Department of Pediatrics, National Research Center, Cairo, Egypt.
Scand J Clin Lab Invest. 2011 Sep;71(5):387-93. doi: 10.3109/00365513.2011.573574. Epub 2011 Apr 8.
To assess bone mineral density (BMD), body composition by dual X-ray absorptiometry (DXA), and various biochemical markers of bone growth and resorption in a group of children with type 1 diabetes mellitus (T1DM).
The study included 47 patients with T1DM and 30 age- and sex-matched controls. Anthropometric measurements, biochemical markers for bone formation, bone resorption and DXA were done for all patients and controls.
Of our diabetes patients, seven (16.7 %), three (7.3 %), and 17 (41.5%) met diagnostic criteria for osteopenia at the right femur, lumbar spine and total body, respectively. On the other hand, osteoporosis as defined by the WHO criteria was diagnosed in 21 patients (51.2%) at the total body by DXA. Lean body mass and lean fat ratio were lower, while, total fat mass, abdominal fat%, soft tissue fat mass%, and fat/lean ratio were higher in diabetics compared to controls. Also, our patients showed lower serum osteocalcin, osteoprotegerin, procollagen type 1, and higher urinary deoxypyridinoline. Pubertal (diabetics and controls) have higher BMD and BMC than prepubertal.
Diabetic patients had a low BMD after adjustment (Z score), low bone formation and high bone resorption markers. Diabetes control and increase in BMI leads to a decrease in the incidence of low bone mineral density. Diabetes causes an increase in body fat especially abdominal fat which leads to an increase in insulin resistance and decrease in lean mass.
评估一组 1 型糖尿病(T1DM)儿童的骨矿物质密度(BMD)、双能 X 线吸收法(DXA)测定的身体成分以及骨生长和吸收的各种生化标志物。
本研究纳入了 47 例 T1DM 患者和 30 名年龄和性别匹配的对照组。对所有患者和对照组进行了人体测量学测量、骨形成、骨吸收的生化标志物以及 DXA。
在我们的糖尿病患者中,分别有 7 名(16.7%)、3 名(7.3%)和 17 名(41.5%)符合右侧股骨、腰椎和全身骨质疏松症的诊断标准。另一方面,根据 WHO 标准,通过 DXA 诊断出 21 名患者(51.2%)患有全身骨质疏松症。与对照组相比,瘦体重和瘦脂肪比降低,而总脂肪量、腹部脂肪%、软组织脂肪量%和脂肪/瘦体重比增加。此外,我们的患者血清骨钙素、骨保护素、I 型前胶原和脱氧吡啶啉水平降低,尿脱氧吡啶啉水平升高。青春期(糖尿病患者和对照组)的 BMD 和 BMC 高于青春期前。
调整(Z 评分)后,糖尿病患者的 BMD 较低,骨形成标志物降低,骨吸收标志物升高。控制糖尿病和增加 BMI 可降低低骨密度的发生率。糖尿病导致体脂增加,特别是腹部脂肪增加,从而导致胰岛素抵抗增加和瘦体重减少。