Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:17333388rdf:typepubmed:Citationlld:pubmed
pubmed-article:17333388lifeskim:mentionsumls-concept:C0422792lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0035647lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0020538lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0017431lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0332281lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0205217lld:lifeskim
pubmed-article:17333388lifeskim:mentionsumls-concept:C0919427lld:lifeskim
pubmed-article:17333388pubmed:issue1-2lld:pubmed
pubmed-article:17333388pubmed:dateCreated2007-7-24lld:pubmed
pubmed-article:17333388pubmed:abstractTextThe goals of our present study were to measure plasma homocysteine levels and determine their association with methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms (C677T and A1298C) in essential hypertensive subjects. Plasma total homocysteine and folic acid levels were measured in essential hypertensive patients (n = 153) before and after oral supplementation with either 5 mg folic acid tablet/day or 5 mg placebo/day for 4 weeks and compared with age and sex matched normotensive controls (n = 133). MTHFR gene polymorphisms (C677T and A1298C) were studied by restriction fragment length polymorphism and correlated with plasma homocysteine levels. Homocysteine levels were significantly higher in hypertensive patients as compared to controls and showed a negative correlation with plasma folate levels. Folic acid supplementation (5 mg/day) for 4 weeks resulted in a significant decrease in plasma homocysteine concentrations in these patients. Patients carrying MTHFR 677T allele (OR = 1.90; 95%CI: 1.14-3.19) or MTHFR 1298C (OR = 2.6, 95%CI: 1.55-4.40) allele were at increased risk of hypertension. The frequency of co-occurrence of MTHFR 677 CT/1298 CC genotypes was significantly higher in the patients compared to controls (P < 0.05) and was associated with increased risk of hypertension (OR = 3.54, 95%CI: 0.37-4.30). Subjects with MTHFR 1298 CC genotype had significantly higher homocysteine levels compared to those with MTHFR 1298 AA genotype (P < 0.05). Our results indicate that MTHFR 677T and 1298C alleles and co-occurrence of MTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension and MTHFR 1298 CC genotype is associated with higher homocysteine levels in our subjects.lld:pubmed
pubmed-article:17333388pubmed:languageenglld:pubmed
pubmed-article:17333388pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:citationSubsetIMlld:pubmed
pubmed-article:17333388pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17333388pubmed:statusMEDLINElld:pubmed
pubmed-article:17333388pubmed:monthAuglld:pubmed
pubmed-article:17333388pubmed:issn0300-8177lld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:JainSanjaySlld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:KhullarMadhuMlld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:KumariSavitaSlld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:SehrawatBadan...lld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:SachdevaMeena...lld:pubmed
pubmed-article:17333388pubmed:authorpubmed-author:MarkanSuchita...lld:pubmed
pubmed-article:17333388pubmed:issnTypePrintlld:pubmed
pubmed-article:17333388pubmed:volume302lld:pubmed
pubmed-article:17333388pubmed:ownerNLMlld:pubmed
pubmed-article:17333388pubmed:authorsCompleteYlld:pubmed
pubmed-article:17333388pubmed:pagination125-31lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:meshHeadingpubmed-meshheading:17333388...lld:pubmed
pubmed-article:17333388pubmed:year2007lld:pubmed
pubmed-article:17333388pubmed:articleTitleMTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension in Indians.lld:pubmed
pubmed-article:17333388pubmed:affiliationDepartment of Experimental Medicine and Biotechnology, Post Graduate Institute of Medical Education and Research, Laboratory no. 2033, Research block B, Chandigarh 160012, India.lld:pubmed
pubmed-article:17333388pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17333388pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:17333388pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
entrez-gene:4524entrezgene:pubmedpubmed-article:17333388lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:17333388lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:17333388lld:entrezgene
lhgdn:association:60516lhgdn:found_inpubmed-article:17333388lld:lhgdn
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17333388lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17333388lld:pubmed