期刊文献+

糖尿病患者血清一氧化氮水平对骨代谢影响 被引量:1

Influence of serum nitric oxide level on bone metabolism in diabetic patients
下载PDF
导出
摘要 目的探讨糖尿病患者血清一氧化氮水平对成骨细胞、Ⅰ型骨胶原代谢的作用。方法 对确诊1型和2型糖尿病的378例患者测定血清一氧化氮(NO)、一氧化氮合酶(NOS)(硝酸还原酶法)、骨钙素《BGP放免法)、尿脱氧吡啶啉(DPD化学发光法)、尿肌酐(Cr酶法),双能X线测定腰椎正位、前臂、髋部骨密度(BMD),并与同期体检的342例健康人群进行比较。结果 糖尿病患者血清NO、NOS显著高于对照组(P<0.001;P<0.05),BGP显著低于对照组(P<0.001),DPD/Cr则显著高于对照组(P<0.001)。糖尿病组和对照组NO与BGP、DPD及各部位BMD均无显著线性相关(P>0.05)。结论糖尿病患者成骨细胞代谢显著低于健康人而Ⅰ型骨胶原分解代谢则显著高于健康人,血清一氧化氮水平与成骨细胞和Ⅰ型骨胶原代谢无显著相关性。 Objective To study the effect of serum nitric oxide levels on osteoblast and type I ossein metabolism in diabetic patients. Methods Nitric oxide ( NO) , nitric oxide synthase ( NOS) and osteocalcin (BGP) were determined by radioimmunoassny, and urine deoxypyridinoline (DPD) by chemiluminescence in 378 patients with type 1 and type 2 diabetes mellitus. Bone mineral density (BMD) of lumbar vertebrae, hip and forearm were measured by dual energy X-ray absorptiometry(DEXA) .The results were compared with those of 342 healthy subjects at the same time. Results The serum levels of NO and NOS in diabetic patients were significantly higher than those in the controls (P < 0. 001, P < 0. 05). BGP was significantly lower than that in the controls but DPD/Cr markedly higher in diabetic patients( P < 0.001). There were no linear correlation between NO and BGP, DPD/Cr and BMD in the two groups( P > 0. 05). Conclusions The osteoblast metabolism in diabetic patients is significantly lower than that in healthy people, whereas the decomposition of type I is significantly higher. The serum NO level has no correlation with osteoblast and type I ossein metabolism.
出处 《中国骨质疏松杂志》 CAS CSCD 2004年第4期459-460,518,共3页 Chinese Journal of Osteoporosis
基金 广西壮族自治区科技厅科学基会资助项目(桂科回9920019)
关键词 血清一氧化氮 糖尿病患者 对照组 骨胶原 成骨细胞 骨代谢 BMD BGP 放免法 尿脱氧吡啶啉 <Keyword>Diabetes mellitus Nitric oxide Bone mineral density Bone metabolism
  • 相关文献

参考文献7

  • 1[1]Miep H, Helfrich, Deborah, et al. Expression of nitric oxide synthase isoforms in bone and bone cell cultures. J bone Miner Res, 1997, 12:1108-1112.
  • 2[2]Kioldrung MB. Skeletal tissue response to cytokines. Clin Orthop, 1990,258: 245-278.
  • 3[3]Ralston SH. The michael mason prize essay 1997, nitric oxide and bone:what a gas. Br J Rheumatol, 1997, 36:831-838.
  • 4[4]Mancini L, Becherini L, Benvenuti S, et al. Bioeffects of a nitric oxide donor in a human preosteoclastic cell line. Int J Clin Pharmacol Res,1997, 17:2-7.
  • 5[5]Robert J, De Marco G, Gangula P, et al. Cytokine induced nitric oxide inhibits bone resorption by inducing apoptosis of osteoclast progenitors and suppressing osteoclast activity.J Bone Miner Res,1997,12:1797-1801.
  • 6徐一甄,沈稚舟,方京冲,杨秀芳,朱禧星.糖尿病大鼠一氧化氮与骨代谢变化的研究[J].中华内分泌代谢杂志,2002,18(3):228-230. 被引量:8
  • 7颜晓东,黄忠,胡映玉,钟华,林碧.糖尿病患者血清钙调节激素及骨密度研究[J].广西医科大学学报,2002,19(5):614-616. 被引量:5

二级参考文献4

共引文献11

同被引文献14

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部