Patten S B, Metz L M
Department of Community Health Sciences, University of Calgary, Alberta, Canada.
Mult Scler. 2001 Aug;7(4):243-8. doi: 10.1177/135245850100700406.
Depression is a suspected side effect of multiple sclerosis (MS) treatment with interferon beta-1a. However, this has not been confirmed by rigorous studies. Several psychological symptom rating scales were completed during the PRISMS clinical trial of subcutaneous interferon beta-1a (Rebif) for relapsing-remitting MS. We conducted an analysis of these data in order to determine whether symptom elevations were associated with treatment. The PRISMS clinical trial included 560 subjects from 22 centres in nine countries. There were two active treatment arms (44 mcg x 3 and 22 mcg x 3 subcutaneously three times per week) and a placebo group. Two hundred and sixty-seven of these subjects were enrolled at English speaking study centres, where psychiatric symptom ratings were obtained at baseline, 6, 12, 18 and 24 months using the Center for Epidemiological Studies Depression Rating Scale (CES-D), the General Health Questionnaire (GHQ) and the Beck Hopelessness Scale (BHS). After randomization, the groups completing these scales were similar in terms of age, gender, EDSS, duration of illness and employment status. Median CES-D scores in the high dose, low dose and placebo groups at baseline were also similar: 8.0, 7.0 and 8.0, respectively. After 6 months of treatment the median change in CES-D score was zero in all three groups. The proportion of subjects exceeding the traditional CES-D cut-point for clinically significant depression (> 15) after 6 months of treatment was strongly associated with pre-treatment depression (RR 2.9, 95% C.I.: 1.8-4.7), but not with treatment group (chi-square=1.64, d.f.=2, P=0.44). The results were comparable at 12, 18 and 24 months and when ratings from the other scales were evaluated. This analysis confirms that depression is common in persons with MS: the incidence of CES-D depression in the first 6 months of follow-up was 15.6%. However, no evidence of increased depressive symptomatology was observed in association with interferon beta-1a (Rebif).
抑郁症被怀疑是多发性硬化症(MS)患者使用β-1a干扰素治疗后的一种副作用。然而,这一点尚未得到严格研究的证实。在皮下注射β-1a干扰素(Rebif)治疗复发缓解型MS的PRISMS临床试验期间,完成了多项心理症状评定量表。我们对这些数据进行了分析,以确定症状升高是否与治疗有关。PRISMS临床试验纳入了来自9个国家22个中心的560名受试者。有两个积极治疗组(分别为每周皮下注射3次44微克和22微克)和一个安慰剂组。其中267名受试者在说英语的研究中心入组,在基线、6个月、12个月、18个月和24个月时使用流行病学研究中心抑郁评定量表(CES-D)、一般健康问卷(GHQ)和贝克绝望量表(BHS)获取精神症状评分。随机分组后,完成这些量表的各组在年龄、性别、扩展残疾状态量表(EDSS)、病程和就业状况方面相似。高剂量组、低剂量组和安慰剂组在基线时的CES-D中位数评分也相似,分别为8.0、7.0和8.0。治疗6个月后,三组的CES-D评分中位数变化均为零。治疗6个月后,超过传统CES-D临床显著抑郁切点(>15)的受试者比例与治疗前抑郁密切相关(相对危险度2.9,95%可信区间:1.8 - 4.7),但与治疗组无关(卡方检验=1.64,自由度=2,P = 0.44)。在12个月、18个月和24个月以及评估其他量表评分时,结果类似。该分析证实抑郁症在MS患者中很常见:随访前6个月CES-D抑郁发生率为15.6%。然而,未观察到与β-1a干扰素(Rebif)相关的抑郁症状增加的证据。