Literature DB >> 21063860

Lactose malabsorption.

Richard J Grand1, Robert K Montgomery.   

Abstract

OPINION STATEMENT: Lactose malabsorption is a syndrome producing constellation of symptoms, including abdominal pain, bloating, flatulence, diarrhea, and sometimes nausea and/or vomiting. Primary causes of lactose malabsorption due to loss of intestinal lactase activity include genetic/racial lactase nonpersistence, congenital lactase deficiency, and developmental lactase deficiency. Secondary lactose malabsorption can be caused by any disorder that injures the small intestinal mucosa, such as viral gastroenteritis, celiac disease, allergic (eosinophilic) gastroenteritis, and radiation enteritis. The diagnosis depends on careful clinical evaluation and is customarily confirmed with a lactose breath hydrogen test. As the symptoms are nonspecific, many adults diagnosed with lactose malabsorption actually have irritable bowel syndrome. Treatment consists of a trial of eliminating lactose-containing dairy foods, with supplementation of alternative calcium and protein sources. Commercial enzyme products containing β-galactosidases can be prescribed to help patients digest dietary lactose. Long-term lactose restriction usually is not necessary and can lead to reduced bone mineral density.

Entities:  

Year:  2008        PMID: 21063860     DOI: 10.1007/s11938-008-0003-0

Source DB:  PubMed          Journal:  Curr Treat Options Gastroenterol        ISSN: 1092-8472


  30 in total

Review 1.  Lactose intolerance.

Authors:  H A Büller; R J Grand
Journal:  Annu Rev Med       Date:  1990       Impact factor: 13.739

2.  Risk of inadequate bone mineralization in diseases involving long-term suppression of dairy products.

Authors:  D Infante; R Tormo
Journal:  J Pediatr Gastroenterol Nutr       Date:  2000-03       Impact factor: 2.839

Review 3.  Adult-type hypolactasia and regulation of lactase expression.

Authors:  Jesper T Troelsen
Journal:  Biochim Biophys Acta       Date:  2005-02-25

4.  Identification of a variant associated with adult-type hypolactasia.

Authors:  Nabil Sabri Enattah; Timo Sahi; Erkki Savilahti; Joseph D Terwilliger; Leena Peltonen; Irma Järvelä
Journal:  Nat Genet       Date:  2002-01-14       Impact factor: 38.330

Review 5.  Lactose intolerance in infants, children, and adolescents.

Authors:  Melvin B Heyman
Journal:  Pediatrics       Date:  2006-09       Impact factor: 7.124

6.  Enzyme replacement therapy for primary adult lactase deficiency. Effective reduction of lactose malabsorption and milk intolerance by direct addition of beta-galactosidase to milk at mealtime.

Authors:  J L Rosado; N W Solomons; R Lisker; H Bourges
Journal:  Gastroenterology       Date:  1984-11       Impact factor: 22.682

7.  The polymorphic expression of lactase in adults is regulated at the messenger RNA level.

Authors:  O Fajardo; H Y Naim; S W Lacey
Journal:  Gastroenterology       Date:  1994-05       Impact factor: 22.682

8.  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.

Authors:  Charlotte A Mulcare; Michael E Weale; Abigail L Jones; Bruce Connell; David Zeitlyn; Ayele Tarekegn; Dallas M Swallow; Neil Bradman; Mark G Thomas
Journal:  Am J Hum Genet       Date:  2004-04-20       Impact factor: 11.025

9.  Prevalence of vitamin D deficiency among healthy adolescents.

Authors:  Catherine M Gordon; Kerrin C DePeter; Henry A Feldman; Estherann Grace; S Jean Emans
Journal:  Arch Pediatr Adolesc Med       Date:  2004-06

10.  A comparison of symptoms after the consumption of milk or lactose-hydrolyzed milk by people with self-reported severe lactose intolerance.

Authors:  F L Suarez; D A Savaiano; M D Levitt
Journal:  N Engl J Med       Date:  1995-07-06       Impact factor: 91.245

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  2 in total

1.  Lactulose hydrogen breath test and functional symptoms in pediatric patients.

Authors:  Ana María Madrid; Glauben Landskron; Gabriela Klapp; Alvaro Reyes; Carolina Pizarro; Carlos Defilippi
Journal:  Dig Dis Sci       Date:  2012-05       Impact factor: 3.199

2.  Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.

Authors:  Lena Diekmann; Katrin Pfeiffer; Hassan Y Naim
Journal:  BMC Gastroenterol       Date:  2015-03-21       Impact factor: 3.067

  2 in total

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