シロシビン療法が神経性やせ症治療に有望性を示す小規模試験(Psilocybin therapy shows potential as a treatment for anorexia nervosa in small trial)

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2026-07-08 インペリアル・カレッジ・ロンドン(ICL)

インペリアル・カレッジ・ロンドンのサイケデリック研究センターは、神経性やせ症(拒食症)患者を対象とした小規模臨床試験で、シロシビン補助療法が有望な治療法となる可能性を示した。対象は平均11年間にわたり治療に十分な効果が得られなかった成人女性21人で、心理療法と組み合わせて6週間にわたりシロシビンを3回投与した。試験の結果、安全性は概ね良好で、主な副作用は頭痛や吐き気だった。体格指数(BMI)に大きな改善はみられなかったものの、摂食障害の症状はほぼ全員で軽減し、3か月後には約半数の参加者で症状が健常者レベルまで改善した。また、回復への意欲は1年間持続した。一方、本研究は対照群を設けていない小規模なパイロット試験であり、効果には個人差も認められたため、有効性を確立するには大規模な無作為化比較試験が必要である。研究チームは、シロシビン療法は専門的な心理的支援を伴う管理された医療環境で実施されるべきであり、新たな拒食症治療法としてさらなる検証が求められるとしている。

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神経性食欲不振症の成人女性に対するシロシビン療法:予備研究 Psilocybin therapy for adult females with anorexia nervosa: pilot study

Hannah M. Douglass,Meg J. Spriggs,Kate Godfrey,Jennifer L. Danby,Frederico J. C. de Magalhaes,Lauren Macdonald,Kirsty L. Alderton,Stephanie Archer,Kirran Ahmad andJonny Martell,…
The British Journal of Psychiatry  Published:08 July 2026
DOI:https://doi.org/10.1192/bjp.2026.10687

シロシビン療法が神経性やせ症治療に有望性を示す小規模試験(Psilocybin therapy shows potential as a treatment for anorexia nervosa in small trial)

Abstract

Background
Anorexia nervosa is a debilitating eating disorder with high mortality and chronicity rates owing to the paucity of effective existing treatments. Several clinical trials using psilocybin therapy have demonstrated therapeutic efficacy and safety in psychiatric conditions, including anorexia nervosa.

Aims
This study aimed to further assess the safety, feasibility and potential efficacy of psilocybin therapy in anorexia nervosa.

Method
This single-blind, within-individual pilot study recruited 21 females with anorexia nervosa, who underwent three dosing sessions with oral psilocybin (COMP360) over 6 weeks in a fixed order (1 mg, 25 mg, 25 mg), alongside talk therapy and adjunctive to treatment as usual. Adverse events were monitored throughout the study. Primary clinical outcome measures were global Eating Disorder Examination Interview (EDE) and Readiness and Motivation Questionnaire (RMQ) precontemplation scores. Primary time points for the EDE were the 6-week final visit, 3-month follow-up and 6-month follow-up; and for the RMQ, they were the 6-week final visit and comparison between dosing days. Global EDE Questionnaire scores were a key secondary outcome. Key time points were the 6-week final visit and comparison between dosing days. There was a 12-month remote follow-up.

Results
Psilocybin was well tolerated by all participants. The most common adverse events were headache, nausea and dizziness. Two serious adverse events (suicide attempts) were reported for one participant within the 6–12-month period. Relative to baseline, participants displayed significant improvements in their eating disorder symptoms (EDE scores: p < 0.0001, d = 0.98, 6 months) and motivation to change (RMQ scores: p = 0.0017, d = 0.65, 12 months). However, there was a large variation in improvement and maintenance during the follow-up.

Conclusions
This study further provides preliminary support for the feasibility, safety and potential efficacy of this intervention to treat adult females with anorexia nervosa, and warrants further investigation in larger and more rigorously designed studies.

医療・健康
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