Department of Biochemistry, Education and Research Hospital of Antalya, TR-07310 Antalya, Turkey.
Aging Clin Exp Res. 2009 Aug-Oct;21(4-5):353-7. doi: 10.1007/BF03324927.
Mildly elevated homocysteine (Hcy) and oxidative stress are novel and potentially modifiable risk factors for post-menopausal osteoporosis. We hypothesized that imbalance of oxidant/ antioxidant status and increased Hcy concentration stimulates osteoporotic activity, leading to increased collagen I breakdown in post-menopausal women.
Patients were divided into 2 groups (NOP and OP). Group NOP had normal bone mineral density (BMD) and group OP low BMD. Thirty-four (69%) were in group OP and 15 (31%) in group NOP. Serum Total Antioxidant Status (TAS) and Total Peroxide (TPx) levels were determined with new automated methods. The study included measurement of Deoxypyridinoline (DPD).
In OP patients plasma t-Hcy, urine deoxypyridinoline and plasma TPx were significantly higher than those in NOP controls. In addition, OP patients also had lower TAS levels than controls, which represent the oxidative imbalance. Pearson's correlation analysis revealed a negative correlation between t-Hcy and TAS (p<0.038). A significant negative correlation was also found between TAS level and BMD values for the spine in OP patients (p<0.035). In contrast, a positive correlation between t-Hcy and TPx in OP patients was demonstrated significantly, r=0.52, p<0.029.
We show that the OP group had reduced TAS, whereas the elevated TPx was different from that in the NOP group. Slightly elevated homocysteinemia may contribute to increasing TPx and reducing TAS in the OP group. However, our results suggest a weak but negative relationship between TAS and BMD. Further investigations are needed to examine the relationship of oxidative stress as an endogenous bioactive agent to bone loss in post-menopausal women. Since oxidative stress is the imbalance between total oxidants and antioxidants in the body, any single oxidant/ antioxidant parameter may not reflect overall oxidative stress. Further studies are needed to understand the underlying mechanisms of these findings.
轻度升高的同型半胱氨酸(Hcy)和氧化应激是绝经后骨质疏松症的新型、潜在可改变的危险因素。我们假设,氧化应激状态的失衡和 Hcy 浓度的增加会刺激骨质疏松症的发生,导致绝经后妇女的 I 型胶原分解增加。
患者分为 2 组(NOP 和 OP)。NOP 组骨密度正常,OP 组骨密度降低。NOP 组 34 例(69%),OP 组 15 例(31%)。采用新的自动化方法测定血清总抗氧化状态(TAS)和总过氧化物(TPx)水平。研究包括测定脱氧吡啶啉(DPD)。
OP 患者的血浆总同型半胱氨酸(t-Hcy)、尿脱氧吡啶啉和血浆 TPx 明显高于 NOP 对照组。此外,OP 患者的 TAS 水平也低于对照组,表明存在氧化失衡。Pearson 相关分析显示,t-Hcy 与 TAS 呈负相关(p<0.038)。OP 患者的 TAS 水平与骨密度呈显著负相关(p<0.035)。相反,OP 患者的 t-Hcy 与 TPx 呈显著正相关,r=0.52,p<0.029。
我们发现 OP 组的 TAS 降低,而 TPx 升高与 NOP 组不同。轻度升高的同型半胱氨酸可能导致 OP 组 TPx 升高和 TAS 降低。然而,我们的结果表明 TAS 与 BMD 之间存在微弱的负相关关系。需要进一步的研究来检查氧化应激作为内源性生物活性物质与绝经后妇女骨丢失的关系。由于氧化应激是体内总氧化剂和抗氧化剂之间的失衡,任何单一的氧化剂/抗氧化剂参数都可能无法反映整体氧化应激。需要进一步的研究来了解这些发现的潜在机制。