Crohn's disease runs a more aggressive course in young Asian patients

被引:26
作者
Thia, KTJ [1 ]
Luman, W [1 ]
Jin, OC [1 ]
机构
[1] Singapore Gen Hosp, Dept Gastroenterol, Infammatory Bowel Dis Ctr, Singapore, Singapore
关键词
Crohn's disease; age; Vienna classification; young; Asian;
D O I
10.1097/01.MIB.0000195390.11645.7d
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Crohn's disease is a heterogeneous inflammatory bowel disease. The impact of age at diagnosis on the clinical course of patients varies widely as reported in the Western literature. Using the Vienna Classification, we seek to determine whether young Crohn's disease patients in an Asian population followed a different clinical course than old patients. Methods: The case records of 100 Crohn's disease patients who were treated at the Inflammatory Bowel Disease Center, Singapore General Hospital, were studied retrospectively. The age group and location of disease and behavior according to the Vienna classification were determined at diagnosis. Results: A1 group (age < 40 years) defined as '' young '' and A2 group (age >= 40) defined as '' old '' contained 65 and 35 patients, respectively Median age for the young group was 27.4 years and that for the old group was 52.6 years. Of the young patients, 66.7% flared at least once compared with 28.6% of the old patients, odds ratio of 5.0 (P < 0.001). Young patients were more likely to be steroid dependent (20.0% of A1 versus 8.6% of A2, P = 0.14), received azathioprine (38.5% of A1 versus 5.7% of A2, P < 0.001) and experienced complications (31% of A1 versus 20% of A2, P = 0.25)-numerically higher rates that did not reach statistical significance. There was no significant difference between the age groups for the location and behavior of disease as well as requirement for surgery. Conclusion: in this first Asian study looking specifically at the impact of age at diagnosis of Crohn's disease, we found that young patients underwent a more aggressive clinical course.
引用
收藏
页码:57 / 61
页数:5
相关论文
共 26 条
[1]  
Achkar JP, 2002, GASTROENTEROLOGY, V122, pA603
[2]  
Beckman I, 1995, IMMUNOLOGY, V86, P533
[3]  
CANTOR RM, 1992, GENETIC BASIS COMMON, P49
[4]   Guidelines for the management of inflammatory bowel disease in adults [J].
Carter, MJ ;
Lobo, AJ ;
Travis, SPL .
GUT, 2004, 53 :v1-v16
[5]   THE EPIDEMIOLOGY OF INFLAMMATORY BOWEL-DISEASE - A LARGE, POPULATION-BASED STUDY IN SWEDEN [J].
EKBOM, A ;
HELMICK, C ;
ZACK, M ;
ADAMI, HO .
GASTROENTEROLOGY, 1991, 100 (02) :350-358
[6]   Inflammatory bowel disease: Etiology and pathogenesis [J].
Fiocchi, C .
GASTROENTEROLOGY, 1998, 115 (01) :182-205
[7]   A simple classification of Crohn's disease: Report of the Working Party for the world congresses of gastroenterology, Vienna 1998 [J].
Gasche, C ;
Scholmerich, J ;
Brynskov, J ;
D'Haens, G ;
Hanauer, SB ;
Irvine, EJ ;
Jewell, DP ;
Rachmilewitz, D ;
Sachar, DB ;
Sandborn, WJ ;
Sutherland, LR .
INFLAMMATORY BOWEL DISEASES, 2000, 6 (01) :8-15
[8]  
HENG TC, 2004, STAT SINGAPORE N SEP, P12
[9]   Crohn's disease in the over-60 age group: a population based study [J].
Heresbach, D ;
Alexandre, JL ;
Bretagne, JF ;
Cruchant, E ;
Dabadie, A ;
Dartois-Hoguin, M ;
Girardot, PM ;
Jouanolle, H ;
Kerneis, J ;
Le Verger, JC ;
Louvain, V ;
Pennognon, L ;
Richecoeur, M ;
Politis, J ;
Robaszkiewicz, M ;
Seyrig, JA ;
Tron, I .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2004, 16 (07) :657-664
[10]   PREVALENCE AND INCIDENCE OF INFLAMMATORY BOWEL-DISEASE IN FAMILY MEMBERS [J].
LASHNER, BA ;
EVANS, AA ;
KIRSNER, JB ;
HANAUER, SB .
GASTROENTEROLOGY, 1986, 91 (06) :1396-1400