mutation at position 20209; this interfered with the polymerase chain reaction product, which needs a C at this position to be able to bind to the wild-type probe present in the test strip.
Conclusion: The homozygous 20209C>T mutation and the presence of the mutation 677C>T in heterozygosity explained the patient’s deep vein thrombosis because the combination of mutations would increase the risk of thrombosis. Suitable genetic counselling should be provided to the patient and first-degree relatives as it important to detect prothrombin gene variants that could increase risk for thrombotic events.

Ključne riječi

thrombosis; prothrombin; deep vein thrombosis; 20209C>T mutation homozygosis

Hrčak ID:

115757

URI

https://hrcak.srce.hr/115757

Datum izdavanja:

15.2.2014.

Posjeta: 1.521 *