Evidence that incidental Lewy body disease is pre-symptomatic Parkinson’s disease

Dennis W. Dickson1, Hiroshige Fujishiro1, Anthony DelleDonne1, Joshua Menke1, Zeshan Ahmed1, Kevin J. Klos2, Keith A. Josephs3, Roberta Frigerio3, Melinda Burnett3, Joseph E. Parisi4, J. Eric Ahlskog3
1Neuropathology Laboratory, Department of Neuroscience, Mayo Clinic, Jacksonville, USA
2Neurological Associates of Tulsa, Tulsa, USA
3Department of Neurology, Mayo Clinic, Rochester, USA
4Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, USA

Tóm tắt

Lewy bodies, the histologic hallmark of Parkinson’s disease (PD), are detected in the brains of about 10% of clinically normal people over the age of 60 years. When Lewy bodies are found in normal individuals, the process is sometimes referred to as incidental Lewy body disease (iLBD). The distribution of Lewy bodies in iLBD is similar to the distribution in PD, but neuronal populations vulnerable to Lewy bodies do not show significant neuronal loss in iLBD. It remains unknown if Lewy bodies in this setting represent pre-symptomatic PD or an age-related change unrelated to PD. To address this question we identified cases of iLBD and used a marker for dopaminergic and noradrenergic neurons, tyrosine hydroxylase (TH), to determine if there were changes similar to those found in PD. TH immunoreactivity in the striatum and the epicardial nerve fibers was decreased in iLBD compared to normal controls, but not to the same extent as in PD. The findings suggest that iLBD is preclinical PD and that the lack of symptoms is due to subthreshold pathology.

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