TY - JOUR
T1 - Most rapid cognitive decline in APOE epsilon 4 negative Alzheimer's disease with early onset
AU - van der Vlies, A.E.
AU - Koedam, E.L.G.E.
AU - Pijnenburg, Y.A.L.
AU - Twisk, J.W.R.
AU - Scheltens, P.
AU - van der Flier, W.M.
PY - 2009
Y1 - 2009
N2 - Background We aimed to compare the rate of cognitive decline in patients with early and late onset Alzheimer's disease (AD) and to investigate the potentially modifying influence of the apolipoprotein E (APOE) genotype.Method We included 99 patients with early onset AD (age 65 years) and 192 patients with late onset AD (age >65 years) who had at least two scores on the Mini-Mental State Examination (MMSE) (range 214) obtained at least 1 year apart. Linear mixed models were performed to investigate the rate of cognitive decline dependent on age at onset (AAO) and APOE genotype.Results The mean (s.d.) age for patients with early onset AD was 57.7 (4.5) years, and 74.5 (5.1) years for patients with late onset AD. AAO was not associated with baseline MMSE [ (s.e.)=0.8 (0.5), p=0.14]. However, patients with early onset showed a faster decline on the MMSE [ (s.e.)=2.4 (0.1) points/year] than those with late onset [ (s.e.)=1.7 (0.1) points/year, p=0.00]. After stratification according to APOE genotype, APOE 4 non-carriers with early onset showed faster cognitive decline than non-carriers with late onset [2.4 (0.3) v. 1.3 (0.3) points/year, p=0.01]. In APOE 4 carriers, no difference in rate of cognitive decline was found between patients with early and late onset [ (s.e.)=0.2 (0.2), p=0.47].Conclusion Patients with early onset AD show more rapid cognitive decline than patients with late onset, suggesting that early onset AD follows a more aggressive course. Furthermore, this effect seems to be most prominent in patients with early onset who do not carry the genetic APOE 4 risk factor for AD. © 2009 Cambridge University Press.
AB - Background We aimed to compare the rate of cognitive decline in patients with early and late onset Alzheimer's disease (AD) and to investigate the potentially modifying influence of the apolipoprotein E (APOE) genotype.Method We included 99 patients with early onset AD (age 65 years) and 192 patients with late onset AD (age >65 years) who had at least two scores on the Mini-Mental State Examination (MMSE) (range 214) obtained at least 1 year apart. Linear mixed models were performed to investigate the rate of cognitive decline dependent on age at onset (AAO) and APOE genotype.Results The mean (s.d.) age for patients with early onset AD was 57.7 (4.5) years, and 74.5 (5.1) years for patients with late onset AD. AAO was not associated with baseline MMSE [ (s.e.)=0.8 (0.5), p=0.14]. However, patients with early onset showed a faster decline on the MMSE [ (s.e.)=2.4 (0.1) points/year] than those with late onset [ (s.e.)=1.7 (0.1) points/year, p=0.00]. After stratification according to APOE genotype, APOE 4 non-carriers with early onset showed faster cognitive decline than non-carriers with late onset [2.4 (0.3) v. 1.3 (0.3) points/year, p=0.01]. In APOE 4 carriers, no difference in rate of cognitive decline was found between patients with early and late onset [ (s.e.)=0.2 (0.2), p=0.47].Conclusion Patients with early onset AD show more rapid cognitive decline than patients with late onset, suggesting that early onset AD follows a more aggressive course. Furthermore, this effect seems to be most prominent in patients with early onset who do not carry the genetic APOE 4 risk factor for AD. © 2009 Cambridge University Press.
U2 - 10.1017/S0033291709005492
DO - 10.1017/S0033291709005492
M3 - Article
SN - 0033-2917
VL - 39
SP - 1907
EP - 1911
JO - Psychological Medicine
JF - Psychological Medicine
IS - 11
ER -