GENETICS OF INFLAMMATORY BOWEL-DISEASE - IMPLICATIONS FOR THE FUTURE

Citation
As. Pena et Jba. Crusius, GENETICS OF INFLAMMATORY BOWEL-DISEASE - IMPLICATIONS FOR THE FUTURE, World journal of surgery, 22(4), 1998, pp. 390-393
Citations number
26
Categorie Soggetti
Surgery
Journal title
ISSN journal
03642313
Volume
22
Issue
4
Year of publication
1998
Pages
390 - 393
Database
ISI
SICI code
0364-2313(1998)22:4<390:GOIB-I>2.0.ZU;2-O
Abstract
There is overwhelming evidence that genetic factors play a role in the predisposition to suffer the development of the chronic inflammatory bowel diseases. The genetic analysis of complex diseases, such as ulce rative colitis and Crohn's disease, is difficult. The presence of dise ase heterogeneity, the relative low frequency in the population, the d egree to which first-degree relatives are affected (approximately 10%) , the presence of genes with minor genetic effects, and ethnic differe nces are some of the difficulties encountered when identifying disease susceptibility loci. Two major approaches to identifying these genes are being followed at present. The first, family-based, consists of st udying linkage analysis in sibling pairs and parental transmission in genome-nide screening using microsatellite markers. These studies are appropriate and helpful for finding genes of major or moderate effects but may provide difficulty when identifying genes with minor effects. Risch and Merikangas have pointed to the power of association studies utilizing candidate genes in families. These studies should be consid ered in the future in genome-wide screens when technologic advances pe rmit. The second approach is based on classic epidemiologic designs, p opulation-based studies, using candidate genes in the framework of a b iologic hypothesis. Recent data using both approaches in both Crohn's disease and ulcerative colitis are reviewed. The results of genome-wid e linkage studies have not reached consensus but suggest that these di seases are different and polygenic in nature. We have started our stud ies with the hypothesis that an abnormal immune dysbalance contributes to the biologic basis of disease. We therefore study polymorphisms in genes encoding proinflammatory and regulatory cytokines. Preliminary data of these association studies suggest the importance of several ge nes with small effects in determining the severity and prognosis of th ese diseases.