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骨相关循环 microRNAs miR-29b-3p、miR-550a-3p 和 miR-324-3p 及其与骨微结构和组织形态计量学的关系。

Bone-related Circulating MicroRNAs miR-29b-3p, miR-550a-3p, and miR-324-3p and their Association to Bone Microstructure and Histomorphometry.

机构信息

Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.

St. Vincent Hospital - Medical Department II, The VINFORCE Study Group, Academic Teaching Hospital of the Medical University of Vienna, Vienna, Austria.

出版信息

Sci Rep. 2018 Mar 20;8(1):4867. doi: 10.1038/s41598-018-22844-2.

DOI:10.1038/s41598-018-22844-2
PMID:29559644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5861059/
Abstract

The assessment of bone quality and the prediction of fracture risk in idiopathic osteoporosis (IOP) are complex prospects as bone mineral density (BMD) and bone turnover markers (BTM) do not indicate fracture-risk. MicroRNAs (miRNAs) are promising new biomarkers for bone diseases, but the current understanding of the biological information contained in the variability of miRNAs is limited. Here, we investigated the association between serum-levels of 19 miRNA biomarkers of idiopathic osteoporosis to bone microstructure and bone histomorphometry based upon bone biopsies and µCT (9.3 μm) scans from 36 patients. Four miRNAs were found to be correlated to bone microarchitecture and seven miRNAs to dynamic histomorphometry (p < 0.05). Three miRNAs, namely, miR-29b-3p, miR-324-3p, and miR-550a-3p showed significant correlations to histomorphometric parameters of bone formation as well as microstructure parameters. miR-29b-3p and miR-324-p were found to be reduced in patients undergoing anti-resorptive therapy. This is the first study to report that serum levels of bone-related miRNAs might be surrogates of dynamic histomorphometry and potentially reveal changes in bone microstructure. Although these findings enhance the potential value of circulating miRNAs as bone biomarkers, further experimental studies are required to qualify the clinical utility of miRNAs to reflect dynamic changes in bone formation and microstructure.

摘要

特发性骨质疏松症(IOP)的骨质量评估和骨折风险预测是一个复杂的问题,因为骨矿物质密度(BMD)和骨转换标志物(BTM)并不能指示骨折风险。microRNAs(miRNAs)是骨疾病有前途的新型生物标志物,但目前对 miRNA 变异性中包含的生物学信息的理解有限。在这里,我们研究了 36 名患者的骨活检和µCT(9.3μm)扫描的血清中 19 种 miRNA 骨标志物与骨微结构和骨组织形态计量学之间的关系。发现有 4 种 miRNA 与骨微结构相关,有 7 种 miRNA 与动态组织形态计量学相关(p<0.05)。三种 miRNA,即 miR-29b-3p、miR-324-3p 和 miR-550a-3p,与骨形成的组织形态计量学参数以及微观结构参数均有显著相关性。miR-29b-3p 和 miR-324-p 在接受抗吸收治疗的患者中发现有降低。这是第一项报道血清中与骨相关的 miRNA 水平可能是动态组织形态计量学的替代物,并可能揭示骨微结构变化的研究。尽管这些发现增强了循环 miRNA 作为骨生物标志物的潜在价值,但需要进一步的实验研究来确定 miRNA 反映骨形成和微结构动态变化的临床实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/1da30daa7828/41598_2018_22844_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/418d7701deab/41598_2018_22844_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/9a398040f943/41598_2018_22844_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/1da30daa7828/41598_2018_22844_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/418d7701deab/41598_2018_22844_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/9a398040f943/41598_2018_22844_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a96/5861059/1da30daa7828/41598_2018_22844_Fig4_HTML.jpg

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