山东大学学报(医学版) ›› 2017, Vol. 55 ›› Issue (5): 103-107.doi: 10.6040/j.issn.1671-7554.0.2016.1681
徐大霞1,侯楠2,李晓峰1,王闯1,孔猛1,焦广俊1,陈允震1
XU Daxia1, HOU Nan2, LI Xiaofeng1, WANG Chuang1, KONG Meng1, JIAO Guangjun1, CHEN Yunzhen1
摘要: 目的 观察骨代谢在糖皮质激素性骨质疏松症(GIOP)进展过程中与糖皮质激素用药时间的关系及变化规律,并依据骨代谢变化趋势探讨GIOP的防治策略。 方法 检测应用GC控制病情的系统红斑狼疮患者117例和健康人群21例骨代谢标志物(β-CTX、T-P1NT、N-MIDOs),测定L1-4椎体骨密度。依据GC使用时间将患者分为7个亚组:Ⅰ组用药1~6个月,Ⅱ组用药7~12个月,Ⅲ组用药13~18个月,Ⅳ组用药19~24个月,Ⅴ组用药25~30个月,Ⅵ组用药31~36个月,Ⅶ组用药>36个月。 结果 Ⅰ组、Ⅱ组和Ⅲ组β-CTX较正常对照组明显升高,差异有统计学意义(P<0.05);Ⅵ组和Ⅶ组β-CTX较正常对照组明显减低,差异有统计学意义(P<0.05);Ⅳ组和Ⅴ组β-CTX较正常对照组无明显差异(P>0.05);应用GC的各亚组T-P1NT、N-MIDOs均较正常对照组明显减低,差异有统计学意义(P<0.05);Ⅱ~Ⅶ组骨密度较正常对照组明显减低,差异有统计学意义(P<0.05)。 结论 GIOP形成过程中,骨代谢是由高分解状态向低分解低成骨低转换状态转变。应用GC 1~18个月的SLE患者骨代谢状态处于高分解低成骨,应用GC 30个月以上的患者骨代谢状态处于低分解低成骨低转换状态。
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