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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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 |
format | Article |
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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
.
Military veterans with traumatic brain injuries who received treatment with the psychoactive compound ibogaine and magnesium experienced improvements in disability, psychiatric symptoms and cognition.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/s41591-023-02705-w</identifier><identifier>PMID: 38182784</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>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</subject><ispartof>Nature medicine, 2024-02, Vol.30 (2), p.373-381</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-f5535f5c48d93cd2c7714724d7a8a0268a344c7e72087d82531e1ad62b3a35503</citedby><cites>FETCH-LOGICAL-c508t-f5535f5c48d93cd2c7714724d7a8a0268a344c7e72087d82531e1ad62b3a35503</cites><orcidid>0000-0001-9203-0730 ; 0000-0001-9122-4525 ; 0000-0001-8376-3406 ; 0000-0002-6153-217X ; 0000-0003-4368-3203</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41591-023-02705-w$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41591-023-02705-w$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38182784$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cherian, Kirsten N.</creatorcontrib><creatorcontrib>Keynan, Jackob N.</creatorcontrib><creatorcontrib>Anker, Lauren</creatorcontrib><creatorcontrib>Faerman, Afik</creatorcontrib><creatorcontrib>Brown, Randi E.</creatorcontrib><creatorcontrib>Shamma, Ahmed</creatorcontrib><creatorcontrib>Keynan, Or</creatorcontrib><creatorcontrib>Coetzee, John P.</creatorcontrib><creatorcontrib>Batail, Jean-Marie</creatorcontrib><creatorcontrib>Phillips, Angela</creatorcontrib><creatorcontrib>Bassano, Nicholas J.</creatorcontrib><creatorcontrib>Sahlem, Gregory L.</creatorcontrib><creatorcontrib>Inzunza, Jose</creatorcontrib><creatorcontrib>Millar, Trevor</creatorcontrib><creatorcontrib>Dickinson, Jonathan</creatorcontrib><creatorcontrib>Rolle, C. E.</creatorcontrib><creatorcontrib>Keller, Jennifer</creatorcontrib><creatorcontrib>Adamson, Maheen</creatorcontrib><creatorcontrib>Kratter, Ian H.</creatorcontrib><creatorcontrib>Williams, Nolan R.</creatorcontrib><title>Magnesium–ibogaine therapy in veterans with traumatic brain injuries</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><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
< 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
.
Military veterans with traumatic brain injuries who received treatment with the psychoactive compound ibogaine and magnesium experienced improvements in disability, psychiatric symptoms and cognition.</description><subject>631/477</subject><subject>692/308/409</subject><subject>Anxiety</subject><subject>Arrhythmia</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Brain Injuries, Traumatic - drug therapy</subject><subject>Cancer Research</subject><subject>Clinical trials</subject><subject>Cognition</subject><subject>Complications</subject><subject>Head injuries</subject><subject>Humans</subject><subject>Ibogaine</subject><subject>Infectious Diseases</subject><subject>Injuries</subject><subject>Magnesium</subject><subject>Magnesium - therapeutic use</subject><subject>Mental depression</subject><subject>Mental disorders</subject><subject>Metabolic Diseases</subject><subject>Military personnel</subject><subject>Military psychology</subject><subject>Molecular Medicine</subject><subject>Neurosciences</subject><subject>Observational studies</subject><subject>Plants</subject><subject>Post traumatic stress disorder</subject><subject>Psychological stress</subject><subject>Signs and symptoms</subject><subject>Substance use</subject><subject>Traumatic brain injury</subject><subject>Treatment Outcome</subject><subject>Veterans - psychology</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kUtOwzAQhi0EoqVwARYoEhs2AT_i2FkhVFFAKmIDEjvLdZzUVeMUO2nVHXfghpwEl5byWLAYzUjzze8Z_wAcI3iOIOEXPkE0QzHEJASDNF7sgC6iSRojBp93Qw0Zj3lG0w448H4CISSQZvugQzjimPGkCwb3srTam7Z6f30zo7qUxuqoGWsnZ8vI2Gium1BbHy1MM44aJ9tKNkZFIxfIAExaZ7Q_BHuFnHp9tMk98DS4fuzfxsOHm7v-1TBWFPImLigltKAq4XlGVI4VYyhhOMmZ5BLilEuSJIpphiFnOceUII1knuIRkYRSSHrgcq07a0eVzpW2YaOpmDlTSbcUtTTid8easSjruUBBkGdspXC2UXD1S6t9IyrjlZ5OpdV16wXOEEfhywgL6OkfdFK3zob7AoU5wyglNFB4TSlXe-90sd0GQbHySax9EsEn8emTWIShk593bEe-jAkAWQM-tGyp3ffb_8h-AEP8n8I</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Cherian, Kirsten N.</creator><creator>Keynan, Jackob N.</creator><creator>Anker, Lauren</creator><creator>Faerman, Afik</creator><creator>Brown, Randi E.</creator><creator>Shamma, Ahmed</creator><creator>Keynan, Or</creator><creator>Coetzee, John P.</creator><creator>Batail, Jean-Marie</creator><creator>Phillips, Angela</creator><creator>Bassano, Nicholas J.</creator><creator>Sahlem, Gregory L.</creator><creator>Inzunza, Jose</creator><creator>Millar, Trevor</creator><creator>Dickinson, Jonathan</creator><creator>Rolle, C. 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E.</au><au>Keller, Jennifer</au><au>Adamson, Maheen</au><au>Kratter, Ian H.</au><au>Williams, Nolan R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnesium–ibogaine therapy in veterans with traumatic brain injuries</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>30</volume><issue>2</issue><spage>373</spage><epage>381</epage><pages>373-381</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>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
.
Military veterans with traumatic brain injuries who received treatment with the psychoactive compound ibogaine and magnesium experienced improvements in disability, psychiatric symptoms and cognition.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>38182784</pmid><doi>10.1038/s41591-023-02705-w</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-9203-0730</orcidid><orcidid>https://orcid.org/0000-0001-9122-4525</orcidid><orcidid>https://orcid.org/0000-0001-8376-3406</orcidid><orcidid>https://orcid.org/0000-0002-6153-217X</orcidid><orcidid>https://orcid.org/0000-0003-4368-3203</orcidid><oa>free_for_read</oa></addata></record> |
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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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T01%3A00%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Magnesium%E2%80%93ibogaine%20therapy%20in%20veterans%20with%20traumatic%20brain%20injuries&rft.jtitle=Nature%20medicine&rft.au=Cherian,%20Kirsten%20N.&rft.date=2024-02-01&rft.volume=30&rft.issue=2&rft.spage=373&rft.epage=381&rft.pages=373-381&rft.issn=1078-8956&rft.eissn=1546-170X&rft_id=info:doi/10.1038/s41591-023-02705-w&rft_dat=%3Cproquest_pubme%3E2918195637%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2928721635&rft_id=info:pmid/38182784&rfr_iscdi=true |