Circulating microRNAs as biomarkers in traumatic brain injury

被引:21
|
作者
Toffolo, Kathryn [1 ]
Osei, Jennifer [1 ]
Kelly, William [1 ]
Poulsen, Austin [1 ]
Donahue, Kaitlynn [1 ]
Wang, Jiefei [2 ]
Hunter, Madison [1 ]
Bard, Jonathan [3 ]
Wang, Jianxin [3 ]
Poulsen, David [1 ]
机构
[1] Univ Buffalo, Jacobs Sch Med & Biomed Sci, Neurosurg Dept, Clin & Translat Res Ctr, Buffalo, NY 14203 USA
[2] Univ Buffalo, Dept Biostat, Buffalo, NY USA
[3] New York State Ctr Bioinformat & Life Sci, Buffalo, NY USA
关键词
Traumatic brain injury; Mirror; Neuroprotection; TERMINAL HYDROLASE-L1; CLINICAL-TRIALS; NEUROPROTECTION; DIAGNOSIS; MODEL; MILD;
D O I
10.1016/j.neuropharm.2018.08.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Preclinical and clinical studies can be greatly improved through the inclusion of diagnostic, prognostic, predictive or pharmacodynamics biomarkers. Circulating microRNAs (miRNAs) represent highly stable targets that respond to physiological and pathological changes. MicroRNA biomarkers can be detected by highly sensitive and absolutely quantitative methods currently available in most clinical laboratories. Here we review preclinical and clinical studies that have examined circulating miRNAs as potential diagnostic and prognostic biomarkers. We also present data that suggests pharmacodynamics biomarkers can be identified that are associated with neuroprotection in general. Although circulating miRNA can serve as useful tools, it is clear their expression profiles are highly sensitive to changing conditions and are influenced by a broad range of parameters including age, sex, body mass index, injury severity, time of collection, as well as methods of processing, purification and detection. Thus, considerable effort will be required to standardize methods and experimental design conditions before circulating miRNAs can prove useful in a heterologous injury like TBI. This article is part of the Special Issue entitled "Novel Treatments for Traumatic Brain Injury".
引用
收藏
页码:199 / 208
页数:10
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