Bone Physiopathology Research Unit, Translational Pediatrics and Clinical Genetics Research Division, Bambino Gesù Children's Hospital, IRCCS, Viale San Paolo 15, 00146, Rome, Italy.
Rare Diseases and Medical Genetic Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
J Endocrinol Invest. 2024 Nov;47(11):2775-2784. doi: 10.1007/s40618-024-02365-8. Epub 2024 Apr 1.
Gorham-Stout disease is a very rare disorder characterized by progressive bone erosion and angiomatous proliferation; its etiopathogenesis is still unknown, and diagnosis is still performed by exclusion criteria. The alteration of bone remodeling activity has been reported in patients; in this study, we characterized circulating osteoclast and osteogenic precursors that could be important to better understand the osteolysis observed in patients.
Flow cytometry analysis of PBMC (Peripheral Blood Mononuclear Cells) was performed to characterize circulating osteoclast and osteogenic precursors in GSD patients (n = 9) compared to healthy donors (n = 55). Moreover, ELISA assays were assessed to evaluate serum levels of bone markers including RANK-L (Receptor activator of NF-κB ligand), OPG (Osteoprotegerin), BALP (Bone Alkaline Phosphatase) and OCN (Osteocalcin).
We found an increase of CD16/CD14CD11b and CD115/CD14CD11b osteoclast precursors in GSD patients, with high levels of serum RANK-L that could reflect the increase of bone resorption activity observed in patients. Moreover, no significant alterations were found regarding osteogenic precursors and serum levels of BALP and OCN.
The analysis of circulating bone cell precursors, as well as of RANK-L, could be relevant as an additional diagnostic tool for these patients and could be exploited for therapeutic purposes.
Gorham-Stout 病是一种非常罕见的疾病,其特征为进行性骨侵蚀和血管性增殖;其病因发病机制尚不清楚,目前仍通过排除标准进行诊断。据报道,患者的骨重塑活性发生改变;在这项研究中,我们对循环破骨细胞和成骨前体细胞进行了特征描述,这可能有助于更好地理解患者中观察到的骨溶解。
对 GSD 患者(n=9)和健康供体(n=55)的外周血单个核细胞(PBMC)进行流式细胞术分析,以对循环破骨细胞和成骨前体细胞进行特征描述。此外,还通过 ELISA 测定评估了包括 RANK-L(核因子-κB 受体激活剂配体)、OPG(骨保护素)、BALP(骨碱性磷酸酶)和 OCN(骨钙素)在内的骨标志物的血清水平。
我们发现 GSD 患者的 CD16/CD14CD11b 和 CD115/CD14CD11b 破骨细胞前体增加,血清 RANK-L 水平升高,这可能反映了患者观察到的骨吸收活性增加。此外,成骨前体细胞和 BALP 及 OCN 的血清水平没有明显变化。
循环骨细胞前体细胞以及 RANK-L 的分析可能作为这些患者的附加诊断工具具有相关性,并可用于治疗目的。