Hunan Provincial Key Laboratory of Metabolic Bone Diseases, National Clinical Research Center for Metabolic Diseases, Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, China.
Department of Endocrinology, The First Hospital of Lanzhou University, Lanzhou, China.
Front Endocrinol (Lausanne). 2022 Jul 22;13:927344. doi: 10.3389/fendo.2022.927344. eCollection 2022.
Clinical vertebral fractures and femoral neck fractures are severe osteoporotic fractures that increase morbidity and mortality. Anthropometric variables are associated with an increased risk of osteoporotic fractures, but it is not clear whether body surface area (BSA) has an effect on clinically severe osteoporotic fractures. The study included total of 3,694 cases of clinical vertebral fractures and femoral neck fractures (2,670 females and 1,024 males) and 3,694 controls without fractures who were matched with the cases by sex and age. There was a significant positive correlation between BSA and bone mineral density (BMD) in female and male fracture patients (females: = 0.430-0.471, < 0.001; males: = 0.338-0.414, < 0.001). There was a significant systematic increase in BMD in both genders at various skeletal sites, grouped by BSA quartile. The osteoporosis rates of the lumbar spine (97.9%), femoral neck (92.4%) and total hip (87.1%) in the female Q1 group were significantly higher than those in the Q4 group ( < 0.001), which were 80.0%, 57.9% and 36.9%, respectively, in the Q4 group; the osteoporosis rates of the lumbar spine, femoral neck, and total hip were 53.9%, 59.4%, and 36.3% in the male Q1 group, and 15.2%, 21.9%, and 7.03% in the Q4 group, which were significantly lower than those in the Q1 group ( < 0.001). In age-adjusted Cox regression models, the risk of fracture in the remaining three groups (Q2, Q3, and Q4) for weight, BMI, and BSA for both genders, compared with the highest quartile (Q1 by descending quartile stratification) were significantly higher. In models adjusted for age and BMD, only men in the BSA Q3 (HR = 1.55, 95% CI = 1.09-2.19) and BSA Q4 groups (HR = 1.41, 95% CI = 1.05-1.87) had significantly higher fracture risks. In models adjusted for age, height, weight, BMI, and BSA, low BMD was the greatest fracture risks for both sexes. Our results showed that BSA was closely related to BMD, prevalence of osteoporosis, and fracture risk, and that a decline in BSA may be a new potential risk factor for osteoporotic fractures in Chinese men.
临床椎体骨折和股骨颈骨折是严重的骨质疏松性骨折,会增加发病率和死亡率。人体测量变量与骨质疏松性骨折的风险增加相关,但尚不清楚体表面积(BSA)是否对临床严重骨质疏松性骨折有影响。该研究共纳入 3694 例临床椎体骨折和股骨颈骨折患者(2670 名女性和 1024 名男性)和 3694 名无骨折的对照者,这些对照者与病例按性别和年龄相匹配。女性和男性骨折患者的 BSA 与骨密度(BMD)之间存在显著的正相关(女性:=0.430-0.471, < 0.001;男性:=0.338-0.414, < 0.001)。在按 BSA 四分位数分组的不同骨骼部位,各性别组的 BMD 均有显著的系统升高。女性 Q1 组的腰椎(97.9%)、股骨颈(92.4%)和全髋(87.1%)的骨质疏松症发生率明显高于 Q4 组( < 0.001),Q4 组分别为 80.0%、57.9%和 36.9%;男性 Q1 组的腰椎、股骨颈和全髋骨质疏松症发生率分别为 53.9%、59.4%和 36.3%,而 Q4 组的发生率分别为 15.2%、21.9%和 7.03%,明显低于 Q1 组( < 0.001)。在年龄调整的 Cox 回归模型中,与最高四分位数(按四分位从高到低分层的 Q1)相比,男女两性剩余三个组(Q2、Q3 和 Q4)的体重、BMI 和 BSA 的骨折风险均显著增加。在调整年龄和 BMD 的模型中,仅男性 BSA Q3 组(HR=1.55,95%CI=1.09-2.19)和 BSA Q4 组(HR=1.41,95%CI=1.05-1.87)的骨折风险显著增加。在调整年龄、身高、体重、BMI 和 BSA 的模型中,低 BMD 是两性最大的骨折风险。我们的结果表明,BSA 与 BMD、骨质疏松症患病率和骨折风险密切相关,BSA 下降可能是中国男性骨质疏松性骨折的一个新的潜在危险因素。