Association between celiac disease and primary lactase deficiency

European Journal of Clinical Nutrition

Volumn 66, Issue 12, 2012, Pages 1364-1365

  Basso, M S ^a   Luciano, R ^a   Ferretti, F ^a   Muraca, M ^a   Panetta, F ^a   Bracci, F ^a   Ottino, S ^a   Diamanti, A ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

celiac disease; children; primary lactase deficiency

Indexed keywords

HLA DQ2 ANTIGEN; HLA DQ8 ANTIGEN; IMMUNOGLOBULIN A; LACTASE; LACTOSE; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE ANTIBODY;

ADOLESCENT; ADULT; ARTICLE; CELIAC DISEASE; CHILD; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC ANALYSIS; GENETIC POLYMORPHISM; HOMOZYGOSITY; HUMAN; INTESTINE BIOPSY; LACTASE DEFICIENCY; LACTOSE INTOLERANCE; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PREVALENCE; SCHOOL CHILD;

ADOLESCENT; CASE-CONTROL STUDIES; CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; DEFICIENCY DISEASES; FEMALE; HOMOZYGOTE; HUMANS; ITALY; LACTASE; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE;

EID: 84870825128     PISSN: 09543007     EISSN: 14765640     Source Type: Journal    
DOI: 10.1038/ejcn.2012.153     Document Type: Article

References (10)

1. American Academy of Pediatrics, Committee on Nutrition. Practical significance of lactose intolerance in children: supplement. Pediatrics 1990; 86: 643-644.
2. Swallow DM. Genetics of lactase persistence and lactose intolerance. Annu Rev Genet 2003; 37: 197-219.
3. Kruse TA, Bolund L, Grzeschik KH, Ropers HH, Sjö ström H, Norén O et al. The human lactase-phlorizin hydrolase gene is located on chromosome 2. FEBS Lett 1988; 240: 123-126.
4. Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Jarvela I. Identification of a variant associated with adulttype hypolactasia. Nat Genet 2002; 30: 233-237.
5. Kuokkanen M, Enattah NS, Oksanen A, Savilahti E, Orpana A, Jarvela I. Transcriptional regulation of the lactasephlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia. Gut 2003; 52: 647-652.
6. Babu J, Kumar S, Babu P, Prasad JH, Ghoshal UC. Frequency of lactose malabsorption among healthy southern and northern Indian opulations by genetic analysis and lactose hydrogen breath and tolerance tests. Am J Clin Nutr 2010; 91: 140-146.
7. Leffler DA, Dennis M, Hyett B, Kelly E, Schuppan D, Kelly CP. Etiologies and predictors of diagnosis in nonresponsive celiac disease. Clinic Gastroenterol Hepatol 2007; 5: 445-450.
8. Hill ID, Dirks MH, Liptak GS, Colletti RB, Fasano A, Guandalini S et al. North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology. Hepatol Nutr J Pediatr Gastroenterol Nutr 2005; 40: 1-19.
9. Kretchmer N. Lactose and lactase: a historical perspective. Gastroenterology 1971; 61: 805-813.
10. Mottes M, Belpinati F, Milani M, Saccomandi D, Petrelli E, Calacoci M et al. Genetic testing for adult-type hypolactasia in Italian families. Clin Chem Lab Med 2008; 46: 980-984.