Saari Laura, Kivinen Katri, Gardberg Maria, Joutsa Juho, Noponen Tommi, Kaasinen Valtteri
From the Division of Clinical Neurosciences (L.S., J.J., V.K.), Turku University Hospital, Turku, Finland; Department of Neurology (L.S., J.J., V.K.) and Turku PET Centre (J.J., T.N., V.K.), University of Turku; and Departments of Pathology (K.K., M.G.) and Clinical Physiology and Nuclear Medicine (T.N.), Turku University Hospital and University of Turku, Finland.
Neurology. 2017 Apr 11;88(15):1461-1467. doi: 10.1212/WNL.0000000000003810. Epub 2017 Mar 10.
To examine possible associations between in vivo brain dopamine transporter SPECT imaging and substantia nigra pars compacta (SNc) neuronal survival in Parkinson disease (PD).
Nigral neuron numbers were calculated for 18 patients (11 patients with neuropathologically confirmed PD) who had been examined with dopamine transporter (DAT) SPECT before death. Correlation analyses between SNc tyrosine hydroxylase (TH)-positive and neuromelanin-containing neuron counts and DAT striatal specific binding ratios (SBRs) were performed with semiquantitative region of interest-based and voxel-based analyses.
Mean putamen SBR did not correlate with the number of substantia nigra TH-positive ( = -0.11, = 0.66) or neuromelanin-containing ( = -0.07, = 0.78) neurons. Correlations remained clearly nonsignificant when the time interval between SPECT and death was used as a covariate, when the voxel-based analysis was used, and when only patients with PD were included.
This cohort study demonstrates that postmortem SNc neuron counts are not associated with striatal DAT binding in PD. These results fit with the theory that there is no correlation between the number of substantia nigra neurons and striatal dopamine after a certain level of damage has occurred. Striatal DAT binding in PD may reflect axonal dysfunction or DAT expression rather than the number of viable neurons.
研究帕金森病(PD)患者体内脑多巴胺转运体SPECT成像与黑质致密部(SNc)神经元存活之间的可能关联。
对18例患者(11例经神经病理学证实为PD的患者)在死亡前进行多巴胺转运体(DAT)SPECT检查,计算黑质神经元数量。采用基于感兴趣区的半定量分析和基于体素的分析,对SNc酪氨酸羟化酶(TH)阳性神经元和含神经黑色素神经元计数与DAT纹状体特异性结合率(SBRs)进行相关性分析。
壳核平均SBR与黑质TH阳性神经元数量(r = -0.11,P = 0.66)或含神经黑色素神经元数量(r = -0.07,P = 0.78)均无相关性。当将SPECT与死亡之间的时间间隔作为协变量、采用基于体素的分析以及仅纳入PD患者时,相关性仍明显无统计学意义。
这项队列研究表明,PD患者死后SNc神经元计数与纹状体DAT结合无关联。这些结果符合以下理论,即在发生一定程度的损伤后,黑质神经元数量与纹状体多巴胺之间不存在相关性。PD患者纹状体DAT结合可能反映轴突功能障碍或DAT表达,而非存活神经元数量。