Review article: Inherited thrombophilia in inflammatory bowel disease

Alfredo Papa, Silvio Danese, Antonino Grillo, Giovanni Gasbarrini, Antonio Gasbarrini

Research output: Contribution to journalArticle

Abstract

Individuals with inflammatory bowel disease frequently experience increased systemic thromboembolic complications, which represent an important cause of morbidity and mortality. Risk factors for thrombosis can be inherited or acquired. The most common inherited risk factors for thromboembolism are factor V Leiden mutation, G20210A mutation in the prothrombin gene, and homozygous C677T mutation in the methylenetetrahydrofolate are reductase gene. In the last few years, a great amount of literature has focused on the prevalence of such genetic mutations and their role in determining thrombosis in IBD patients. In this review, we summarize the results of these studies.

Original languageEnglish
Pages (from-to)1247-1251
Number of pages5
JournalAmerican Journal of Gastroenterology
Volume98
Issue number6
DOIs
Publication statusPublished - Jun 1 2003

ASJC Scopus subject areas

  • Gastroenterology

Fingerprint Dive into the research topics of 'Review article: Inherited thrombophilia in inflammatory bowel disease'. Together they form a unique fingerprint.

  • Cite this