Source:http://linkedlifedata.com/resource/pubmed/id/19152396
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017337,
umls-concept:C0020094,
umls-concept:C0076560,
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umls-concept:C1442734,
umls-concept:C1527148,
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umls-concept:C1704619,
umls-concept:C1705603,
umls-concept:C1880355,
umls-concept:C1882417
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pubmed:issue |
3
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pubmed:dateCreated |
2009-1-22
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pubmed:abstractText |
The development of HTLV-1 associated clinical manifestations, such as TSP/HAM and ATLL, occur in 2-4% of the infected population and it is still unclear why this infection remains asymptomatic in most infected carriers. Recently, it has been demonstrated that HTLV uses the Glucose transporter type 1 (GLUT1) to infect T-CD4(+) lymphocytes and that single nucleotide polymorphisms (SNP) in the GLUT1 gene are associated with diabetic nephropathy in patients with diabetes mellitus in different populations. These polymorphisms could contribute to a higher GLUT1 protein expression on cellular membrane, facilitating the entry of HTLV and its transmission cell by cell. This could result in a higher provirus load and consequently in the development of TSP/HAM. To evaluate the role of GLUT1 gene polymorphisms in the development of TSP/HAM in HTLV-1 infected individuals, the g.22999G > T, g.15339T > C and c.-2841A > T sites were analyzed by PCR/RFLP or sequencing in 244 infected individuals and 102 normal controls. The proviral load of the HTLV-1 infected patients was also analyzed using Real Time Quantitative PCR. Genotypic and allelic frequencies of the three sites did not differ significantly between controls and HTLV-1 infected individuals. There was no difference in genotypic and allelic distributions among patients as to the presence or absence of HTLV-1 associated clinic manifestations. As regards the quantification of the provirus load, we observed a significant reduction in the asymptomatic individuals compared with the oligosymptomatic and TSP/HAM individuals. These results suggest that g.22999G > T, g.15339T > C, and c.-2841A > T SNP do not contribute to HTLV-1 infection nor to the genetic susceptibility of TSP/HAM in Brazilian HTLV-1 infected individuals.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1096-9071
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pubmed:author |
pubmed-author:AlcantaraLuiz Carlos JúniorLC,
pubmed-author:AzevedoRocheleR,
pubmed-author:CostaGiselle Calasans SouzaGC,
pubmed-author:CovasDimas TadeuDT,
pubmed-author:GadelhaSandra RochaSR,
pubmed-author:Galvão-CastroBernardoB,
pubmed-author:KashimaSimone HaddadSH,
pubmed-author:MuricyGabrielG,
pubmed-author:OlavarriaViviana NilaVN,
pubmed-author:TakayanaguiOsvaldo MassaitiOM
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pubmed:copyrightInfo |
Copyright 2009 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
81
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
552-7
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pubmed:meshHeading |
pubmed-meshheading:19152396-Brazil,
pubmed-meshheading:19152396-Gene Frequency,
pubmed-meshheading:19152396-Genotype,
pubmed-meshheading:19152396-Glucose Transporter Type 1,
pubmed-meshheading:19152396-HTLV-I Infections,
pubmed-meshheading:19152396-Human T-lymphotropic virus 1,
pubmed-meshheading:19152396-Humans,
pubmed-meshheading:19152396-Paraparesis, Tropical Spastic,
pubmed-meshheading:19152396-Polymerase Chain Reaction,
pubmed-meshheading:19152396-Polymorphism, Genetic,
pubmed-meshheading:19152396-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:19152396-Proviruses
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pubmed:year |
2009
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pubmed:articleTitle |
Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in Brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene.
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pubmed:affiliation |
Laboratório Avançado de Saúde Pública, Centro de Pesquisa Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Bahia, Brazil.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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