Abstract

Heroin use disorder is a chronic and relapsing disease that induces persistent changes in the brain. The diagnoses of heroin use disorders are mainly based on subjective reports and no valid biomarkers available. Recent researches have revealed that circulating miRNAs are useful non-invasive biomarkers for diagnosing brain diseases such as Alzheimer's disease, multiple sclerosis, schizophrenia, and bipolar disorder. However, studies on circulating miRNAs for the diagnosis of heroin use disorders are rarely reported. In this study, we investigated the differential expression of plasma miRNAs in 57 heroin-dependent patients. Based on literature research and microarray analysis, two candidate miRNAs, miR-320a and let-7b-5p, were selected and analyzed by quantitative real-time RT-PCR. The results showed miR-320a and let-7b were significantly upregulated in plasma of the heroin-dependent patients compared to that in healthy controls. The area under curves (AUCs) of receiver operating characteristic (ROC) curves of miR-320a and let-7b-5p were 0.748 and 0.758, respectively. The sensitivities of miR-320a and let-7b-5p were 71.9 and 70.2%, while the specificities of miR-320a and let-7b-5p were 76.1 and 78.3%, respectively. The combination of these two miRNAs predicted heron dependence with an AUC of 0.782 (95% CI 0.687–0.876), with 73.7% sensitivity and 82.6% specificity. Our findings suggest a potential use for circulating miRNAs as biomarkers for the diagnosis of heroin abuse.

Highlights

  • Heroin, a morphine derivative, is one of the most powerfully addictive drugs abused in the world

  • MiRNAs are abundantly expressed in the nervous system, suggesting they may be important for neural development and function [27]

  • Chronic morphine treatment increases let-7 and miRNA23b expression in a time- and dose-dependent manner and suppresses the association of MOR1 mRNA with polysomes [8, 13, 28]

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Summary

Introduction

A morphine derivative, is one of the most powerfully addictive drugs abused in the world. People who abused heroin are among the most marginalized and disadvantaged drug users. They experience poor health outcomes with a greater chance of premature death, increased risk of both non-fatal and fatal drug overdoses, and high rates of potentially life-threatening infectious diseases, such as tuberculosis, hepatitis, and HIV. Heroin addiction is a relapsing and chronic brain disorder that causes persistent alterations in synaptic plasticity [1,2,3]. The underlying molecular mechanisms that lead to addiction remain poorly understood.

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