Table 1.
Pathological Correlation of In Vivo PiB Retention
| Clinical Diagnosis |
PiB Status |
Scan-PM Intervala |
Autopsy | Aβ ELISA or IHCb |
Path Dx | Reference | |||
|---|---|---|---|---|---|---|---|---|---|
| Braak Stage |
Diffuse Plaques |
Neuritic Plaques |
CAA | ||||||
| DLB | Pos. | 3 mos. | IV | Moderate | Sparse | Severe | High | DLB, Poss. ADc | (Bacskai et al., 2007) |
| AD | Pos. | 10 mos. | V/VI | Frequent | Frequent | Mild | High | Def. ADc | (Ikonomovic et al., 2008) |
| CJD | Neg. | 2 wks | n/ad | None | None | None | None | CJD | (Villemagne et al., 2009) |
| CJD | Neg. | 4 wks | n/a | Sparse, frontal only | None | None | Low-None | CJD | (Villemagne et al., 2009) |
| Very mild AD | Neg. | 2.5 yrs | III | Moderate | Sparse | Mild | High | Poss. ADc | (Cairns et al., 2009a) |
| PDD | Pos. | <15 mos. | V/VI | Frequent | Sparse | Moderate | High | PDD, Poss ADc | (Burack et al., 2010) |
| PDD | Pos. | <15 mos. | V/VI | Frequent | Sparse | Mild | High | PDD, Poss. ADc | (Burack et al., 2010) |
| PDD | Neg. | <15 mos. | III/IV | Sparse | None | None | Few-None | PDD | (Burack et al., 2010) |
| A: CDR=0 | Neg. | 1.7 yrs | IV | n/a | None | None | Low | Normal Brain | (Sojkova et al., 2011) |
| B: CDR=0 | Neg. | 2.4 yrs | III | n/a | Moderate | None | Low | Poss. ADc | (Sojkova et al., 2011) |
| C: CDR=0 | Pos. | 2.4 yrs | IV | n/a | Moderate | None | High | Poss. ADc | (Sojkova et al., 2011) |
| D: CDR=0.5 | Pos. | 1.1 yrs | III | n/a | Moderate | Present | Low | Poss. ADc | (Sojkova et al., 2011) |
| E: CDR=0 | Pos. | 1.4 yrs | IV | Frequent | Sparse | Present | High | Normal Brain | (Sojkova et al., 2011) |
| F: CDR=2–4.5e | Pos. | 2 mos. | III | n/a | Moderate | Present | High | Poss. ADc | (Sojkova et al., 2011) |
| 1: CDR=0.5f | Neg. | 36 mos. | gHP− | n/a | 0 | n/a | 0h | n/a | (Leinonen et al., 2008) |
| 2: CDR=0f | Neg. | 23 mos. | gHP− | n/a | 0 | n/a | 0h | n/a | (Leinonen et al., 2008) |
| 3: CDR=0f | Neg. | 15 mos. | gHP− | n/a | 0 | n/a | 0h | n/a | (Leinonen et al., 2008) |
| 4: CDR=1f | Neg. | 2 mos. | gHP− | n/a | 0 | n/a | 0h | n/a | (Leinonen et al., 2008) |
| 5: CDR=1f | Neg. | 5 mos. | gHP− | n/a | 0 | n/a | 1 (fleecy)h | n/a | (Leinonen et al., 2008) |
| 6: CDR=1f | Neg. | 20 mos. | gHP− | n/a | 1 | n/a | 39h | n/a | (Leinonen et al., 2008) |
| 7: CDR=1f | Pos. | 12 mos. | gHP− | n/a | 0 | n/a | 42h | n/a | (Leinonen et al., 2008) |
| 8: CDR=0.5f | Pos. | 26 mos | gHP+ | n/a | 2 | n/a | 45h | n/a | (Leinonen et al., 2008) |
| 9; CDR=2f | Pos. | 27 mos. | gHP+ | n/a | 3 | n/a | 66h | n/a | (Leinonen et al., 2008) |
| 10: CDR=1f | Pos. | 28 mos. | gHP+ | n/a | 0 | n/a | 80h | n/a | (Leinonen et al., 2008) |
Interval between PiB scan and postmortem analysis.
Level of Aβ by enzyme-linked immunosorbant assay or anti-Aβ immunohistochemistry (IHC).
Possible or Definite AD dementia by CERAD criteria (Mirra et al., 1991).
Not assessed
Subject F had three assessments.
Biopsy study of subjects with suspected NPH
Positive or negative for hyperphosphorylated tau (HP)
Aβ plaques per ×100 field detected with (IHC)