| Literature DB >> 28934429 |
Sandrine Cabantous1, Ogobara Doumbo2, Belco Poudiougou2, Laurence Louis3, Abdoulaye Barry4, Aboubacar A Oumar5, Abdoualye Traore4, Sandrine Marquet1, Alain Dessein1.
Abstract
Cerebral malaria, a reversible encephalopathy affecting young children, is a medical emergency requiring urgent clinical assessment and treatment. We performed a whole-transcriptomic analysis of blood samples from Malian children with cerebral or uncomplicated malaria. We focused on transcripts from pathways for which dysfunction has been associated with neurodegenerative disorders. We found that SNCA, SIAH2, UBB, HSPA1A, TUBB2A, and PINK1 were upregulated (fold-increases, ≥2.6), whereas UBD and PSMC5 were downregulated (fold-decreases, ≤4.39) in children with cerebral malaria, compared with those with uncomplicated malaria. These findings provide the first evidence for pathogenic mechanisms common to human cerebral malaria and neurodegenerative disorders.Entities:
Keywords: PBMCs; cerebral malaria; common pathways; expression; human; mRNA; neurodegenerative disorders
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Year: 2017 PMID: 28934429 DOI: 10.1093/infdis/jix359
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226