A biopsy-based quick test in the diagnosis of duodenal hypolactasia in upper gastrointestinal endoscopy

Endoscopy

Volumn 38, Issue 7, 2006, Pages 708-712

  Kuokkanen, M ^a   Myllyniemi, M ^b   Vauhkonen, M ^c   Helske, T ^c   Kaariainen I ^c   Karesvuori, S ^c   Linnala, A ^b   Harkonen M ^b   Jarvela I ^d   Sipponen, Pentti ^b,c  

^a UNIVERSITY OF HELSINKI   (Finland)

^b Biohit Oyj   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^d Helsinki University   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; DNA; LACTASE; LACTOSE; SUCRASE;

ADULT; ARTICLE; BIOASSAY; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIAGNOSTIC ERROR; DIAGNOSTIC KIT; DIAGNOSTIC PROCEDURE; DISEASE SEVERITY; DNA EXTRACTION; DNA SEQUENCE; DUODENUM BIOPSY; DUODENUM DISEASE; ENZYME ACTIVITY; FEMALE; GASTROINTESTINAL ENDOSCOPY; GENOME ANALYSIS; GENOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; INCUBATION TIME; LACTASE DEFICIENCY; MAJOR CLINICAL STUDY; MALE; OUTPATIENT CARE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROSPECTIVE STUDY; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS; STATISTICAL ANALYSIS; STOMACH BIOPSY; TREATMENT INDICATION;

BIOPSY; DUODENUM; ENDOSCOPY, GASTROINTESTINAL; FEMALE; HUMANS; LACTASE; LACTOSE INTOLERANCE; LACTOSE TOLERANCE TEST; MALE; MIDDLE AGED; REAGENT KITS, DIAGNOSTIC; SENSITIVITY AND SPECIFICITY;

EID: 33745874090     PISSN: 0013726X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-925354     Document Type: Article

References (13)

1. Dahlqvist A, Hammond JB, Crane RK et al. Intestinal lactase deficiency and lactose intolerance in adults: preliminary report. Gastroenterology 1963; 45: 488-491
2. Simoons FJ. Primary adult lactose intolerance and the milking habit: a problem in biologic and cultural interrelations, 2: a culture historical hypothesis. Am J Dig Dis 1970; 15: 695-710
3. Sahi T, Isokoski M, Jussila J et al. Recessive inheritance of adult-type lactose malabsorption. Lancet 1973; ii: 823-826
4. Flatz G, Rotthauwe HW. The human lactase polymorphism: physiology and genetics of lactose absorption and malabsorption. Prog Med Genet 1977; 2: 205-249.
5. Simoons FJ. The geographic hypothesis and lactose malabsorption: a weighing of the evidence. Am J Dig Dis 1978; 23: 963-980
6. Enattah NS, Sahi T, Savilahti E et al. Identification of a variant associated with adult-type hypolactasia. Nat Genet 2002; 30: 233-237
7. Kuokkanen M, Enattah NS, Oksanen A et al. Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia. Gut 2003; 52: 647-652
8. Olds LC, Sibley E. Lactase persistence DNA variant enhances lactase promoter activity in vitro: functional role as a cis regulatory element. Hum Mol Genet 2003; 12: 2333-2340
9. Troelsen JT, Olsen J, Moller J et al. An upstream polymorphism associated with lactase persistence has increased enhancer activity. Gastroenterology 2003; 125: 1686-1694
10. Arola H. Diagnosis of hypolactasia and lactose malabsorption. Scand J Gastroenterol Suppl 1994; 202: 26-35
11. Dahlqvist A. Assay of intestinal disaccharidases. Scand J Clin Lab Invest 1984; 44: 169-172
12. Härkönen MHA, Passonneau JV, Lowry OH. Relationship between energy reserves and function in rat superior cervical ganglion. J Neurochem 1969; 16: 1439-1450
13. Carroccio A, Montalto G, Cavera G et al. Lactose intolerance and self-reported milk intolerance: relationship with lactose maldigestion and nutrient intake. J Am Coll Nutr 1998; 17: 631-636