Evidence map›Paper›PMID 27051654›Full record

ArticleVascular specialist international2016

Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis.

Habib Ghaznavi, Zahra Soheili, Shahram Samiei, Mohammad Soleiman Soltanpour

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Article in Vascular specialist international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 35% of its field
1 · What the graph read from it

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 4 institutions in 1 country.

Habib GhaznaviCellular and Molecular Research Centre, Zahedan University of Medical Sciences, Zahedan.
Zahra SoheiliDepartment of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran.
Shahram SamieiIranian Blood Transfusion Organization, Tehran.
Mohammad Soleiman SoltanpourDepartment of Laboratory Sciences, Faculty of Paramedical Sciences, Zanjan University of Medical Sciences, Zanjan, Iran.
Iranian Legal Medicine Organization · IRNational Institute of Genetic Engineering and Biotechnology · IRZahedan University of Medical Sciences · IRZanjan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePortal vein thrombosis (PVT) is a rare and life-threatening vascular disorder characterized by obstruction or narrowing of the portal vein. Hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism has been studied in PVT patients with conflicting results. In the present study the association of hyperhomocysteinemia and MTHFR C677T polymorphism with PVT risk was investigated in Iranians. MATERIALS AND

methodsOur study population consisted of 10 idiopathic PVT patients and 80 healthy control subjects matched for age and sex. MTHFR C677T polymorphism was genotyped by the polymerase chain reaction technique combined with restriction enzyme fragment length polymorphism (PCR-RFLP) technique and plasma total homocysteine (tHcy) levels were determined by enzyme immunoassay method.

resultsMean plasma tHcy levels were significantly higher in PVT patients (20.2±6.8) than control subjects (10.9±4.7) (P=0.001). Moreover, plasma tHcy levels were significantly higher in 677T allele carriers relative to 677C allele carriers in both PVT patients (P=0.01) and control subjects (P=0.03). Neither homozygote nor heterozygote genotypes of MTHFR C677T polymorphism correlated significantly with PVT risk (P>0.05). Moreover, MTHFR C677T polymorphism didn't increase the risk of PVT under dominant (CT+TT vs. CC) or recessive (TT vs. CC+CT) genetic models analyzed (P>0.05). The difference in frequency of minor 677T allele between PVT patients and control subjects was not statistically significant (P>0.05).

conclusionBased on the current study, we suggest that hyperhomocysteinemia constitutes a significant and common risk factor for PVT. Also, MTHFR C677T polymorphism is not a risk factor for PVT but is a contributing factor for elevated plasma tHcy levels.

Indexed as

Genetic polymorphismHomocysteineMethylene tetrahydrofolate reductasePortal vein thrombosis

Identifiers

PMID27051654
PMCPMC4816019
OpenAlexW2321194574

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