Alcohol Consumption Modulates the Development of Chronic Pain in COVID-19 Patients: A Network Meta-Analysis.

IF 3.7 Q1 CHEMISTRY, MEDICINAL ACS Pharmacology and Translational Science Pub Date : 2025-02-04 eCollection Date: 2025-02-14 DOI:10.1021/acsptsci.4c00479
Muhammed Bishir, Michael Vigorito, Ming-Huan Chan, Mohammed A S Khan, Sulie L Chang
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Abstract

The mechanisms underlying the onset and progression of chronic pain in COVID-19 patients have been understudied. Using network meta-analysis, we previously demonstrated that alcohol augments COVID-19 symptoms and pathologies possibly by inducing a severe cytokine storm. We and others have also reported that acute alcohol consumption produces analgesic effects, while chronic alcohol consumption results in hyperalgesia and chronic pain. This study aimed to identify the influence of alcohol consumption and COVID-19 on pain. Using publicly available curated gene expression data sets of differentially expressed genes (DEGs) in the prefrontal cortex (PFC) and amygdala of COVID-19 patients, we employed a bioinformatics application, QIAGEN ingenuity pathway analysis (IPA), to identify the key signaling pathways, upstream regulators, and biological functions in these brain areas known to play a role in pain. Canonical pathway analysis revealed activation of the neuropathic pain pathway and signaling pathways involving the cytokine storm, S100 family, IL-6, and neuroinflammation. IPA's network builder was employed to construct a network map of shared molecules between alcohol and pain-related constructs (discomfort, neuropathic pain, and inflammatory pain). The simulation of alcohol consumption inhibited pain in this network map. To study the influence of COVID-19, we overlaid the DEGs from the PFC and amygdala onto these networks, mimicking alcohol consumption during SARS-CoV-2 infection. Upregulation of molecules in the amygdala and PFC predicted an increase in neuropathic pain, as well as an increase in inflammatory pain in the PFC. Our results suggest that while alcohol consumption directly inhibits pain, the presence of COVID-19 exaggerates impaired cytokine signaling, neuroinflammation, and neuropathic pain signaling in the CNS providing novel insights into the signaling pathways associated with chronic pain of the COVID-19 patients.

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酒精消费调节COVID-19患者慢性疼痛的发展:一项网络荟萃分析
COVID-19患者慢性疼痛发生和进展的机制尚未得到充分研究。通过网络荟萃分析,我们之前证明了酒精可能通过诱导严重的细胞因子风暴来增强COVID-19的症状和病理。我们和其他人也报道了急性饮酒会产生镇痛作用,而慢性饮酒会导致痛觉过敏和慢性疼痛。这项研究旨在确定饮酒和COVID-19对疼痛的影响。利用可公开获得的COVID-19患者前额叶皮层(PFC)和杏仁核中差异表达基因(DEGs)的基因表达数据集,我们采用生物信息学应用QIAGEN独创性途径分析(IPA)来确定这些已知在疼痛中起作用的大脑区域的关键信号通路、上游调节因子和生物功能。典型通路分析显示,神经性疼痛通路和涉及细胞因子风暴、S100家族、IL-6和神经炎症的信号通路被激活。IPA的网络构建器被用来构建酒精和疼痛相关结构(不适、神经性疼痛和炎症性疼痛)之间共享分子的网络图。在这个网络图中,酒精消耗的模拟抑制了疼痛。为了研究COVID-19的影响,我们将PFC和杏仁核的deg覆盖到这些网络上,模拟SARS-CoV-2感染期间的酒精消耗。杏仁核和PFC分子的上调预示着神经性疼痛的增加,以及PFC中炎症性疼痛的增加。我们的研究结果表明,虽然饮酒直接抑制疼痛,但COVID-19的存在会加剧中枢神经系统中受损的细胞因子信号、神经炎症和神经性疼痛信号,这为COVID-19患者慢性疼痛相关的信号通路提供了新的见解。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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