Dooley Ming
Holistic Resonance Center, 2525 Camino Del Rio S #130, San Diego, CA 92108, USA.
Int J Mol Sci. 2025 Jul 28;26(15):7284. doi: 10.3390/ijms26157284.
Chronic inflammatory response syndrome (CIRS) and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) are debilitating multisystem illnesses that share overlapping symptoms and molecular patterns, including immune dysregulation, mitochondrial impairment, and vascular dysfunction. This review provides a chronological synthesis of biomarker development in CIRS, tracing its evolution from early functional tests such as visual contrast sensitivity (VCS) to advanced transcriptomic profiling. Drawing on peer-reviewed studies spanning two decades, we examine the layered integration of neuroendocrine, immunologic, metabolic, and genomic markers that collectively support a multisystem model of innate immune activation specific to environmentally acquired illness. Particular focus is given to the Gene Expression: Inflammation Explained (GENIE) platform's use of transcriptomics to classify disease stages and distinguish CIRS from other fatiguing conditions. While ME/CFS research continues to explore overlapping pathophysiologic features, it has yet to establish a unified diagnostic model with validated biomarkers or exposure-linked mechanisms. As a result, many patients labeled with ME/CFS may, in fact, represent unrecognized CIRS cases. This review underscores the importance of structured biomarker timelines in improving differential diagnosis and guiding treatment in complex chronic illness and highlights the reproducibility of the CIRS framework in contrast to the diagnostic ambiguity surrounding ME/CFS.
慢性炎症反应综合征(CIRS)和肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是使人衰弱的多系统疾病,它们有重叠的症状和分子模式,包括免疫失调、线粒体损伤和血管功能障碍。本综述按时间顺序综合了CIRS中生物标志物的发展,追溯其从早期功能测试如视觉对比敏感度(VCS)到先进转录组分析的演变。借鉴二十年来的同行评审研究,我们研究了神经内分泌、免疫、代谢和基因组标志物的分层整合,这些标志物共同支持了一种针对环境获得性疾病的先天性免疫激活多系统模型。特别关注基因表达:炎症解析(GENIE)平台利用转录组学对疾病阶段进行分类并将CIRS与其他疲劳状况区分开来。虽然ME/CFS研究继续探索重叠的病理生理特征,但尚未建立一个具有经过验证的生物标志物或暴露相关机制的统一诊断模型。因此,许多被诊断为ME/CFS的患者实际上可能是未被识别的CIRS病例。本综述强调了结构化生物标志物时间线在改善复杂慢性疾病的鉴别诊断和指导治疗方面的重要性,并突出了CIRS框架的可重复性,与之形成对比的是围绕ME/CFS的诊断模糊性。