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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. Roslavtseva
National Medical Research Center for Children’s Health
Russian 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
National Medical Research Center for Children’s Health
Russian Federation


Olga I. Simonova
National Medical Research Center for Children’s Health; I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation


Tatiana V. Bushueva
National Medical Research Center for Children’s Health; Academician N.P. Bochkov Medical Genetic Scientific Center
Russian Federation


Tatiana E. Borovik
National Medical Research Center for Children’s Health; I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation


Ivan E. Smirnov
National Medical Research Center for Children’s Health
Russian Federation


Vera P. Chernevich
National Medical Research Center for Children’s Health
Russian Federation


Maksim M. Lokhmatov
National Medical Research Center for Children’s Health; I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation


References

1. Kapranov N.I., Kashirskaya N.Yu., eds. Cystic Fibrosis [Mukovistsidoz]. Moscow: Medpraktika-M; 2014. (in Russian)

2. Bell S.C., Mall M.A., Gutierrez H., Macek M., Madge S., Davies J.C., et al. The future of cystic fibrosis care: a global perspective. Lancet Respir. Med. 2020; 8(1): 65–124. https://doi.org/10.1016/S2213-2600(19)30337-6

3. Bergeron C., Cantin A.M. Cystic fibrosis: pathophysiology of lung disease. Semin. Respir. Crit. Care Med. 2019; 40(6): 715–26. https://doi.org/10.1055/s-0039-1694021

4. Egan M.E. Genetics of cystic fibrosis: clinical implications. Clin. Chest Med. 2016; 37(1): 9–16. https://doi.org/10.1016/j.ccm.2015.11.002

5. Munk A. Cystic Fibrosis: evidence for gut inflammation. Int. J. Biochem. Cell Biol. 2014; 52: 180–3. https://doi.org/10.1016/j.biocel.2014.02.005

6. Khavkin A.I. Lactose intolerance: current approaches to diagnosis and treatment. Voprosy dietologii. 2020; 10(1): 59–67. https://doi.org/10.20953/2224-5448-2020-10-59-67 (in Russian)

7. Bogdanova N.M. Lactase deficiency and intolerance to lactose: the main factors of development and the principles of diet therapy. Meditsina: teoriya i praktika. 2020; 5(1): 62–70. (in Russian)

8. Ziatdinova N.V., Malanicheva T.G., Bareeva L.A. Lactase deficiency and gastrointestinal allergy in young children. Meditsinskiy sovet. 2020; (10): 86–90. https://doi.org/10.21518/2079-701X-2020-10-86-90 (in Russian)

9. Ipatova M.G., Dubrovskaya M.I., Korneva T.I., Kurgasheva E.K., Mukhina Yu.G. Infantile lactase deficiency and dietary habits. Clinical cases. Voprosy sovremennoy pediatrii. 2012; 11(1): 119–23. (in Russian)

10. Anguita-Ruiz A., Aguilera C.M., Gil Á. Genetics of lactose intolerance: an updated review and online interactive world maps of phenotype and genotype frequencies. Nutrients. 2020; 12(9): 2689. https://doi.org/10.3390/nu12092689

11. Ugidos-Rodríguez S., Matallana-González M.C., Sánchez-Mata M.C. Lactose malabsorption and intolerance: a review. Food Funct. 2018; 9(8): 4056–68. https://doi.org/10.1039/c8fo00555a

12. Wanes D., Husein D.M., Naim H.Y. Congenital lactase deficiency: mutations, functional and biochemical implications, and future perspectives. Nutrients. 2019; 11(2): 461. https://doi.org/10.3390/nu11020461

13. Mukhina Yu.G., Chubarova A.I., Geras’kina V.P., Bel’mer S.V., Gasilina T.V., Borovik T.E., et al. Working protocol for the diagnosis and treatment of lactase deficiency in children. Voprosy detskoy dietologii. 2016; 14(1): 64–9. (in Russian)

14. Guidelines. Optimization Program for feeding of children of the first year of life in Russian Federation. Moscow; 2019. (in Russian)

15. Babayan M.L. Lactase deficiency: latest diagnostic methods and treatment. Meditsinskiy sovet. 2013; (1-1): 24–7. (in Russian)

16. Mukhina Yu.G., Shumilov P.V., Dubrovskaya M.I. Modern approaches to the diagnosis and treatment of disaccharidase deficiency in children. Trudnyy patsient. 2006; 4(9-1): 12–6. (in Russian)

17. Dahlqvist A. Method for assay of intestinal disaccharidases. Anal. Biochem. 1964; 7: 18–25. https://doi.org/10.1016/0003-2697(64)90115-0.

18. Fidler-Witon E., Lisowska A., Walkowiak J. Lactose intolerance in cystic fibrosis. Pediatria polska. 2010; 85(6): 629–32.

19. Antonowicz I., Reddy V., Khaw K.T., Scwachmann H. Lactase deficiency in cystic fibrosis. Pediatrics. 1968; 42(3): 492–500.

20. Mądry E., Fidler E., Sobczyńska-Tomaszewska A., Lisowska A., Krzyżanowska P., Pogorzelski A., et al. Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis. Eur. J. Hum. Genet. 2011; 19(7): 748–52. https://doi.org/10.1038/ejhg.2011.36

21. Modiano G., Cimineli B., Pignatti P.E. Cystic fibrosis and lactase persistence: a possible correlation. Eur. J. Hum. Genetics. 2007; 15(3): 225–9. https://doi.org/10.1038/sj.ejhg.5201749

22. Roslavtseva E., Simonova O., Lokhmatov M., Tupylenko A., Ignatova A., Gorinova Y. Lactase activity in small intestinal biopsies in cystic fibrosis (CF) children. J. Cyst. Fibrosis. 2017; 16(S1): S135. https://doi.org/10.1016/S1569-1993(17)30626-4

23. Roslavtseva E., Simonova O., Lokhmatov M., Gordeeva I. Lactase activity in biopsy specimens of the small intestine mucosa in children with CF (continued). J. Cyst. Fibrosis. 2018; 17(3): 108


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

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ISSN 1560-9561 (Print)
ISSN 2413-2918 (Online)