氧化应激和抗氧化剂在老年骨质疏松性髋部骨折中的作用。

Mustafa Aydın, Emre Avcı
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引用次数: 0

摘要

背景:骨质疏松症的特征定义为骨密度和骨量的减少,伴随着骨结构的恶化,这增加了骨的脆弱性和骨折的风险。骨质疏松症常随年龄增长而发展。在高危人群中,氧化损伤是一种常见的病理状况。氧化应激在骨质疏松症的发展和骨质疏松相关骨折的形成中起着关键作用。本研究旨在探讨氧化应激和抗氧化剂在老年骨质疏松性髋部骨折,特别是股骨粗隆间骨折和股骨颈骨折患者骨组织代谢中的作用。方法:采用幂次分析方法,选取24例65岁以上因跌倒后出现髋部疼痛,经x线检查诊断为髋部骨折(股骨粗隆间骨折或股骨颈骨折),在骨科创伤科住院并行手术治疗的患者。对照组由24名年龄和性别匹配的健康个体组成,没有骨折史,符合相同的排除标准。采用分光光度法测定血清样品的氧化应激水平和抗氧化参数,包括总抗氧化状态(TAS)、总氧化状态(TOS)、氧化应激指数(OSI)和对氧磷酶-1 (PON-1)。结果:患者组TAS (p=0.189)、OSI (p=0.110)水平明显低于对照组。相反,患者组的TOS (p=0.002)和PON-1 (p=0.013)水平显著高于对照组。结论:数据表明氧化负荷增加导致氧化平衡被破坏,从而导致抗氧化剂缺乏。更好地了解疾病的病理生理学,以及替代治疗方法和疾病标志物的发展,将有助于文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of oxidative stress and antioxidants in older individuals with osteoporotic hip fractures.

Background: Osteoporosis is characteristically defined as a decrease in bone density and mass, accompanied by the deterioration of bone structure, which increases bone fragility and the risk of fractures. Osteoporosis frequently develops with age. In high-risk populations, oxidative damage is a common pathological condition. Oxidative stress plays a critical role in the development of osteoporosis and the formation of osteoporosis-related fractures. This study aimed to investigate the role of oxidative stress and antioxidants in bone tissue metabolism among elderly individuals with osteoporotic hip fractures, specifically intertrochanteric femur fractures and femoral neck fractures, who presented to our department.

Methods: Based on power analysis, 24 patients over the age of 65 who presented with hip pain following a fall, were diagnosed with hip fractures (intertrochanteric or femoral neck fractures) on X-ray, were hospitalized in the Orthopedics and Traumatology Department, and underwent surgery were included in the study. A control group consisting of 24 healthy individuals matched for age and gender, with no history of fractures and meeting the same exclusion criteria, was also included. Levels of oxidative stress and antioxidant parameters, including total antioxidant status (TAS), total oxidant status (TOS), oxidative stress index (OSI), and paraoxonase-1 (PON-1), were measured in serum samples using spectrophotometric methods.

Results: The TAS (p=0.189) and OSI (p=0.110) levels in the patient group were significantly lower compared to the control group. Conversely, the TOS (p=0.002) and PON-1 (p=0.013) levels in the patient group were significantly higher than those in the control group.

Conclusion: The data indicate that oxidative balance is disrupted due to increased oxidative load and the resulting antioxidant deficiency. A better understanding of the pathophysiology of the disease, along with the development of alternative treatment approaches and disease markers, will contribute to the literature.

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