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Serum homocysteine

dc.contributor.authorCascalheira, Jose F.
dc.contributor.authorJoao, Sara S.
dc.contributor.authorPinhancos, Sandra S.
dc.contributor.authorCastro, Rita
dc.contributor.authorPalmeira, Manuela
dc.contributor.authorAlmeida, Sofia
dc.contributor.authorFaria, Maria C.
dc.contributor.authorDomingues, Fernanda C.
dc.date.accessioned2015-12-30T10:18:13Z
dc.date.available2015-12-30T10:18:13Z
dc.date.issued2009
dc.description.abstractObjectives: To study the interplay between serum concentrations of homocysteine, steroid hormones and vitamins B and mutations in 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, in association to Alzheimer's type dementia (ATD). Design and methods: Case-control study including 19 individuals diagnosed with ATD and 36 healthy controls. Serum concentrations of the analytes were determined and MTHFR 1298A - C mutation was screened by PCR-RFLP. Results: Multivariable logistic regression analysis identified homocysteine (OR=1.92, P0.01), cholesterol (OR C mutation (OR=6.01, P0.04) as independent predictors of ATD. Positive interaction between homocysteine and uric acid, creatinine, urea or cortisol (P0.02) and negative interaction between homocysteine and vitamin B-12 or MTHFR 1298A - C mutation (P0.03) were observed. Conclusions: High serum concentrations of homocysteine, cholesterol and uric acid, and low concentrations of estradiol and vitamin B-12, as well as the MTHFR 1298A - C mutation are simultaneously associated to ATD. (C) 2009 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
dc.formatapplication/pdf
dc.identifier.citationCLINICAL BIOCHEMISTRY. - Vol. 42, n. 9 (JUN 2009), p. 783-790
dc.identifier.doihttp://dx.doi.org/10.1016/j.clinbiochem.2009.02.006
dc.identifier.issn0009-9120
dc.identifier.urihttp://hdl.handle.net/10451/21475
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.subjectMedical Laboratory Technology
dc.titleSerum homocysteine
dc.titleInterplay with other circulating and genetic factors in association to Alzheimer's type dementia
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage790por
oaire.citation.startPage783por
oaire.citation.titleCLINICAL BIOCHEMISTRYpor
oaire.citation.volumeVol. 42por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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