2 型糖尿病患者股骨颈的微硬度较低,异质矿化较少,表明骨折风险较高

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2024-01-15 DOI:10.1093/jbmrpl/ziae005
Aleksandar Cirovic, Felix N Schmidt, Marko Vujačić, P. Sihota, Bojan Petrovic, Vladimir Živković, Zoran Bascarevic, S. Nikolić, D. Djonic, M. Djuric, Björn Busse, Petar Milovanovic
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引用次数: 0

摘要

人们对 2 型糖尿病(T2DM)患者更易骨折的微观结构原因的了解还很有限。在这项研究中,我们检测了 18 名发生低能量骨折的 T2DM 患者(T2DMFx:78 ± 7 岁,15 名女性和 3 名男性)和 20 名对照组患者(74 ± 7 岁,16 名女性和 4 名男性)的骨矿化、骨细胞裂隙参数和股骨颈小梁的微硬度。T2DMFx受试者的股骨颈是在一家三级骨科医院采集的,而对照组受试者的股骨颈是在尸检时采集的。与对照组相比,T2DMFx患者的骨小梁微硬度(p = 0.023)和矿化异质性(p = 0.001)较低,矿化度高于第95百分位数(p = 0.058)的骨面积也较低。每个骨面积的骨细胞裂隙数、每个骨面积的矿化裂隙数和每个骨面积的总裂隙数在组间无明显差异(均 p > 0.05)。根据血管并发症(VD)的存在将 T2DMFx 组划分为 T2DMFxVD(VD 存在)和 T2DMFxNVD(VD 不存在)后,我们观察到 T2DMFxVD 组的微硬度尤其降低(与对照组相比,p = 0.02),而矿化异质性在两个 T2DMFx 亚组中均显著降低(T2DMFxNVD 与对照组相比,p = 0.002;T2DMFxVD 与对照组相比,p = 0.038)。观察到的矿化和微硬度变化可能是导致 T2DM 患者髋部骨折易感性增加的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lower microhardness along with less heterogeneous mineralization in the femoral neck of individuals with type 2 diabetes mellitus indicates higher fracture risk
There is still limited understanding of the microstructural reasons for the higher susceptibility to fractures in individuals with type 2 diabetes mellitus (T2DM). In this study, we examined bone mineralization, osteocyte lacunar parameters, and microhardness of the femoral neck trabeculae in 18 individuals with T2DM who sustained low-energy fracture (T2DMFx: 78 ± 7 years, 15 women and 3 men) and 20 controls (74 ± 7 years, 16 women and 4 men). Femoral necks of the T2DMFx subjects were obtained at a tertiary orthopedic hospital, while those of the controls were collected at autopsy. T2DMFx individuals had lower trabecular microhardness (p = 0.023) and mineralization heterogeneity (p = 0.001), and a tendency to a lower bone area with mineralization above 95th percentile (p = 0.058) than the controls. There were no significant intergroup differences in the numbers of osteocyte lacunae per bone area, mineralized lacunae per bone area, and total lacunae per bone area (each p > 0.05). After dividing the T2DMFx group based on the presence of vascular complications (VD) to T2DMFxVD (VD present) and T2DMFxNVD (VD absent), we observed that microhardness was particularly reduced in the T2DMFxVD group (vs. control group, p = 0.02), while mineralization heterogeneity was significantly reduced in both T2DMFx subgroups (T2DMFxNVD vs. control, p = 0.002; T2DMFxVD vs. control, p = 0.038). The observed changes in mineralization and microhardness may contribute to the increased hip fracture susceptibility in individuals with T2DM.
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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