
In patients with comorbid major depressive disorder (MDD) and obesity, adding simvastatin to escitalopram does not appear to produce additional antidepressive effects despite improving the cardiovascular risk profile, according to a study.
For the study, patients with MDD and comorbid obesity were randomly assigned to receive treatment with simvastatin 40 mg per day or placebo as add-on to escitalopram (10 mg for the first 2 weeks, then increased to 20 mg until the end of study) for 12 weeks. Researchers assessed the change in Montgomery-Åsberg Depression Rating Scale (MADRS) score from baseline to week 12 as the primary endpoint.
A total of 160 patients were included in the intention-to-treat analysis, including 81 in the simvastatin group and 79 in the placebo group (mean age 39.0 years; 79 percent female). At week 12, the MADRS scores did not significantly differ between the simvastatin and placebo groups (mean difference, 0.47 points, 95 percent confidence interval [CI], −2.08 to 3.02; p=0.71). Likewise, simvastatin did not produce any improvements in any of the mental health–related secondary endpoints relative to placebo.
However, compared with placebo, simvastatin was associated with significantly greater reductions in low-density lipoprotein cholesterol (−40.37 vs −3.78 mg/dL; p<0.001), total cholesterol (−39.07 vs −4.89 mg/dL; p<0.001), and C-reactive protein (−1.04 vs 0.57 mg/L; p=0.003).
There were four cases of serious adverse events, with no difference between the two groups.
Overall, blinding was effectively maintained, and the retention rate was 95.6 percent.