Artaloytia Juan Francisco, Arango Celso, Lahti Adrienne, Sanz Javier, Pascual Ana, Cubero Pedro, Prieto David, Palomo Tomás
Hospital Universitario 12 de Octobre, Madrid, Spain.
Am J Psychiatry. 2006 Mar;163(3):488-93. doi: 10.1176/appi.ajp.163.3.488.
Despite the clinical observation that antipsychotics can produce negative symptoms, no previous controlled study, to our knowledge, has evaluated this action in healthy subjects. The present study assessed observer-rated and self-rated negative symptoms produced by conventional and second-generation antipsychotics in healthy volunteers.
The authors used a double-blind, placebo-controlled trial of single doses of haloperidol (5 mg) and risperidone (2.5 mg) in normal subjects. Thirty-two subjects were administered haloperidol, risperidone, and placebo in a random order. Motor variables and observer-rated negative symptoms were assessed after 3-4 hours and subjective negative symptoms and drowsiness after 24 hours.
Neither of the active drugs caused significant motor extrapyramidal symptoms after administration. Haloperidol caused significantly more negative signs and symptoms than placebo on the Scale for the Assessment of Negative Symptoms (SANS) and two self-rated negative symptom scales: the Subjective Deficit Syndrome Scale total score and an analog scale that evaluates subjective negative symptoms. Risperidone caused significantly more negative signs and symptoms than placebo on the Brief Psychiatric Rating Scale (BPRS), the SANS, the Subjective Deficit Syndrome Scale total score, and the analog scale for subjective negative symptoms. After control for drowsiness, risperidone but not haloperidol produced more negative symptoms than placebo on the BPRS and the SANS. Significance was lost for the subjective negative symptoms with both drugs.
Single doses of both haloperidol and risperidone produce negative symptoms in normal individuals. Drowsiness may be an important confounding factor in the assessment of negative symptoms in antipsychotic trials.
尽管临床观察发现抗精神病药物可引发阴性症状,但据我们所知,此前尚无对照研究在健康受试者中评估这一作用。本研究评估了传统及第二代抗精神病药物在健康志愿者中引发的、由观察者评定和自我评定的阴性症状。
作者对正常受试者进行了一项单剂量氟哌啶醇(5毫克)和利培酮(2.5毫克)的双盲、安慰剂对照试验。32名受试者按随机顺序接受氟哌啶醇、利培酮和安慰剂治疗。在3至4小时后评估运动变量和观察者评定的阴性症状,在24小时后评估主观阴性症状和嗜睡情况。
两种活性药物给药后均未引起明显的运动性锥体外系症状。在阴性症状评定量表(SANS)以及两个自我评定的阴性症状量表上,氟哌啶醇比安慰剂导致了显著更多的阴性体征和症状,这两个量表分别是主观缺陷综合征量表总分以及一个评估主观阴性症状的类似量表。在简明精神病评定量表(BPRS)、SANS、主观缺陷综合征量表总分以及主观阴性症状类似量表上,利培酮比安慰剂导致了显著更多的阴性体征和症状。在控制嗜睡因素后,在BPRS和SANS上,利培酮比安慰剂产生了更多的阴性症状,而氟哌啶醇则未出现此情况。两种药物的主观阴性症状差异不再显著。
单剂量的氟哌啶醇和利培酮均可在正常个体中产生阴性症状。嗜睡可能是抗精神病药物试验中阴性症状评估的一个重要混杂因素。