Serum Proteome Alterations in Patients with Cognitive Impairment after Traumatic Brain Injury Revealed by iTRAQ-Based Quantitative Proteomics.
Xin-Gui XiongQinghua LiangChunhu ZhangYang WangWei HuangWei-Jun PengZhe WangZi-An XiaPublished in: BioMed research international (2017)
Background. Cognitive impairment is the leading cause of traumatic brain injury- (TBI-) related disability; however, the underlying pathogenesis of this dysfunction is not completely understood. Methods. Using an isobaric tagging for relative and absolute quantitation- (iTRAQ-) based quantitative proteomic approach, serum samples from healthy control subjects, TBI patients with cognitive impairment, and TBI patients without cognitive impairment were analysed to identify differentially expressed proteins (DEPs) related to post-TBI cognitive impairment. In addition, DEPs were further analysed using bioinformatic platforms and validated using enzyme-linked immunosorbent assays (ELISA). Results. A total of 56 DEPs were identified that were specifically related to TBI-induced cognitive impairment. Bioinformatic analysis revealed that a wide variety of cellular and metabolic processes and some signaling pathways were involved in the pathophysiology of cognitive deficits following TBI. Five randomly selected DEPs were validated using ELISA in an additional 105 cases, and the results also supported the experimental findings. Conclusions. Despite limitations, our findings will facilitate further studies of the pathological mechanisms underlying TBI-induced cognitive impairment and provide new methods for the research and development of neuroprotective agents. However, further investigation on a large cohort is warranted.
Keyphrases
- cognitive impairment
- traumatic brain injury
- severe traumatic brain injury
- mild traumatic brain injury
- end stage renal disease
- mass spectrometry
- drug induced
- multiple sclerosis
- signaling pathway
- chronic kidney disease
- ejection fraction
- high resolution
- diabetic rats
- high glucose
- oxidative stress
- epithelial mesenchymal transition
- single cell
- high throughput
- label free
- data analysis
- pi k akt
- case control
- stress induced