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Circulating microRNAs in malaria infection: bench to bedside.

Supat ChamnanchanuntSuthat FucharoenTsukuru Umemura
Published in: Malaria journal (2017)
Severe malaria has a poor prognosis with a morbidity rate of 80% in tropical areas. The early parasite detection is one of the effective means to prevent severe malaria of which specific treatment strategies are limited. Many clinical characteristics and laboratory testings have been used for the early diagnosis and prediction of severe disease. However, a few of these factors could be applied to clinical practice. MicroRNAs (miRNAs) were demonstrated as useful biomarkers in many diseases such as malignant diseases and cardiovascular diseases. Recently it was found that plasma miR-451 and miR-16 were downregulated in malaria infection at parasitic stages or with multi-organ failure involvement. MiR-125b, -27a, -23a, -150, 17-92 and -24 are deregulated in malaria patients with multiple organ failures. Here, the current findings of miRNAs were reviewed in relation to clinical severity of malaria infection and emphasized that miRNAs are potential biomarkers for severe malaria infection.
Keyphrases
  • plasmodium falciparum
  • poor prognosis
  • long non coding rna
  • cell proliferation
  • early onset
  • clinical practice
  • cardiovascular disease
  • metabolic syndrome
  • drug induced
  • long noncoding rna
  • cardiovascular risk factors