Coryell W, Turner R D, Sherman A
J Clin Psychopharmacol. 1987 Jun;7(3):138-42.
Twenty-six outpatients with major depression completed a 6-week, fixed dose trial of desipramine and provided plasma samples. Recovery after 6 weeks, defined in either of two ways, corresponded to lower desipramine levels, while clinical status at 4 weeks bore no apparent relationship to plasma levels. Upper limits of 140 or 155 ng/ml emerged depending on the outcome measure used. Patients with endogenous depression, those with primary depression, and those with abnormal dexamethasone suppression test results yielded similar therapeutic thresholds, while the sharpest blood level/response relationship emerged in the subgroup with an abnormal escape from dexamethasone.
26名重度抑郁症门诊患者完成了为期6周的地昔帕明固定剂量试验,并提供了血浆样本。以两种方式之一定义的6周后康复与较低的地昔帕明水平相对应,而4周时的临床状态与血浆水平无明显关系。根据所使用的结果测量方法,出现了140或155 ng/ml的上限。内源性抑郁症患者、原发性抑郁症患者以及地塞米松抑制试验结果异常的患者产生了相似的治疗阈值,而在地塞米松异常撤药亚组中出现了最明显的血药浓度/反应关系。