Schwarz Johannes, Storch Alexander, Koch Walter, Pogarell Oliver, Radau Perry E, Tatsch Klaus
Department of Neurology, University of Leipzig, Leipzig, Germany.
J Nucl Med. 2004 Oct;45(10):1694-7.
Imaging of L-dopa uptake or dopamine transporter binding can monitor the progression of Parkinson's disease. Most follow-up studies have provided data best fitted by a linear decline of their outcome measure. However, in these studies, patients were repeatedly scanned during their first years after a diagnosis had been established.
We followed 6 patients with early Parkinson's disease for 7.5 y using 123I-labeled N-(3-iodopropene-2-yl)-2beta-carbomethoxy-3beta-(4-chlorophenyl) tropane and SPECT.
Loss of dopamine transporter binding was best fitted using a single exponential approximation. A 63% loss (tau [time constant tau]) was calculated as 5.18 +/- 7.62 y in the putamen and 10.62 +/- 31.4 y in the caudate nucleus when a 3-parameter fit was used.
These data approximate, for what is to our knowledge the first time, the decline of dopamine transporter binding as expected in biologic systems and may allow for models that correct for exponential decline to be developed and for disease-modifying effects in patients with advanced disease to be determined.
左旋多巴摄取或多巴胺转运体结合的成像可监测帕金森病的进展。大多数随访研究提供的数据最适合用其结果测量的线性下降来拟合。然而,在这些研究中,患者在确诊后的头几年内被反复扫描。
我们使用123I标记的N-(3-碘丙烯-2-基)-2β-甲氧基羰基-3β-(4-氯苯基)托烷和单光子发射计算机断层扫描(SPECT)对6例早期帕金森病患者进行了7.5年的随访。
多巴胺转运体结合的丧失最适合用单指数近似来拟合。当使用三参数拟合时,壳核中63%的丧失(时间常数τ)计算为5.18±7.62年,尾状核中为10.62±31.4年。
据我们所知,这些数据首次近似了生物系统中预期的多巴胺转运体结合的下降情况,并可能有助于开发校正指数下降的模型,以及确定晚期疾病患者的疾病修饰效应。