Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study

被引:17
|
作者
Pertusa, Clara [1 ]
Tarin, Juan J. [2 ]
Cano, Antonio [3 ]
Angel Garcia-Perez, Miguel [1 ,4 ]
Mifsut, Damian [5 ]
机构
[1] INCLIVA Hlth Res Inst, Res Unit, Valencia 46010, Spain
[2] Univ Valencia, Dept Cellular Biol Funct Biol & Phys Anthropol, Burjassot 46100, Spain
[3] Univ Valencia, Dept Pediat Obstet & Gynecol, Valencia 46010, Spain
[4] Univ Valencia, Dept Genet, Burjassot 46100, Spain
[5] INCLIVA Inst Hlth Res, Clin Hosp, Orthoped Surg & Traumatol, Valencia 46010, Spain
关键词
CIRCULATING MICRORNAS; MIRNA SIGNATURES; DIFFERENTIATION; STANDARDIZATION; EXPRESSION; DENSITY; PLASMA; TISSUE;
D O I
10.1038/s41598-021-98789-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The rising incidence of bone pathologies such as osteoporosis and osteoarthritis is negatively affecting the functional status of millions of patients worldwide. The genetic component of these multifactorial pathologies is far from being fully understood, but in recent years several epigenetic mechanisms involved in the pathophysiology of these bone diseases have been identified. The aim of the present study was to compare the serum expression of four miRNAs in women with hip fragility fracture (OF group), osteoarthritis requiring hip replacement (OA group) and control women (Ctrl group). Serum expression of miR-497-5p, miR-155-5p, miR-423-5p and miR-365-3p was determined in a sample of 23 OA women, 25 OF women and 52 Ctrl women. Data shown that women with bone pathologies have higher expression of miR-497 and miR-423 and lower expression of miR-155 and miR-365 than control subjects. Most importantly, miR-497 was identified as an excellent discriminator between OA group and control group (AUC: 0.89, p < 0.000) and acceptable in distinguishing from the OF group (AUC: 0.76, p = 0.002). Our data suggest that circulating miR-497 may represent a significant biomarker of OA, a promising finding that could contribute towards future early-stage diagnosis of this disease. Further studies are required to establish the role of miR-155, miR-423 and miR-365 in bone pathologies.
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页数:9
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