Cell-Free Mitochondrial DNA in Acute Brain Injury

被引:5
|
作者
Kayhanian, Saeed [1 ,2 ,3 ]
Glynos, Angelos [1 ,2 ]
Mair, Richard [1 ,3 ]
Lakatos, Andras [1 ,4 ]
Hutchinson, Peter J. A. [1 ,3 ]
Helmy, Adel E. [1 ,3 ]
Chinnery, Patrick F. [1 ,2 ,4 ,5 ]
机构
[1] Univ Cambridge, Dept Clin Neurosci, Cambridge, England
[2] Univ Cambridge, MRC Mitochondrial Biol Unit, Cambridge, England
[3] Cambridge Univ Hosp, Dept Neurosurg, Cambridge, England
[4] Cambridge Univ Hosp, Dept Neurol, Cambridge, England
[5] Univ Cambridge, Addenbrookes Hosp, Dept Clin Neurosci, Cambridge CB2 0QQ, England
来源
NEUROTRAUMA REPORTS | 2022年 / 3卷 / 01期
基金
英国工程与自然科学研究理事会; 英国惠康基金; 英国医学研究理事会;
关键词
acute brain injury; brain inflammation; DAMP; mitochondrial DNA; subarachnoid hemorrhage; traumatic brain injury; CEREBROSPINAL-FLUID; RESPONSES;
D O I
10.1089/neur.2022.0032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traumatic brain injury and aneurysmal subarachnoid haemorrhage are a major cause of morbidity and mortality worldwide. Treatment options remain limited and are hampered by our understanding of the cellular and molecular mechanisms, including the inflammatory response observed in the brain. Mitochondrial DNA (mtDNA) has been shown to activate an innate inflammatory response by acting as a damage-associated molecular pattern (DAMP). Here, we show raised circulating cell-free (ccf) mtDNA levels in both cerebrospinal fluid (CSF) and serum within 48 h of brain injury. CSF ccf-mtDNA levels correlated with clinical severity and the interleukin-6 cytokine response. These findings support the use of ccf-mtDNA as a biomarker after acute brain injury linked to the inflammatory disease mechanism.
引用
收藏
页码:415 / 420
页数:6
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