Evidence map›Paper›PMID 41318439›Full record

ArticleBMC musculoskeletal disorders2025

miR-29a-3p serves as a potential biomarker for diagnosing spinal tuberculosis: a comprehensive analysis integrating clinical data and molecular markers.

Mengqi Zhu, Rong Fu, YuXing Gao, Linan Wang, NingKui Niu

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Article in BMC musculoskeletal disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mengqi Zhu *Department of Orthopedic, General Hospital of Ningxia Medical University, Ningxia Hui Autonomous Region, No.804 Shengli Street, Yinchuan, 750004, China.
Rong Fu *Shenyang Medical College, Shenyang, 110034, China.
YuXing GaoDepartment of Orthopedic, General Hospital of Ningxia Medical University, Ningxia Hui Autonomous Region, No.804 Shengli Street, Yinchuan, 750004, China.
Linan WangDepartment of Orthopedic, General Hospital of Ningxia Medical University, Ningxia Hui Autonomous Region, No.804 Shengli Street, Yinchuan, 750004, China.
NingKui NiuDepartment of Orthopedic, General Hospital of Ningxia Medical University, Ningxia Hui Autonomous Region, No.804 Shengli Street, Yinchuan, 750004, China. niuningkui6743242@163.com.

Funding

National Natural Science Foundation of China 82260436
6 · The paper itself

Abstract

backgroundSpinal tuberculosis (STB), the most common bone and joint tuberculosis, often causes spinal deformity and impairs quality of life. While microRNAs (miRNAs) regulate various disease pathogenesis, their expression and function in STB remain poorly understood.

methods100 STB patients (observation group) from Ningxia Medical University Affiliated Hospital (Jan 2021-Dec 2024) and 100 healthy controls were enrolled. miRNA high-throughput sequencing of 3 samples per group identified differentially expressed miRNAs, validated via known STB signaling pathways. Real-time fluorescence quantitative reverse transcription PCR(RT-qPCR) quantified peripheral blood miR-29a-3p in all participants. Clinical data were collected. Independent samples t-tests, linear regression, Spearman correlation, and receiver operating characteristic(ROC) curves analyzed miR-29a-3p's expression differences, associations with clinical parameters, and diagnostic performance (alone or combined with conventional indicators).

resultsPeripheral blood miR-29a-3p was significantly lower in STB patients (AUC = 0.864). It negatively correlated with erythrocyte sedimentation rate(ESR) and C-reactive protein(CRP) but not with white blood cell count, disease duration, or neutrophil percentage. Combining miR-29a-3p with bacteriological testing, T-cell spot test(T-SPOT), and imaging significantly improved diagnostic performance.

conclusionmiR-29a-3p shows distinct low expression in STB patients' peripheral blood, associated with inflammation activity and conventional diagnostic indicators, making it a promising auxiliary biomarker. Critically, integrating miR-29a-3p into combined detection strategies enhances and optimizes current STB diagnostic frameworks, addressing unmet clinical needs for more accurate and efficient diagnosis, thus holding substantial value for improving STB management.

Indexed as

MicroRNAsTuberculosis, SpinalAdultBiomarkersBlood SedimentationCase-Control StudiesFemaleHumansMaleMiddle AgedBiomarkersMicroRNAsMIRN29a microRNA, humanBiomarkerMiR-29a-3pMiRNA-seqSpinal tuberculosis

Identifiers

PMID41318439
PMCPMC12772068

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.