Interest-activity symptom severity predicts response to ketamine infusion in treatment-resistant depression

被引:6
作者
Chen, Mu-Hong [1 ,2 ,3 ]
Lin, Wei-Chen [1 ,2 ,3 ]
Wu, Hui-Ju [2 ]
Bai, Ya-Mei [1 ,2 ]
Li, Cheng-Ta [1 ,2 ,3 ]
Tsai, Shih-Jen [1 ,2 ,3 ]
Hong, Chen-Jee [1 ,2 ,3 ]
Tu, Pei-Chi [1 ,2 ,4 ]
Su, Tung-Ping [1 ,2 ,3 ,4 ,5 ]
机构
[1] Taipei Vet Gen Hosp, Dept Psychiat, 201,Sec 2,Shih Pai Rd, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Fac Med, Dept Psychiat, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Brain Sci, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Med Res, Taipei, Taiwan
[5] Cheng Hsin Gen Hosp, Dept Psychiat, Taipei, Taiwan
关键词
Ketamine; Treatment-resistant depression; Interest-activity; RATING-SCALE; ANHEDONIA; INDIVIDUALS; STIMULATION;
D O I
10.1007/s00213-020-05737-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background Interest and activity are part of the positive mood domain. Evidence suggests the symptom domain of interest-activity at baseline as a clinical predictor for treatment response to traditional antidepressants. However, whether this domain is related to the response to a single low-dose ketamine infusion remains unclear. Methods Seventy-one patients with treatment-resistant depression were randomized to 3 treatment groups: a single 0.5 or 0.2 mg/kg ketamine or normal saline placebo infusion. Depressive symptoms were measured using the 17-item Hamilton Depression Rating Scale before infusions and at postinfusion period (at 40 min and up to 2 weeks). Low (mild) versus medium versus high (severe) interest-activity symptom domain groups were classified on the basis of the cutoff point of +/- 0.4 standard deviation. The effect of baseline interest-activity symptoms on outcomes was tested using generalized estimating equation models. Results The interest-activity symptom domain as a continuous variable (beta = 8.413, p = .016) was related to the trajectory of depressive symptoms. Stratified by levels of the interest-activity symptom domain, in the low interest-activity, 0.2 mg/kg ketamine infusion (beta = 0.013) demonstrated the greatest antidepressant effect (p < .01) compared with 0.5 mg/kg ketamine (beta = 0.739) and placebo infusions; however, in the high interest-activity, 0.5 mg/kg ketamine infusion (beta = 0.001) demonstrated the best antidepressant effect (p < .01) compared with 0.2 mg/kg ketamine (beta = 1.372) and placebo infusions. Discussion The symptom domain of interest-activity was an independent predictor for the treatment response to a single low-dose ketamine infusion.
引用
收藏
页码:857 / 865
页数:9
相关论文
共 28 条
[1]   Comparison of Beck Depression Inventories-IA and -II in psychiatric outpatients [J].
Beck, AT ;
Steer, RA ;
Ball, R ;
Ranieri, WF .
JOURNAL OF PERSONALITY ASSESSMENT, 1996, 67 (03) :588-597
[2]   Adjunctive Treatment with Asenapine Augments the Escitalopram-Induced Effects on Monoaminergic Outflow and Glutamatergic Neurotransmission in the Medial Prefrontal Cortex of the Rat [J].
Bjorkholm, Carl ;
Franberg, Olivia ;
Malmerfelt, Anna ;
Marcus, Monica M. ;
Konradsson-Geuken, Asa ;
Schilstrom, Bjorn ;
Jardemark, Kent ;
Svensson, Torgny H. .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2015, 18 (03)
[3]   Efficacy of low-dose ketamine infusion in anxious vs nonanxious depression: revisiting the Adjunctive Ketamine Study of Taiwanese Patients with Treatment-Resistant Depression [J].
Chen, Mu-Hong ;
Lin, Wei-Chen ;
Wu, Hui-Ju ;
Bai, Ya-Mei ;
Li, Cheng-Ta ;
Tsai, Shih-Jen ;
Hong, Chen-Jee ;
Tu, Pei-Chi ;
Cheng, Chih-Ming ;
Su, Tung-Ping .
CNS SPECTRUMS, 2021, 26 (04) :362-367
[4]   The Impact of (the Concept of) Treatment-Resistant Depression: An Opinion Review [J].
Demyttenaere, Koen ;
Van Duppen, Zeno .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2019, 22 (02) :85-92
[5]   Anhedonia and Reward-Circuit Connectivity Distinguish Nonresponders from Responders to Dorsomedial Prefrontal Repetitive Transcranial Magnetic Stimulation in Major Depression [J].
Downar, Jonathan ;
Geraci, Joseph ;
Salomons, Tim V. ;
Dunlop, Katharine ;
Wheeler, Sarah ;
McAndrews, Mary Pat ;
Bakker, Nathan ;
Blumberger, Daniel M. ;
Daskalakis, Zafiris J. ;
Kennedy, Sidney H. ;
Flint, Alastair J. ;
Giacobbe, Peter .
BIOLOGICAL PSYCHIATRY, 2014, 76 (03) :176-185
[6]   Clinical, behavioral, and neural measures of reward processing correlate with escitalopram response in depression: a Canadian Biomarker Integration Network in Depression (CAN-BIND-1) Report [J].
Dunlop, Katharine ;
Rizvi, Sakina J. ;
Kennedy, Sidney H. ;
Hassel, Stefanie ;
Strother, Stephen C. ;
Harris, Jacqueline K. ;
Zamyadi, Mojdeh ;
Arnott, Stephen R. ;
Davis, Andrew D. ;
Mansouri, Farrokh ;
Schulze, Laura ;
Ceniti, Amanda K. ;
Lam, Raymond W. ;
Milev, Roumen ;
Rotzinger, Susan ;
Foster, Jane A. ;
Frey, Benicio N. ;
Parikh, Sagar V. ;
Soares, Claudio N. ;
Uher, Rudolf ;
Turecki, Gustavo ;
MacQueen, Glenda M. ;
Downar, Jonathan .
NEUROPSYCHOPHARMACOLOGY, 2020, 45 (08) :1390-1397
[7]   Ketamine treatment reverses behavioral and physiological alterations induced by chronic mild stress in rats [J].
Garcia, Leda S. B. ;
Comim, Clarissa M. ;
Valvassori, Samira S. ;
Reus, Gislaine Z. ;
Stertz, Laura ;
Kapczinski, Flavio ;
Gavioli, Elaine C. ;
Quevedo, Joao .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2009, 33 (03) :450-455
[8]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[9]   Combining clinical variables to optimize prediction of antidepressant treatment outcomes [J].
Iniesta, Raquel ;
Malki, Karim ;
Maier, Wolfgang ;
Rietschel, Marcella ;
Mors, Ole ;
Hauser, Joanna ;
Henigsberg, Neven ;
Dernovsek, Mojca Zvezdana ;
Souery, Daniel ;
Stahl, Daniel ;
Dobson, Richard ;
Aitchison, Katherine J. ;
Farmer, Anne ;
Lewis, Cathryn M. ;
McGuffin, Peter ;
Uher, Rudolf .
JOURNAL OF PSYCHIATRIC RESEARCH, 2016, 78 :94-102
[10]  
Kadriu B, 2020, ADV PHARMACOL, V89, P195, DOI 10.1016/bs.apha.2020.05.003