Serum lipid profile changes after successful treatment with electroconvulsive therapy in major depression: A prospective pilot trial

- Total Cholesterol and cholesterol subtypes were increased after the ECT treatment.
- Apolipoprotein A1 was also increased after ECT, whereas apolipoprotein B was not.
- Indices for the prediction of cardiovascular diseases were unchanged after ECT.
- Clinical improvement of depression correlated with HDL cholesterol increase.

BackgroundCholesterol is reduced in depressed patients, however, these patients have a higher risk for cardiovascular diseases. Electroconvulsive therapy (ECT) is a highly effective treatment option for specific forms of depression. Like for other non-pharmacological therapies targeting depression such as psychotherapy or sleep deprivation, there is a lack of evidence about the effects on peripheral lipid parameters. Our objective was to study the impact of ECT as a non-pharmacological treatment on the peripheral lipid pattern in depressive patients.MethodPeripheral lipid profile composition before and after a course of ECT was analysed in 27 non-fasting inpatients at a university psychiatric hospital with DSM-IV major depressive episode. For the impact of ECT treatment on each lipid parameter a multivariate repeated measurement regression analysis was performed and computed separately for every dependent variable.ResultsTotal Cholesterol and the cholesterol subtypes HDL and LDL were increased after the treatment compared to baseline. Apolipoprotein A1 was also increased after ECT, whereas apolipoprotein B was not. Indices for the prediction of cardiovascular diseases were unchanged after successful treatment by ECT. The reduction of depressive psychopathology negatively correlated with increases of HDL cholesterol and apolipoprotein A1.LimitationsSubjects received several antidepressants and other psychotropic medication before and during the ECT.ConclusionsIn our preliminary pilot study ECT as a non-pharmacological, effective treatment of depression led to distinct effects on the peripheral lipid pattern.