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DOI 10.1007/s11845-026-04570-1

Медицинская библиотека · Irish journal of medical science · 2026

LncH19 regulates osteoclast activation by targeting miR-196a-5p to diagnose postmenopausal osteoporosis.

Wei Ye, Ren Li, Chen Zhen, Tan Ruiquan, Dai Yong, Wen Yuhao, Zhong Cheng, Lin Danxia, Chen Weibing

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Аннотация

BACKGROUND

Postmenopausal women have a higher prevalence of osteoporosis (OP) due to age related factors and hormonal changes. This study aims to investigate the interactions between lncH19 and miR-196a-5p, as well as their roles in the diagnosis and management of OP.

AIMS: The ultimate goal is to identify novel biomarkers and potential therapeutic targets for this disease.

METHODS

The relative expression levels of lncH19 and miR-196a-5p were measured using RT-qPCR. The diagnostic potential of lncH19 for OP was evaluated via receiver operating characteristic (ROC) curve analysis. The interaction between lncH19 and miR-196a-5p was verified by a luciferase reporter assay. To explore the regulatory effect of lncH19 in the pathogenesis of OP, PMA-induced THP-1 cells were used as an in vitro model.

RESULTS

In postmenopausal women with OP, serum lncH19 levels were decreased, whereas miR-196a-5p levels were increased, and the two exhibited a negative correlation. LncH19 showed significant clinical diagnostic value for OP. It was confirmed that lncH19 directly targets miR-196a-5p and can suppress PMA induced inflammatory responses in macrophages. However, miR-196a-5p mimics could attenuate the anti-inflammatory effect of lncH19.

CONCLUSIONS

This study provides new insights into the pathogenesis of OP, clarifies the important value of lncH19 as a predictive biomarker, and offers a new direction for the treatment and prognostic evaluation of OP.

Для цитирования: Wei Ye, Ren Li, Chen Zhen, Tan Ruiquan, Dai Yong, Wen Yuhao, Zhong Cheng, Lin Danxia, Chen Weibing. LncH19 regulates osteoclast activation by targeting miR-196a-5p to diagnose postmenopausal osteoporosis.. Irish journal of medical science. 2026. DOI: 10.1007/s11845-026-04570-1.
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