Magnesium-ibogaine therapy in veterans with traumatic brain injuries.
Kirsten N CherianNimrod Jackob KeynanLauren A AnkerAfik FaermanRandi E BrownAhmed ShammaOr KeynanJohn P CoetzeeJean-Marie BatailAngela PhillipsNicholas J BassanoGregory L SahlemJose InzunzaTrevor MillarJonathan DickinsonC E RolleJennifer KellerMaheen AdamsonIan H KratterNolan R WilliamsPublished in: Nature medicine (2024)
Traumatic brain injury (TBI) is a leading cause of disability. Sequelae can include functional impairments and psychiatric syndromes such as post-traumatic stress disorder (PTSD), depression and anxiety. Special Operations Forces (SOF) veterans (SOVs) may be at an elevated risk for these complications, leading some to seek underexplored treatment alternatives such as the oneirogen ibogaine, a plant-derived compound known to interact with multiple neurotransmitter systems that has been studied primarily as a treatment for substance use disorders. Ibogaine has been associated with instances of fatal cardiac arrhythmia, but coadministration of magnesium may mitigate this concern. In the present study, we report a prospective observational study of the Magnesium-Ibogaine: the Stanford Traumatic Injury to the CNS protocol (MISTIC), provided together with complementary treatment modalities, in 30 male SOVs with predominantly mild TBI. We assessed changes in the World Health Organization Disability Assessment Schedule from baseline to immediately (primary outcome) and 1 month (secondary outcome) after treatment. Additional secondary outcomes included changes in PTSD (Clinician-Administered PTSD Scale for DSM-5), depression (Montgomery-Åsberg Depression Rating Scale) and anxiety (Hamilton Anxiety Rating Scale). MISTIC resulted in significant improvements in functioning both immediately (P corrected < 0.001, Cohen's d = 0.74) and 1 month (P corrected < 0.001, d = 2.20) after treatment and in PTSD (P corrected < 0.001, d = 2.54), depression (P corrected < 0.001, d = 2.80) and anxiety (P corrected < 0.001, d = 2.13) at 1 month after treatment. There were no unexpected or serious adverse events. Controlled clinical trials to assess safety and efficacy are needed to validate these initial open-label findings. ClinicalTrials.gov registration: NCT04313712 .
Keyphrases
- traumatic brain injury
- clinical trial
- sleep quality
- open label
- social support
- depressive symptoms
- spinal cord injury
- posttraumatic stress disorder
- stem cells
- heart failure
- left ventricular
- mental health
- metabolic syndrome
- type diabetes
- combination therapy
- adipose tissue
- bone marrow
- mesenchymal stem cells
- squamous cell carcinoma
- white matter
- phase ii
- resting state
- rectal cancer
- cell therapy
- aortic dissection
- locally advanced