Register for email alerts and news feeds:
This journal | BMJ Group
rss
Published Online First: 14 December 2005. doi:10.1136/gut.2005.083964
Gut 2006;55:803-808
Copyright © 2006 BMJ Publishing Group Ltd & British Society of Gastroenterology.

COELIAC DISEASE

Concordance, disease progression, and heritability of coeliac disease in Italian twins

L Nisticò1, C Fagnani1, I Coto2, S Percopo2, R Cotichini1, M G Limongelli2, F Paparo2, S D’Alfonso3, M Giordano3, C Sferlazzas4, G Magazzù4, P Momigliano-Richiardi3, L Greco2, M A Stazi1

1 Genetic Epidemiology Unit, National Centre of Epidemiology, Surveillance and Health Promotion (CNESPS), Istituto Superiore di Sanità, Rome, Italy
2 Department of Paediatrics, University of Naples Federico II, Naples and European Laboratory of Food Induced Disease (ELFID), Naples, Italy
3 Department of Medical Sciences, Eastern Piedmont University "A Avogadro" and Interdisciplinary Research Center for Autoimmune Diseases (IRCAD), Novara, Italy
4 Department of Paediatric Sciences, University of Messina, Messina, Italy

Correspondence to:
Dr L Nisticò
Genetic Epidemiology Unit, CNESPS, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Roma, Italia; lnistico{at}iss.it

Background and aims: We adopted the twin method to disentangle the genetic and environmental components of susceptibility to coeliac disease (CD). We estimated disease concordance rate by zygosity and HLA genotypes, discordance times, progression rates to disease, and heritability.

Methods: We crosslinked the Italian Twin Registry with the membership lists of the Italian Coeliac Disease Association and recruited 23 monozygotic (MZ) and 50 dizygotic (DZ) twin pairs with at least one affected member. Zygosity was assigned by DNA fingerprinting, and HLA-DQ and DR alleles were genotyped. Disease status was ascertained by antiendomysial, anti-human tissue transglutaminase antibodies, and bowel biopsy.

Results: Concordance was significantly higher in MZ (83.3% probandwise, 71.4% pairwise) than in DZ (16.7% probandwise, 9.1% pairwise) pairs. Concordance was not affected by sex or HLA genotype of the co-twin and being MZ was significantly associated with the occurrence of CD (Cox adjusted hazard ratio 14.3 (95% confidence interval 4.0–50.3)). In 90% of concordant pairs the discordance time was <=2 years. MZ and DZ co-twins had 70% and 9% cumulative probability of having symptomatic or silent forms of CD, respectively, within five years. Under ACE (additive genetic, common, and unshared environmental factors) models, with CD population prevalences of 1/91 and 1/1000, heritability estimates were 87% and 57%, respectively.

Conclusion: MZ pairs have a high probability of being concordant, regardless of sex or HLA genotype. Most of the affected co-twins receive a diagnosis within two years. A remarkable proportion of phenotypic variance is due to genetic factors.

Abbreviations: CD, coeliac disease; MZ, monozygotic, DZ, dizygotic; AIC, Italian Coeliac Disease Association; anti-tTG, anti-human tissue transglutaminase antibodies; ACE, additive genetic, common, and unshared environmental factors

Keywords: twins; coeliac disease; concordance; disease progression; heritability


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Relevant Article

Digest
Robin Spiller and Alastair Watson
Gut 2006 55: 749. [Extract] [Full Text] [PDF]

This article has been cited by other articles:

  • Heap, G. A., van Heel, D. A. (2009). The genetics of chronic inflammatory diseases. Hum Mol Genet 18: R101-R106 [Abstract] [Full Text]  
  • Pastore, L., Campisi, G., Compilato, D., Muzio, L. L. (2008). Orally Based Diagnosis of Celiac Disease: Current Perspectives. JDR 87: 1100-1107 [Abstract] [Full Text]  
  • Olsson, C., Hernell, O., Hornell, A., Lonnberg, G., Ivarsson, A. (2008). Difference in Celiac Disease Risk Between Swedish Birth Cohorts Suggests an Opportunity for Primary Prevention. Pediatrics 122: 528-534 [Abstract] [Full Text]  
  • Bourgey, M., Calcagno, G., Tinto, N., Gennarelli, D., Margaritte-Jeannin, P., Greco, L., Limongelli, M. G., Esposito, O., Marano, C., Troncone, R., Spampanato, A., Clerget-Darpoux, F., Sacchetti, L. (2007). HLA related genetic risk for coeliac disease. Gut 56: 1054-1059 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Cardiology Jobs

Gastroenterology Jobs