Positron emission tomography after fetal transplantation in Huntington's disease.

Furtado, Sarah; Sossi, Vesna; Hauser, Roberta A; Samii, Ali; Schulzer, Michael; Murphy, Colleen B; Freeman, Thomas B; Stoessl, A Jon · Ann Neurol · 2005

prospective_cohort · Level II

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Abstract

Huntington's disease (HD) is a progressive disorder with no known cure. We report two-year postoperative positron emission tomography (PET) data from 7 HD patients who underwent intrastriatal fetal transplantation. Patients showed widespread reductions in glucose uptake with no significant change over 2 years. Dopamine receptor binding was significantly reduced in HD striatum. D1 binding did not change significantly following transplantation, but there was a significant loss of D2 binding. These findings may reflect loss of graft viability and/or disease progression. There was no significant relationship between changes in PET and clinical function. In summary, there was no benefit from transplantation.

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