Circulating microRNAs in serum as novel biomarkers for osteoporosis: a case-control study

Aims: Osteoporosis is underdiagnosed because of the lack of a convenient diagnostic method. Circulating microRNAs (miRNAs) emerge as novel biomarkers for disease diagnosis. Here, we conducted a case-control study that included a total of 448 serum samples collected from 182 healthy participants, 132...

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Veröffentlicht in:Therapeutic advances in musculoskeletal disease 2020, Vol.12, p.1759720X20953331-1759720X20953331
Hauptverfasser: Shuai, Yi, Liao, Li, Su, Xiaoxia, Sha, Nanxi, Li, Xiaobo, Wu, Yutao, Jing, Huan, Kuang, Huijuan, Deng, Zhihong, Li, Yongqi, Jin, Yan
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Sprache:eng
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Zusammenfassung:Aims: Osteoporosis is underdiagnosed because of the lack of a convenient diagnostic method. Circulating microRNAs (miRNAs) emerge as novel biomarkers for disease diagnosis. Here, we conducted a case-control study that included a total of 448 serum samples collected from 182 healthy participants, 132 osteopenia participants, and 134 osteoporosis patients. Methods: Circulating miRNAs dysregulated during osteoporosis were screened and analyzed in three randomly determined sub-cohorts: the discovery cohort identified 22 candidate miRNAs; the training cohort tested the candidate miRNAs and constructed Index 1, comprising five miRNAs by logistic regression, and Index 2, comprising four miRNAs, was developed by linear combination. Results: Both indices were tested in the validation cohort and showed statistically significant results in distinguishing osteoporosis patients from healthy and osteopenic patients. Moreover, Index 1 also showed improved performance over traditional bone turnover biomarkers type I pro-collagen (tPINP) and type I collagen (β-CTx). Conclusion: In conclusion, circulating miRNAs are potential biomarkers for osteoporosis. The diagnostic panel of circulating miRNAs could be a complementary method for dual-energy X-ray absorptiometry (DXA) in mass screening and routine examination to enhance the osteoporosis detection rate.
ISSN:1759-720X
1759-7218
DOI:10.1177/1759720X20953331