Skip to main content

Advertisement

Log in

Disease severity and treatment requirements in familial inflammatory bowel disease

  • Original Article
  • Published:
International Journal of Colorectal Disease Aims and scope Submit manuscript

Abstract

Purpose

Several studies demonstrate an increased prevalence and concordance of inflammatory bowel disease among the relatives of patients. Other studies suggest that genetic influence is over-estimated. The aims of this study are to evaluate the phenotypic expression and the treatment requirements in familial inflammatory bowel disease, to study the relationship between number of relatives and degree of kinship with disease severity and to quantify the impact of family aggregation compared to other environmental factors.

Methods

Observational analytical study of 1211 patients followed in our unit. We analyzed, according to the existence of familial association, number and degree of consanguinity, the phenotypic expression, complications, extraintestinal manifestations, treatment requirements, and mortality. A multivariable analysis considering smoking habits and non-steroidal-anti-inflammatory drugs was performed.

Results

14.2% of patients had relatives affected. Median age at diagnosis tended to be lower in the familial group, 32 vs 29, p = 0.07. In familial ulcerative colitis, there was a higher proportion of extraintestinal manifestations: peripheral arthropathy (OR = 2.3, p = 0.015) and erythema nodosum (OR = 7.6, p = 0.001). In familial Crohn’s disease, there were higher treatment requirements: immunomodulators (OR = 1.8, p = 0.029); biologics (OR = 1.9, p = 0.011); and surgery (OR = 1.7, p = 0.044). The abdominal abscess increased with the number of relatives affected: 5.1% (sporadic), 7.0% (one), and 14.3% (two or more), p=0.039. These associations were maintained in the multivariate analysis.

Conclusions

Familial aggregation is considered a risk factor for more aggressive disease and higher treatment requirements, a tendency for earlier onset, more abdominal abscess, and extraintestinal manifestations, remaining a risk factor analyzing the influence of some environmental factors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Trier F et al (2015) Familial risk of inflammatory bowel disease: a population-based cohort study 1977-2011. Am J Gastroenterol 110:564–571

    Article  Google Scholar 

  2. Andreu M et al (2014) Disease severity in familial cases of IBD. J Crohn’s Colitis 8:234–239

    Article  CAS  Google Scholar 

  3. Colombel J-F et al (1996) Clinical characteristics of Crohn’s disease in 72 families. Gastroenterol 111:604–607

    Article  CAS  Google Scholar 

  4. Peeters M et al (1996) Familial aggregation in Crohn’s disease: increased age-adjusted risk and concordance in clinical characteristics. Gastroenterol 11:597–603

    Article  Google Scholar 

  5. Orholm M et al (1991) Familial occurrence of inflammatory bowel disease. N Engl J Med 324:84–88

    Article  CAS  PubMed  Google Scholar 

  6. Cabré E et al (2014) Phenotypic concordance in familial inflammatory bowel disease (IBD). Result of a nationwide IBD Spanish database. J Crohn’s Colitis 8:654–661

    Article  Google Scholar 

  7. Steven R. Brant (2011). Update on the heritability of inflammatory bowel disease: the importance of twin studies. Inflamm Bowel Dis.

  8. Bayless T et al (1996) Crohn’s disease: concordance for site and clinical type in affected family members- potential hereditary influences. Gastroenterol 111:573–579

    Article  CAS  Google Scholar 

  9. Halfvarson J et al (2011) Genetic in twins with Chron’s disease: less pronounced than previously believed? Inflamm Bowel Dis 17:6–12

    Article  PubMed  Google Scholar 

  10. John C et al (1996) Inflammatory bowel disease in 97 families each with three or more affected first-degree relatives. Gastroenterol 111:587–596

    Article  Google Scholar 

  11. Dignass A et al (2012) The second European evidence-based consensus on the diagnosis and management of ulcerative colitis part 1: definitions and diagnosis. J Crohn’s Colitis 6:965–990

    Article  Google Scholar 

  12. Van Assche G et al (2010) The second European evidence-based consensus on the diagnosis and management of Crohn’s disease: definitions and diagnosis. J Crohn’s Colitis 4:7–27

    Article  Google Scholar 

  13. Silverberg MS et al (2005) Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: report of a working party of the 2005 Montreal Congress of Gastroenterology. Can J Gastroenterol 19:5–36

    Article  Google Scholar 

  14. Satsangi J et al (1996) Clinical patterns of familial inflammatory bowel disease. Gut 38:738–741

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Loddo I et al (2015) Inflammatory bowel disease: genetics, epigenetics, and pathogenesis. Front Immunol 6:551

    Article  PubMed  PubMed Central  Google Scholar 

  16. Gordon H et al (2015) Heritability in inflammatory bowel disease: from the first twin study to genome-wide association studies. Inflamm Bowel Dise 21:1428–1434

    Google Scholar 

Download references

Acknowledgement

To all the people who collaborated in the study:

Data collection: Joan Tosca, Marta Maia Bosca-Watts, Ana Sanahuja, Pablo Navarro, Isabel Pascual, Rosario Antón, Francisco Mora, Miguel Mínguez.

Study design: María Pilar Ballester, David Martí, Miguel Minguez.

Literature search: María Pilar Ballester, David Martí.

Data analysis and interpretation: María Pilar Ballester, Joan Tosca.

Writing: María Pilar Ballester, David Martí, Joan Tosca, Marta Maia Bosca-Watts, Miguel Minguez.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to María Pilar Ballester.

Ethics declarations

The study was approved by the institutional ethics committee of the hospital.

Funding statement

The authors declare no funding support.

Conflict of interest

The authors declare that they have no conflicts of interest.

Additional information

Spanish Gastroenterology conference (Spanish Gastroenterology Association) in Madrid, March 2016 and Digestive Disease Week (American Gastroenterology Association) in San Diego, May 2016.

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ballester, M.P., Martí, D., Tosca, J. et al. Disease severity and treatment requirements in familial inflammatory bowel disease. Int J Colorectal Dis 32, 1197–1205 (2017). https://doi.org/10.1007/s00384-017-2791-y

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00384-017-2791-y

Keywords

Navigation