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Similar clinical characteristics of familial and sporadic inflammatory bowel disease in South Korea.
DC Field | Value | Language |
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dc.contributor.author | Chung, SH | - |
dc.contributor.author | Park, SJ | - |
dc.contributor.author | Lee, HS | - |
dc.contributor.author | Hong, SP | - |
dc.contributor.author | Cheon, JH | - |
dc.contributor.author | Kim, TI | - |
dc.contributor.author | Kim, WH | - |
dc.date.accessioned | 2016-04-05T07:32:37Z | - |
dc.date.available | 2016-04-05T07:32:37Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1007-9327 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/12349 | - |
dc.description.abstract | AIM: To investigate differences of clinical characteristics and disease courses
between familial and sporadic inflammatory bowel disease (IBD) patients. METHODS: We obtained clinical data on Crohn's disease (CD) (n = 691) and ulcerative colitis (n = 1113) from a tertiary referral medical center between 2005 and 2012. Seventeen patients (2.5%) with CD and 27 patients (2.4%) with ulcerative colitis (UC) were identified as having a familial history of IBD, including the first and second degree relatives. For each control case, three times the number of age-, sex-, and diagnosis year-matched CD and UC patients, without a family history of IBD, were randomly selected in this case control study. RESULTS: There were no significant differences in age or main symptom at diagnosis, extraintestinal manifestation, location/extent, behavior of disease activity, number of hospitalizations, number of operations, operation type, number of relapses, or oral medical treatment between familial and sporadic CD and UC patients. Median (min-max) follow-up periods after diagnosis of familial CD and sporadic CD patients were 84 (24-312) and 36 (8-240) mo, respectively (P = 0.008). Familial CD patients more frequently used anti-tumor necrosis factor (TNF) antibodies compared to sporadic CD patients (17.6% vs 0%, P = 0.014). CONCLUSION: In conclusion, a family history of IBD does not seem to be an important predictive factor affecting clinical characteristics or disease course even if there is a more frequent use of anti-TNF antibodies in familial CD patients compared to sporadic CD patients. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adolescent | - |
dc.subject.MESH | Anti-Inflammatory Agents | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Colitis, Ulcerative | - |
dc.subject.MESH | Crohn Disease | - |
dc.subject.MESH | Digestive System Surgical Procedures | - |
dc.subject.MESH | Disease Progression | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Gastrointestinal Agents | - |
dc.subject.MESH | Genetic Predisposition to Disease | - |
dc.subject.MESH | Heredity | - |
dc.subject.MESH | Hospitalization | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Pedigree | - |
dc.subject.MESH | Phenotype | - |
dc.subject.MESH | Recurrence | - |
dc.subject.MESH | Registries | - |
dc.subject.MESH | Remission Induction | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Tertiary Care Centers | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Tumor Necrosis Factor-alpha | - |
dc.subject.MESH | Young Adult | - |
dc.title | Similar clinical characteristics of familial and sporadic inflammatory bowel disease in South Korea. | - |
dc.type | Article | - |
dc.identifier.pmid | 25493025 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258581/ | - |
dc.contributor.affiliatedAuthor | 정, 숙희 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3748/wjg.v20.i45.17120 | - |
dc.citation.title | World journal of gastroenterology | - |
dc.citation.volume | 20 | - |
dc.citation.number | 45 | - |
dc.citation.date | 2014 | - |
dc.citation.startPage | 17120 | - |
dc.citation.endPage | 17126 | - |
dc.identifier.bibliographicCitation | World journal of gastroenterology, 20(45). : 17120-17126, 2014 | - |
dc.identifier.eissn | 2219-2840 | - |
dc.relation.journalid | J010079327 | - |
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