Kuroda Tatsuhiko, Shiraki Masataka, Tanaka Shiro, Ohta Hiroaki
Department of Obstetrics and Gynecology, Tokyo Women's Medical University, Tokyo, Japan.
Bone. 2009 Jan;44(1):168-72. doi: 10.1016/j.bone.2008.03.023. Epub 2008 Apr 10.
It was reported that low bone mineral density (BMD), osteoporotic fractures and low serum 25-hydroxyvitamin D (25-OHVD) levels increase the risk of mortality in elderly Caucasian people. However, there is no data available on the relationship between bone mineral density or 25-OHVD levels and mortality in elderly Asian women. To determine whether or not low bone mineral density (BMD) or low 25-OHVD levels contribute to increased mortality risk, we conducted a prospective observational study in 1232 ambulatory postmenopausal female volunteers. Information was obtained from the subjects on baseline BMD, the serum levels of biochemical indices including 25-OHVD, prevalent fractures, co-morbidities and lifestyle variables. The participants were observed for a total of 6.9+/-3.6 years (mean+/-SD) and a total of 107 participants (8.7%) were dead during the observation. Mortality was assessed and confirmed on the certificates or hospital records or information from their family. In addition to traditional risks for mortality, such as age (Hazard ratio, 1.73, 95% CI, 1.51-1.98, P<0.01), 25-OHVD level <50 nmol/l (HR 2.17, 1.27-3.72, P=0.01), prevalent malignancies (HR 5.60, 3.36-9.31, P<0.01) and existing osteoporosis (HR 2.14, 1.22-3.75, P=0.01) were found to be significant independent risk factors for all-cause mortality by using multivariate Cox's regression analysis. It is suggested that prevalent osteoporosis, prevalent malignancy or lower levels of 25-OHVD represent powerful risk factors for mortality.
据报道,低骨矿物质密度(BMD)、骨质疏松性骨折和低血清25-羟基维生素D(25-OHVD)水平会增加老年白种人的死亡风险。然而,关于老年亚洲女性骨矿物质密度或25-OHVD水平与死亡率之间的关系尚无可用数据。为了确定低骨矿物质密度(BMD)或低25-OHVD水平是否会增加死亡风险,我们对1232名绝经后门诊女性志愿者进行了一项前瞻性观察研究。从受试者那里获取了关于基线BMD、包括25-OHVD在内的生化指标血清水平、既往骨折、合并症和生活方式变量的信息。参与者总共被观察了6.9±3.6年(平均值±标准差),在观察期间共有107名参与者(8.7%)死亡。根据死亡证明、医院记录或其家人提供的信息对死亡率进行评估和确认。除了传统的死亡风险因素外,通过多变量Cox回归分析发现,年龄(风险比,1.73,95%可信区间,1.51 - 1.98,P<0.01)、25-OHVD水平<50 nmol/l(HR 2.17,1.27 - 3.72,P = 0.01)、既往恶性肿瘤(HR 5.60,3.36 - 9.31,P<0.01)和现患骨质疏松症(HR 2.14,1.22 - 3.75,P = 0.01)是全因死亡率的显著独立风险因素。提示现患骨质疏松症、既往恶性肿瘤或较低的25-OHVD水平是死亡的有力风险因素。