Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9186545 | Autonomic Neuroscience | 2005 | 5 Pages |
Abstract
We compared MIBG uptake at various parts of the body in controls and patients with Parkinson's disease and multiple system atrophy. In the heart, MIBG uptake in Parkinson's disease (early H/M: 1.668 ± 0.325, late H/M: 1.500 ± 0.402) was less than that in multiple system atrophy (early H/M: 2.395 ± 0.186, late H/M: 2.530 ± 0.391) and controls (early H/M: 2.635 ± 0.508, late H/M: 2.575 ± 0.635) (early: P < 0.0001, late: P < 0.0001). There were no significant differences in uptake by the lung, thyroid, or liver in the three groups. Only on early images, uptake in the shoulder in multiple system atrophy (early S/M: 0.473 ± 0.78) and Parkinson's disease (early S/M: 0.470 ± 0.710) was decreased compared to that in controls (early S/M: 0.560 ± 0.118) (P = 0.0252). MIBG is reported to be taken up in the terminal part of sympathetic nerves and demonstrates sympathetic nerve activity, especially on late images. The cause of differences between the heart and other parts of the body remains unknown. We consider the following possibilities: (a) differences in the sympathetic nervous system between Parkinson's disease and multiple system atrophy are more subtle in organs other than the heart; (b) the cause of MIBG uptake reduction by the heart in Parkinson's disease involves factors in addition to sympathetic nervous system damage; and (c) MIBG uptake by organs other than the heart involves not only the sympathetic nervous system but also non-neuronal components. In conclusion, MIBG uptake by organs other than the heart cannot differentiate Parkinson's disease from multiple system atrophy at present.
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Authors
Hideaki Matsui, Fukashi Udaka, Masaya Oda, Tamotsu Kubori, Kazuto Nishinaka, Masakuni Kameyama,