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神经性厌食症患者胃肠道内感受改变预示复发。

Altered Gastrointestinal Interoception in Anorexia Nervosa Predicts Relapse.

作者信息

Verdonk Charles, Mink Keller, Choquette Emily, Moseman Scott E, Mayeli Ahmad, Stewart Jennifer L, Paulus Martin P, Smith Ryan, Khalsa Sahib S

机构信息

Laureate Institute for Brain Research, Tulsa, Oklahoma, United States.

UMR VIFASOM, Université de Paris, Paris, France.

出版信息

medRxiv. 2025 Sep 18:2025.09.16.25335842. doi: 10.1101/2025.09.16.25335842.

Abstract

Anorexia nervosa (AN) is a deadly psychiatric disorder, yet relapse remains common after weight restoration and no objective tools exist to track recovery. AN involves profound disturbances of gastrointestinal interoception, but no clinical tests assess this dysfunction. In this single-blind, randomized-crossover study, 62 weight-restored females with restrictive AN and 57 matched healthy comparisons completed a gastrointestinal detection task using an ingestible vibrating capsule while behavioral, electroencephalographic, and peripheral physiological signals were recorded. AN participants showed reduced perceptual accuracy and higher miss-rates despite intact neural and physiological responses. Computational modeling revealed stronger prior beliefs against perceiving gut sensations, diminished interoceptive precision, and maladaptive learning. Capsule stimulation also induced larger hunger increases in AN. Initial priors, response bias, and stomach unpleasantness predicted six-month relapse, while miss-rate and precision shifts predicted symptom severity. These findings reveal mechanistic disruptions in gastrointestinal interoception that predict relapse, offering scalable biomarkers to personalize treatment and prevent recurrence.

摘要

神经性厌食症(AN)是一种致命的精神疾病,然而体重恢复后复发仍然很常见,并且没有客观工具来跟踪康复情况。AN涉及胃肠道内感受的严重紊乱,但尚无临床测试评估这种功能障碍。在这项单盲、随机交叉研究中,62名体重恢复的限制型AN女性和57名匹配的健康对照者使用可摄入振动胶囊完成了一项胃肠道检测任务,同时记录行为、脑电图和外周生理信号。尽管神经和生理反应完好,但AN参与者的感知准确性降低,漏报率更高。计算模型显示,对感知肠道感觉的先验信念更强,内感受精度降低,以及适应不良的学习。胶囊刺激在AN中也引起更大的饥饿感增加。初始先验、反应偏差和胃部不适感可预测六个月后的复发,而漏报率和精度变化可预测症状严重程度。这些发现揭示了胃肠道内感受中预测复发的机制性破坏,为个性化治疗和预防复发提供了可扩展的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca30/12458608/61cd776f02d2/nihpp-2025.09.16.25335842v1-f0001.jpg

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