Chen Li-Zhen, Cai Qi, Zheng Peng-Fei
Department of Pharmacy, The First Hospital of Putian City, Putian, Fujian, China.
College of Environmental and Biological Engineering, Putian University, Putian, Fujian, China.
Front Immunol. 2025 May 23;16:1597370. doi: 10.3389/fimmu.2025.1597370. eCollection 2025.
Post-COVID-19 Condition (PCC), impacting 30-90% of survivors, is characterized by persistent fatigue and metabolic dysfunction, often linked to underlying mitochondrial impairment. This review examines current evidence on mitochondrial-targeted nutrition therapies, with a focus on magnetic resonance spectroscopy (MRS) as a tool for assessing metabolic recovery. Key findings highlight reduced adenosine triphosphate (ATP) production, heightened oxidative stress, and disrupted mitochondrial biogenesis- metabolic abnormalities that closely mirror those seen in chronic fatigue syndromes. While mitochondrial dysfunction is recognized as central, debate continues on whether systemic inflammation or direct viral damage primarily drives these abnormalities. Current evidence supports nutrients, such as, CoQ10, NAC, and creatine for restoring energy metabolism and reducing oxidative stress. MRS biomarkers (τPCr, Qmax), offer valuable tools for monitoring personalized intervention. However, several limitations persist, including variability in nutritional protocols, inconsistencies in MRS methodologies, and limited consideration of microbiome-psychosocial interactions. Most clinical trials focus on short-term outcomes, lacking data on long-term efficacy or stratification based on mitochondrial dysfunction severity. Future research priorities include multi-omics investigations into mitochondrial-epigenetic interactions, the development of targeted antioxidants, and exploration of engineered microbial metabolites. Standardizing MRS protocols, validating composite endpoints, and optimizing nutrient delivery systems require interdisciplinary collaboration. This review advocates for a precision medicine approach, combining MRS-based metabolic profiling with personalized nutritional strategies, to address the multifactorial nature of PCC and advance clinical translation.
新冠后状况(PCC)影响着30%-90%的幸存者,其特征为持续疲劳和代谢功能障碍,常与潜在的线粒体损伤有关。本综述审视了当前关于线粒体靶向营养疗法的证据,重点关注磁共振波谱(MRS)作为评估代谢恢复的工具。主要发现突出了三磷酸腺苷(ATP)生成减少、氧化应激增强以及线粒体生物发生紊乱——这些代谢异常与慢性疲劳综合征中所见的异常极为相似。虽然线粒体功能障碍被认为是核心问题,但关于全身炎症或直接病毒损伤是否主要导致这些异常仍存在争议。目前的证据支持使用辅酶Q10、N-乙酰半胱氨酸(NAC)和肌酸等营养素来恢复能量代谢并减轻氧化应激。MRS生物标志物(磷酸肌酸恢复时间常数、最大反应量)为监测个性化干预提供了有价值的工具。然而,仍存在一些局限性,包括营养方案的可变性、MRS方法的不一致性以及对微生物组-心理社会相互作用的考虑有限。大多数临床试验关注短期结果,缺乏关于长期疗效的数据或基于线粒体功能障碍严重程度的分层数据。未来的研究重点包括对线粒体-表观遗传相互作用的多组学研究、靶向抗氧化剂的开发以及对工程化微生物代谢产物的探索。标准化MRS方案、验证复合终点以及优化营养输送系统需要跨学科合作。本综述提倡采用精准医学方法,将基于MRS的代谢谱分析与个性化营养策略相结合,以应对PCC的多因素性质并推进临床转化。