Neumeyer Ann M, Cano Sokoloff Natalia, McDonnell Erin, Macklin Eric A, McDougle Christopher J, Misra Madhusmita
Lurie Center for Autism, Massachusetts General Hospital, Lexington, MA; Harvard Medical School, Boston, MA.
Lurie Center for Autism, Massachusetts General Hospital, Lexington, MA.
J Pediatr. 2017 Feb;181:195-201.e6. doi: 10.1016/j.jpeds.2016.10.080. Epub 2016 Nov 22.
To test the hypothesis that bone accrual over a 4-year period is reduced in boys with autism spectrum disorder (ASD) compared with typically developing controls.
Twenty-five boys with ASD and 24 controls were assessed for bone outcomes. Fourteen boys with ASD and 11 controls were assessed both at baseline and after 4 years. The mean subject age was 11.0 ± 1.6 years at study initiation and 14.9 ± 1.6 years at follow-up. Bone mineral density (BMD) was measured at the spine, hip, and whole body using dual-energy X-ray absorptiometry and normalized for age, race, and sex (BMD z-scores). Height adjustments were performed as well. We assessed medical history, physical activity using questionnaires, vitamin D and calcium intake using food records, and serum calcium, phosphorus, 25(OH)-vitamin D, and pubertal hormone levels.
Boys with ASD had lower spine, hip, and whole body BMD z-scores compared with controls. In those subjects assessed both at baseline and after 4 years, bone accrual rates did not differ between the 2 groups; however, spine and hip BMD z-scores remained lower in the boys with ASD than in controls at follow-up. Notably, the ASD group was less physically active at both time points.
Although pubertal bone accrual was similar to that in controls, BMD in children with ASD remained low over a 4-year follow-up period, suggesting that low BMD is a consequence of prepubertal factors, such as low physical activity. Studies are needed to investigate the causes and consequences of decreased BMD, to assess BMD in females and adults with ASD, and to evaluate therapeutic interventions.
检验以下假设:与发育正常的对照组相比,患有自闭症谱系障碍(ASD)的男孩在4年期间的骨质积累减少。
对25名患有ASD的男孩和24名对照组进行了骨骼指标评估。14名患有ASD的男孩和11名对照组在基线和4年后均接受了评估。研究开始时受试者的平均年龄为11.0±1.6岁,随访时为14.9±1.6岁。使用双能X线吸收法测量脊柱、髋部和全身的骨密度(BMD),并根据年龄、种族和性别进行标准化(BMD z评分)。还进行了身高调整。我们评估了病史、使用问卷评估身体活动、使用食物记录评估维生素D和钙的摄入量,以及血清钙、磷、25(OH)-维生素D和青春期激素水平。
与对照组相比,患有ASD的男孩脊柱、髋部和全身的BMD z评分较低。在那些在基线和4年后均接受评估的受试者中,两组之间的骨质积累率没有差异;然而,随访时患有ASD的男孩脊柱和髋部的BMD z评分仍低于对照组。值得注意的是,ASD组在两个时间点的身体活动都较少。
尽管青春期骨质积累与对照组相似,但在4年的随访期内,患有ASD的儿童的BMD仍然较低,这表明低BMD是青春期前因素的结果,如身体活动不足。需要开展研究来调查BMD降低的原因和后果,评估患有ASD的女性和成年人的BMD,并评估治疗干预措施。