Progression from MCI to AD: Predictive value of CSF Aβ42 is modified by APOE genotype

Abstract: Objective: To 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). Methods: In 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. Results: Cox 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. Conclusions: Aβ42 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. [Copyright &y& Elsevier]