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人体胫骨皮质中无酶糖基化、吸收与微损伤之间的关联。

Association between non-enzymatic glycation, resorption, and microdamage in human tibial cortices.

作者信息

Ural Ani, Janeiro Colleen, Karim Lamya, Diab Tamim, Vashishth Deepak

机构信息

Department of Mechanical Engineering, Villanova University, 800 Lancaster Avenue, Villanova, PA 19085, USA.

Department of Biomedical Engineering, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

出版信息

Osteoporos Int. 2015 Mar;26(3):865-873. doi: 10.1007/s00198-014-2938-4. Epub 2014 Oct 18.

Abstract

UNLABELLED

To better understand the association between different components of bone quality, we investigated the relationship among in vivo generated non-enzymatic glycation, resorption, and microdamage. The results showed negative correlation between advanced glycation end-products (AGEs) and resorption independent of age highlighting the interaction between these parameters that may lead to bone fragility.

INTRODUCTION

Changes in the quality of bone material contribute significantly to bone fragility. In order to establish a better understanding of the interaction of the different components of bone quality and their influence on bone fragility, we investigated the relationship between non-enzymatic glycation, resorption, and microdamage generated in vivo in cortical bone using bone specimens from the same donors.

METHODS

Total fluorescent advanced glycation end-products (AGEs) were measured in 96 human cortical bone samples from 83 donors. Resorption pit density, average resorption pit area, and percent resorption area were quantified in samples from 48 common donors with AGE measurements. Linear microcrack density and diffuse damage were measured in 21 common donors with AGE and resorption measurements. Correlation analyses were performed between all measured variables to establish the relationships among them and their variation with age.

RESULTS

We found that average resorption pit area and percent resorption area decreased with increasing AGEs independently of age. Resorption pit density and percent resorption area demonstrated negative age-adjusted correlation with diffuse damage. Furthermore, average resorption pit area, resorption pit density, and percent resorption area were found to decrease significantly with age.

CONCLUSIONS

The current study demonstrated the in vivo interrelationship between the organic constituents, remodeling, and damage formation in cortical bone. In addition to the age-related reduction in resorption, there is a negative correlation between AGEs and resorption independent of age. This inverse relationship indicates that AGEs alter the resorption process and/or accumulate in the tissue as a result of reduced resorption and may lead to bone fragility by adversely affecting fracture resistance through altered bone matrix properties.

摘要

未标注

为了更好地理解骨质量不同成分之间的关联,我们研究了体内产生的非酶糖基化、骨吸收和微损伤之间的关系。结果显示,晚期糖基化终产物(AGEs)与骨吸收之间存在负相关,且不受年龄影响,突出了这些参数之间的相互作用,这可能导致骨脆性增加。

引言

骨材料质量的变化对骨脆性有显著影响。为了更好地理解骨质量不同成分之间的相互作用及其对骨脆性的影响,我们使用来自相同供体的骨标本,研究了皮质骨中体内产生的非酶糖基化、骨吸收和微损伤之间的关系。

方法

在来自83名供体的96份人类皮质骨样本中测量总荧光晚期糖基化终产物(AGEs)。在48名有AGE测量值的共同供体的样本中,对骨吸收陷窝密度、平均骨吸收陷窝面积和骨吸收面积百分比进行量化。在21名有AGE和骨吸收测量值的共同供体中,测量线性微裂纹密度和弥漫性损伤。对所有测量变量进行相关性分析,以确定它们之间的关系及其随年龄的变化。

结果

我们发现,平均骨吸收陷窝面积和骨吸收面积百分比随AGEs增加而降低,且不受年龄影响。骨吸收陷窝密度和骨吸收面积百分比与弥漫性损伤呈负相关,且经年龄调整。此外,平均骨吸收陷窝面积、骨吸收陷窝密度和骨吸收面积百分比随年龄显著降低。

结论

当前研究证明了皮质骨中有机成分、重塑和损伤形成之间的体内相互关系。除了与年龄相关的骨吸收减少外,AGEs与骨吸收之间存在不受年龄影响的负相关。这种反向关系表明,AGEs改变骨吸收过程和/或由于骨吸收减少而在组织中积累,并可能通过改变骨基质特性对骨折抗性产生不利影响,从而导致骨脆性增加。

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