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微小病毒B19在肌痛性脑脊髓炎/慢性疲劳综合征患者亚组中的过度表达:一项初步研究。

Over-Representation of Torque Teno Mini Virus 9 in a Subgroup of Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Pilot Study.

作者信息

Giménez-Orenga Karen, Martín-Martínez Eva, Oltra Elisa

机构信息

Escuela de Doctorado, Universidad Católica de Valencia San Vicente Mártir, 46001 Valencia, Spain.

National Health Service, Manises Hospital, 46940 Valencia, Spain.

出版信息

Pathogens. 2024 Sep 1;13(9):751. doi: 10.3390/pathogens13090751.

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic disorder classified by the WHO as postviral fatigue syndrome (ICD-11 8E49 code). Diagnosing ME/CFS, often overlapping with fibromyalgia (FM), is challenging due to nonspecific symptoms and lack of biomarkers. The etiology of ME/CFS and FM is poorly understood, but evidence suggests viral infections play a critical role. This study employs microarray technology to quantitate viral RNA levels in immune cells from ME/CFS, FM, or co-diagnosed cases, and healthy controls. The results show significant overexpression of the Torque Teno Mini Virus 9 (TTMV9) in a subgroup of ME/CFS patients which correlate with abnormal HERV and immunological profiles. Increased levels of TTMV9 transcripts accurately discriminate this subgroup of ME/CFS patients from the other study groups, showcasing its potential as biomarker for patient stratification and the need for further research into its role in the disease. Validation of the findings seems granted in extended cohorts by continuation studies.

摘要

肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是一种慢性疾病,被世界卫生组织归类为病毒后疲劳综合征(ICD-11编码8E49)。由于症状不具特异性且缺乏生物标志物,诊断ME/CFS颇具挑战,该病症常与纤维肌痛(FM)重叠。ME/CFS和FM的病因尚不清楚,但有证据表明病毒感染起着关键作用。本研究采用微阵列技术对ME/CFS、FM或共诊断病例以及健康对照的免疫细胞中的病毒RNA水平进行定量。结果显示,在一部分ME/CFS患者中,微小病毒B19(TTMV9)显著过表达,这与异常的人内源性逆转录病毒(HERV)和免疫谱相关。TTMV9转录本水平的升高能够准确地将这一亚组ME/CFS患者与其他研究组区分开来,显示出其作为患者分层生物标志物的潜力,以及对其在疾病中作用进行进一步研究的必要性。通过后续研究,在更大的队列中对这些发现进行验证似乎是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0f/11435283/9011d3999f12/pathogens-13-00751-g001.jpg

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