Surgical Sciences and Technologies, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Int J Mol Sci. 2024 May 28;25(11):5879. doi: 10.3390/ijms25115879.
Aging comes with the loss of muscle and bone mass, leading to a condition known as osteosarcopenia. Circulating, cellular, and tissue biomarkers research for osteosarcopenia is relatively scarce and, currently, no established biomarkers exist. Here we find that osteosarcopenic patients exhibited elevated basophils and TNFα levels, along with decreased aPPT, PT/INR, IL15, alpha-Klotho, DHEA-S, and FGF-2 expression and distinctive bone and muscle tissue micro-architecture and biomarker expressions. They also displayed an increase in osteoclast precursors with a concomitant imbalance towards spontaneous osteoclastogenesis. Similarities were noted with osteopenic and sarcopenic patients, including a lower neutrophil percentage and altered cytokine expression. A linear discriminant analysis (LDA) on models based on selected biomarkers showed a classification accuracy in the range of 61-78%. Collectively, our data provide compelling evidence for novel biomarkers for osteosarcopenia that may hold potential as diagnostic tools to promote healthy aging.
衰老是伴随着肌肉和骨量的丧失而来的,导致一种被称为骨质疏松-肌少症的情况。用于骨质疏松-肌少症的循环、细胞和组织生物标志物研究相对较少,目前尚无既定的生物标志物。在这里,我们发现骨质疏松-肌少症患者表现出嗜碱性粒细胞和 TNFα 水平升高,同时伴有 aPPT、PT/INR、IL15、alpha-Klotho、DHEA-S 和 FGF-2 表达降低,以及独特的骨骼和肌肉组织微观结构和生物标志物表达。他们还表现出破骨细胞前体增加,自发性破骨细胞形成失衡。与骨质疏松症和肌少症患者有相似之处,包括中性粒细胞百分比降低和细胞因子表达改变。基于选定生物标志物的模型的线性判别分析(LDA)显示分类准确率在 61-78%之间。总的来说,我们的数据为骨质疏松-肌少症的新型生物标志物提供了有力的证据,这些生物标志物可能具有作为促进健康衰老的诊断工具的潜力。