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. Author manuscript; available in PMC: 2010 May 1.
Published in final edited form as: Parkinsonism Relat Disord. 2008 Sep 18;15(4):300–306. doi: 10.1016/j.parkreldis.2008.07.010

Table 1.

Results of PET Studies in Cases 1 and 2 Compared with Normal and Sporadic PD Controls

PET results*
Measure Location Normal controls (n=33) sPD controls (n=67) Sagamihara family members
Case 1 Case 2
Kocc, min−1 Caudate nucleus 0.0116±0.0010 0.0085±0.0017 (74%) 0.0055 (47%) 0.0070 (60%)
Putamen 0.0104±0.0011 0.0046±0.0017 (44%) 0.0027 (26%) 0.0036 (35%)
BP (DTBZ) Caudate nucleus 0.967±0.008 0.539 (56%) 0.41 (42%) 0.44 (45%)
Putamen 0.979±0.009 0.353 (36%) 0.20 (20%) 0.21 (21%)
BP (MP) Caudate nucleus 1.460±0.002 0.848±0.252 (58%) 0.43 (37%) 0.45 (39%)
Putamen 1.319±0.002 0.490±0.236 (37%) 0.23 (26%) 0.25 (27%)
BP (RAC) Caudate nucleus 2.28±0.24§ 2.08±0.32// 2.89 2.59
Putamen 2.27±0.27 2.39±0.4 3.11 2.84

BP, binding potential; DTBZ, 11C-α-dihydrotetrabenazine; Kocc, uptake rate constant of 18F-6-fluoro-L-dopa; MP, 11C-d-threo-methylphenidate; PD, Parkinson disease; RAC, 11C-raclopride; sPD, sporadic PD.

*

Values shown are mean±SD or value (% of normal) for each tracer.

Data from Adams et al (8), except for BP (RAC), which are unpublished data (normal controls) and from de la Fuente-Fernandez R, Sossi V, Huang Z, Furtado S, Lu J-Q, Calne DB, et al. Levodopa-induced changes in synaptic dopamine levels increase with progression of Parkinson’s disease: implications for dyskinesias. Brain 2004;127:2747–54 (sPD controls).

Age-adjusted.

§

N=10. Mean±SD age, 51.3±16.4 y.

//

N=8. Mean±SD age, 64.4±11.2 y.