Abstract

BackgroundTo verify the differential expression of miR‐30c and miR‐142‐3p between tuberculosis patients and healthy controls and to investigate the performance of microRNA (miRNA) and subsequently models for the diagnosis of tuberculosis (TB).MethodsWe followed up 460 subjects suspected of TB, and finally enrolled 132 patients, including 60 TB patients, 24 non‐TB disease controls (TB‐DCs), and 48 healthy controls (HCs). The differential expression of miR‐30c and miR‐142‐3p in serum samples of the TB patients, TB‐DCs, and HCs were identified by reverse transcription–quantitative real‐time PCR. Diagnostic models were developed by analyzing the characteristics of miRNA and electronic health records (EHRs). These models evaluated by the area under the curves (AUC) and calibration curves were presented as nomograms.ResultsThere were differential expression of miR‐30c and miR‐142‐3p between TB patients and HCs (p < 0.05). Individual miRNA has a limited diagnostic value for TB. However, diagnostic performance has been both significantly improved when we integrated miR‐142‐3p and ordinary EHRs to develop two models for the diagnosis of tuberculosis. The AUC of the model for distinguishing tuberculosis patients from healthy controls has increased from 0.75 (95% CI: 0.66–0.84) to 0.96 (95% CI: 0.92–0.99) and the model for distinguishing tuberculosis patients from non‐TB disease controls has increased from 0.67 (95% CI: 0.55–0.79) to 0.94 (95% CI: 0.89–0.99).ConclusionsIntegrating serum miR‐142‐3p and EHRs is a good strategy for improving TB diagnosis.

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