中华外科杂志
中華外科雜誌
중화외과잡지
CHINESE JOURNAL OF SURGERY
2010年
17期
1305-1308
,共4页
石少辉%李子荣%王佰亮%孙伟%程立明%潘琳%王冉东
石少輝%李子榮%王佰亮%孫偉%程立明%潘琳%王冉東
석소휘%리자영%왕백량%손위%정립명%반림%왕염동
股骨头坏死%骨形态发生蛋白质类%硬化带%个性化治疗
股骨頭壞死%骨形態髮生蛋白質類%硬化帶%箇性化治療
고골두배사%골형태발생단백질류%경화대%개성화치료
Femur head necrosis%Bone morphogenetic proteins%Sclerosis rim%Individualized treatment
目的 通过对股骨头坏死(ONFH)患者硬化带形成情况进行回顾性分析及其组织学观察,探讨骨形态蛋白(BMP4)与硬化带关系,为股骨头坏死个性化治疗提供理论依据.方法 2005年11月至2007年11月共治疗激素性ONFH全髋关节置换患者184髋,患者平均年龄(47±7)岁,依此把患者分为高(>54岁)、中(40~54岁)和低(<40岁)3个年龄组,分析比较3组患者硬化带形成比率.从184髋中选取部分股骨头标本,包括高年龄组患者股骨头18髋,低年龄组11髋,中年龄组股骨头标本20髋(有无硬化带形成者各10髋).股骨头冠状面正中剖开,在负重区和非负重区取材,行常规HE染色、苦味酸-天狼星红染色、电镜制备和BMP4蛋白免疫组化染色.BMP4蛋白免疫组化染色强度用图像分析软件计算其平均光密度.结果 硬化带在组织学上表现为骨小梁增粗,结构紊乱,但骨细胞结构同正常骨细胞,且处于高分泌状态.中年龄组ONFH患者硬化带形成比例为71.4%(105/147),显著高于低年龄组患者(45.5%,5/11)和高年龄组患者(38.5%,10/26)(P均<0.01).中年组患者股骨头BMP4平均光密度为0.32±0.14,明显高于低年龄组0.20±0.17和高年龄组0.19±0.27,且差异具有统计学意义(P均<0.05);中年龄组患者无硬化带形成者BMP4平均光密度分别为0.16±0.1l,有硬化带形成患者为0.28±0.13,差异具有统计学意义(P<0.01).有硬化带形成患者出现髋关节疼痛到关节置换时间为(49±11)个月,显著长于无硬化带形成者(15±2)个月,差异具有统计学意义(P<0.01).结论 ONFH患者硬化带形成与BMP4表达强弱呈正相关,BMP的高表达可能促进硬化带的形成.
目的 通過對股骨頭壞死(ONFH)患者硬化帶形成情況進行迴顧性分析及其組織學觀察,探討骨形態蛋白(BMP4)與硬化帶關繫,為股骨頭壞死箇性化治療提供理論依據.方法 2005年11月至2007年11月共治療激素性ONFH全髖關節置換患者184髖,患者平均年齡(47±7)歲,依此把患者分為高(>54歲)、中(40~54歲)和低(<40歲)3箇年齡組,分析比較3組患者硬化帶形成比率.從184髖中選取部分股骨頭標本,包括高年齡組患者股骨頭18髖,低年齡組11髖,中年齡組股骨頭標本20髖(有無硬化帶形成者各10髖).股骨頭冠狀麵正中剖開,在負重區和非負重區取材,行常規HE染色、苦味痠-天狼星紅染色、電鏡製備和BMP4蛋白免疫組化染色.BMP4蛋白免疫組化染色彊度用圖像分析軟件計算其平均光密度.結果 硬化帶在組織學上錶現為骨小樑增粗,結構紊亂,但骨細胞結構同正常骨細胞,且處于高分泌狀態.中年齡組ONFH患者硬化帶形成比例為71.4%(105/147),顯著高于低年齡組患者(45.5%,5/11)和高年齡組患者(38.5%,10/26)(P均<0.01).中年組患者股骨頭BMP4平均光密度為0.32±0.14,明顯高于低年齡組0.20±0.17和高年齡組0.19±0.27,且差異具有統計學意義(P均<0.05);中年齡組患者無硬化帶形成者BMP4平均光密度分彆為0.16±0.1l,有硬化帶形成患者為0.28±0.13,差異具有統計學意義(P<0.01).有硬化帶形成患者齣現髖關節疼痛到關節置換時間為(49±11)箇月,顯著長于無硬化帶形成者(15±2)箇月,差異具有統計學意義(P<0.01).結論 ONFH患者硬化帶形成與BMP4錶達彊弱呈正相關,BMP的高錶達可能促進硬化帶的形成.
목적 통과대고골두배사(ONFH)환자경화대형성정황진행회고성분석급기조직학관찰,탐토골형태단백(BMP4)여경화대관계,위고골두배사개성화치료제공이론의거.방법 2005년11월지2007년11월공치료격소성ONFH전관관절치환환자184관,환자평균년령(47±7)세,의차파환자분위고(>54세)、중(40~54세)화저(<40세)3개년령조,분석비교3조환자경화대형성비솔.종184관중선취부분고골두표본,포괄고년령조환자고골두18관,저년령조11관,중년령조고골두표본20관(유무경화대형성자각10관).고골두관상면정중부개,재부중구화비부중구취재,행상규HE염색、고미산-천랑성홍염색、전경제비화BMP4단백면역조화염색.BMP4단백면역조화염색강도용도상분석연건계산기평균광밀도.결과 경화대재조직학상표현위골소량증조,결구문란,단골세포결구동정상골세포,차처우고분비상태.중년령조ONFH환자경화대형성비례위71.4%(105/147),현저고우저년령조환자(45.5%,5/11)화고년령조환자(38.5%,10/26)(P균<0.01).중년조환자고골두BMP4평균광밀도위0.32±0.14,명현고우저년령조0.20±0.17화고년령조0.19±0.27,차차이구유통계학의의(P균<0.05);중년령조환자무경화대형성자BMP4평균광밀도분별위0.16±0.1l,유경화대형성환자위0.28±0.13,차이구유통계학의의(P<0.01).유경화대형성환자출현관관절동통도관절치환시간위(49±11)개월,현저장우무경화대형성자(15±2)개월,차이구유통계학의의(P<0.01).결론 ONFH환자경화대형성여BMP4표체강약정정상관,BMP적고표체가능촉진경화대적형성.
Objectives To analyze retrospectively the formation and histological changes of sclerosis rim in patients with osteonecrosis of the femoral head ( ONFH), and to study the relationship between bone morphogenetic proteins (BMP4) and sclerosis rim, so as to acquire experimental and theoretical basis on individualized treatment for ONFH patients. Methods From November 2005 to November 2007,184 hips of steroid-induced ONFH inpatients were collected. The mean age was (47 ± 7 ) years, the patients weredivided into high ( more than 54 years old), middle (40-54 years old) and low ( less than 40 years old) age groups. Their clinical data were analyzed retrospectively according to gender and age. Parts of the femoral heads were selected for the study, including 18 hips in high age group,11 hips in low age group and 20 hipsin middle age group. Each 10 hips were selected with or without sclerosis rim. The femoral heads were cut along middle coronal plane, their weight-bearing and non-weight-bearing areas were used for the study. The specimens were processed by routine HE staining and picric acid-Sirius red staining and electron microscopy preparation and immunohistocheministry stain. The average optical density of BMP4 protein was calculated by image analysis software. Results The trabecular of sclerosis rim was thickening and disorder. But its osteocytes were normal and with high secretion. The ratio of sclerosis rim was 71.4% (105/147) in middle age ONFH patients, which was significantly higher than the low age group patients (45. 5% ,5/11 ) and high age group patients ( 38.5%, 10/26 ) ( P < 0. 01 ). The optical density of BMP4 in middle age ONFH patients was 0. 32 ±0. 14, which was significantly higher than the low age group 0. 20 ±0. 17 and high age patients 0. 19 ±0. 27 ( P < 0. 05 ). The optical density was 0. 16 ± 0. 11 in ONFH patients without sclerosis rim,which was significantly lower than with sclerosis rim (0. 28 ± 0. 13 ) (P <0. 01 ). The time from hip pain to joint replacement in patients with sclerosis rim was ( 49 ± 11 ) months, and ( 15 ± 2 ) months without sclerosis rim. There was significant difference between the two groups ( P < 0. 01 ). Conclusions The formation of sclerosis rim is positively related to the expression of BMP4, and high expression of BMP maybe promote the formation of sclerosis rim.