| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 330973 | Neurobiology of Aging | 2011 | 7 Pages |
ObjectiveTo study CSF biomarkers amyloid-beta 1–42 (Aβ42) and total tau (tau) in relation to APOE genotype in their ability to predict progression from mild cognitive impairment (MCI) to Alzheimer's disease (AD).MethodsIn 100 MCI patients CSF Aβ42, tau and APOE genotype were determined. At follow-up of 18 (13–24) months 58 patients remained non-progressive and 42 progressed to AD.ResultsCox proportional hazards models showed an interaction between Aβ42 and APOE genotype (p < 0.05). Stratification for APOE revealed HR (95% CI) for abnormal Aβ42 of 8.2 (2.1–31.9) for ε4 non-carriers, 3.9 (0.8–18.5) for heterozygotes and 0.3 (0.0–1.7) for homozygotes. Inversely, stratification for Aβ42 revealed that in patients with normal levels of Aβ42, ε4 homozygotes had a strongly increased risk of progression to AD with HR (95% CI) 20.8 (2.4–182.8). Tau and APOE independently predicted progression to AD.ConclusionsAβ42 was a stronger predictor of progression to AD in APOE ε4 non-carriers than in carriers. Furthermore, the risk of progression for ε4 homozygotes was very high, also in patients with normal levels of Aβ42.
