Magnesium–ibogaine therapy in veterans with traumatic brain injuries

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 complicatio...

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Veröffentlicht in:Nature medicine 2024-02, Vol.30 (2), p.373-381
Hauptverfasser: Cherian, Kirsten N., Keynan, Jackob N., Anker, Lauren, Faerman, Afik, Brown, Randi E., Shamma, Ahmed, Keynan, Or, Coetzee, John P., Batail, Jean-Marie, Phillips, Angela, Bassano, Nicholas J., Sahlem, Gregory L., Inzunza, Jose, Millar, Trevor, Dickinson, Jonathan, Rolle, C. E., Keller, Jennifer, Adamson, Maheen, Kratter, Ian H., Williams, Nolan R.
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container_end_page 381
container_issue 2
container_start_page 373
container_title Nature medicine
container_volume 30
creator Cherian, Kirsten N.
Keynan, Jackob N.
Anker, Lauren
Faerman, Afik
Brown, Randi E.
Shamma, Ahmed
Keynan, Or
Coetzee, John P.
Batail, Jean-Marie
Phillips, Angela
Bassano, Nicholas J.
Sahlem, Gregory L.
Inzunza, Jose
Millar, Trevor
Dickinson, Jonathan
Rolle, C. E.
Keller, Jennifer
Adamson, Maheen
Kratter, Ian H.
Williams, Nolan R.
description 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  
doi_str_mv 10.1038/s41591-023-02705-w
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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  &lt; 0.001, Cohen’s d  = 0.74) and 1 month ( P corrected  &lt; 0.001, d  = 2.20) after treatment and in PTSD ( P corrected  &lt; 0.001, d  = 2.54), depression ( P corrected  &lt; 0.001, d  = 2.80) and anxiety ( P corrected  &lt; 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 . 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ispartof Nature medicine, 2024-02, Vol.30 (2), p.373-381
issn 1078-8956
1546-170X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10878970
source MEDLINE; Nature; SpringerLink Journals - AutoHoldings
subjects 631/477
692/308/409
Anxiety
Arrhythmia
Biomedical and Life Sciences
Biomedicine
Brain
Brain Injuries, Traumatic - drug therapy
Cancer Research
Clinical trials
Cognition
Complications
Head injuries
Humans
Ibogaine
Infectious Diseases
Injuries
Magnesium
Magnesium - therapeutic use
Mental depression
Mental disorders
Metabolic Diseases
Military personnel
Military psychology
Molecular Medicine
Neurosciences
Observational studies
Plants
Post traumatic stress disorder
Psychological stress
Signs and symptoms
Substance use
Traumatic brain injury
Treatment Outcome
Veterans - psychology
title Magnesium–ibogaine therapy in veterans with traumatic brain injuries
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