中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2014年
21期
1643-1646
,共4页
朱浪静%欧阳霞%郑东辉%马剑达%陈乐锋%韦秀宁%莫颖倩%戴冽
硃浪靜%歐暘霞%鄭東輝%馬劍達%陳樂鋒%韋秀寧%莫穎倩%戴冽
주랑정%구양하%정동휘%마검체%진악봉%위수저%막영천%대렬
类风湿关节炎%滑膜%TRAF6%骨代谢标志物
類風濕關節炎%滑膜%TRAF6%骨代謝標誌物
류풍습관절염%활막%TRAF6%골대사표지물
Rheumatoid arthritis%Synovium%TRAF6%Bone metabolism marker
目的:了解类风湿关节炎( RA)患者滑膜肿瘤坏死因子受体相关因子6( TRAF6)表达及其与血清骨代谢标志物的相关性。方法2010年4月至2012年12月在中山大学孙逸仙纪念医院采用电化学发光法检测51例确诊RA患者和102例健康对照者的血清骨代谢标志物I型前胶原氨基端前肽( PINP)、骨钙素降解产物( N-MID.OC)和I型胶原C末端肽( CTX-I)的水平并分析其与临床疾病活动指标的相关性。免疫组化染色检测30例活动期RA患者滑膜TRAF6表达,评估TRAF6+细胞数并分析其与骨代谢标志物之间的相关性。结果 RA患者血清CTX-I水平明显高于健康对照组[(0.53±0.33)×10-3比(0.33±0.16)×10-3 g/L,P<0.01]。 RA患者血清PINP和N-MID.OC与晨僵时间、健康评估问卷HAQ评分、疼痛VAS评分呈负相关( P<0.05)。 RA患者血清PINP与双手平均握力呈正相关( r=0.296, P<0.05)。 RA滑膜衬里层和衬里下层均见TRAF6表达,且TRAF6表达在重度滑膜炎组高于轻度滑膜炎组。 RA患者滑膜组织TRAF6表达与PINP和N-MID.OC呈正相关(r=0.381,0.345, P<0.05)。结论 RA患者存在骨吸收增加、骨代谢失衡,其滑膜TRAF6表达增加可能与RA代偿性骨形成增加有关,TRAF6可能通过介导滑膜炎症参与了RA的骨代谢失衡。
目的:瞭解類風濕關節炎( RA)患者滑膜腫瘤壞死因子受體相關因子6( TRAF6)錶達及其與血清骨代謝標誌物的相關性。方法2010年4月至2012年12月在中山大學孫逸仙紀唸醫院採用電化學髮光法檢測51例確診RA患者和102例健康對照者的血清骨代謝標誌物I型前膠原氨基耑前肽( PINP)、骨鈣素降解產物( N-MID.OC)和I型膠原C末耑肽( CTX-I)的水平併分析其與臨床疾病活動指標的相關性。免疫組化染色檢測30例活動期RA患者滑膜TRAF6錶達,評估TRAF6+細胞數併分析其與骨代謝標誌物之間的相關性。結果 RA患者血清CTX-I水平明顯高于健康對照組[(0.53±0.33)×10-3比(0.33±0.16)×10-3 g/L,P<0.01]。 RA患者血清PINP和N-MID.OC與晨僵時間、健康評估問捲HAQ評分、疼痛VAS評分呈負相關( P<0.05)。 RA患者血清PINP與雙手平均握力呈正相關( r=0.296, P<0.05)。 RA滑膜襯裏層和襯裏下層均見TRAF6錶達,且TRAF6錶達在重度滑膜炎組高于輕度滑膜炎組。 RA患者滑膜組織TRAF6錶達與PINP和N-MID.OC呈正相關(r=0.381,0.345, P<0.05)。結論 RA患者存在骨吸收增加、骨代謝失衡,其滑膜TRAF6錶達增加可能與RA代償性骨形成增加有關,TRAF6可能通過介導滑膜炎癥參與瞭RA的骨代謝失衡。
목적:료해류풍습관절염( RA)환자활막종류배사인자수체상관인자6( TRAF6)표체급기여혈청골대사표지물적상관성。방법2010년4월지2012년12월재중산대학손일선기념의원채용전화학발광법검측51례학진RA환자화102례건강대조자적혈청골대사표지물I형전효원안기단전태( PINP)、골개소강해산물( N-MID.OC)화I형효원C말단태( CTX-I)적수평병분석기여림상질병활동지표적상관성。면역조화염색검측30례활동기RA환자활막TRAF6표체,평고TRAF6+세포수병분석기여골대사표지물지간적상관성。결과 RA환자혈청CTX-I수평명현고우건강대조조[(0.53±0.33)×10-3비(0.33±0.16)×10-3 g/L,P<0.01]。 RA환자혈청PINP화N-MID.OC여신강시간、건강평고문권HAQ평분、동통VAS평분정부상관( P<0.05)。 RA환자혈청PINP여쌍수평균악력정정상관( r=0.296, P<0.05)。 RA활막츤리층화츤리하층균견TRAF6표체,차TRAF6표체재중도활막염조고우경도활막염조。 RA환자활막조직TRAF6표체여PINP화N-MID.OC정정상관(r=0.381,0.345, P<0.05)。결론 RA환자존재골흡수증가、골대사실형,기활막TRAF6표체증가가능여RA대상성골형성증가유관,TRAF6가능통과개도활막염증삼여료RA적골대사실형。
Objective To evaluate the correlation between synovial tumor necrosis factor receptor -associated factor ( TRAF) 6 expression and serum bone metabolism markers in rheumatoid arthritis ( RA).Methods Serum biochemical markers of bone formation ( N-terminal propeptide of type I collagen , PINP and N-terminal midfragment of osteocalcin , N-MID.OC) and bone resorption ( C-terminal telopeptide of type I collagen, CTX-I) were detected by chemiluminescence in 51 RA patients and 102 age and gender-matched healthy controls from Sun Yat-sen Memorial Hospital during the period of April 2010 to December 2012.Clinical and other serological parameters of reflecting RA activity and severity were collected and correlated with bone metabolism markers.TRAF6 was stained immunohistochemically in synovium from 30 active RA patients and the intensity of TRAF 6 +cells was analyzed semiquantitatively.Correlation between synovial TRAF6 expression and serum bone metabolism markers was analyzed.Results Serum CTX-I level was significantly higher in RA patients than healthy controls ( ( 0.53 ±0.33 ) ×10 -3 vs ( 0.33 ±0.16 ) × 10 -3 g/L, P<0.01 ).Serum PINP and N-MID.OC levels of RA patients were correlated negatively with morning stiffness (P<0.05), Health Assessment Questionnaire (HAQ) score (P<0.05) and pain visual analogue scales ( VAS) score ( P <0.05 ).Serum PINP level of RA patients correlated positively with gripping power (r=0.296, P<0.05).TRAF6 expression was observed in lining and sublining area of RA synovium and a higher expression of TRAF 6 was seen in patients with severe synovitis than those with mild synovitis.Significant correlation was found between synovial TRAF 6 expression and serum PINP level ( r=0.381, P<0.05), as well as serum N-MID.OC level (r=0.345, P<0.05).Conclusion Increased bone resorption and altered skeletal bone metabolism are present in RA.An elevated expression of synovial TRAF6 may be correlated with increased compensatory bone formation.And TRAF6 is probably involved in the pathogenesis of bone metabolism imbalance through modulating synovial inflammation in RA .