Chevalley Thierry, Bonjour Jean-Philippe, Ferrari Serge, Rizzoli Rene
Division of Bone Diseases, Department of Rehabilitation and Geriatrics, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
J Bone Miner Res. 2009 Jan;24(1):144-52. doi: 10.1359/jbmr.080815.
Late menarche is a risk factor for fragility fractures. We hypothesized that pubertal timing-dependent alterations in bone structural components would persist from peak bone mass to menopause, independent of premenopausal bone loss. We studied the influence of menarcheal age (MENA) on femoral neck BMD (FN aBMD) by DXA and microstructure of distal tibia by HR-pQCT in healthy young adult (YAD; 20.4 +/- 0.6 [SD] yr, n = 124) and premenopausal middle-aged (PREMENO; 45.8 +/- 3.4 yr, n = 120) women. Median of MENA was 13.0 +/- 1.2 and 13.1 +/- 1.7 yr in YAD and PREMENO, respectively. In YAD and PREMENO (n = 244), FN aBMD (R = -0.29, p = 0.013), as well as total volumetric BMD (Dtot; R = -0.23, p = 0.006) and cortical thickness (Ct.Th; R = -0.18, p = 0.011) of distal tibia were inversely correlated to MENA. After segregation by the median of MENA in EARLY and LATE subgroups, the significant influences of both MENA (p = 0.004) and chronological age (p < 0.0001) were observed for FN aBMD and trabecular bone volume fraction of the distal tibia with similar differences in T-scores between LATE and EARLY subgroups in YAD (-0.36 and -0.31 T-scores) and PREMENO (-0.35 and -0.42 T-scores) women. Ct.Th was negatively influenced by MENA, whereas trabecular thickness (Tb.Th) was negatively influenced by chronological age. There was a striking inverse relationship between cross-sectional area and Ct.Th (R = -0.57, p < 0.001). In conclusion, the negative influence of late menarcheal age at weight-bearing sites as observed by the end of skeletal growth remains unattenuated a few years before menopause and is independent of premenopausal bone loss. Alterations in both bone mineral mass and microstructural components may explain the increased risk of fragility fractures associated with later menarcheal age.
初潮延迟是脆性骨折的一个风险因素。我们假设,青春期时间依赖性的骨结构成分改变会从骨量峰值持续到绝经,且独立于绝经前的骨质流失。我们通过双能X线吸收法(DXA)研究了初潮年龄(MENA)对健康年轻成年女性(YAD;20.4±0.6[标准差]岁,n = 124)和绝经前中年女性(PREMENO;45.8±3.4岁,n = 120)股骨颈骨密度(FN aBMD)的影响,并通过高分辨率外周定量CT(HR-pQCT)研究了胫骨远端的微观结构。YAD组和PREMENO组的MENA中位数分别为13.0±1.2岁和13.1±1.7岁。在YAD组和PREMENO组(n = 244)中,FN aBMD(R = -0.29,p = 0.013)以及胫骨远端的总体积骨密度(Dtot;R = -0.23,p = 0.006)和皮质厚度(Ct.Th;R = -0.18,p = 0.011)与MENA呈负相关。在根据MENA中位数分为早期和晚期亚组后,观察到MENA(p = 0.004)和实际年龄(p < 0.0001)对FN aBMD和胫骨远端小梁骨体积分数均有显著影响,YAD组(-0.36和-0.31 T值)和PREMENO组(-0.35和-0.42 T值)的晚期和早期亚组之间的T值存在相似差异。Ct.Th受MENA的负面影响,而小梁厚度(Tb.Th)受实际年龄的负面影响。横截面积与Ct.Th之间存在显著的负相关关系(R = -0.57,p < 0.001)。总之,在骨骼生长结束时观察到的初潮延迟对负重部位的负面影响在绝经前几年仍未减弱,且独立于绝经前的骨质流失。骨矿物质质量和微观结构成分的改变可能解释了与初潮延迟相关的脆性骨折风险增加的原因。