Literature DB >> 24803813

Prediction of Crohn's disease aggression through NOD2/CARD15 gene sequencing in an Australian cohort.

Maneesha Bhullar1, Finlay Macrae1, Gregor Brown1, Margie Smith1, Ken Sharpe1.   

Abstract

AIM: To investigate the association between mutations in oligomerisation domain 2/caspase recruitment domains 15 (NOD2/CARD15) and the natural history of Crohn's disease (CD) to identify patients who would benefit from early aggressive medical intervention.
METHODS: We recruited thirty consecutive unrelated CD patients with a history of ileo-caecal or small bowel resection during the period 1980-2000; Fifteen patients of these had post-operative relapse that required further surgery and fifteen did not. Full sequencing of the NOD2/CARD15 gene using dHPLC for exons 3, 5, 7, 10 and 12 and direct sequencing for exons 2, 4, 6, 8, 9 and 11 was conducted. CD patients categorized as carrying variants were anyone with at least 1 variant of the NOD2/CARD15 gene.
RESULTS: About 13.3% of the cohort (four patients) carried at least one mutant allele of 3020insC of the NOD2/CARD15 gene. There were 20 males and 10 females with a mean age of 43.3 years (range 25-69 years). The mean follow up was 199.6 mo and a median of 189.5 mo. Sixteen sequence variations within the NOD2/CARD15 gene were identified, with 9 of them occurring with an allele frequency of greater than 10 %. In this study, there was a trend to suggest that patients with the 3020insC mutation have a higher frequency of operations compared to those without the mutation. Patients with the 3020insC mutation had a significantly shorter time between the diagnosis of CD and initial surgery. This study included Australian patients of ethnically heterogenous background unlike previous studies conducted in different countries.
CONCLUSION: These findings suggest that patients carrying NOD2/CARD15 mutations follow a rapid and more aggressive form of Crohn's disease showing a trend for multiple surgical interventions and significantly shorter time to early surgery.

Entities:  

Keywords:  Crohn’s disease; Genotyping; Inflammatory bowel disease; Natural history; Oligomerisation domain 2/caspase recruitment domains 15

Mesh:

Substances:

Year:  2014        PMID: 24803813      PMCID: PMC4009534          DOI: 10.3748/wjg.v20.i17.5008

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  44 in total

Review 1.  Biological therapies in inflammatory bowel disease: top-down or bottom-up?

Authors:  Bas Oldenburg; Daan Hommes
Journal:  Curr Opin Gastroenterol       Date:  2007-07       Impact factor: 3.287

2.  CARD15 gene variants and risk of reoperation in Crohn's disease patients.

Authors:  Giovanni Maconi; Elisabetta Colombo; Gianluca Matteo Sampietro; Francesca Lamboglia; Renata D'Incà; Marco Daperno; Andrea Cassinotti; Giacomo Carlo Sturniolo; Sandro Ardizzone; Piergiorgio Duca; Gabriele Bianchi Porro; Vito Annese
Journal:  Am J Gastroenterol       Date:  2009-07-28       Impact factor: 10.864

3.  NOD2/CARD15 and TNFA, but not IL1B and IL1RN, are associated with Crohn's disease.

Authors:  António Carlos Ferreira; Susana Almeida; Marta Tavares; Paulo Canedo; Fábio Pereira; Gonçalo Regalo; Céu Figueiredo; Eunice Trindade; Raquel Seruca; Fátima Carneiro; Jorge Amil; José Carlos Machado; Fernando Tavarela-Veloso
Journal:  Inflamm Bowel Dis       Date:  2005-04       Impact factor: 5.325

4.  Carriage of CARD15 variants and smoking as risk factors for resective surgery in patients with Crohn's ileal disease.

Authors:  L Laghi; S Costa; S Saibeni; P Bianchi; P Omodei; A Carrara; L Spina; E Contessini Avesani; M Vecchi; R De Franchis; A Malesci
Journal:  Aliment Pharmacol Ther       Date:  2005-09-15       Impact factor: 8.171

5.  Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.

Authors:  Julia Seiderer; Fabian Schnitzler; Stephan Brand; Tanja Staudinger; Simone Pfennig; Karin Herrmann; Katrin Hofbauer; Julia Dambacher; Cornelia Tillack; Michael Sackmann; Burkhard Göke; Peter Lohse; Thomas Ochsenkühn
Journal:  Scand J Gastroenterol       Date:  2006-12       Impact factor: 2.423

6.  Association of NOD2/CARD15 mutations with previous surgical procedures in Crohn's disease.

Authors:  M Barreiro; C Núñez; J E Domínguez-Muñoz; A Lorenzo; F Barreiro; J Potel; A S Peña
Journal:  Rev Esp Enferm Dig       Date:  2005-08       Impact factor: 2.086

7.  NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Authors:  Martin Lacher; Johanna Helmbrecht; Sebastian Schroepf; Sibylle Koletzko; Antje Ballauff; Martin Classen; Holm Uhlig; Jochen Hubertus; Dominik Hartl; Peter Lohse; Dietrich von Schweinitz; Roland Kappler
Journal:  J Pediatr Surg       Date:  2010-08       Impact factor: 2.545

8.  Identification of NOD2/CARD15 mutations in Malaysian patients with Crohn's disease.

Authors:  Kek Heng Chua; Ida Hilmi; Ching Ching Ng; Tzy Lui Eng; Shanthi Palaniappan; Way Seah Lee; Khean-Lee Goh
Journal:  J Dig Dis       Date:  2009-05       Impact factor: 2.325

9.  Common NOD2 mutations are absent in patients with Crohn's disease in India.

Authors:  Srinivasan Pugazhendhi; Aneesh Amte; Ramadass Balamurugan; Venkataraman Subramanian; Balakrishnan S Ramakrishna
Journal:  Indian J Gastroenterol       Date:  2008 Sep-Oct

10.  OCTN and CARD15 gene polymorphism in Chinese patients with inflammatory bowel disease.

Authors:  Mei Li; Xiang Gao; Chang-Cun Guo; Kai-Chun Wu; Xin Zhang; Pin-Jin Hu
Journal:  World J Gastroenterol       Date:  2008-08-21       Impact factor: 5.742

View more
  5 in total

Review 1.  Prognostic factors affecting outcomes in fistulating perianal Crohn's disease: a systematic review.

Authors:  G C Braithwaite; M J Lee; D Hind; S R Brown
Journal:  Tech Coloproctol       Date:  2017-06-20       Impact factor: 3.781

2.  NOD2/CARD15 mutations in Polish and Bosnian populations with and without Crohn's disease: prevalence and genotype-phenotype analysis.

Authors:  Nermin N Salkic; Grazyna Adler; Iwona Zawada; Ervin Alibegovic; Beata Karakiewicz; Anna Kozlowska-Wiechowska; Michał Wasilewicz; Violetta Sulzyc-Bielicka; Dariusz Bielicki
Journal:  Bosn J Basic Med Sci       Date:  2015-05-25       Impact factor: 3.363

Review 3.  NOD2 mutations and colorectal cancer - Where do we stand?

Authors:  Diogo Branquinho; Paulo Freire; Carlos Sofia
Journal:  World J Gastrointest Surg       Date:  2016-04-27

Review 4.  Identifying the Neurogenetic Framework of Crohn's Disease Through Investigative Analysis of the Nucleotide-binding Oligomerization Domain-containing Protein 2 Gene Mutation.

Authors:  Md Sakibuzzaman; Syed Ahmad Moosa; Mahabuba Akhter; Ipsita Hamid Trisha; Khandokar A Talib
Journal:  Cureus       Date:  2019-09-17

5.  Long-Term Follow-Up, Association between CARD15/NOD2 Polymorphisms, and Clinical Disease Behavior in Crohn's Disease Surgical Patients.

Authors:  Francesco Giudici; Tiziana Cavalli; Cristina Luceri; Edda Russo; Daniela Zambonin; Stefano Scaringi; Ferdinando Ficari; Marilena Fazi; Amedeo Amedei; Francesco Tonelli; Cecilia Malentacchi
Journal:  Mediators Inflamm       Date:  2021-02-24       Impact factor: 4.711

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.