Diagnostic possibilities of lactase deficiency in children with cystic fibrosis
https://doi.org/10.46563/1560-9561-2021-24-3-157-162
EDN: ahawgf
Abstract
Introduction. Children with cystic fibrosis often have gastrointestinal symptoms despite properly selected primary therapy and pancreatic substitution therapy. A possible reason is lactase deficiency.
Aim is to determine the frequency of lactase deficiency in children with cystic fibrosis and the need for appropriate dietary correction of their diets.
Materials and methods. In 213 children with cystic fibrosis, during esophagogastroduodenoscopy in biopsies of the small intestinal mucosa 359 rapid tests, «Lactose intolerance quick test” were performed. According to the results of an express test, some patients diagnosed with hypolactasia to determine their tolerance to lactose underwent a glycemic load test with lactose and measured the level of fecal calprotectin to assess the level of faecal calprotectin the degree of chronic intestinal inflammation.
Results. Normal lactase activity was observed in 129 (36%) biopsies studied, moderate hypolactasia in 91 (25%) biopsies, severe hypolactasia in 139 (39%) biopsies. In patients with moderate hypolactasia, according to the express test results, 20% confirmed intolerance to lactose as a result of the load test. In patients with severe hypolactasia, 72% were confirmed to be lactose intolerant, according to the results of an express test. There was no correlation between the level of calprotectin and the results of the glycemic load test with lactose.
Conclusion. Lactase deficiency is observed in a significant proportion of patients with cystic fibrosis, which may be a consequence of primary adult hypolactasia and chronic intestinal inflammation. In children with cystic fibrosis with dyspeptic symptoms persisted despite correctly prescribed basic therapy and pancreatic enzymes, it is necessary to exclude lactose intolerance and prescribe a low-lactose diet.
Contribution:
Roslavtseva E.А., Simonova O.I. — concept and design of the study;
Sokolov I., Lokhmatov M.M. — collection of material;
Sokolov I., Bushueva T.V. — statistical processing;
Roslavtseva E.А., Sokolov I., Simonova O.I., Borovik T.E., Chernevich V.P. — writing of the text;
Simonova O.I., Smirnov I.E., Borovik T.E., Bushueva T.V. — editing.
All authors — approval of the final version of the manuscript, responsibility for integrity.
Acknowledgement. The study had no sponsorship.
Conflict of interest. The authors declare no conflict of interest.
Received: May 24, 2021
Accepted: June 23, 2021
Published: July 16, 2021
About the Authors
Elena A. RoslavtsevaRussian Federation
MD, PhD, leading researcher of the National Medical Research Center for Children’s Health, Moscow, 119991, Russian Federation
e-mail: roslikea@gmail.com
Ina Sokolov
Russian Federation
Olga I. Simonova
Russian Federation
Tatiana V. Bushueva
Russian Federation
Tatiana E. Borovik
Russian Federation
Ivan E. Smirnov
Russian Federation
Vera P. Chernevich
Russian Federation
Maksim M. Lokhmatov
Russian Federation
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Review
For citations:
Roslavtseva E.A., Sokolov I., Simonova O.I., Bushueva T.V., Borovik T.E., Smirnov I.E., Chernevich V.P., Lokhmatov M.M. Diagnostic possibilities of lactase deficiency in children with cystic fibrosis. Russian Pediatric Journal. 2021;24(3):157-162. (In Russ.) https://doi.org/10.46563/1560-9561-2021-24-3-157-162. EDN: ahawgf