Valero C, Olmos J M, Rivera F, Hernández J L, Vega M E, Macías J González
Department of Internal Medicine, University Hospital Marqués de Valdecilla, University of Cantabria, Avenida de Valdecilla s/n, 39008, Santander, Spain.
Calcif Tissue Int. 2006 Jun;78(6):343-7. doi: 10.1007/s00223-005-0237-y. Epub 2006 Jun 21.
Osteoprotegerin (OPG) is considered one of the main regulators of bone remodeling. Various patterns of serum OPG levels have been described in different types of tumors. We undertook this study to determine serum OPG levels in patients with squamous cell head and neck cancer (SCHNC), analyzing their relationship with other metabolic bone parameters and bone mineral density (BMD), as well as the possible influence of chemotherapy. Forty male patients with localized SCHNC were studied, and their results were compared with those of 40 healthy male controls. The type of treatment followed by each patient was noted. Age, weight, height, and lifestyle habits were recorded; and OPG, Ca(2+), intact parathyroid hormone (iPTH), 25-Hydroxyvitamin D (25OHD) and 1,25-Dihydroxyvitamin D (1,25(OH)(2)D), bone alkaline phosphatase, osteocalcin, and serum C-terminal cross-links telopeptide of type I collagen (ICTP) were determined. Dual-energy X-ray absorptiometry BMD at the lumbar spine, femoral neck, and hip was also measured. Serum OPG was higher in patients than in controls (91.7 +/- 25.8 vs. 77.2 +/- 26.3, P = 0.02). ICTP (a bone resorption marker) was 37% higher in patients (P = 0.007). Bone mass was lower in patients at the lumbar spine, femoral neck, and total hip. Lumbar spine Z-score showed a significant progressive decrease in controls, stage I-III patients, and stage IV patients. Logistic regression analysis showed a significant association between the disease and serum OPG levels, the odds ratio per standard deviation increase of this being 1.9 (95% confidence interval 1.1-3.8, P = 0.04) after adjusting for bone mass and ICTP serum levels, as well as for alcohol and smoking history. Adjustment for alcohol intake and tobacco use did not cancel out BMD differences between patients and controls. Patients with SCHNC show increased OPG serum levels, increased bone resorption, and decreased bone mass. The OPG rise appears to be unrelated to the BMD decrease, and the BMD decrease seems to be, at least in part, independent of smoking and drinking habits. No differences in either OPG or BMD were seen between patients with and without chemotherapy. Further studies are needed to clarify the mechanisms responsible for OPG and BMD changes in SCHNC.
骨保护素(OPG)被认为是骨重塑的主要调节因子之一。在不同类型的肿瘤中已描述了血清OPG水平的各种模式。我们开展这项研究以确定头颈部鳞状细胞癌(SCHNC)患者的血清OPG水平,分析其与其他代谢性骨参数及骨密度(BMD)的关系,以及化疗的可能影响。研究了40例局限性SCHNC男性患者,并将其结果与40例健康男性对照者的结果进行比较。记录每位患者所采用的治疗类型。记录年龄、体重、身高和生活习惯;并测定OPG、钙(Ca2+)、完整甲状旁腺激素(iPTH)、25-羟基维生素D(25OHD)和1,25-二羟基维生素D(1,25(OH)2D)、骨碱性磷酸酶、骨钙素以及I型胶原血清C末端交联肽(ICTP)。还测量了腰椎、股骨颈和髋部的双能X线吸收法骨密度。患者的血清OPG高于对照者(91.7±25.8对77.2±26.3,P = 0.02)。患者的ICTP(一种骨吸收标志物)高37%(P = 0.007)。患者腰椎、股骨颈和全髋部的骨量较低。腰椎Z评分在对照者、I-III期患者和IV期患者中呈显著的逐渐下降。逻辑回归分析显示疾病与血清OPG水平之间存在显著关联,在调整骨量和ICTP血清水平以及饮酒和吸烟史后,每标准差增加的优势比为1.9(95%置信区间1.1 - 3.8,P = 0.04)。调整酒精摄入量和烟草使用并未消除患者与对照者之间的骨密度差异。SCHNC患者显示血清OPG水平升高、骨吸收增加和骨量减少。OPG升高似乎与骨密度降低无关,而骨密度降低似乎至少部分独立于吸烟和饮酒习惯。接受化疗和未接受化疗的患者在OPG或骨密度方面均未观察到差异。需要进一步研究以阐明SCHNC中OPG和骨密度变化的机制。