BACKGROUND:Modic changes (MC) are associated with low back pain (LBP). In this study, we compared changes in size and type of MC, after a single intravenous infusion of 5 mg zoledronic acid (ZA) or placebo, among chronic LBP patients with MC on magnetic resonance imaging (MRI), and evaluated whether the MRI changes correlate with symptoms. METHODS:All patients (N = 19 in ZA, 20 in placebo) had MRI at baseline (0.23-1.5 T) and at one year (1.5-3 T). We evaluated the level, type and volume of all the MC. The MC were classified into M1 (M1 (100%)), predominating M1 (M1/2 (65:35%)) or predominating M2 (M1/2 (35:65%)), and M2 (M2 (100%)). The first two were considered M1-dominant, and the latter two M2-dominant. Volumes of M1 and M2 were calculated separately for the primary MC, which was assumed to cause the symptoms, and the other MC. We analysed the one-year treatment differences in M1 and M2 volumes using analysis of covariance with adjustments for age, sex, body mass index, and smoking. The correlations between the MRI changes and the changes in LBP symptoms were analysed using Pearson correlations. RESULTS:In the ZA group, 84.2% of patients had M1-dominant primary MC at baseline, compared to 50% in the placebo group (p = 0.041). The primary MC in the ZA group converted more likely to M2-dominant (42.1% ZA, 15% placebo; p = 0.0119). The other MC (15 ZA, 8 placebo) were on average 42% smaller and remained largely M2-dominant. The M1 volume of the primary MC decreased in the ZA group, but increased in the placebo group (-0.83 cm3 vs 0.91 cm3; p = 0.21). The adjusted treatment difference for M1 volume was -1.9 cm3 (95% CI -5.0 to 1.2; p = 0.22) and for M2 volume 0.23 cm3 (p = 0.86). In the MC that remained M1-dominant, volume change correlated positively with increased symptoms in the placebo group, whereas the correlations were negative and weak in the ZA group. CONCLUSIONS:Zoledronic acid tended to speed up the conversion of M1-dominant into M2-dominant MC and decrease the volume of M1-dominant MC, although statistical significance was not demonstrated. TRIAL REGISTRATION:The registration number in ClinicalTrials.gov is NCT01330238 and the date of registration February 11, 2011.

译文

背景:Modic change(MC)与下背痛(LBP)相关。在这项研究中,我们比较了在接受磁共振成像(MRI)的MC的慢性LBP患者中,单次静脉注射5 mg唑来膦酸(ZA)或安慰剂后MC的大小和类型的变化,并评估了MRI是否改变与症状相关。
方法:所有患者(ZA中N = 19,安慰剂中20)在基线(0.23-1.5 T)和一年(1.5-3 T)均接受MRI检查。我们评估了所有MC的级别,类型和体积。 MC分为M1(M1(100%)),M1(M1 / 2(65:35%))或M2(M1 / 2(35:65%))以及M2(M2(100%) )。前两个被认为是M1主导,后两个被认为是M2主导。 M1和M2的体积分别针对假定会引起症状的主MC和其他MC进行计算。我们使用年龄,性别,体重指数和吸烟调整的协方差分析,分析了M1和M2量在一年治疗中的差异。使用Pearson相关性分析MRI变化与LBP症状变化之间的相关性。
结果:在ZA组中,有84.2%的患者在基线时具有M1为主的原发性MC,而在安慰剂组中则为50%(p = 0.041)。 ZA组中的主要MC更有可能转化为M2型(42.1%ZA,15%安慰剂; p = 0.0119)。另一个MC(15 ZA,8个安慰剂)平均缩小了42%,并且仍以M2为主。在ZA组中,主要MC的M1体积减少,但在安慰剂组中增加(-0.83 cm3对0.91 cm3; p = 0.21)。 M1体积的调整后治疗差异为-1.9 cm3(95%CI -5.0至1.2; p = 0.22),M2体积为0.23 cm3(p = 0.86)。在以M1为主的MC中,安慰剂组的体量变化与症状增加呈正相关,而ZA组的相关性为负而微弱。
结论:唑来膦酸具有加速M1主导型向M2主导型MC转化的作用,并降低M1主导型MC的体积,尽管没有统计学意义。
试用注册:ClinicalTrials.gov中的注册号为NCT01330238,注册日期为2011年2月11日。

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