Lactose intolerance:: Lactose tolerance test versus genotyping

被引:46
作者
Ridefelt, P [1 ]
Håkansson, LD [1 ]
机构
[1] Univ Hosp, Dept Med Sci, SE-75185 Uppsala, Sweden
关键词
diagnostic techniques; digestive system; genotype; lactose intolerance; lactose tolerance test; polymorphism; single nucleotide;
D O I
10.1080/00365520510015764
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective. Adult lactose intolerance, which affects the majority of the population in the world, has been associated with a single nucleotide polymorphism, C-13910T, located upstream of the lactase gene. Material and methods. Adult patients undergoing lactose tolerance tests with lactose challenge and plasma glucose measurements were included in the study comprising 44 Swedes and 7 non-Swedish individuals. A real-time PCR method was established for the genotyping. Results. Out of 51 patients 48 had concordant results on genotyping and lactose tolerance tests, e. g. - 13910T/T and - 13910C/T genotypes had high glucose elevations. All patients with the heterozygous genotype, - 13910C/T, had high glucose elevations, and no gene - dose relationship was observed when comparing maximal glucose increases for cases with - 13910C/T and - 13910T/T genotypes. Conclusions. Genotyping could replace lactose challenge as a first-stage screening test in adults of European descent, but should be used together with tolerance tests in children and patients where secondary lactose intolerance is suspected.
引用
收藏
页码:822 / 826
页数:5
相关论文
共 15 条
[1]   Genetic signatures of strong recent positive selection at the lactase gene [J].
Bersaglieri, T ;
Sabeti, PC ;
Patterson, N ;
Vanderploeg, T ;
Schaffner, SF ;
Drake, JA ;
Rhodes, M ;
Reich, DE ;
Hirschhorn, JN .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (06) :1111-1120
[2]   The C/C-13910 and G/G-22018 genotypes for adult-type hypolactasia are not associated with inflammatory bowel disease [J].
Büning, C ;
Ockenga, J ;
Krüger, S ;
Jurga, J ;
Baier, P ;
Dignass, A ;
Vogel, A ;
Strassburg, C ;
Weltrich, R ;
Genschel, J ;
Lochs, H ;
Schmidt, H .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2003, 38 (05) :538-542
[3]   Identification of a variant associated with adult-type hypolactasia [J].
Enattah, NS ;
Sahi, T ;
Savilahti, E ;
Terwilliger, JD ;
Peltonen, L ;
Järvelä, I .
NATURE GENETICS, 2002, 30 (02) :233-237
[4]   Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia [J].
Kuokkanen, M ;
Enattah, NS ;
Oksanen, A ;
Savilahti, E ;
Orpana, A ;
Järvelä, I .
GUT, 2003, 52 (05) :647-652
[5]   The T allele of a single-nucleotide polymorphism 13.9 kb upstream of the lactase gene (LCT) (C-13.9kbT) does not predict or cause the lactase-persistence phenotype in Africans [J].
Mulcare, CA ;
Weale, ME ;
Jones, AL ;
Connell, B ;
Zeitlyn, D ;
Tarekegn, A ;
Swallow, DM ;
Bradman, N ;
Thomas, MG .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (06) :1102-1110
[6]   A novel method for diagnosis of adult hypolactasia by genotyping of the-13910 C/T polymorphism with Pyrosequencing™ technology [J].
Nilsson, TK ;
Johansson, CA .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2004, 39 (03) :287-290
[7]  
NILSSONEHLE P, 2003, LAURELLS KLINISK KEM, P529
[8]   Lactase persistence DNA variant enhances lactase promoter activity in vitro:: functional role as a cis regulatory element [J].
Olds, LC ;
Sibley, E .
HUMAN MOLECULAR GENETICS, 2003, 12 (18) :2333-2340
[9]   The causal element for the lactase persistence/non-persistence polymorphism is located in a 1 Mb region of linkage disequilibrium in Europeans [J].
Poulter, M ;
Hollox, E ;
Harvey, CB ;
Mulcare, C ;
Peuhkuri, K ;
Kajander, K ;
Sarner, M ;
Korpela, R ;
Swallow, DM .
ANNALS OF HUMAN GENETICS, 2003, 67 :298-311
[10]  
Risch Neil, 2002, GENOME BIOL, V7, P1