Joseph M H, Baker H F, Johnstone E C, Crow T J
Psychopharmacology (Berl). 1979 Jun 28;64(1):35-40. doi: 10.1007/BF00427342.
Urinary MHPG excretion in patients with acute schizophrenia was studied before and during a trial of the isomers of flupenthixol and placebo. Pretrial MHPG excretion was not related to severity of illness before the trial or to other pretrial clinical variables. In male subjects higher pretrial MHPG excretion was associated with a better outcome 1 year post-trial. However in females no relationship between MHPG excretion and outcome was established. During the trial there was a reduction in MHPG excretion in patients treated with beta-flupenthixol but no decrease in the group treated with alpha-flupenthixol or chlorpromazine. In patients on placebo there was a reduction in MHPG excretion in those who did well clinically, but not in those who did poorly. Thus low MHPG excretion may be a predictor of poor outcome in schizophrenia, but MHPG excretion also changes both as a function of clinical state and of neuroleptic drug administration.
在氟哌噻吨异构体和安慰剂试验之前及期间,对急性精神分裂症患者的尿中3-甲氧基-4-羟基苯乙二醇(MHPG)排泄情况进行了研究。试验前的MHPG排泄与试验前疾病严重程度或其他试验前临床变量无关。在男性受试者中,试验前较高的MHPG排泄与试验后1年较好的预后相关。然而,在女性中,未确立MHPG排泄与预后之间的关系。试验期间,接受β-氟哌噻吨治疗的患者MHPG排泄减少,但接受α-氟哌噻吨或氯丙嗪治疗的组未减少。服用安慰剂的患者中,临床情况良好者MHPG排泄减少,但情况不佳者未减少。因此,低MHPG排泄可能是精神分裂症预后不良的一个预测指标,但MHPG排泄也会随临床状态和抗精神病药物给药而变化。