Yamaguchi Katsuyuki, Masuhara Kensaku, Yamasaki Satoshi, Fuji Takeshi, Seino Yoshiki
Department of Orthopaedic Surgery, Kaizuka City Hospital, Hori, Kaizuka, Osaka 597-0015, Japan.
Bone. 2004 Jul;35(1):217-23. doi: 10.1016/j.bone.2004.03.017.
We previously reported the effects of cyclic therapy with etidronate (CTE) on periprosthetic bone mineral density (BMD) after cementless total hip arthroplasty (THA). This study aimed to evaluate the effects of withdrawal and intervention of CTE after cementless THA. The control group consisted of 24 patients without osteoactive drugs. Sixteen patients continued on CTE (i.e., 400 mg/day oral etidronate for 2 weeks followed by 12 weeks of 500 mg/day calcium lactate, repeated every 14 weeks) for the first 12 months followed by no treatment for 18 months (early-etidronate group). Fifteen patients received no treatment for the first 18 months followed by CTE for 12 months (late-etidronate group). Periprosthetic BMD in seven regions of interest based on the zones of Gruen et al. was measured with dual energy X-ray absorptiometry at 3 weeks, 6, 12, 18, 24, and 30 months postoperatively. At 12 months after operation (off therapy point in the early-etidronate group), postoperative decreases of BMD in the early-etidronate group were significantly smaller than those in the control group in zones 1, 2, 5, 6, and 7 and those in the late-etidronate group in zones 1, 5, 6, and 7 (P < 0.05 for each). In the early-etidronate group, significant decreases in BMD were found during months 12-30 (off therapy period) after withdrawal of CTE in zones 1 and 7 (P < 0.05 for each). In the late-etidronate group, BMD increased significantly in zones 4 and 6 (P < 0.05 for each) during months 18-30 (on therapy period) after intervention trial, while in the controls, BMD decreased significantly in zone 3 (P < 0.05) over this period. At the final follow-up (30 months), BMD loss in zone 7 was significantly less in the early-etidronate group than in the other groups (P < 0.05). BMD changes in the early-etidronate group and late-etidronate group were associated with changes in biochemical bone markers.
我们之前报道了依替膦酸循环疗法(CTE)对非骨水泥型全髋关节置换术(THA)后假体周围骨密度(BMD)的影响。本研究旨在评估非骨水泥型THA后CTE停药及再次干预的效果。对照组由24例未使用骨活性药物的患者组成。16例患者在最初12个月持续接受CTE治疗(即口服依替膦酸400mg/天,持续2周,随后口服乳酸钙500mg/天,持续12周,每14周重复一次),之后18个月不接受治疗(早期依替膦酸组)。15例患者在最初18个月不接受治疗,之后接受CTE治疗12个月(晚期依替膦酸组)。术后3周、6个月、12个月、18个月、24个月和30个月时,采用双能X线吸收法测量基于Gruen等分区的七个感兴趣区域的假体周围骨密度。术后12个月(早期依替膦酸组的停药时间点),早期依替膦酸组1区、2区、5区、6区和7区的术后骨密度降低幅度显著小于对照组,1区、5区、6区和7区的术后骨密度降低幅度也显著小于晚期依替膦酸组(各区域P<0.05)。在早期依替膦酸组,CTE停药后12 - 30个月(停药期)期间,1区和7区的骨密度显著降低(各区域P<0.05)。在晚期依替膦酸组,干预试验后18 - 30个月(治疗期)期间,4区和6区的骨密度显著增加(各区域P<0.05),而在此期间对照组3区的骨密度显著降低(P<0.05)。在最终随访(30个月)时,早期依替膦酸组7区的骨密度损失显著低于其他组(P<0.05)。早期依替膦酸组和晚期依替膦酸组的骨密度变化与生化骨标志物的变化相关。