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DOI 10.1002/mds.26247

Медицинская библиотека · Movement disorders : official journal of the Movement Disorder Society · 2015

Brain alterations with deep brain stimulation: New insight from a neuropathological case series.

Kronenbuerger Martin, Nolte Kay Wilhelm, Coenen Volker Arnd, Burgunder Jean-Marc, Krauss Joachim K, Weis Joachim

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Previous studies on human brain tissue alterations caused by deep brain stimulation described glial and reactive inflammatory changes. In the current pathoanatomical study, we extended the analysis to signs of axonal changes and the influence of concomitant disease.

METHODS

Brains of 10 patients with Parkinson's disease or essential tremor and a total of 18 electrodes were systematically examined up to 7.5 y after surgery.

RESULTS

In general, tissue that had long-term contact with the electrode material exhibited astrogliosis in all, T-lymphocytes in 93%, and multinucleated giant cells in 68% of patients. Immunohistochemistry showed an increase in amyloid precursor protein immunoreactive axonal swellings in the brain at the electrically active parts of the electrodes. Patients who died of septicemia showed a more severe astrogliosis and giant cell reaction than patients who died of cardiovascular events. Parkinson's disease or essential tremor did not differentially produce histopathological changes around the electrodes.

CONCLUSION

Long-term electrical stimulation by deep brain stimulation causes minor axonal changes. The cause of death, but not the underlying neurological disease, affects the histopathological changes around the electrode. The findings need to be reproduced by examining larger patient subgroups.

Для цитирования: Kronenbuerger Martin, Nolte Kay Wilhelm, Coenen Volker Arnd, Burgunder Jean-Marc, Krauss Joachim K, Weis Joachim. Brain alterations with deep brain stimulation: New insight from a neuropathological case series.. Movement disorders : official journal of the Movement Disorder Society. 2015. DOI: 10.1002/mds.26247.

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