Fecal Microbiota Transplantation for Sleep Disturbance in Post-acute COVID-19 Syndrome

医学 2019年冠状病毒病(COVID-19) 粪便细菌疗法 病因学 微生物群 扰动(地质) 2019-20冠状病毒爆发 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 移植 前瞻性队列研究 睡眠(系统调用) 肠道菌群 睡眠障碍 重症监护医学 内科学 免疫学 精神科 微生物学 生物信息学 爆发 病理 艰难梭菌 失眠症 疾病 抗生素 传染病(医学专业) 计算机科学 操作系统 古生物学 生物
作者
Raphaela Iris Lau,Qi Su,Jessica Y. L. Ching,Rashid N. Lui,Ting Ting Chan,Marc Wong,Louis Ho Shing Lau,Yun Kwok Wing,Ngan Yin Chan,Hanson Kwok,Agnes H. Ho,Yee Kit Tse,Chun Pan Cheung,Moses K.T. Li,Wan Ying Siu,Chengyu Liu,Wenqi Lu,Yun Wang,Emily Chiu,Pui Kuan Cheong
出处
期刊:Clinical Gastroenterology and Hepatology [Elsevier BV]
被引量:3
标识
DOI:10.1016/j.cgh.2024.06.004
摘要

Background & Aims Post-acute COVID-19 syndrome (PACS) is associated with sleep disturbance but treatment options are limited. The aetiology of PACS may be secondary to alterations in the gut microbiome. Here, we report the efficacy of faecal microbiota transplantation (FMT) in alleviating post-COVID insomnia symptoms in a non-randomised, open-label prospective interventional study. Methods Between September 22, 2022 and May 22, 2023, we recruited 60 PACS patients with insomnia defined as Insomnia Severity Index (ISI) ≥ 8 and assigned them to the FMT group (FMT at weeks 0, 2, 4 and 8; n=30) or the control group (n=30). The primary outcome was clinical remission defined by an ISI of less than eight at 12 weeks. Secondary outcomes included changes in the Pittsburgh Sleep Quality Index (PSQI), Generalised Anxiety Disorder-7 scale (GAD-7), Epworth Sleepiness Scale (ESS), Multidimensional Fatigue Inventory (MFI), blood cortisol and melatonin, and gut microbiome analysis on metagenomic sequencing. Results At week 12, more patients in the FMT than the control group had insomnia remission (37.9% vs 10.0%; p=0.018). The FMT group showed a decrease in ISI score (p<0.0001), PSQI (p<0.0001), GAD-7 (p=0.0019), ESS (p=0.0057) and blood cortisol concentration (p=0.035) from baseline to week 12, but there was no significant change in the control group. There was enrichment of bacteria such as Gemmiger formicilis and depletion of microbial pathways producing menaquinol derivatives after FMT. Gut microbiome profile resembled that of the donor in FMT responders but not in non-responders at week 12. There was no serious adverse event. Conclusion This pilot study showed that FMT could be effective and safe in alleviating post-COVID insomnia and further clinical trials are warranted. ClinicalTrials.gov identifier: NCT05556733.
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