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Mode of Delivery Does Not Affect the Risk of Inflammatory Bowel Disease

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Abstract

Background

Recent evidence suggests that exposures in early life that are known to influence microbiome development may affect the risk of developing inflammatory bowel disease (IBD). Cesarean section has been associated with altered colonization of commensal gut flora and is thought to predispose to immune-mediated diseases later in life.

Aims

To evaluate the risk of IBD, Crohn’s Disease (CD), and Ulcerative Colitis (UC) according to mode of delivery (C-section vs vaginal delivery).

Methods

A systematic search was performed in PubMed and Embase. The primary outcome was the risk of IBD in individuals delivered vaginally compared to those born by C-section. Secondary outcomes were UC and CD risk according to mode of delivery and IBD risk in individuals born by emergent compared to elective C-section. Publication bias was evaluated by funnel plots and Egger’s test. Study’s quality was characterized using the Newcastle–Ottawa Scale.

Results

Ten studies fulfilled the inclusion criteria, of which seven were population-based. No publication bias was detected. Overall, 14.164 IBD patients and 4.206.763 controls were included. Being born by C-section was not associated with increased risk of IBD [OR 1.01, 95% CI (0.81–1.27), p = 0.92], CD [OR 1.15, 95% CI (0.94–1.42), p = 0.18] or UC [OR 0.94, 95% CI (0.61–1.45), p = 0.79]. No differences were found between emergent and elective C-section in IBD [OR 1.05, 95% CI (0.59–1,87), p = 0.87]. Substantial heterogeneity was found in statistical analysis, and further studies are needed.

Conclusion

Overall, the risk of developing IBD was not affected by mode of delivery.

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References

  1. Abraham C, Cho JH. Inflammatory bowel disease. New Engl J Med. 2009;361:2066–2078.

    Article  CAS  Google Scholar 

  2. Zhang YZ, Li YY. Inflammatory bowel disease: pathogenesis. World J Gastroenterol. 2014;20:91–99.

    Article  Google Scholar 

  3. Hold GL, Smith M, Grange C, et al. Role of the gut microbiota in inflammatory bowel disease pathogenesis: what have we learnt in the past 10 years? World J Gastroenterol. 2014;20:1192–1210.

    Article  Google Scholar 

  4. Molodecky NA, Soon IS, Rabi DM, et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology. 2012;142:46–54.e42.

    Article  Google Scholar 

  5. Benchimol EI, Fortinsky KJ, Gozdyra P, et al. Epidemiology of pediatric inflammatory bowel disease: a systematic review of international trends. Inflamm Bowel Dis. 2011;17:423–439.

    Article  Google Scholar 

  6. Benchimol EI, Bernstein CN, Bitton A, et al. Trends in epidemiology of pediatric inflammatory bowel disease in Canada: distributed network analysis of multiple population-based provincial health administrative databases. Am J Gastroenterol. 2017;112:1120–1134.

    Article  Google Scholar 

  7. Milani C, Duranti S, Bottacini F, et al. The first microbial colonizers of the human gut: composition, activities, and health implications of the infant gut microbiota. Microbiol Mol Biol Rev. 2017;81:e00017–e00036.

    Article  Google Scholar 

  8. Ley D, Desseyn JL, Mischke M, Knol J, Turck D, Gottrand F. Early-life origin of intestinal inflammatory disorders. Nutr Rev. 2017;75:175–187.

    Article  Google Scholar 

  9. Rutayisire E, Huang K, Liu Y, Tao F. The mode of delivery affects the diversity and colonization pattern of the gut microbiota during the first year of infants’ life: a systematic review. BMC Gastroenterol. 2016;16:86.

    Article  Google Scholar 

  10. Koloski NA, Bret L, Radford-Smith G. Hygiene hypothesis in inflammatory bowel disease: a critical review of the literature. World J Gastroenterol. 2008;14:165–173.

    Article  Google Scholar 

  11. Neu J. Dysbiosis in the neonatal period: role of cesarean section. Nestle Nutr Inst Workshop Ser. 2017;88:57–65.

    Article  Google Scholar 

  12. Renz-Polster H, David M, Buist A, et al. Caesarean section delivery and the risk of allergic disorders in childhood. Clin Exp Allergy. 2005;35:1466–1472.

    Article  CAS  Google Scholar 

  13. Sevelsted A, Stokholm J, Bønnelykke K, Bisgaard H. Cesarean section and chronic immune disorders. Pediatrics. 2018;135:e92–e98.

    Article  Google Scholar 

  14. Bager P, Simonsen J, Nielsen NM, Frisch M. Cesarean section and offspring’s risk of inflammatory bowel disease: a national cohort study. Inflamm Bowel Dis. 2012;18:857–862.

    Article  Google Scholar 

  15. Malmborg P, Bahmanyar S, Grahnquist L, Hildebrand H, Montgomery S. Cesarean section and the risk of pediatric Crohn’s disease. Inflamm Bowel Dis. 2012;18:703–708.

    Article  Google Scholar 

  16. Decker E, Engelmann G, Findeisen A, et al. Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children. Pediatrics. 2010;125:e1433–e1440.

    Article  Google Scholar 

  17. Bernstein CN, Banerjee A, Targownik LE, et al. Cesarean section delivery is not a risk factor for development of inflammatory bowel disease: a population-based analysis. Clin Gastroenterol Hepatol. 2016;14:50–57.

    Article  Google Scholar 

  18. Kristensen K, Henriksen L. Cesarean section and disease associated with immune function. J Allergy Clin Immunol. 2016;137:587–590.

    Article  Google Scholar 

  19. Andersen V, Erichsen R, Froslev T, Sorensen H, Ehrenstein V. Differential risk of ulcerative colitis and crohn’s disease among boys and girls after cesarean delivery. Inflamm Bowel Dis. 2013;19:e8–e10.

    Article  Google Scholar 

  20. Roberts SE, Wotton CJ, Williams JG, Griffith M, Goldacre MJ. Perinatal and early life risk factors for inflammatory bowel disease. World J Gastroenterol. 2011;17:743–749.

    Article  Google Scholar 

  21. Hutfless S, Melvin DL, Herrinton LJ. Prenatal and perinatal characteristics associated with pediatric-onset inflammatory bowel disease. Dig Dis Sci. 2012;57:2149–2156. https://doi.org/10.1007/s10620-012-2128-1.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Bengtson MB, Solberg IC, Aamodt G, et al. Relationships between inflammatory bowel disease and perinatal factors: both maternal and paternal disease are related to preterm birth of offspring. Inflamm Bowel Dis. 2010;16:847–855.

    Article  Google Scholar 

  23. Ponsonby A, Catto-smith AG, Pezic A, et al. Association between early-life factors and risk of child-onset. Inflamm Bowel Dis. 2009;15:858–866.

    Article  Google Scholar 

  24. Sonntag B, Stolze B, Heinecke A, et al. Preterm birth but not mode of delivery is associated with an increased risk of developing inflammatory bowel disease later in life. Inflamm Bowel Dis. 2007;13:1385–1390.

    Article  Google Scholar 

  25. Black M, Bhattacharya S, Philip S, Norman JE, McLernon DJ. Planned cesarean delivery at term and adverse outcomes in childhood health. JAMA. 2015;314:2271–2279.

    Article  CAS  Google Scholar 

  26. Ananthakrishnan A, Bernestein C, Iliopoulos D, et al. Environmental triggers in IBD: a review of progress and evidence. Nat Rev Gastroenterol Hepatol. 2018;15:39–49.

    Article  Google Scholar 

  27. Biasucci G, Rubini M, Riboni S, Morelli L, Bessi E, Retetangos C. Early human development mode of delivery affects the bacterial community in the newborn gut. Early Hum Dev. 2010;86:13–15.

    Article  Google Scholar 

  28. Dominguez-bello MG, Blaser MJ. Development of the human gastrointestinal microbiota and insights from the high-throughput sequencing. Gastroenterology. 2011;140:1713–1719.

    Article  CAS  Google Scholar 

  29. Vatanen T, Kostic AD, Hennezel E, et al. Variation in microbiome LPS immunogenicity contributes to autoimmunity in humans article variation in microbiome LPS immunogenicity contributes to autoimmunity in humans. Cell. 2016;165:842–853.

    Article  CAS  Google Scholar 

  30. Riedler J, Braun-Faharlander C, Eder W, et al. Exposure to farming in early life and development of asthma and allergy: a cross-sectional survey. Lancet. 2001;358:1129–1133.

    Article  CAS  Google Scholar 

  31. Bruce A, Black M, Bhattacharya S. Mode of delivery and risk of inflammatory bowel disease in the offspring: systematic review and meta-analysis of observational studies. Inflamm Bowel Dis. 2014;20:1217–1226.

    Article  Google Scholar 

  32. Li YI, Tian YUN, Zhu W, et al. Cesarean delivery and risk of inflammatory bowel disease: a systematic review and meta-analysis. Scand J Gastroenterol. 2014;49:834–844.

    Article  Google Scholar 

  33. Stokholm J, Thorsen J, Chawes B, et al. Cesarean section changes neonatal gut colonization. J Allergy Clin Immunol. 2016;138:881–889.

    Article  Google Scholar 

  34. Torres J, Hu J, Seki A, et al. Infants born to mothers with IBD present with altered gut microbiome that transfers abnormalities of the adaptive immune system to germ-free mice. Gut. 2019;0:1–10.

    Google Scholar 

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Contributions

All authors contributed to the manuscript’s concept and design. CG and BM independently extracted the data. Disagreements were solved through consensus or, if needed, by a third author (JT). NN performed the statistical analysis. CG wrote the manuscript. All authors critically revised the manuscript. All authors have approved the final version of the manuscript.

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Correspondence to Joana Torres.

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Frias Gomes, C., Narula, N., Morão, B. et al. Mode of Delivery Does Not Affect the Risk of Inflammatory Bowel Disease. Dig Dis Sci 66, 398–407 (2021). https://doi.org/10.1007/s10620-020-06204-7

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  • DOI: https://doi.org/10.1007/s10620-020-06204-7

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