Key result
Levomilnacipran ER improves noradrenergic response by ~56% versus placebo in major depressive disorder.
Why the study?
Does levomilnacipran extended-release improve noradrenergic symptoms, anxiety symptoms, and functional impairment in adults with major depressive disorder?
Does levomilnacipran extended-release improve noradrenergic symptoms, anxiety symptoms, and functional impairment in adults with major depressive disorder?
In adults with major depressive disorder, levomilnacipran extended-release improves functional impairment indirectly, primarily through improvements in noradrenergic symptoms.
Supports levomilnacipran ER for noradrenergic symptoms in MDD; extends evidence for targeted use and indirect functional gains.
To evaluate the effects of levomilnacipran extended-release (LVM-ER; 40–120 mg/day) on noradrenergic (NA) and anxiety-related symptoms in adults with major depressive disorder (MDD) and explore the relationship between these symptoms and functional impairment. Data were pooled from 5 randomized, double-blind, placebo-controlled trials (N=2598). Anxiety and NA Cluster scores were developed by adding selected item scores from the Montgomery-Åsberg Depression Rating Scale (MADRS) and 17-item Hamilton Depression Rating Scale (HAMD17). A path analysis was conducted to estimate the direct effects of LVM-ER on functional impairment (Sheehan Disability Scale [SDS] total score) and the indirect effects through changes in NA and Anxiety Cluster scores. Mean improvements from baseline in NA and Anxiety Cluster scores were significantly greater with LVM-ER versus placebo (both P<0.001), as were the response rates (≥50% score improvement): NA Cluster (44% vs 34%; odds ratio=1.56; P<0.0001); Anxiety Cluster (39% vs 36%; odds ratio=1.19; P=0.041). Mean improvement in SDS total score was also significantly greater with LVM-ER versus placebo (−7.3 vs −5.6; P<0.0001). LVM-ER had an indirect effect on change in SDS total score that was mediated more strongly through NA Cluster score change (86%) than Anxiety Cluster score change (18%); the direct effect was negligible. NA and Anxiety Cluster scores, developed based on the face validity of individual MADRS and HAMD17 items, were not predefined as efficacy outcomes in any of the studies. In adults with MDD, LVM-ER indirectly improved functional impairment mainly through improvements in NA symptoms and less so via anxiety symptoms.
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Blier et al. (2016) studied major depressive disorder (MDD) (n=2,598). levomilnacipran extended-release (LVM-ER) vs. placebo was evaluated on Noradrenergic (NA) Cluster response rate (≥50% score improvement) (OR 1.56, p=<0.0001). Levomilnacipran extended-release significantly improved noradrenergic cluster response rates compared to placebo (44% vs 34%; OR 1.56; P<0.0001) in adults with major depressive disorder.
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