Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice


Autoria(s): MATTAR, Rejane; MONTEIRO, Maria do Socorro; VILLARES, Cibele Aparecida; SANTOS, Anibal Ferreira dos; CARRILHO, Flair Jose
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Objectives: To validate C/T-13910 polymorphism associated with primary hypolactasia for clinical practice. Design and methods: Lactose breath test and PCR-RFLP for the C/T-13910 polymorphism were performed. Results: Twenty-seven of 28 patients with genotype CC had positive breath tests, all twenty-two patients with genotypes CT or TT had negative breath tests. Agreement of tests was high (p<0.0001; Kappa Index 0.96). Conclusion: C/T-13910 polymorphism detection may be a new tool for primary hypolactasia diagnosis. (C) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

Identificador

CLINICAL BIOCHEMISTRY, v.41, n.7/Ago, p.628-630, 2008

0009-9120

http://producao.usp.br/handle/BDPI/22141

10.1016/j.clinbiochem.2008.01.006

http://dx.doi.org/10.1016/j.clinbiochem.2008.01.006

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Clinical Biochemistry

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #hypolactasia #lactase persistence #lactose malabsorption #single nucleotide polymorphism #hydrogen breath test #LACTOSE-INTOLERANCE #PERSISTENCE #DNA #DIAGNOSIS #ELEMENT #TESTS #Medical Laboratory Technology
Tipo

article

original article

publishedVersion