Translational Research, Lysosomal and Rare Disorders Research and Treatment Center, Fairfax, VA, United States.
Front Endocrinol (Lausanne). 2022 Nov 24;13:1029130. doi: 10.3389/fendo.2022.1029130. eCollection 2022.
Patients with Gaucher disease (GD) have progressive bone involvement that clinically presents with debilitating bone pain, structural bone changes, bone marrow infiltration (BMI), Erlenmeyer (EM) flask deformity, and osteoporosis. Pain is referred by the majority of GD patients and continues to persist despite the type of therapy. The pain in GD is described as chronic deep penetrating pain; however, sometimes, patients experience severe acute pain. The source of bone pain is mainly debated as nociceptive pain secondary to bone pathology or neuropathic or inflammatory origins. Osteocytes constitute a significant source of secreted molecules that coordinate bone remodeling. Osteocyte markers, sclerostin (SOST) and Dickkopf-1 (DKK-1), inactivate the canonical Wnt signaling pathway and lead to the inhibition of bone formation. Thus, circulated sclerostin and DKK-1 are potential biomarkers of skeletal abnormalities. This study aimed to assess the circulating levels of sclerostin and DKK-1 in patients with GD and their correlation with clinical bone pathology parameters: pain, bone mineral density (BMD), and EM deformity. Thirty-nine patients with GD were classified into cohorts based on the presence and severity of bone manifestations. The serum levels of sclerostin and DKK-1 were quantified by enzyme-linked immunosorbent assays. The highest level of sclerostin was measured in GD patients with pain, BMI, and EM deformity. The multiparameter analysis demonstrated that 95% of GD patients with pain, BMI, and EM deformity had increased levels of sclerostin. The majority of patients with elevated sclerostin also have osteopenia or osteoporosis. Moreover, circulating sclerostin level increase with age, and GD patients have elevated sclerostin levels when compared with healthy control from the same age group. Pearson's linear correlation analysis showed a positive correlation between serum DKK-1 and sclerostin in healthy controls and GD patients with normal bone mineral density. However, the balance between sclerostin and DKK-1 waned in GD patients with osteopenia or osteoporosis. In conclusion, the osteocyte marker, sclerostin, when elevated, is associated with bone pain, BMI, and EM flask deformity in GD patients. The altered sclerostin/DKK-1 ratio correlates with the reduction of bone mineral density. These data confirm that the Wnt signaling pathway plays a role in GD-associated bone disease. Sclerostin and bone pain could be used as biomarkers to assess patients with a high risk of BMI and EM flask deformities.
戈谢病(GD)患者存在进行性骨骼受累,临床上表现为骨痛、结构性骨骼改变、骨髓浸润(BMI)、厄尔勒姆(EM)烧瓶畸形和骨质疏松症。大多数 GD 患者都有疼痛症状,并持续存在,尽管接受了治疗。GD 患者的疼痛被描述为慢性深穿透性疼痛;然而,有时患者会经历严重的急性疼痛。骨痛的来源主要有争议,认为是继发于骨骼病理学的伤害性疼痛或神经源性或炎症性来源。骨细胞是协调骨骼重塑的分泌分子的重要来源。骨细胞标志物,骨硬化蛋白(SOST)和 Dickkopf-1(DKK-1),可使经典 Wnt 信号通路失活,并导致骨形成抑制。因此,循环中的骨硬化蛋白和 DKK-1 是骨骼异常的潜在生物标志物。本研究旨在评估 GD 患者的循环骨硬化蛋白和 DKK-1 水平及其与临床骨骼病理学参数(疼痛、骨密度(BMD)和 EM 畸形)的相关性。根据骨骼表现的存在和严重程度,将 39 名 GD 患者分为两组。通过酶联免疫吸附试验定量测定骨硬化蛋白和 DKK-1 的血清水平。在有疼痛、BMI 和 EM 畸形的 GD 患者中,骨硬化蛋白水平最高。多参数分析表明,95%的有疼痛、BMI 和 EM 畸形的 GD 患者的骨硬化蛋白水平升高。大多数骨硬化蛋白升高的患者也有骨质疏松症或骨质疏松症。此外,循环骨硬化蛋白水平随年龄增长而增加,与同年龄组的健康对照组相比,GD 患者的骨硬化蛋白水平升高。Pearson 线性相关分析显示,在健康对照组和骨密度正常的 GD 患者中,血清 DKK-1 与骨硬化蛋白呈正相关。然而,在骨质疏松症或骨质疏松症的 GD 患者中,骨硬化蛋白和 DKK-1 之间的平衡减弱。总之,在 GD 患者中,当骨细胞标志物骨硬化蛋白升高时,与骨痛、BMI 和 EM 烧瓶畸形相关。骨硬化蛋白/ DKK-1 比值的改变与骨密度的降低相关。这些数据证实,Wnt 信号通路在 GD 相关的骨骼疾病中起作用。骨硬化蛋白和骨痛可作为评估 BMI 和 EM 烧瓶畸形高风险患者的生物标志物。