Henry Yvette M, Fatayerji Diana, Eastell Richard
Bone Metabolism Group, Division of Clinical Science (North), Northern General Hospital, Herries Road, S5 7AU, Sheffield, UK.
Osteoporos Int. 2004 Apr;15(4):263-73. doi: 10.1007/s00198-003-1542-9. Epub 2004 Feb 24.
The age at which peak bone mineral content (peak BMC) is reached remains controversial and the mechanism underlying bone mass "consolidation" is still undefined. The aims of this study were to investigate; (1) the timing of peak BMC by studying bone size and volumetric BMD (vBMD) as separate entities and (2) to determine the relative contributions of bone size and vBMD to bone mass "consolidation". A total of 132 healthy Caucasian children (63 boys and 69 girls, ages 11-19 years) and 134 healthy Caucasian adults (66 men and 68 women, ages 20-50 years) were studied. BMC was measured by DXA at the AP and lateral lumbar spine (LS) femoral neck (FN) and ultradistal radius (UDR). vBMD and bone volume (size) were estimated. Bone mass "consolidation" was examined between age 16 years to the age peak bone values were attained. During growth, BMC and bone size increased steeply with age and approximately 80-90% of peak values were achieved by late adolescence. vBMD at the spine and UDR (in women) increased gradually, but vBMD at the FN and UDR in men remained almost constant. During "consolidation", bone size continued to increase with little change in vBMD. Peak vBMD at the lumbar spine was reached at 22 and 29 years in men and women, respectively, but earlier at the FN at 12 years. At the UDR peak vBMD was achieved at age 19 years in women, with little change in men. In conclusion, peak vBMD and bone size are almost fully attained during late adolescence. Although speculative, the lack of change in vBMD during consolidation implies that the continued increase in bone mass may primarily be due to increases in bone size rather than increases in either trabecular volume, cortical thickness or the degree of mineralisation of existing bone matrix (vBMD). Skeletal growth and maturation is heterogeneous, but crucial in understanding how the origins of osteoporosis may begin during childhood and young adulthood.
达到峰值骨矿物质含量(峰值骨密度)的年龄仍存在争议,骨量“巩固”的潜在机制也尚未明确。本研究的目的是调查:(1)通过将骨大小和体积骨密度(vBMD)作为独立的实体进行研究来确定峰值骨密度的时间,以及(2)确定骨大小和vBMD对骨量“巩固”的相对贡献。共研究了132名健康的白种儿童(63名男孩和69名女孩,年龄11 - 19岁)和134名健康的白种成年人(66名男性和68名女性,年龄20 - 50岁)。通过双能X线吸收法(DXA)测量了前后位和侧位腰椎(LS)、股骨颈(FN)和桡骨远侧端(UDR)的骨密度。估算了vBMD和骨体积(大小)。在16岁至达到峰值骨值的年龄之间检查骨量“巩固”情况。在生长过程中,骨密度和骨大小随年龄急剧增加,到青春期后期达到峰值的约80 - 90%。脊柱和UDR(女性)的vBMD逐渐增加,但男性FN和UDR的vBMD几乎保持不变。在“巩固”过程中,骨大小持续增加,而vBMD变化不大。男性和女性腰椎的峰值vBMD分别在22岁和29岁时达到,但FN的峰值vBMD在12岁时更早达到。在UDR,女性在19岁时达到峰值vBMD,男性变化不大。总之,峰值vBMD和骨大小在青春期后期几乎完全达到。虽然只是推测,但在巩固过程中vBMD缺乏变化意味着骨量的持续增加可能主要是由于骨大小的增加,而不是小梁体积、皮质厚度或现有骨基质矿化程度(vBMD)的增加。骨骼生长和成熟是异质性的,但对于理解骨质疏松症如何在儿童期和青年期开始至关重要。