Literature DB >> 29491758

Variable Use of Disaccharidase Assays When Evaluating Abdominal Pain.

Stanley A Cohen1, Hannah Oloyede1.   

Abstract

Background and Aims: Patients with a disaccharidase deficiency typically present with abdominal discomfort and often with diarrhea. However, disaccharidase deficiency is often overlooked as a cause of these complaints. Therefore, we sought to determine the prevalence of lactase and sucrase deficiencies in a pediatric population undergoing diagnostic esophagogastroduodenoscopy (EGD) and to describe disaccharidase testing practices among pediatric gastroenterologists.
Methods: Endoscopic records from patients undergoing diagnostic EGD and disaccharidase analysis (DA) were retrospectively reviewed. Diagnostic EGDs performed over a 5-year period (2010 through 2014) at a freestanding endoscopy center serving 13 pediatric gastroenterologists were assessed. Demographic and clinical data on patients were collected and grouped; patients with primary sucrase-isomaltase deficiency (SID) were the main focus. The data were stratified by the physician performing the procedures.
Results: Over the 5-year study period, 5368 EGDs were performed, with abdominal pain as the primary indication in 3235 cases (60.2%). DAs were performed on 963 patients (17.9% of the total cohort; 29.8% of those with abdominal pain). Lactase deficiencies, sucrase deficiencies, and primary SID were found in 44.7%, 7.6%, and 3.5% of DAs, respectively. The number of DAs performed varied widely among physicians, ranging from 1.6% to 64.5% of EGDs evaluating patients with abdominal pain. Univariate regression analysis revealed significant correlations between the number of DAs performed and the number of SID and lactase deficiencies found (P<.001 for both).
Conclusion: Rates of DAs vary widely among pediatric gastroenterologists performing diagnostic EGDs in children with abdominal pain. Physician education and clinical practice guidelines regarding the use of DAs are warranted.

Entities:  

Keywords:  Sucrase-isomaltase deficiency; disaccharidase deficiency; lactase deficiency; physician variability

Year:  2018        PMID: 29491758      PMCID: PMC5824592     

Source DB:  PubMed          Journal:  Gastroenterol Hepatol (N Y)        ISSN: 1554-7914


  21 in total

1.  Patients with irritable bowel syndrome-diarrhea have lower disease-specific quality of life than irritable bowel syndrome-constipation.

Authors:  Prashant Singh; Kyle Staller; Kenneth Barshop; Elaine Dai; Jennifer Newman; Sonia Yoon; Shahar Castel; Braden Kuo
Journal:  World J Gastroenterol       Date:  2015-07-14       Impact factor: 5.742

2.  Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization.

Authors:  Yael Haberman; Ayelet Di Segni; Nurit Loberman-Nachum; Ortal Barel; Vered Kunik; Eran Eyal; Nitzan Kol; Goni Hout-Siloni; Brigitte Kochavi; Camila Avivi; Michael Schvimer; Gideon Rechavi; Yair Anikster; Iris Barshack; Batia Weiss
Journal:  J Pediatr Gastroenterol Nutr       Date:  2017-05       Impact factor: 2.839

Review 3.  Disaccharidase deficiency in health and disease.

Authors:  R Herber
Journal:  Calif Med       Date:  1972-06

4.  Assay of intestinal disaccharidases.

Authors:  A Dahlqvist
Journal:  Scand J Clin Lab Invest       Date:  1984-04       Impact factor: 1.713

5.  Impact of the Bowel Management Program on the quality of life in children with fecal incontinence.

Authors:  João H F Colares; Marionescu Purcaru; Guilherme P F da Silva; Mirna A Frota; Carlos A B da Silva; Antônio A Melo-Filho; Andrea Bischoff; Alberto Peña
Journal:  Pediatr Surg Int       Date:  2016-02-13       Impact factor: 1.827

6.  Congenital sucrase-isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy.

Authors:  J W L Puntis; V Zamvar
Journal:  Arch Dis Child       Date:  2015-07-10       Impact factor: 3.791

Review 7.  Enzyme replacement as an effective treatment for the common symptoms of complex carbohydrate intolerance.

Authors:  Barbara Levine; Steven Weisman
Journal:  Nutr Clin Care       Date:  2004 Apr-Jun

8.  Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.

Authors:  Marwan Alfalah; Markus Keiser; Tosso Leeb; Klaus-Peter Zimmer; Hassan Y Naim
Journal:  Gastroenterology       Date:  2008-11-19       Impact factor: 22.682

9.  Fructose intolerance in children presenting with abdominal pain.

Authors:  Robert E Gomara; Michael S Halata; Leonard J Newman; Howard E Bostwick; Stuart H Berezin; Lynnette Cukaj; Mary C See; Marvin S Medow
Journal:  J Pediatr Gastroenterol Nutr       Date:  2008-09       Impact factor: 2.839

10.  13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.

Authors:  Claudia C Robayo-Torres; Antone R Opekun; Roberto Quezada-Calvillo; Xavier Villa; E O Smith; Marilyn Navarrete; Susan S Baker; Buford L Nichols
Journal:  J Pediatr Gastroenterol Nutr       Date:  2009-04       Impact factor: 2.839

View more
  3 in total

Review 1.  Carbohydrate Intolerance and Disaccharidase Measurement - a Mini-Review.

Authors:  Matthew Burke
Journal:  Clin Biochem Rev       Date:  2019-11

2.  Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.

Authors:  Su Bin Kim; Fernando H Calmet; Jose Garrido; Monica T Garcia-Buitrago; Baharak Moshiree
Journal:  Dig Dis Sci       Date:  2019-09-06       Impact factor: 3.199

Review 3.  The Role of Disaccharidase Deficiencies in Functional Abdominal Pain Disorders-A Narrative Review.

Authors:  Mora V Puertolas; Amanda C Fifi
Journal:  Nutrients       Date:  2018-11-29       Impact factor: 5.717

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.