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老年人肋骨皮质中线性微裂纹积累的变异性。

Variability of linear microcrack accumulation in the cortex of elderly human ribs.

作者信息

Agnew Amanda M, Dominguez Victoria M, Sciulli Paul W, Stout Sam D

机构信息

Skeletal Biology Research Lab, Injury Biomechanics Research Center, The Ohio State University, 333 W. 10th Ave., Columbus, OH 43210, USA; Department of Anthropology, The Ohio State University, 174 W. 18th Ave., Columbus, OH 43210, USA.

Skeletal Biology Research Lab, Injury Biomechanics Research Center, The Ohio State University, 333 W. 10th Ave., Columbus, OH 43210, USA.

出版信息

Bone Rep. 2017 Feb 21;6:60-63. doi: 10.1016/j.bonr.2017.02.004. eCollection 2017 Jun.

Abstract

Excessive accumulation of microdamage in the skeleton is believed to contribute to fragility and risk of fracture, particularly in the elderly. Current knowledge of how much damage accrual varies between individuals, if at all, is lacking. In this study, paired sixth ribs from five male and five female elderly individuals (76-92 years, mean age = 84.7 years) were examined using staining and fluorescent microcopy to quantify linear microcracks present at the time of death ( microdamage). Crack number, crack length, crack density, and crack surface density were measured for each complete cross-section, with densities calculated using the variable of bone area (which accounts for the influence of porosity on the cortex, unlike the more frequently used cortical area), and analyzed using a two-way mixed model analysis of variance. Results indicate that while microcracks between individuals differ significantly, differences between the left and right corresponding pairs within individuals and the pleural and cutaneous cortices within each rib did not. These results suggest that systemic influences, such as differential metabolic activity, affect the accumulation of linear microcracks. Furthermore, variation in remodeling rates between individuals may be a major factor contributing to differential fracture risk in the elderly. Future work should expand to include a wider age range to examine differences in microdamage accumulation across the lifespan, as well as considering the influence of bisphosphonates on microdamage accumulation in the context of compromised remodeling rates in the elderly.

摘要

骨骼中微损伤的过度积累被认为会导致骨骼脆弱和骨折风险增加,尤其是在老年人中。目前对于个体间微损伤积累量是否存在差异(若存在差异)的了解还很缺乏。在本研究中,对五名老年男性和五名老年女性(年龄76 - 92岁,平均年龄 = 84.7岁)的配对第六肋骨进行了检查,使用染色和荧光显微镜来量化死亡时存在的线性微裂纹(微损伤)。对每个完整横截面测量裂纹数量、裂纹长度、裂纹密度和裂纹表面密度,密度计算使用骨面积变量(该变量考虑了孔隙率对皮质的影响,与更常用的皮质面积不同),并采用双向混合方差分析模型进行分析。结果表明,虽然个体间的微裂纹存在显著差异,但个体内左右对应肋骨之间以及每根肋骨内的胸膜和皮肤皮质之间的差异并不显著。这些结果表明,诸如代谢活动差异等系统性影响会影响线性微裂纹的积累。此外,个体间重塑率的差异可能是导致老年人骨折风险差异的一个主要因素。未来的研究应扩大到包括更广泛的年龄范围,以研究整个生命周期中微损伤积累的差异,同时考虑双膦酸盐在老年人重塑率受损情况下对微损伤积累的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcd9/5365308/eedc2fb95d1c/gr1.jpg

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