抗治疗性抑郁症外消旋氯胺酮和艾氯胺酮输注后抑郁症状缓解和反应的临床预测因素

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Human Psychopharmacology: Clinical and Experimental Pub Date : 2022-02-18 DOI:10.1002/hup.2836
Ana Paula Jesus-Nunes, Gustavo C. Leal, Fernanda S. Correia-Melo, Flávia Vieira, Rodrigo P. Mello, Ana Teresa Caliman-Fontes, Mariana V. F. Echegaray, Roberta F. Marback, Lívia N. F. Guerreiro-Costa, Breno Souza-Marques, Cassio Santos-Lima, Lucca S. Souza, Igor D. Bandeira, Flavio Kapczinski, Acioly L. T. Lacerda, Lucas C. Quarantini
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引用次数: 8

摘要

背景:重度抑郁症(MDD)是世界范围内致残的主要原因,大多数人无法实现症状缓解。难治性抑郁症(TRD)的特点是,在适当的时间和剂量下,对一大类抗抑郁药进行至少一次适当的试验失败。我们的目的是确定外消旋氯胺酮和艾氯胺酮输注后24小时和7天抑郁症状缓解和反应的临床预测因素。方法采用氯胺酮和艾氯胺酮治疗TRD的随机、双盲、主动对照、非劣效性试验。根据《精神障碍诊断与统计手册》第四版诊断为重度抑郁症并符合TRD标准的个体于2017年3月至2018年6月被招募。参与者接受单次亚麻醉剂量氯胺酮(0.5 mg/kg)或艾氯胺酮(0.25 mg/kg)治疗40分钟。使用Montgomery-Åsberg抑郁评定量表(MADRS)评估抑郁症状,在输注后24小时和7天,MADRS评分≤7分定义为症状缓解,反应定义为抑郁症状严重程度减轻≥50%。临床变量根据既往临床试验选取。采用逐步后向逻辑回归,考虑置信水平为95%。结果共纳入61例患者:女性39例(63.9%),平均年龄(47.2±14.9)岁。治疗失败率较高(优势比(OR) = 0.677;95%可信区间(CI): 0.47-0.97)和更高的疾病严重程度(OR = 0.912;95% CI: 0.83-0.99)与干预后7天抑郁症状缓解较少相关,并且与干预后24小时的反应较少相关(OR = 0.583;95% ci: 0,40;0,84, OR = 0.909;95% ci: 0,83;分别为0,99)。结论治疗失败次数和疾病严重程度是该TRD人群抑郁症状缓解和缓解较少的预测因素。缓解预测因素的研究可能有助于更好地选择可能受益于接受氯胺酮的患者。
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Clinical predictors of depressive symptom remission and response after racemic ketamine and esketamine infusion in treatment-resistant depression

Background

Major depressive disorder (MDD) is a leading cause of disability worldwide and most people do not achieve symptom remission. Treatment-resistant depression (TRD) is characterized by the failure of at least one adequate trial of a major class of antidepressant, with adequate time and dosage. We aimed to identify clinical predictors of depressive symptom remission and response 24 h and 7 days after racemic ketamine and esketamine infusions.

Methods

A randomized, double-blind, active-controlled, non-inferiority trial using ketamine and esketamine in TRD. Individuals diagnosed with MDD according to Diagnostic and Statistical Manual of Mental Disorders version IV and fulfilling TRD criteria were recruited from March 2017 to June 2018. Participants received a single subanesthetic dose of ketamine (0.5 mg/kg) or esketamine (0.25 mg/kg) for 40 min. Depressive symptoms were assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) and symptom remission was defined as a MADRS score ≤7 and response defined as ≥50% reduction in depressive symptom severity, 24 h and 7 days after the infusion. Clinical variables were selected based on previous clinical trials. Stepwise backward logistic regression was used, considering a confidence level of 95%.

Results

61 subjects were included: 39 (63.9%) were females with a mean age of 47.2 ± 14.9. Higher number of therapeutic failures (Odds Ratio (OR) = 0.677; 95% confidence interval (CI): 0.47–0.97) and higher severity of illness (OR = 0.912; 95% CI: 0.83–0.99) were associated with fewer remissions of depressive symptoms 7 days after intervention, and with fewer response in 24 h (OR = 0.583; 95% CI: 0,40; 0,84 and OR = 0.909; 95% CI: 0,83; 0,99, respectively).

Conclusion

Number of treatment failures and severity of illness were predictors of fewer remissions and responses of depressive symptoms in this TRD population. Study of predictors of remission may contribute to better selection patients that may benefit from receiving ketamine.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
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