Service de Neurochirurgie.
Inserm U955 Team 14;
J Neurosurg. 2016 Aug;125(2):472-80. doi: 10.3171/2015.7.JNS15379. Epub 2016 Jan 8.
OBJECTIVE Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is a well-established therapy for motor symptoms in patients with pharmacoresistant Parkinson's disease (PD). However, the procedure, which requires multimodal perioperative exploration such as imaging, electrophysiology, or clinical examination during macrostimulation to secure lead positioning, remains challenging because the STN cannot be reliably visualized using the gold standard, T2-weighted imaging (T2WI) at 1.5 T. Thus, there is a need to improve imaging tools to better visualize the STN, optimize DBS lead implantation, and enlarge DBS diffusion. METHODS Gradient-echo sequences such as those used in T2WI suffer from higher distortions at higher magnetic fields than spin-echo sequences. First, a spin-echo 3D SPACE (sampling perfection with application-optimized contrasts using different flip angle evolutions) FLAIR sequence at 3 T was designed, validated histologically in 2 nonhuman primates, and applied to 10 patients with PD; their data were clinically compared in a double-blind manner with those of a control group of 10 other patients with PD in whom STN targeting was performed using T2WI. RESULTS Overlap between the nonhuman primate STNs segmented on 3D-histological and on 3D-SPACE-FLAIR volumes was high for the 3 most anterior quarters (mean [± SD] Dice scores 0.73 ± 0.11, 0.74 ± 0.06, and 0.60 ± 0.09). STN limits determined by the 3D-SPACE-FLAIR sequence were more consistent with electrophysiological edges than those determined by T2WI (0.9 vs 1.4 mm, respectively). The imaging contrast of the STN on the 3D-SPACE-FLAIR sequence was 4 times higher (p < 0.05). Improvement in the Unified Parkinson's Disease Rating Scale Part III score (off medication, on stimulation) 12 months after the operation was higher for patients who underwent 3D-SPACE-FLAIR-guided implantation than for those in whom T2WI was used (62.2% vs 43.6%, respectively; p < 0.05). The total electrical energy delivered decreased by 36.3% with the 3D-SPACE-FLAIR sequence (p < 0.05). CONCLUSIONS 3D-SPACE-FLAIR sequences at 3 T improved STN lead placement under stereotactic conditions, improved the clinical outcome of patients with PD, and increased the benefit/risk ratio of STN-DBS surgery.
深部脑刺激(DBS)对丘脑底核(STN)的刺激是治疗抗药性帕金森病(PD)患者运动症状的一种成熟疗法。然而,该手术需要在宏观刺激期间进行多模态围手术期探索,例如成像、电生理学或临床检查,以确保导联定位,这仍然具有挑战性,因为 STN 不能使用 T2 加权成像(T2WI)等金标准在 1.5T 下可靠地可视化。因此,需要改进成像工具以更好地可视化 STN,优化 DBS 导联植入,并扩大 DBS 扩散。方法:梯度回波序列(如 T2WI 中使用的那些)在更高的磁场下比自旋回波序列具有更高的失真。首先,设计了一种在 3T 下使用的自旋回波 3D SPACE(使用不同的翻转角演化进行应用优化对比的采样完美)FLAIR 序列,在 2 只非人类灵长类动物中进行了组织学验证,并应用于 10 名 PD 患者;以双盲方式将他们的数据与另一组 10 名 PD 患者的数据进行了临床比较,这些患者使用 T2WI 进行了 STN 靶向治疗。结果:在 3 只非人类灵长类动物的 STN 中,3D 组织学和 3D-SPACE-FLAIR 体积分割之间的重叠很高,前 3 个四分之一的 Dice 评分分别为 0.73 ± 0.11、0.74 ± 0.06 和 0.60 ± 0.09。由 3D-SPACE-FLAIR 序列确定的 STN 边界比由 T2WI 确定的边界更符合电生理边缘(分别为 0.9 毫米和 1.4 毫米)。STN 的成像对比度在 3D-SPACE-FLAIR 序列上高 4 倍(p < 0.05)。术后 12 个月,接受 3D-SPACE-FLAIR 引导植入的患者的统一帕金森病评定量表第三部分评分(停药、刺激)改善程度高于接受 T2WI 治疗的患者(分别为 62.2%和 43.6%;p < 0.05)。3D-SPACE-FLAIR 序列的总电能输送减少了 36.3%(p < 0.05)。结论:3T 下的 3D-SPACE-FLAIR 序列改善了立体定向条件下的 STN 导联放置,改善了 PD 患者的临床预后,并提高了 STN-DBS 手术的获益/风险比。