Impacts of metabolic disruption, body mass index and inflammation on cognitive function in post-COVID-19 condition: a randomized controlled trial on vortioxetine.

IF 3.6 3区 医学 Q1 PSYCHIATRY Annals of General Psychiatry Pub Date : 2024-02-29 DOI:10.1186/s12991-024-00494-1
Angela T H Kwan, Gia Han Le, Ziji Guo, Felicia Ceban, Kayla M Teopiz, Taeho Greg Rhee, Roger Ho, Joshua D Di Vincenzo, Sebastian Badulescu, Shakila Meshkat, Bing Cao, Joshua D Rosenblat, Donovan A Dev, Lee Phan, Mehala Subramaniapillai, Roger S McIntyre
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Abstract

Background: Post-COVID-19 Condition (PCC), as defined by the World Health Organization (WHO), currently lacks any regulatory-approved treatments and is characterized by persistent and debilitating cognitive impairment and mood symptoms. Additionally, metabolic dysfunction, chronic inflammation and the associated risks of elevated body mass index (BMI) have been reported. In this study, we aim to investigate the efficacy of vortioxetine in improving cognitive deficits in individuals with PCC, accounting for the interaction of metabolic dysfunction, elevated inflammation and BMI.

Methods: This is a post-hoc analysis of an 8-week randomized, double-blind, placebo-controlled trial that was conducted among adults aged 18 years and older living in Canada who were experiencing WHO-defined PCC symptoms. The recruitment of participants began in November 2021 and concluded in January 2023. A total of 200 individuals were enrolled, where 147 were randomized in a 1:1 ratio to receive either vortioxetine (5-20 mg, n = 73) or placebo (n = 74) for daily treatment under double-blind conditions. The primary outcome measure was the change in the Digit Symbol Substitution Test (DSST) score from baseline to endpoint.

Results: Our findings showed significant effects for time (χ2 = 7.771, p = 0.005), treatment (χ2 = 7.583, p = 0.006) and the treatment x time x CRP x TG-HDL x BMI interaction (χ2 = 11.967, p = 0.018) on cognitive function. Moreover, the between-group analysis showed a significant improvement with vortioxetine at endpoint (mean difference = 0.621, SEM = 0.313, p = 0.047).

Conclusion: Overall, vortioxetine demonstrated significant improvements in cognitive deficits among individuals with baseline markers of metabolic dysfunction, elevated inflammation and higher BMI at endpoint as compared to placebo.

Trial registration: NCT05047952 (ClinicalTrials.gov; Registration Date: September 17, 2021).

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代谢紊乱、体重指数和炎症对 COVID-19 后认知功能的影响:关于伏替西汀的随机对照试验。
背景:根据世界卫生组织(WHO)的定义,"COVID-19 后症状"(PCC)目前缺乏任何经监管机构批准的治疗方法,其特征是持续存在令人衰弱的认知障碍和情绪症状。此外,代谢功能障碍、慢性炎症和体重指数(BMI)升高的相关风险也有报道。在本研究中,我们旨在调查伏替西汀在改善 PCC 患者认知障碍方面的疗效,同时考虑代谢功能障碍、炎症升高和体重指数的相互作用:这是一项为期 8 周的随机、双盲、安慰剂对照试验的事后分析,该试验的对象是居住在加拿大的 18 岁及以上、出现世界卫生组织定义的 PCC 症状的成年人。参与者招募始于 2021 年 11 月,结束于 2023 年 1 月。共招募了 200 人,其中 147 人按 1:1 的比例随机接受伏替西汀(5-20 毫克,n = 73)或安慰剂(n = 74),在双盲条件下接受每日治疗。主要结果是数字符号替换测试(DSST)得分从基线到终点的变化:我们的研究结果表明,时间(χ2 = 7.771,p = 0.005)、治疗(χ2 = 7.583,p = 0.006)和治疗 x 时间 x CRP x TG-HDL x BMI 交互作用(χ2 = 11.967,p = 0.018)对认知功能有显着影响。此外,组间分析显示,伏替西汀在终点有显著改善(平均差 = 0.621,SEM = 0.313,p = 0.047):总体而言,与安慰剂相比,伏替西汀在终点时能明显改善基线代谢功能障碍标记物、炎症升高和体重指数较高者的认知缺陷:NCT05047952(ClinicalTrials.gov;注册日期:2021年9月17日)。
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来源期刊
CiteScore
6.60
自引率
2.70%
发文量
43
审稿时长
>12 weeks
期刊介绍: Annals of General Psychiatry considers manuscripts on all aspects of psychiatry, including neuroscience and psychological medicine. Both basic and clinical neuroscience contributions are encouraged. Annals of General Psychiatry emphasizes a biopsychosocial approach to illness and health and strongly supports and follows the principles of evidence-based medicine. As an open access journal, Annals of General Psychiatry facilitates the worldwide distribution of high quality psychiatry and mental health research. The journal considers submissions on a wide range of topics including, but not limited to, psychopharmacology, forensic psychiatry, psychotic disorders, psychiatric genetics, and mood and anxiety disorders.
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