Researchers at the Max Planck Institute of Psychiatry discovered when suicidality occurred it happened within two weeks of beginning treatment, or increasing dosage, for 59% of patients. Altogether, 8.1% of patients studied suffered from this adverse side effect of antidepressant medications. Since 2005, in the United States, Canada and some European countries, antidepressants have carried a warning alerting the doctor and the patient to the serious risk of medication-induced suicidality.
Up until now, however, doctors have had no indications as to which patients may be at risk. Sundance CEO Kim Bechthold stated, “Our hope is that the new test will assist the physician in significantly reducing the risk of suicide emerging from antidepressant drug use and will provide patients and families with valuable personal information to use with their doctors in weighing the risks and benefits of the medications.”
Scientists at the Max Planck Institute of Psychiatry in Munich have now discovered 79 genetic biomarkers that had a 91% probability of correctly classifying patients at risk of antidepressant-induced suicide.
The researchers also discovered that the increased risk for suicide is not limited to individuals under the age of 25, as described in the warning by the American regulatory agency FDA. Instead, the risk was found in the studies to be present across all ages from 18 to 75. In the United States, more than 9 million new antidepressant drugs are prescribed annually (IMS 2006 National Prescription Drug Audit).
The licensing agreement with Sundance Diagnostics was concluded with Max-Planck-Innovation, the Max Planck Society’s technology transfer organization.