Table 1.
Clinical characteristics of the patient and the control groups.
| Patient group (n = 103) | Control group (n = 114) | P | |
|---|---|---|---|
| Mean age(yr) | 46.4 ± 13.5 | 43.2 ± 13.2 | .073 |
| Sex | |||
| Female | 52 (50.5%) | 56 (49.1%) | .841 |
| Male | 51 (49.5%) | 58 (50.9%) | |
| CDAI | |||
| Inactive | 63 (61.2%) | ||
| Mild | 24 (23.3%) | ||
| Moderate | 16 (15.5%) | ||
| Duration of disease | |||
| 0–5 yr | 31 (30.1%) | ||
| 6–10 yr | 25 (24.3%) | ||
| >10 yr | 47 (45.6%) | ||
| Montreal Classification | |||
| A1 | 4 (3.9%) | ||
| A2 | 59 (57.3%) | ||
| A3 | 40 (38.8%) | ||
| L1 | 51 (49.5%) | ||
| L2 | 12 (11.7%) | ||
| L3 | 40 (38.8%) | ||
| B1 | 67 (65%) | ||
| B2 | 18 (17.5%) | ||
| B3 | 13 (12.6%) | ||
| Perineal disease | 5 (4.9%) | ||
| Upper gastrointestinal disease | 0 (0%) | ||
| Prior ileal or ileocolic resection | 31 (30.1%) | ||
| Treatment of CD | |||
| 5-ASA | 52 (50.5%) | ||
| AZA | 28 (27.2%) | ||
| Biologic + AZA | 12 (11.7%) | ||
| Biologic agents | 6 (5.8%) | ||
| Sulfasalazin | 2 (1.9%) | ||
| 5-ASA + AZA | 2 (1.9%) | ||
| Sulfasalazin + AZA | 1 (1%) |
ASA = 5-aminosalicylic acid, AZA = azathioprine, CD = Crohn’s disease, CDAI = Crohn’s disease activity index.