Persoons P, Vermeire S, Demyttenaere K, Fischler B, Vandenberghe J, Van Oudenhove L, Pierik M, Hlavaty T, Van Assche G, Noman M, Rutgeerts P
Department of Neurosciences and Psychiatry, Psychiatry Section, Katholieke Universiteit Leuven, Leuven, Belgium.
Aliment Pharmacol Ther. 2005 Jul 15;22(2):101-10. doi: 10.1111/j.1365-2036.2005.02535.x.
Major depressive disorder is the most common psychiatric diagnosis in Crohn's disease. In other chronic diseases, evidence suggests that depression influences the course of the disease. Strong evidence of such a mediating role of major depressive disorder in Crohn's disease has never been found.
To assess the relationship between major depressive disorder and outcome of treatment of luminal Crohn's disease with infliximab.
In this prospective study, 100 consecutive unselected patients underwent assessment of psychosocial, demographical disease-related biological and clinical parameters at baseline and at 4 weeks after infliximab. Major depressive disorder was diagnosed using the Patient Health Questionnaire. Subsequently, the patients were followed up clinically until the next flare or during 9 months.
The Crohn's disease responded in 75% of the patients, and remission was achieved in 60%. The presence of major depressive disorder at baseline predicted a lower remission rate (OR = 0.166, 95% CI = 0.049-0.567, P = 0.004). At follow-up, 88% of the patients needed retreatment. At univariate regression analysis, major depressive disorder significantly decreased time to retreatment (P = 0.001). Multivariate Cox regression confirmed major depressive disorder as an independent determinant of active disease both at baseline and at re-evaluation (hazard ratio = 2.271, 95% CI: 1.36-3.79, P = 0.002).
Major depressive disorder is a risk factor for failure to achieve remission with infliximab and for earlier retreatment in patients with active luminal Crohn's disease. Assessment and management of major depressive disorder should be part of the clinical approach to patients with Crohn's disease.
重度抑郁症是克罗恩病最常见的精神疾病诊断。在其他慢性疾病中,有证据表明抑郁症会影响疾病进程。但从未发现重度抑郁症在克罗恩病中起这种中介作用的确凿证据。
评估重度抑郁症与英夫利昔单抗治疗管腔型克罗恩病疗效之间的关系。
在这项前瞻性研究中,100例未经挑选的连续患者在基线期及英夫利昔单抗治疗4周后接受了心理社会、人口统计学、疾病相关生物学和临床参数评估。使用患者健康问卷诊断重度抑郁症。随后,对患者进行临床随访直至下次病情复发或9个月期间。
75%的患者克罗恩病有反应,60%实现缓解。基线期存在重度抑郁症预示缓解率较低(比值比=0.166,95%置信区间=0.049-0.567,P=0.004)。随访时,88%的患者需要再次治疗。单因素回归分析显示,重度抑郁症显著缩短再次治疗时间(P=0.001)。多因素Cox回归证实,重度抑郁症在基线期和重新评估时均为活动性疾病的独立决定因素(风险比=2.271,95%置信区间:1.36-3.79,P=0.002)。
重度抑郁症是管腔型活动性克罗恩病患者使用英夫利昔单抗治疗未达缓解及早期再次治疗的危险因素。对重度抑郁症的评估和管理应成为克罗恩病患者临床治疗方法的一部分。