MiR-150 levels are related to in-hospital mortality in non-HIV Pneumocystis pneumonia patients

Med Mycol. 2024 May 3;62(5):myae022. doi: 10.1093/mmy/myae022.

Abstract

Pneumocystis pneumonia (PCP) is a common opportunistic infection that occurs in immunocompromised patients. Compared with HIV patients, PCP in non-HIV patients tends to follow up a more urgent course and poorer prognosis. Therefore, markers that could predict survival of PCP patients in non-HIV population are of great value. MiRNA-150 has been widely studied in many diseases since it has been identified as a vital regulator of immune cell differentiation and activation. We thus conduct this study aiming to evaluate the prognostic value of miR-150 level in non-HIV PCP. First, the expression levels of miR-150 were compared between PCP patients and healthy volunteers. The miR-150 levels in immune cells were also detected in PCP mouse models. Then the prognostic value of miR-150 was further assessed in another PCP population (n = 72). The expression levels of miR-150 were measured by reverse transcription real-time PCR (RT-PCR) technique. Our data demonstrated significantly decreased miR-150 expression levels in PCP patients and mouse models compared to controls. The miR-150 levels also decreased in various immune cells of PCP mouse models. With a cut-off value of 3.48, the area under the curve, sensitivity, specificity of miR-150 to predicate PCP mortality were 0.845, 68.2% and 96.0%, respectively. In conclusion, miR-150 expression value might serve as a potential biomarker to identify PCP patients at high risk of death.

Keywords: Pneumocystis Pneumonia; microRNA; mortality; prognostic value.

Plain language summary

Pneumocystis pneumonia (PCP) remains a fatal risk for immunosuppressed patients. MiR-150 takes part in immune regulation, and thus is involved in infection control. Our study indicated that the miR-150 expression may act as a potential biomarker for predicting mortality of PCP patients.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Biomarkers
  • Disease Models, Animal
  • Female
  • Hospital Mortality
  • Humans
  • Male
  • Mice
  • MicroRNAs* / genetics
  • Middle Aged
  • Pneumonia, Pneumocystis* / immunology
  • Pneumonia, Pneumocystis* / microbiology
  • Pneumonia, Pneumocystis* / mortality
  • Prognosis