• Individualisation of indications for anti-Helicobacter pylori therapy and evaluation of its efficacy in children with functional dyspepsia
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Individualisation of indications for anti-Helicobacter pylori therapy and evaluation of its efficacy in children with functional dyspepsia

PERINATOLOGY AND PEDIATRIC. UKRAINE. 2017.3(71):108-114; doi 10.15574/PP.2017.71.108

Ali Sameh Ali
Bohomolets National Medical University, Kyiv, Ukraine

Objective. To analyze the indications for bismuth-based anti-H. pylori therapy and to study its efficacy in children with functional dyspepsia (FD) taking into account H. pylori CagA-status and serum vitamin D levels.
Material and methods. Sixty children (main group) aged 6-17 years diagnosed with H. pylori-associated functional dyspepsia underwent different modified bismuth-based anti-H. pylori treatment regimens comparing to children in the control group (n=62), where 32 patients received no treatment and 30 children received standard 7-day lansoprazole-based triple anti-H. pylori therapy. The common diagnostic algorithm was used. Children with FD who had H. pylori infection confirmed in subsequent non-invasive tests were included in the study. At the pre-treatment stage, we analyzed the disease course to establish its main factors, not considering the presence of H. pylori infection, and weighed the risks and benefits of anti-H. pylori therapy. To verify H. pylori infection in children with FD, from 4 to 6 biopsy samples from gasrtric mucosa were taken during duodenoscopy for further microscopic examination and rapid urease analysis: once H. pylori infection was detected, the final decision concerning anti-H. pylori therapy in each particular case was made. In all children tests for total serum anti-H. pylori CagA antibodies as well as serum 25-hydroxycholecalciferol (vitamin D) were performed.
Results. In the main group H. pylori CagA antibodies were detected in 40 patients and were not detected in 20: 40 children had H. pylori CagA_positive (CagA+) status and 20 children had H. pylori CagA-negative (CagA-) status. In the main group, 22 children had serum vitamin D levels within the normal range and 38 children had vitamin D deficiency. In the main group the rate of successful eradication was 78.3%. A comparison of the efficacy of 10-day bismuth-based sequential eradication therapy with vitamin D as an adjuvant and 7-day bismuth-based triple therapy showed the rates of eradication 73.3% and 83.3%, respectively. In the main group, the rates of successful eradication depending on H. pylori CagA+ and H. pylori CagA-status were 92.5% and 50%, respectively; depending on vitamin D supply: in children who had vitamin D deficiency – 76.3%, in those who had serum vitamin D levels within the normal range – 81.8%. The rate of successful eradication of standard 7-day triple therapy was 70%: depending on H. pylori CagA+ or H. pylori CagA-status: 95.2% and 11.1%, respectively; depending on vitamin D supply: 66.7% in children who had vitamin D deficiency, in those who had serum vitamin D levels within the normal range – 80%.
Conclusions. The indications for anti-H. pylori therapy in children with FD should be individualized taking into consideration its risks and benefits: simultaneous eradication in family members who have first- or second-degree relatives with H. pyloridependent conditions; detection of H. pylori in gastric samples; self-contamination with H. pylori CagA+. In children with FD both bismuth-based therapies, 7-day triple and 10-day sequential, provide a high rate of eradication. H. pylori CagA-status and serum vitamin D level can serve as predictors of effective H. pylori eradication. The rate of successful eradication does not depend on clinical forms of functional dyspepsia. Children with H. pylori CagA-status who have insufficient supply of vitamin D or vitamin D deficiency should obtain vitamin D exogenously as an adjuvantto 10-day bismuth_based sequential eradication therapy. The above-mentioned combined scheme may increase the efficacy of H. pylori eradication.
Key words: functional dyspepsia, H. pylori CagA-status, sequential anti-H. pylori therapy, bismuth subcitrate, 25-hydroxycholecalciferol, children.

References

1. Pechkurov D, Tyazheva A, Allenova Y, Shakhmatova E. (2014). Biopsychosocial model of functional disorders of the gastrointestinal tract: what is new in etiology, pathogenesis, diagnosis and treatment? Voprosy detskoy diyetologii. 12(1): 61-65.

2. Vasiliev Y. (2013). Functional dyspepsia. Contemporary ideas about the problem and the possibilities of therapy. Meditsinskiy sovet. 10.

3. Volosovets O, Saltanova S. (2012). Influence of antibacterial therapy for H. pylori-infected parents on the level of H. pylori reinfection in children with achieved eradication. Zdorovʹe rebenka. 2(37): 25-27.

4. Voloshyn K. (2015). Comparative analysis of motor-evacuation and acid-forming functions of the stomach in children with various clinical variants of functional dyspepsia. Aktual'ní problemi suchasnoyi medytsyny. Visnyk ukrayins'koyi medychnoyi stomatologichnoyi akademiyi. 4(52): 50-56.

5. Maydannyk V. (2007). Rome criteria III (2006) diagnosis of functional gastrointestinal disorders in children. Pediatrics, Obstetrics and Gynecology. 3: 5-14.

6. Maydannyk V. (2016). Rome Criteria IV (2016): What's New? World J. of Pediatrics, Obstetrics and Gynecology. 10(1): 8-18.

7. Hata T, Kato M, Kudo T, Ono S et al. (2013). Comparison of gastric relaxation and sensory functions between functional dyspepsia and healthy subjects using novel drinking-ultrasonography test. Digestion. 87: 34–39. https://doi.org/10.1159/000343935; PMid:23343967

8. Drossman D. (2006). The functional gastrosntestinal disorders and the Rome III process. Gastroenterology. 130(5): 1377-1390. https://doi.org/10.1053/j.gastro.2006.03.008; PMid:16678553

9. Drossman D. (2016). Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features, and Rome IV. Gastroenterology. 150(6): 1262-1279. https://doi.org/10.24890/pc

10. Koletzko S, Jones N, Goodman K et al. (2011). Evidence-based guidelines from ESPGHAN and NASPGHAN for Helicobacter pylori infection in children. J Pediatr Gastroenterol Nutr. 53: 230–43. https://doi.org/10.1097/MPG.0b013e3182227e90

11. Hyams J, Di Lorenzo C, Saps M et al. (2016). Functional gastrointestinal disorders: child/adolescent. Gastroenterology. 150: 1456-1468. https://doi.org/10.1053/j.gastro.2016.02.015; PMid:27144632

12. Malfertheiner P, Mossner J, Fischbach W et al. (2003). Helicobacter pylori eradication is beneficial in the treatment of functional dyspepsia. Aliment Pharmacol Ther. 18: 615–25. https://doi.org/10.1046/j.1365-2036.2003.01695.x; PMid:12969088

13. Chiesa C, Anania C, Pacifico L et al. (2011). Helicobacter pylori therapy in children: a focus on proton pump inhibitors. Chemotherapy. 57(1): 85-93. https://doi.org/10.1159/000323619; PMid:21346353

14. Jones N, Koletzko S, Goodman K et al. (2017). Joint ESPGHAN/ NASPGHAN Guidelines for the Management of Helicobacter pylori in Children and Adolescents (Update 2016). J Pediatr Gastroenterol Nutr. 64(6): 991-1003. https://doi.org/10.1097/MPG.0000000000001594; PMid:28541262

15. Sugano K, Tack J, Kuipers E et al. (2016). Kyoto global consensus report on Helicobacter pylori gastritis. Gut. 64(9): 1353-67. https://doi.org/10.1136/gutjnl-2015-309252; PMid:26187502 PMCid:PMC4552923

16. Malfertheiner P, Megraud F, O’Morain C et al. (2016). Management of Helicobacter pylori infection – the Maastricht V/Florence Consensus Report. Gut. 0: 1–25. https://doi.org/10.1136/gutjnl-2016-312288

17. Saps M, Nichols-Vinueza D, Rosen J, Velasco-Benítez C. (2014). Prevalence of functional gastrointestinal disorders in Colombian school children. J Pediatr. 164: 542–545. https://doi.org/10.1016/j.jpeds.2013.10.088; PMid:24332822

18. Drossman D, Corazziari E, Talley N et al. (1999). Rome II: A multinational consensus document on functional gastrointestinal disorders. Gut. 45(2); II: 1-1181.

19. Fischbach W, Malfertheiner P, Hoffmann J et al. (2009). S3-Leitlinie «Helicobacter pylori und gastroduodenale Ulcuskrankheit» der DGVS. Z. Gastroenterol. 47: 68-102. https://doi.org/10.1055/s-0028-1109062; PMid:19156594

20. Zullo A, Hassan C, Ridola L et al. (2013). Standard triple and sequential therapies for Helicobacter pylori eradication: an update. Eur J Intern Med. 24(1): 16-19. https://doi.org/10.1016/j.ejim.2012.07.006; PMid:22877993