Detailed Information on Publication Record
2019
The role of the NOD2/CARD15 gene in surgical treatment prediction in patients with Crohn’s disease
KUNOVSKÝ, Lumír, Zdeněk KALA, Filip MAREK, Jiří DOLINA, Karolina POREDSKÁ et. al.Basic information
Original name
The role of the NOD2/CARD15 gene in surgical treatment prediction in patients with Crohn’s disease
Authors
KUNOVSKÝ, Lumír (203 Czech Republic, belonging to the institution), Zdeněk KALA (203 Czech Republic, belonging to the institution), Filip MAREK (203 Czech Republic, guarantor, belonging to the institution), Jiří DOLINA (203 Czech Republic, belonging to the institution), Karolina POREDSKÁ (203 Czech Republic, belonging to the institution), Lenka KUČEROVÁ (203 Czech Republic, belonging to the institution), Klára BENEŠOVÁ (203 Czech Republic, belonging to the institution) and Ladislav MITÁŠ (203 Czech Republic, belonging to the institution)
Edition
International Journal of Colorectal Disease, New York, Springer, 2019, 0179-1958
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30212 Surgery
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.108
RIV identification code
RIV/00216224:14110/19:00108963
Organization unit
Faculty of Medicine
UT WoS
000455824400018
Keywords in English
Crohn’s disease; Czech cohort; Disease course; Genetics; Inflammatory bowel disease; Intestinal resection; NOD2/CARD15; Surgery
Tags
International impact, Reviewed
Změněno: 11/5/2020 08:16, Mgr. Tereza Miškechová
Abstract
V originále
Purpose: Crohn’s disease (CD) belongs to chronic disorders with unpredictable disease course. The aim of this study was to identify how genetic testing (NOD2/CARD15) can be used in patients with CD to predict the need for surgical treatment (to define an aggressive type of disease where the patient can profit from early surgery). Methods: The patients who were tested genetically had undergone a surgery due to CD at the Department of Surgery University Hospital Brno Bohunice between 2010 and 2016. The control group consisted of patients with CD who had been diagnosed with CD at least 5 years prior to the testing and had not required any surgical intervention. The second control group was healthy subjects. Results: In total, there were 117 operated patients for CD, 77 patients with CD that had not undergone surgery for CD and 30 healthy subjects. For patients with at least one genetic mutation, the risk of the necessity of surgical treatment of CD is 1.96 times higher than for patients with no mutation. Patients with two or more mutations were generally operated on at a younger age, in a shorter time after being diagnosed and each patient had a partial resection of the ileum. Conclusion: The group of operated patients with CD had a significantly higher distribution of at least one genetic mutation as opposed to the non-operated group. In patients with two or more mutations, the disease course was more aggressive. This group of patients might profit from the conservative top-down or early surgical therapy.