Clinical Cell Biology, Vejle Hospital - Lillebaelt Hospital, Department of Regional Health Research, University of Southern Denmark, Vejle, Denmark; Orthopaedic Research Laboratory, Department of Orthopaedic Surgery & Traumatology, Odense University Hospital, Department of Clinical Research, University of Southern Denmark, Denmark.
Clinical Cell Biology, Vejle Hospital - Lillebaelt Hospital, Department of Regional Health Research, University of Southern Denmark, Vejle, Denmark.
Bone. 2018 Dec;117:70-82. doi: 10.1016/j.bone.2018.09.011. Epub 2018 Sep 18.
Cortical bone is remodeled by intracortical basic multicellular units (BMUs), whose end result can be observed as quiescent osteons in histological sections. These osteons offer a unique opportunity to investigate the BMU balance between the magnitude of bone resorption and subsequent bone formation at the BMU level. Our main objective was to investigate whether the latter parameters change between defined categories of osteons and with age, and to which extend these changes contribute to age-induced cortical porosity. Cortices of iliac bone specimens from 35 women (aged 16-78 years) with a higher porosity with age were investigated. A total of 3084 quiescent osteons reflecting 75% of the intracortical pores were histological examined. The osteons diameter, pore diameter, wall thickness, prevalence and contribution to the porosity were highly variable, but unchanged with age. Next, the osteons were categorized according to whether they reflected the remodeling of existing canals (type 2Q osteons) or the generation of new canals (type 1Q osteons). Type 2Q osteons versus type 1Q osteons: (i) had more frequently a pore diameter > 75 μm (7.4 vs. 1.3%; p < 0.001); (ii) had a larger mean pore diameter (40 ± 10 vs. 25 ± 4 μm; p < 0.001), osteon diameter (120 ± 21 vs. 94 ± 21 μm; p < 0.001) and wall thickness (40 ± 10 vs. 35 ± 9; p < 0.05); (iii) had a larger contribution to the cortical porosity (29 ± 18 vs. 8 ± 8%; p < 0.001); (iv) were more prevalent (44 ± 10 vs. 31 ± 11%; p < 0.001); and (v) were more prevalent with age. Collectively, this study demonstrates that quiescent osteons with age more frequently result from remodeling of existing canals, which in some cases had a more negative BMU balance. Still, the osteons showed no overall age-related change in their pore diameter i.e. BMU balance. In contrast to conventional wisdom, these data show that non-quiescent pores, not pores of quiescent osteons, were the main contributor to a higher cortical porosity.
皮质骨由皮质内基本多细胞单位(BMU)重塑,其最终结果可在组织学切片中观察到静止的骨单位。这些骨单位为研究 BMU 在骨吸收和随后的骨形成之间的平衡提供了独特的机会。我们的主要目的是研究这些参数是否在定义的骨单位类别之间以及随年龄而变化,以及这些变化在多大程度上导致皮质骨的年龄相关性多孔性。研究了来自 35 名女性(年龄 16-78 岁)的髂骨标本的皮质,这些女性的皮质随年龄增长而出现更高的多孔性。对 3084 个反映 75%皮质内孔的静止骨单位进行了组织学检查。骨单位直径、孔直径、壁厚度、发生率和对孔隙率的贡献高度可变,但不随年龄变化。接下来,根据骨单位是否反映了现有管腔的重塑(2Q 型骨单位)或新管腔的生成(1Q 型骨单位)对骨单位进行分类。2Q 型骨单位与 1Q 型骨单位相比:(i)更频繁地具有大于 75μm 的孔直径(7.4%比 1.3%;p<0.001);(ii)具有更大的平均孔直径(40±10μm 比 25±4μm;p<0.001)、骨单位直径(120±21μm 比 94±21μm;p<0.001)和壁厚度(40±10μm 比 35±9μm;p<0.05);(iii)对皮质孔隙率的贡献更大(29±18%比 8±8%;p<0.001);(iv)更常见(44±10%比 31±11%;p<0.001);(v)随年龄增长而更常见。总的来说,这项研究表明,随年龄增长的静止骨单位更频繁地来自于现有管腔的重塑,在某些情况下,这种重塑的 BMU 平衡更具负性。尽管如此,骨单位的孔径即 BMU 平衡并没有随年龄发生整体变化。与传统观点相反,这些数据表明,非静止的孔,而不是静止骨单位的孔,是皮质骨更高多孔性的主要原因。