Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2008
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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 |
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 |