Department of Gerontology, Neurosciences, Head and Neck and Orthopedics, Catholic University of the Sacred Heart, Largo Agostino Gemelli, 8, 00168, Rome, Italy.
Aging Research Center, Karolinska Institutet and Stockholm University, Stockholm, Sweden.
Osteoporos Int. 2017 Oct;28(10):2929-2934. doi: 10.1007/s00198-017-4133-x. Epub 2017 Jul 6.
This study analyzed data of bone mineral density (BMD) from a large cohort of adults with Down syndrome (DS). BMD was found to decrease with age more rapidly in these subjects than in the general population, exposing adults with DS to an increased risk of osteoporosis and bone fracture.
Down syndrome (DS) in adulthood presents with a high prevalence of osteoporosis. However, in DS, bone mineral density (BMD) can be underestimated due to short stature. Furthermore, the rate of age-related decline in BMD and its association with gender in DS has been rarely evaluated or compared with the general population. The present study is aimed at assessing the variation of BMD with age and gender in a sample of adults with DS and to compare these data with those of the general population, after adjusting for anthropometric differences.
Adults with DS, aged 18 or older, were assessed dual-energy-X-ray-absorptiometry (DXA) at the femoral neck and at the lumbar spine. They were compared with the general population enrolled in the National Health and Nutrition Examination Survey (NHANES) 2009-2010 dataset. Bone mineral apparent density (BMAD) was calculated for each individual.
DXA was evaluated in 234 subjects with DS (mean age 36.93 ± 11.83 years, ranging from 20 to 69 years; 50.4% females). In the lumbar spine both mean BMD (DS 0.880 ± 0.141 vs. NHANES 1.062 ± 0.167, p < 0.001) and BMAD (DS 0.138 ± 0.020 vs. NHANES 0.152 ± 0.020, p < 0.001) were significantly lower in the DS sample than in the NAHNES cohort. The same trend was observed at the femoral neck in both BMD (DS 0.658 ± 0.128 vs. NHANES 0.835 ± 0.137, p < 0.001) and BMAD (DS 0.151 ± 0.030 vs. NHANES 0.159 ± 0.028, p<0.001). Age was associated with lower femoral neck BMAD in both samples; importantly, this association was significantly stronger in the DS sample. In the lumbar spine region, no significant association between BMAD and age could be observed in both samples.
Adults with DS have lower bone mineral density compared to the general population and they experience a steeper decline with age. Early screening programs are needed in DS population.
本研究分析了一大群唐氏综合征(DS)成年人的骨密度(BMD)数据。结果发现,这些患者的 BMD 随年龄增长的下降速度快于普通人群,使 DS 成年人面临更高的骨质疏松症和骨折风险。
对年龄在 18 岁及以上的 DS 成年人进行双能 X 线吸收法(DXA)检测,测量股骨颈和腰椎的 BMD。并将这些数据与 2009-2010 年全国健康和营养调查(NHANES)数据库中的普通人群数据进行比较,以调整身高差异。
234 例 DS 患者接受了 DXA 评估(平均年龄 36.93±11.83 岁,年龄范围为 20-69 岁;女性占 50.4%)。在腰椎部位,DS 患者的平均 BMD(0.880±0.141 比 NHANES 0.1062±0.167,p<0.001)和 BMAD(0.138±0.020 比 NHANES 0.152±0.020,p<0.001)均显著低于 NHANES 队列。同样的趋势也出现在股骨颈部位,BMD(0.658±0.128 比 NHANES 0.835±0.137,p<0.001)和 BMAD(0.151±0.030 比 NHANES 0.159±0.028,p<0.001)均低于 NHANES 队列。年龄与两组的股骨颈 BMAD 降低相关;重要的是,这种关联在 DS 组更为明显。在腰椎部位,两组均未观察到 BMAD 与年龄之间的显著相关性。
与普通人群相比,DS 成年人的骨密度较低,且随年龄增长而下降的速度更快。DS 人群需要早期筛查计划。