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Plasma microRNA signature of patients with IgA nephropathy
Jingjing Wu1, Huo Zhang2, Weiwei Wang3
1Department of Nephrology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, PR China.
Abstract:
We looked for differentially expressed MicroRNAs (miRNAs) in Immunoglobulin A nephropathy (IgAN). Forty-eight miRNAs were identified through the initial screening phase (2 IgAN pools vs. 1 normal control (NC) pool) using quantitative reverse transcription polymerase chain reaction (qRT-PCR) based Exiqon panel (miRCURY-Ready-to-Use-PCR-Human-panel-I + II-V1.M). By qRT-PCR, these miRNAs were further assessed in the training (32 IgAN VS. 31 NCs) and testing stages (51 IgAN VS. 51 NCs). The renal pathological lesions of patients with IgAN were evaluated according to Lee's grading system. We discovered a plasma miRNA signature including four up-regulated miRNAs (miR-148a-3p, miR-150-5p, miR-20a-5p and miR-425-3p) and the areas under the receiver operating characteristic (ROC) curve (AUC) were 0.80 and 0.76 for the training and testing stage, respectively. The expression of the four miRNAs in IgAN grade I-II subgroups (according to Lee's grading system) was obviously higher than that in IgAN grade III-V (P < .05). In summary, the plasma expression of miR-148a-3p, miR-150-5p, miR-20a-5p and miR-425-3p were up-regulated in patients with IgAN, especially the early-stage disease. Further studies are needed to explore the roles of the four miRNAs in the pathogenesis and progression of IgAN.
Insights
Researchers identified four plasma microRNAs (miRNAs) that are upregulated in Immunoglobulin A nephropathy (IgAN) patients. These miRNAs may serve as biomarkers, particularly for early-stage IgAN disease.
Area of Science:
- Nephrology
- Molecular Biology
- Biomarker Discovery
Background:
- Immunoglobulin A nephropathy (IgAN) is a common primary glomerulonephritis.
- Identifying reliable biomarkers for IgAN diagnosis and staging is crucial.
- MicroRNAs (miRNAs) are small non-coding RNAs with regulatory roles in various diseases.
Purpose of the Study:
- To identify differentially expressed miRNAs in the plasma of IgAN patients.
- To evaluate the diagnostic potential of identified miRNAs as biomarkers for IgAN.
- To investigate the correlation between miRNA expression and disease severity in IgAN.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) using a comprehensive miRNA panel.
- Screening of 48 miRNAs in pooled samples, followed by validation in training and testing cohorts.
- Plasma samples from 32 IgAN patients and 31 normal controls (NCs) for training, and 51 IgAN patients and 51 NCs for testing.
- Assessment of renal pathology using Lee's grading system.
Main Results:
- A plasma miRNA signature comprising four upregulated miRNAs (miR-148a-3p, miR-150-5p, miR-20a-5p, and miR-425-3p) was identified.
- The miRNA signature achieved an area under the receiver operating characteristic curve (AUC) of 0.80 in the training set and 0.76 in the testing set.
- Higher expression of these four miRNAs was observed in early-stage IgAN (Lee's grade I-II) compared to advanced stages (grade III-V).
Conclusions:
- Plasma levels of miR-148a-3p, miR-150-5p, miR-20a-5p, and miR-425-3p are significantly upregulated in IgAN patients.
- This miRNA signature shows potential as a non-invasive biomarker for IgAN, especially in early disease stages.
- Further research is warranted to elucidate the specific roles of these miRNAs in IgAN pathogenesis and progression.
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