BACKGROUND: The 17-item Hamilton depression rating scale (HAMD(17)) is the standard efficacy outcome in antidepressant clinical trials. It is criticized for multidimensionality and poorly discriminating treatment from placebo. HAMD subscales may overcome these limitations and reduce the sample size of clinical trials. This study compared the discriminative performance of the HAMD(17) and three established HAMD subscales (Bech, Maier-Philipp, Gibbons) across a range of antidepressants with different mechanisms of action. METHODS: We analyzed data from 24 clinical trials including 3692 patients randomized totricyclic or tetracyclic antidepressants (TCAs or TeCAs), selective serotonin reuptake inhibitors (SSRIs) or placebo. Data were analyzed using a mixed model for repeated measurements (MMRM). Standardized effect sizes for the HAMD(17) and subscales were derived for every time-point, and their effect on sample size was evaluated. RESULTS: For TCAs and TeCAs vs. placebo, the HAMD(17) consistently provided the highest standardized effects. The sample size to establish efficacy at week six was >25 percent smaller than for any of the subscales. However, for SSRIs vs. placebo, the HAMD(17) provided slightly smaller standardized effects and was the least efficient outcome. There were no relevant differences between the subscales. LIMITATIONS: Data were derived exclusively from mirtazapine trials. Conclusions are restricted to clinical trial settings. CONCLUSIONS: Comparative performance of the HAMD(17) and various subscales strongly depends on type of antidepressant. Results support using HAMD(17) as primary endpoint in clinical trials, but it will be beneficial to pro-actively include subscales as additional endpoints to successfully establish treatment effects of new antidepressants.
RCT Entities:
BACKGROUND: The 17-item Hamilton depression rating scale (HAMD(17)) is the standard efficacy outcome in antidepressant clinical trials. It is criticized for multidimensionality and poorly discriminating treatment from placebo. HAMD subscales may overcome these limitations and reduce the sample size of clinical trials. This study compared the discriminative performance of the HAMD(17) and three established HAMD subscales (Bech, Maier-Philipp, Gibbons) across a range of antidepressants with different mechanisms of action. METHODS: We analyzed data from 24 clinical trials including 3692 patients randomized to tricyclic or tetracyclic antidepressants (TCAs or TeCAs), selective serotonin reuptake inhibitors (SSRIs) or placebo. Data were analyzed using a mixed model for repeated measurements (MMRM). Standardized effect sizes for the HAMD(17) and subscales were derived for every time-point, and their effect on sample size was evaluated. RESULTS: For TCAs and TeCAs vs. placebo, the HAMD(17) consistently provided the highest standardized effects. The sample size to establish efficacy at week six was >25 percent smaller than for any of the subscales. However, for SSRIs vs. placebo, the HAMD(17) provided slightly smaller standardized effects and was the least efficient outcome. There were no relevant differences between the subscales. LIMITATIONS: Data were derived exclusively from mirtazapine trials. Conclusions are restricted to clinical trial settings. CONCLUSIONS: Comparative performance of the HAMD(17) and various subscales strongly depends on type of antidepressant. Results support using HAMD(17) as primary endpoint in clinical trials, but it will be beneficial to pro-actively include subscales as additional endpoints to successfully establish treatment effects of new antidepressants.
Authors: Maurizio Fava; Marlene P Freeman; Martina Flynn; Bettina B Hoeppner; Richard Shelton; Dan V Iosifescu; James W Murrough; David Mischoulon; Cristina Cusin; Mark Rapaport; Boadie W Dunlop; Madhukar H Trivedi; Manish Jha; Gerard Sanacora; Gretchen Hermes; George I Papakostas Journal: Brain Stimul Date: 2017-09-23 Impact factor: 8.955
Authors: Lucas Primo de Carvalho Alves; Marcelo Pio de Almeida Fleck; Aline Boni; Neusa Sica da Rocha Journal: PLoS One Date: 2017-01-23 Impact factor: 3.240
Authors: Wenling Zhao; Yiman Wang; Xuming Mao; Aimee S Payne; Suying Feng; Wei Li; Yanhong Wang; Di Wang; Hongzhong Jin; Jing Yuan; Li Li Journal: Ann Transl Med Date: 2020-11