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Effect of mirtazapine on metabolism and energy substrate partitioning in healthy men
Johannes M. Hennings, Sarah Heel, Katharina Lechner, Manfred Uhr, Tatjana Dose, Ludwig Schaaf, Florian Holsboer, Susanne Lucae, Stephany Fulda, Stefan Kloiber
Johannes M. Hennings, Sarah Heel, Katharina Lechner, Manfred Uhr, Tatjana Dose, Ludwig Schaaf, Florian Holsboer, Susanne Lucae, Stephany Fulda, Stefan Kloiber
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Clinical Research and Public Health Metabolism Neuroscience

Effect of mirtazapine on metabolism and energy substrate partitioning in healthy men

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Abstract

BACKGROUND. Weight gain and metabolic changes during treatment with antidepressant drugs have emerged as an important concern, particularly in long-term treatment. It is still a matter of ongoing debate whether weight gain and metabolic perturbations with antidepressant use are the consequence of increased appetite and weight gain, respectively, or represents direct pharmacological effects of the drug on metabolism. METHODS. We therefore conducted a proof-of-concept, open-label clinical trial, hypothesizing that in exceptionally healthy men no change of metabolic parameters would occur under mirtazapine, when environmental factors such as nutrition, sleep, and physical exercise were controlled and kept constant. Over a 3-week preparation phase, 10 healthy, young men were attuned to a standardized diet adjusted to their individual caloric need, to a regular sleep/wake cycle and moderate exercise. Continuing this protocol, we administered 30 mg mirtazapine daily for 7 days. RESULTS. While no significant weight gain or changes in resting energy expenditure were observed under these conditions, hunger and appetite for sweets increased with mirtazapine, accompanied by a shift in energy substrate partitioning towards carbohydrate substrate preference as assessed by indirect calorimetry. Furthermore, with mirtazapine, insulin and C-peptide release increased in response to a standardized meal. CONCLUSION. Our findings provide important insights into weight-independent metabolic changes associated with mirtazapine and allow a better understanding of the long-term metabolic effects observed in patients treated with antidepressant drugs. TRIAL REGISTRATION. ClinicalTrials.gov NCT00878540. FUNDING. Nothing to declare.

Authors

Johannes M. Hennings, Sarah Heel, Katharina Lechner, Manfred Uhr, Tatjana Dose, Ludwig Schaaf, Florian Holsboer, Susanne Lucae, Stephany Fulda, Stefan Kloiber

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Figure 2

Appetite and satiety under baseline and mirtazapine.

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Appetite and satiety under baseline and mirtazapine.
Hunger (A), satiety...
Hunger (A), satiety (B), appetite for sweets (C) and fatty and salty food (D and E) are shown using mean intraday visual analog scales (VAS, 0–100 mm). The mean of 3 consecutive baseline days (baseline) is subsequently followed by drug days (M1 = day after the first given dose of mirtazapine; M2 = day after the second given dose of mirtazapine; and so forth). A repeated-measures ANOVA with a Greenhouse-Geisser correction indicated statistically significant day-to-day differences for hunger and satiety ratings (F[2.59, 23.30] = 5.27, P = 0.008 and F[2.57, 23.16] = 7.55, P = 0.002, respectively), with asterisks in A and B indicating significant differences compared with baseline ratings (post hoc Bonferroni corrected). *P < 0.05, **P < 0.01, ***P < 0.001. There was no statistically significant time effect for ratings of appetite for sweets and salty and fatty food in the repeated-measures ANOVA (P = 0.072, P = 0.067, P = 0.063, respectively). Individual values are indicated as circles. Lower and upper hinges of box plots represent first and third quartiles. Whisker lines correspond to highest and lowest values no further than 1.5 interquartile range from the hinges; outliers are beyond this line. Median lines are indicated across the boxes, and mean values are indicated with an ×.

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