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男孩中轴骨与附属骨骼生长的异质性:对男性骨脆性发病机制的影响

Heterogeneity in the growth of the axial and appendicular skeleton in boys: implications for the pathogenesis of bone fragility in men.

作者信息

Bradney M, Karlsson M K, Duan Y, Stuckey S, Bass S, Seeman E

机构信息

Department of Medicine, Austin and Repatriation Medical Center, University of Melbourne, Australia.

出版信息

J Bone Miner Res. 2000 Oct;15(10):1871-8. doi: 10.1359/jbmr.2000.15.10.1871.

Abstract

Men with spine fractures have reduced vertebral body (VB) volume and volumetric bone mineral density (vBMD). Men with hip fractures have reduced femoral neck (FN) volume and vBMD, site-specific deficits that may have their origins in growth. To describe the tempo of growth in regional bone size, bone mineral content (BMC), and vBMD, we measured bone length, periosteal and endocortical diameters, BMC, and vBMD using dual-energy X-ray absorptiometry in 184 boys aged between 7 and 17 years. Before puberty, growth was more rapid in the legs than in the trunk. During puberty, leg growth slowed while trunk length accelerated. Bone size was more advanced than BMC in all regions, being approximately 70% and approximately 35% of their predicted peaks at 7 years of age, respectively. At 16 years of age, bone size had reached its adult peak while BMC was still 10% below its predicted peak. The legs accounted for 48%, whereas the spine accounted for 10%, of the 1878 g BMC accrued between 7 and 17 years. Peripubertal growth contributed (i) 55 % of the increase in leg length but 78% of the mineral accrued and (ii) 69% of the increase in spine length but 87% of the mineral accrued. Increased metacarpal and midfemoral cortical thickness was caused by respective periosteal expansion with minimal change in the endocortical diameter. Total femur and VB vBMD increased by 30-40% while size and BMC increased by 200-300%. Thus, growth builds a bigger but only slightly denser skeleton. We speculate that effect of disease or a risk factor during growth depends on the regions maturational stage at the time of exposure. The earlier growth of a regions size than mass, and the differing growth patterns from region to region, predispose to site-specific deficits in bone size, vBMD, or both. Regions further from their peak may be more severely affected by illness than those nearer completion of growth. Bone fragility in old age is likely to have its foundations partly established during growth.

摘要

脊柱骨折的男性椎体(VB)体积和骨体积密度(vBMD)降低。髋部骨折的男性股骨颈(FN)体积和vBMD降低,这些特定部位的缺陷可能源于生长过程。为了描述区域骨大小、骨矿物质含量(BMC)和vBMD的生长节奏,我们使用双能X线吸收法测量了184名7至17岁男孩的骨长度、骨膜和内皮质直径、BMC和vBMD。青春期前,腿部生长比躯干生长更快。青春期期间,腿部生长放缓而躯干长度加速。所有区域的骨大小比BMC发育得更早,在7岁时分别约为其预测峰值的70%和约35%。16岁时,骨大小已达到成人峰值,而BMC仍比其预测峰值低10%。在7至17岁累积的1878克BMC中,腿部占48%,而脊柱占10%。青春期前后的生长贡献如下:(i)腿部长度增加的55%,但矿物质累积的78%;(ii)脊柱长度增加的69%,但矿物质累积的87%。掌骨和股骨中段皮质厚度增加分别是由于骨膜扩张,而内皮质直径变化最小。股骨和VB的总vBMD增加了30 - 40%,而大小和BMC增加了200 - 300%。因此,生长构建了一个更大但密度仅略有增加的骨骼。我们推测,生长期间疾病或风险因素的影响取决于暴露时各区域的成熟阶段。一个区域的大小比质量更早生长,且各区域生长模式不同,这易导致骨大小、vBMD或两者出现特定部位的缺陷。距离峰值较远的区域可能比接近生长完成的区域更容易受到疾病的严重影响。老年时的骨脆性可能部分在生长期间就已奠定基础。

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