4.6 Review

Pharmacological Interventions to Treat Antipsychotic-Induced Dyslipidemia in Schizophrenia Patients: A Systematic Review and Meta Analysis

Journal

FRONTIERS IN PSYCHIATRY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2021.642403

Keywords

schizophrenia; antipsychotics; dyslipidemia; systematic review; meta-analysis

Categories

Funding

  1. Department of Psychiatry, University of Toronto
  2. Canadian Institutes of Health Research
  3. PSI foundation, Ontario
  4. CAMH
  5. Canadian Institutes of Health Research (CIHR)
  6. University of Toronto
  7. Research Hospital Fund-Canada Foundation for Innovation (RHFCFI)
  8. HLS Therapeutics Inc.
  9. Banting and Best Diabetes Center, University of Toronto
  10. Ontario Graduate Scholarship
  11. Institute of Medical Science, University of Toronto

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Pharmacological interventions are effective in reducing LDL cholesterol, triglycerides, and total cholesterol levels while increasing HDL cholesterol levels in patients with schizophrenia. Certain interventions such as antipsychotic switching, antipsychotic add-ons, and off label lipid-lowering agents may be more effective in improving specific lipid parameters. Future studies should explore novel interventions for managing antipsychotic-induced dyslipidemia.
Introduction: Antipsychotic-induced dyslipidemia represents a common adverse effect faced by patients with schizophrenia that increases risk for developing further metabolic complications and cardiovascular disease. Despite its burden, antipsychotic-induced dyslipidemia is often left untreated, and the effectiveness of pharmacological interventions for mitigating dyslipidemia has not been well-addressed. This review aims to assess the effectiveness of pharmacological interventions in alleviating dyslipidemia in patients with schizophrenia. Methods: Medline, PsychInfo, and EMBASE were searched for all relevant English articles from 1950 to November 2020. Randomized placebo-controlled trials were included. Differences in changes in triglycerides, HDL cholesterol, LDL cholesterol, and VLDL cholesterol levels between treatment and placebo groups were meta-analyzed as primary outcomes. Results: Our review identified 48 randomized controlled trials that comprised a total of 3,128 patients and investigated 29 pharmacological interventions. Overall, pharmacological interventions were effective in lowering LDL cholesterol, triglycerides, and total cholesterol levels while increasing the levels of HDL cholesterol. Within the intervention subgroups, approved lipid-lowering agents did not reduce lipid parameters other than total cholesterol level, while antipsychotic switching and antipsychotic add-on interventions improved multiple lipid parameters, including triglycerides, LDL cholesterol, HDL cholesterol, and total cholesterol. Off label lipid lowering agents improved triglycerides and total cholesterol levels, with statistically significant changes seen with metformin. Conclusion: Currently available lipid lowering agents may not work as well in patients with schizophrenia who are being treated with antipsychotics. Additionally, antipsychotic switching, antipsychotic add-ons, and certain off label interventions might be more effective in improving some but not all associated lipid parameters. Future studies should explore novel interventions for effectively managing antipsychotic-induced dyslipidemia.

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