AI Article Synopsis

  • The study explored the role of the let-7 family of microRNAs in anti-NMDAR encephalitis by analyzing blood samples from patients and controls.
  • Results showed significant down-regulation of let-7a, let-7b, let-7d, and let-7f in anti-NMDAR encephalitis patients compared to controls, with let-7b showing potential as a diagnostic marker.
  • Furthermore, let-7 levels were also decreased in other nervous system diseases, but let-7b did not show significant changes post-treatment, highlighting its specific relevance to anti-NMDAR encephalitis.

Article Abstract

The study aimed to investigate the expression and significance of the plasma let-7 family in anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. Blood samples from 5 anti-NMDAR encephalitis patients and 5 negative controls were collected for microarray analysis. Blood samples from10 anti-NMDAR encephalitis patients, 10 anti-NMDAR encephalitis patients whose physical conditions have improved after 3 months of immunotherapy, 20 virus (meningitis) encephalitis patients, 20 tuberculosis (meningitis) encephalitis patients, 10 purulent (meningitis) encephalitis patients, 20 cerebral cysticercosis patients, 20 ischemic stroke patients, 20 intracerebral hemorrhage patients, 15 neuromyelitis optica patients, 15 multiple sclerosis patients, 15 moyamoya disease patients, and 20 negative controls were collected for real-time quantitative PCR (qRT-PCR) analysis. The expression levels of let-7a, let-7b, let-7d, and let-7f were significantly down-regulated in anti-NMDAR encephalitis compared with the negative controls (NC). The expression levels of let-7a, let-7d, and let-7f were significantly down-regulated in other nervous system diseases compared with the NC group while the expression level of let-7b was statistically insignificant in other nervous system diseases compared with the NC group. In addition, there was no significant dysregulation of let-7b in the anti-NMDAR encephalitis treatment group compared with the NC. Let-7b may be a potential diagnostic marker and an indicator that reflected the molecular mechanism of anti-NMDAR encephalitis.

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Source
http://dx.doi.org/10.1007/s12031-015-0489-6DOI Listing

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