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不宁腿综合征患者的突触前多巴胺能功能:与早期帕金森病有共同特征吗?

Presynaptic dopaminergic function in patients with restless legs syndrome: are there common features with early Parkinson's disease?

作者信息

Linke Rainer, Eisensehr Ilonka, Wetter Thomas-Christian, Gildehaus Franz-Josef, Pöpperl Gabriele, Trenkwalder Claudia, Noachtar Soheyl, Tatsch Klaus

机构信息

Department of Nuclear Medicine, University of Munich, Munich, Germany.

出版信息

Mov Disord. 2004 Oct;19(10):1158-62. doi: 10.1002/mds.20226.

Abstract

The cause of restless legs syndrome (RLS) is unknown, but an involvement of the dopaminergic system and a possible relation to Parkinson's disease (PD) is suggested by the positive response to dopaminergic treatment. We imaged the striatal dopamine transporter with [(123)I] N-(3-iodopropen-2-yl)-2beta-carbomethoxy-3beta-(chloro-phenyl) tropane ([(123)I]IPT) and single-photon emission computed tomography (SPECT) in 28 RLS patients, and compared the results with transporter binding in 29 patients with early PD and 23 age-matched controls. No difference in IPT binding was found between RLS patients and controls. IPT binding was correlated significantly with age in RLS patients and controls, whereas there was no relation with the duration of symptoms or severity of RLS. PD patients presented significant lower presynaptic IPT binding ipsi- and contralateral to the affected body side compared with RLS patients or controls. We found no common characteristics between RLS patients and patients with early PD detectable by dopamine transporter SPECT. Our results do not strengthen an identical pathophysiologic pathway between RLS and PD on the level of nigrostriatal presynaptic terminal function.

摘要

不宁腿综合征(RLS)的病因尚不清楚,但多巴胺能治疗的阳性反应提示多巴胺能系统受累且可能与帕金森病(PD)有关。我们用[(123)I] N-(3-碘丙烯-2-基)-2β-甲氧羰基-3β-(氯苯基)托烷([(123)I] IPT)和单光子发射计算机断层扫描(SPECT)对28例RLS患者的纹状体多巴胺转运体进行成像,并将结果与29例早期PD患者和23例年龄匹配的对照者的转运体结合情况进行比较。RLS患者与对照者之间未发现IPT结合存在差异。RLS患者和对照者中,IPT结合与年龄显著相关,而与RLS症状持续时间或严重程度无关。与RLS患者或对照者相比,PD患者患侧身体同侧和对侧的突触前IPT结合均显著降低。我们发现,通过多巴胺转运体SPECT检测,RLS患者与早期PD患者之间没有共同特征。我们的结果并未在黑质纹状体突触前终末功能水平上强化RLS与PD之间相同的病理生理途径。

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