Aino M Kuusela, Emma A Honkanen, Elina Jaakkola, Elina Myller, Mikael Eklund, Simo Nuuttila, Kirsi-Marja Murtomäki, Tuomas Mertsalmi, Reeta Levo, Toni Ihalainen, Tommi Noponen, Tero Vahlberg, Juho Joutsa, Filip Scheperjans, Valtteri Kaasinen
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This link seems particularly meaningful in ET patients with additional neurological signs, such as slowness of movements, rigidity, or rest tremor (ET+).</p><p><strong>Objectives: </strong>To investigate the potential dopaminergic pathophysiology of ET+ and to compare it to PD.</p><p><strong>Methods: </strong>Fourty-three ET+ patients, 115 PD patients and 40 healthy controls were studied using [<sup>123</sup>I]FP-CIT SPECT imaging and clinical examinations. A median follow-up of 3.0 years was carried out to confirm the diagnoses. ET+ patients underwent an extended follow-up with a median of 7.7 years (range 4.3-9.8 years). Region-specific binding ratios of striatal DAT binding were compared among the groups and correlated with the MDS-UPDRS motor scores.</p><p><strong>Results: </strong>Bradykinesia scores were negatively associated with posterior putamen DAT binding in both the ET+ and PD groups, with the strongest correlation observed in finger tapping (F = 11.1, β = -0.10, 95%CI -0.16 to -0.04, P = 0.001). In ET+ patients, kinetic tremor asymmetry correlated with posterior putamen DAT binding asymmetry (r = 0.33, P = 0.043), indicating a relationship between more severe tremor and subtle contralateral DAT loss.</p><p><strong>Conclusions: </strong>In ET+, subtle increases in bradykinesia scores correlate with striatal dopaminergic dysfunction, while kinetic tremor asymmetry is associated with hemispheric DAT binding asymmetry. 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引用次数: 0
摘要
背景:虽然先前的影像学研究普遍显示特发性震颤(ET)的纹状体多巴胺转运体(DAT)结合正常,但新出现的证据表明,在这种情况下,部分多巴胺能机制和ET与帕金森病(PD)之间存在流行病学联系。这种联系在伴有其他神经学症状的ET患者中似乎特别有意义,如运动缓慢、僵硬或静止性震颤(ET+)。目的:探讨ET+的潜在多巴胺能病理生理机制,并与PD进行比较。方法:对43例ET+患者、115例PD患者和40例健康对照者进行[123I]FP-CIT SPECT显像和临床检查。中位随访时间为3.0年以确认诊断。ET+患者接受了中位数为7.7年(4.3-9.8年)的延长随访。比较各组间纹状体DAT结合的区域特异性结合率,并与MDS-UPDRS运动评分相关。结果:在ET+组和PD组中,运动迟缓评分与后壳核DAT结合呈负相关,其中在手指敲打中相关性最强(F = 11.1, β = -0.10, 95%CI -0.16 ~ -0.04, P = 0.001)。在ET+患者中,运动性震颤不对称与后壳核数据结合不对称相关(r = 0.33, P = 0.043),表明更严重的震颤与轻微的对侧数据丢失有关。结论:在ET+中,运动迟缓评分的轻微增加与纹状体多巴胺能功能障碍有关,而运动性震颤不对称与半球DAT结合不对称有关。这些发现支持部分多巴胺能参与ET+病理生理的概念。
Striatal Dopaminergic Function and Motor Slowing in Essential Tremor Plus.
Background: While previous imaging studies have generally shown normal striatal dopamine transporter (DAT) binding in essential tremor (ET), emerging evidence suggests a partial dopaminergic mechanism in this condition and an epidemiological link between ET and Parkinson's disease (PD). This link seems particularly meaningful in ET patients with additional neurological signs, such as slowness of movements, rigidity, or rest tremor (ET+).
Objectives: To investigate the potential dopaminergic pathophysiology of ET+ and to compare it to PD.
Methods: Fourty-three ET+ patients, 115 PD patients and 40 healthy controls were studied using [123I]FP-CIT SPECT imaging and clinical examinations. A median follow-up of 3.0 years was carried out to confirm the diagnoses. ET+ patients underwent an extended follow-up with a median of 7.7 years (range 4.3-9.8 years). Region-specific binding ratios of striatal DAT binding were compared among the groups and correlated with the MDS-UPDRS motor scores.
Results: Bradykinesia scores were negatively associated with posterior putamen DAT binding in both the ET+ and PD groups, with the strongest correlation observed in finger tapping (F = 11.1, β = -0.10, 95%CI -0.16 to -0.04, P = 0.001). In ET+ patients, kinetic tremor asymmetry correlated with posterior putamen DAT binding asymmetry (r = 0.33, P = 0.043), indicating a relationship between more severe tremor and subtle contralateral DAT loss.
Conclusions: In ET+, subtle increases in bradykinesia scores correlate with striatal dopaminergic dysfunction, while kinetic tremor asymmetry is associated with hemispheric DAT binding asymmetry. These findings support the concept of partial dopaminergic involvement in the pathophysiology of ET+.
期刊介绍:
Movement Disorders Clinical Practice- is an online-only journal committed to publishing high quality peer reviewed articles related to clinical aspects of movement disorders which broadly include phenomenology (interesting case/case series/rarities), investigative (for e.g- genetics, imaging), translational (phenotype-genotype or other) and treatment aspects (clinical guidelines, diagnostic and treatment algorithms)