Identification of differentially expressed exosome proteins in serum as potential biomarkers for cognitive impairments in cerebral small vessel disease

• Published in: Neuroscience letters Vol. 822; p. 137631
• Main Authors: Feng, Qian, Lu, Yanjing, Zhang, Ruyang, Li, Yifan, Zhao, Zhong, Zhou, Hua
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 06.02.2024
• Subjects: Cerebral small vessel disease; Cognitive impairments; CSVD; Exosomes; Proteomics analysis; Cognitive impairments; CSVD; Proteomics analysis; Exosomes; Cerebral small vessel disease
• ISSN: 0304-3940; 1872-7972; 1872-7972
• DOI: 10.1016/j.neulet.2024.137631

•The 30 differentially expressed plasma exosome proteins identified in our study are promising as biomarkers for diagnosing cognitive impairments resulting from CSVD.•These proteins are involved in various biological processes, such as cellular movement, protein metabolism, and immune responses.•The differentially expressed plasma exosome proteins, including histone, proteasome, clusterin and coagulation factor XIII, hold promise as diagnostic biomarkers for cognitive impairment associated with CSVD. Cognitive impairment arising from cerebral small vessel disease (CSVD) represents a critical subtype of vascular cognitive impairments (VCI) and is the primary cause of vascular dementia. However, identifying reliable clinical and laboratory indicators for this disease remain elusive. We hypothesize that plasma exosome proteins hold the potential to serve as biomarkers for the onset of cognitive dysfunction associated with cerebrovascular diseases. We employed TMT-based proteomics to discern variations in serum exosome proteomes between individuals with cognitive impairments due to CSVD and healthy volunteers. Each group comprised 18 subjects, and through differential expression analysis, we identified 22 down-regulated and 8 up-regulated proteins between the two groups. Our research revealed 30 differentially expressed plasma exosome proteins, including histone, proteasome, clusterin and coagulation factor XIII, in individuals with cognitive impairments caused by CSVD. The 30 differentially expressed plasma exosome proteins identified in our study are promising as biomarkers for diagnosing cognitive impairments resulting from CSVD. These findings may help us better understand the underlying pathological mechanisms involved in the diseases.