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Published Online: 1 April 2011

Huntington's Disease: Effect of Memantine on FDG-PET Brain Metabolism?

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences

Abstract

In this open-label pilot study, the authors evaluated the effect of memantine on the distribution of brain glucose metabolism in four Huntington's disease (HD) patients as determined by serial 18-fluoro-deoxyglucose [F18]FDG-PET scans over a period of 3–4 months (90–129 days, with one patient choosing to continue treatment over the 18-month follow-up period). The treatment regimen was well tolerated. No significant differences on neuropsychological parameters before and after treatment were detected; but the patient who continued treatment did not deteriorate at 18 months' reevaluation, whereas the three patients who had stopped treatment after 3 to 4 months had minor progression in all cognitive domains on re-evaluation 12 months after the end of treatment.

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Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: 206 - 210
PubMed: 21677252

History

Received: 6 October 2009
Revision received: 22 January 2010
Accepted: 29 March 2010
Published online: 1 April 2011
Published in print: Spring 2011

Authors

Details

Lena Elisabeth Hjermind, M.D.
From the Neurogenetics Clinic, Memory Disorders Research Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; the Section of Neurogenetics, Institute of Cellular & Molecular Medicine, University of Copenhagen, The Panum Institute, Copenhagen, Denmark; the Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; and Kennedy Center, Glostrup, Denmark.
Ian Law, M.D.
From the Neurogenetics Clinic, Memory Disorders Research Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; the Section of Neurogenetics, Institute of Cellular & Molecular Medicine, University of Copenhagen, The Panum Institute, Copenhagen, Denmark; the Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; and Kennedy Center, Glostrup, Denmark.
Aia Jønch, M.D.
From the Neurogenetics Clinic, Memory Disorders Research Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; the Section of Neurogenetics, Institute of Cellular & Molecular Medicine, University of Copenhagen, The Panum Institute, Copenhagen, Denmark; the Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; and Kennedy Center, Glostrup, Denmark.
Jette Stokholm, M.Sc.
From the Neurogenetics Clinic, Memory Disorders Research Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; the Section of Neurogenetics, Institute of Cellular & Molecular Medicine, University of Copenhagen, The Panum Institute, Copenhagen, Denmark; the Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; and Kennedy Center, Glostrup, Denmark.
Jørgen Erik Nielsen, M.D.
From the Neurogenetics Clinic, Memory Disorders Research Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; the Section of Neurogenetics, Institute of Cellular & Molecular Medicine, University of Copenhagen, The Panum Institute, Copenhagen, Denmark; the Department of Clinical Physiology, Nuclear Medicine and PET, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; and Kennedy Center, Glostrup, Denmark.

Notes

Send correspondence to Lena Elisabeth Hjermind, M.D., Neurogenetics Clinic, Memory Disorders Research Group, Section 6702, Copenhagen University Hospital, Rigshospitalet, Blegdamsvej 9, DK-2100 Copenhagen Denmark; [email protected] (e-mail).

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