Author(s)

Nanyao Chen¹, Min Guo^2*, Dan Yu³, Feng Zhou³

¹The Fourth People’s Hospital of Haikou, Haikou, China.
²Hainan General Hospital, Haikou, China.
³Central South University Xiangya School of Medical Affiliated Haikou Hospital, Haikou, China.

Objective: To investigate the bioinformatics of differentially expressed proteins in plasma in patients with acute cerebral infarction associated with H-type hypertension. Methods: Gene chip public database (gene expression omnibus, GEO) GDS4521 chip data, in the chip in 30 cases of H patients with acute cerebral infarction with high blood pressure and age, gender, matching the 20 H hypertension patients as the research object, collects the mononuclear cells (PBMCs) is used to detect the gene chip, using the GO (gene Ontology, GO), protein function analysis tools such as KEGG, screening and analysis of enrichment of differentially expressed genes function and related signaling pathway. Results: 31 genes in PBMCs were significantly changed in h-type hypertension and H-type hypertension with acute cerebral infarction, 32 of which were increased and 2 of which were decreased. GO analysis showed that in terms of biological processes, the genes related to inflammatory response and neutrophil chemotaxis were the most. In terms of molecular function, chemokine activity-related genes are the most. KEGG signaling pathway analysis showed that the most differentially expressed genes were located in the TNF signaling pathway. Conclusion: H-type hypertension with acute cerebral infarction has a variety of functional proteins and signaling pathways changes, suggesting that inflammatory response in H-type hypertension with acute cerebral infarction recovery period may still play a role in the prognosis and reactivation of the disease.

Acute Cerebral Infarction, Proteomics, ITRAQ Technology, Immunohistochemical

Chen, N. , Guo, M. , Yu, D. and Zhou, F. (2021) Bioinformatics Study of Plasma Differentially Expressed Proteins in H-Type Hypertension with or without Acute Cerebral Infarction. Journal of Behavioral and Brain Science, 11, 1-9. doi: 10.4236/jbbs.2021.111001.