Wang Weijun, Li Sisheng, Niu Dongsheng
Department of Orthopaedics, No.7 People's Hospital of Zibo, Zibo Shandong, 255040, PR China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2010 Sep;24(9):1072-7.
To explore the significance and the relationship between osteoporosis and the mRNA expressions of vascular endothelial growth factor (VEGF) and bone morphogenetic protein 2 (BMP-2) in nontraumatic avascular necrosis of the femoral head (NONFH), so as to provide a theoretical basis for the pathogenesis and the clinical treatment of NONFH.
Sixty-nine specimens of femoral head were collected from voluntary donators undergoing total hip arthroplasty, including 37 cases of NONFH (NONFH group) and 32 cases of fresh femoral neck fracture (control group). In NONFH group, there were 26 males and 11 females with an average age of 57.3 years (range, 43-75 years), including 19 cases of steroid-induced avascular necrosis of the femoral head (ANFH), 16 cases of alcoholic ANFH, and 2 cases of idiopathic ANFH; according to Ficat staging system, there were 23 cases at stage III and 14 cases at stage IV. In control group, there were 23 males and 9 females with an average age of 58.6 years (range, 46-79 years). The NO level of serum, the Q value of femur, and the bone mineral density (BMD) of weight-bearing area were measured firstly. The bone tissues were harvested from weightbearing necrosis area and healthy area. The pathological change was observed by HE staining, the percentage of empty bone lacuna and the percentage of trabecular bone area were calculated. The mRNA expressions of VEGF and BMP-2 in femoral head were detected through in situ hybridization technique.
There were significant differences (P < 0.05) in the NO level of serum, the Q value of femur, and the BMD between NONFH group and control group. In NONFH group, the femoral head showed irregular shape, the articular cartilage exfoliated and collapsed. In weight-bearing necrosis area, the bone trabeculae were sparse and non-intact with a great number of empty lacuna; necrotic bone trabeculae were decomposed and absorbed; no obvious bone regeneration and repair were observed. In weight-bearing healthy area, the fat cells in bone marrow showed proliferation and hypertrophy. In control group, the femoral head had normal appearance, intact articular cartilage, and intact bone trabeculae with a regular arrange, and osteocytes were clearly seen. There were significant differences in the percentage of empty bone lacuna and the percentage of trabecular bone area between NONFH group and control group (P < 0.05). The mRNA expressions of VEGF and BMP-2 were positive in 2 groups. The positive area ratio, the absorbance value, and integral absorbance value of VEGF mRNA and BMP-2 mRNA in NONFH group were significantly lower than those in control group (P < 0.05); the grey scales of VEGF mRNA and BMP-2 mRNA in NONFH group were significantly higher than that in control group (P < 0.05).
The pathological stage of osteoporosis may play an important role in the mechanism of the NONFH. The decrease of mRNA expressions of VEGF and BMP-2 in femoral head of NONFH is important reason that affect its bone mass, osteoporosis, rehabilitation, and reconstruction. It may be benefit to the reparative process of the necrosis femoral head to increase the mRNA expressions of VEGF and BMP-2 in the femoral head.
探讨骨质疏松症与非创伤性股骨头缺血性坏死(NONFH)中血管内皮生长因子(VEGF)和骨形态发生蛋白2(BMP - 2)mRNA表达之间的关系及意义,为NONFH的发病机制及临床治疗提供理论依据。
收集69例接受全髋关节置换术的自愿捐献者的股骨头标本,其中37例为NONFH(NONFH组),32例为新鲜股骨颈骨折(对照组)。NONFH组中,男26例,女11例,平均年龄57.3岁(范围43 - 75岁),其中激素性股骨头缺血性坏死(ANFH)19例,酒精性ANFH 16例,特发性ANFH 2例;按Ficat分期系统,Ⅲ期23例,Ⅳ期14例。对照组中,男23例,女9例,平均年龄58.6岁(范围46 - 79岁)。首先检测血清NO水平、股骨Q值及负重区骨密度(BMD)。从负重坏死区和健康区获取骨组织。通过HE染色观察病理变化,计算空骨陷窝百分比和小梁骨面积百分比。采用原位杂交技术检测股骨头中VEGF和BMP - 2的mRNA表达。
NONFH组与对照组血清NO水平、股骨Q值及BMD比较,差异有统计学意义(P < 0.05)。NONFH组股骨头外形不规则,关节软骨剥脱、塌陷。负重坏死区骨小梁稀疏、不完整,大量空陷窝;坏死骨小梁分解吸收,未见明显骨再生及修复。负重健康区骨髓脂肪细胞增生肥大。对照组股骨头外观正常,关节软骨完整,骨小梁完整且排列规则,可见骨细胞。NONFH组与对照组空骨陷窝百分比和小梁骨面积百分比比较,差异有统计学意义(P < 0.05)。两组VEGF和BMP - 2的mRNA表达均为阳性。NONFH组VEGF mRNA和BMP - 2 mRNA的阳性面积比、吸光度值及积分吸光度值均显著低于对照组(P < 0.05);NONFH组VEGF mRNA和BMP - 2 mRNA的灰度值显著高于对照组(P < 0.05)。
骨质疏松症的病理阶段可能在NONFH的发病机制中起重要作用。NONFH股骨头中VEGF和BMP - 2 mRNA表达降低是影响其骨量、骨质疏松、修复及重建的重要原因。增加股骨头中VEGF和BMP - 2 mRNA的表达可能有利于坏死股骨头的修复过程。