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FDG PET Imaging in Patients with Pathologically Verified Dementia

John M. Hoffman, Kathleen A. Welsh-Bohmer, Michael Hanson, Barbara Crain, Christine Hulette, Nancy Earl and R. Edward Coleman
Journal of Nuclear Medicine November 2000, 41 (11) 1920-1928;
John M. Hoffman
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Kathleen A. Welsh-Bohmer
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Michael Hanson
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Barbara Crain
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Christine Hulette
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Nancy Earl
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R. Edward Coleman
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  • FIGURE 1.
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    FIGURE 1.

    FDG PET scan of 54-y-old woman with progressive dementing illness (patient 7; Table 1). Note significant reduction in FDG in parietal, temporal, and frontal cortices (arrows). The metabolic pattern noted on this particular study would be considered classic for AD. The patient had AD, verified by pathological examination.

  • FIGURE 2.
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    FIGURE 2.

    FDG PET scans of 60-y-old man with a rapidly progressive dementia syndrome (patient 2; Table 1). Patient had both biopsy and autopsy confirmation of diagnosis of Creutzfeldt-Jacob disease. FDG PET scans at 2 levels show marked reduction in FDG uptake in temporo-parietal (A) and parietal (B) regions bilaterally. A pattern very similar to AD has been reported in previous cases of Creutzfeldt-Jacob disease studied with FDG PET imaging (31–33).

  • FIGURE 3.
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    FIGURE 3.

    (A–C) FDG PET scans at 3 transaxial levels of 64-y-old man with progressive dementing illness (patient 5; Table 1). Pathologic diagnosis was nonspecific neuronal degeneration. FDG PET scan was interpreted as abnormal but not AD pattern. FDG PET images at 3 levels are shown. Note asymmetric FDG uptake, particularly in the left frontal area (arrow) on multiple imaging levels. Temporo-parietal hypometabolism was not a prominent finding in this patient with non–Alzheimer's type dementia.

  • FIGURE 4.
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    FIGURE 4.

    FDG PET scan of 66-y-old man with progressive dementia with extrapyramidal features (patient 13; Table 1). This individual had histologically proven progressive supranuclear palsy. FDG PET scan was interpreted as abnormal but not AD pattern. FDG PET image showed reduction in FDG uptake in frontal regions bilaterally. Prominent frontal hypometabolism has been previously described in patients with progressive supranuclear palsy with FDG PET (34–36).

Tables

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    TABLE 1.

    Summary Data

    Subject no.SexAge at PET (y)Age at path. (y)Clinical diagnosisPath. diagnosisBiopsy or autopsyInterpreter PET grade*Interval PET to path. (mo)
    1F5660DementiaADAutopsy344
    2M6061CJDCJDBiopsy & autopsy325
    3M6465DementiaADAutopsy317
    4M6264Probable ADADBiopsy3−65
    5M6466DementiaNeuronal deg.Autopsy423
    6M6971Possible ADADAutopsy228
    7F5454Probable ADADBiopsy3−2
    8M7375Possible ADADAutopsy231
    9F5960Probable ADADAutopsy316
    10F6971Probable ADADAutopsy327
    11M5759Probable ADADAutopsy333
    12M6467Probable ADAD + LewyAutopsy344
    13M6669DementiaPSPAutopsy446
    14F6868DementiaADBiopsy22
    15M7276Probable ADADAutopsy348
    16F7476PSPPSP + ADAutopsy434
    17M7373Probable ADADAutopsy35
    18F8081PD/Lewy bodyLewy bodyAutopsy322
    19M7778Probable ADADAutopsy49
    20M7276Probable ADADAutopsy351
    21M3739Toxic enceph.PreamyloidAutopsy422
    22M6876Pick'sMLCDAutopsy487
    • Path, pathologic diagnosis; CJD, Creutzfeldt-Jacob disease; Neuronal deg., neuronal degeneration; Lewy, Lewy body disease; PSP, progressive supranuclear palsy; PD, Parkinson's disease; enceph., encephalopathy; MLCD, mesio–limbo cortical dementia.

    • ↵* See methods for description of PET score.

    • View popup
    TABLE 2.

    Clinical Diagnosis Versus Pathologic Diagnosis Results

    ResultsSensitivitySpecificityPV positivePV negativeAccuracy
    Prob. AD only clinically: AD + other on path.62.5% (10/16)100% (6/6)100% (10/10)50% (6/12)72.7% (16/22)
    Poss. or prob. AD clinically: AD + other on path.75.0% (12/16)100% (6/6)100% (12/12)60% (6/10)81.8% (18/22)
    Prob. AD only clinically: AD only on path.64.3% (9/14) 87.5% (7/8)90% (9/10)  58.3% (7/12)72.7% (16/22)
    Poss. or prob. AD clinically: AD only on path.78.6% (11/14)87.5% (7/8)91.7% (11/12)70% (7/10)81.8% (18/22)
    • PV, predictive value; Prob., probable; poss., possible; path., pathology.

    • View popup
    TABLE 3.

    FDG PET Interpreter Results Versus Pathologic Diagnosis

    ResultsSensitivitySpecificityPV positivePV negativeAccuracy
    PET grade 2 or 3: path. AD only92.9% (13/14)62.5% (5/8)81.3% (13/16)83.3% (5/6)81.8% (18/22)
    PET grade 2 or 3: path. AD and other87.5% (14/16)66.7% (4/6)87.5% (14/16)66.7% (4/6)81.8% (18/22)
    • PV, predictive value; Path., pathology.

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Journal of Nuclear Medicine
Vol. 41, Issue 11
November 1, 2000
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FDG PET Imaging in Patients with Pathologically Verified Dementia
John M. Hoffman, Kathleen A. Welsh-Bohmer, Michael Hanson, Barbara Crain, Christine Hulette, Nancy Earl, R. Edward Coleman
Journal of Nuclear Medicine Nov 2000, 41 (11) 1920-1928;

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FDG PET Imaging in Patients with Pathologically Verified Dementia
John M. Hoffman, Kathleen A. Welsh-Bohmer, Michael Hanson, Barbara Crain, Christine Hulette, Nancy Earl, R. Edward Coleman
Journal of Nuclear Medicine Nov 2000, 41 (11) 1920-1928;
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