FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |   Search Term  Advanced Search

Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe

Previous Volume 361:255-263 July 16, 2009 Number 3 Next

Longitudinal Modeling of Age-Related Memory Decline and the APOE 4 Effect

	Full Text PDF PDA Full Text PowerPoint Slide Set Supplementary Material Purchase this article Letters Add to Personal Archive Add to Citation Manager Notify a Friend E-mail When Cited E-mail When Letters Appear PubMed Citation

ABSTRACT

Background The APOE 4 allele is associated with the risk of late-onset Alzheimer's disease. The age at which memory decline diverges among persons who are homozygous for the APOE 4 allele, those who are heterozygous for the allele, and noncarriers is unknown.

Methods Using local advertisements, we recruited cognitively normal subjects between the ages of 21 and 97 years, who were grouped according to their APOE 4 status. We then followed the subjects with longitudinal neuropsychological testing. Anyone in whom mild cognitive impairment or dementia developed during follow-up was excluded. We compared the rates of decline in predetermined cognitive measures between carriers and noncarriers of the APOE 4 allele, using a mixed model for longitudinal change with age.

Results We analyzed 815 subjects: 317 APOE 4 carriers (79 who were homozygous for the APOE 4 allele and 238 who were heterozygous) and 498 noncarriers. Carriers, as compared with noncarriers, were generally younger (mean age, 58.0 vs. 61.4 years; P<0.001) and were followed for a longer period (5.3 vs. 4.7 years, P=0.01), with an equivalent duration of formal education (15.4 years) and proportion of women (69%). Longitudinal decline in memory in carriers began before the age of 60 years and showed greater acceleration than in noncarriers (P=0.03), with a possible allele–dose effect (P=0.008). We observed similar although weaker effects on measures of visuospatial awareness and general mental status.

Conclusions Age-related memory decline in APOE 4 carriers diverges from that of noncarriers before the age of 60 years, despite ongoing normal clinical status.

Source Information

From the Mayo Clinic Arizona, Scottsdale (R.J.C., A.C.D., D.O., B.K.W., D.E.C.L., C.H.S.); Sun Health Research Institute, Sun City (M.N.S., D.J.C.); the University of Arizona, Tucson (G.L.A., S.Z.R., G.E.A., E.M.R.); Barrow Neurological Institute, Phoenix (L.C.B., J.S.); and Banner Alzheimer's Institute and Translational Genomics Research Institute, Phoenix (E.M.R.) — all in Arizona; and the Mayo Clinic, Jacksonville, FL (R.R.).

Address reprint requests to Dr. Caselli at the Department of Neurology, Mayo Clinic Arizona, 13400 E. Shea Blvd., Scottsdale, AZ 85259, or at caselli.richard{at}mayo.edu.

Full Text of this Article

Related Letters:

Age-Related Memory Decline and the APOE 4 Effect
Chuang J.-Y., Ma L., Zhao G., Xia F., Caselli R. J., Dueck A. C., Reiman E. M.
Extract | Full Text | PDF  
N Engl J Med 2009; 361:1996-1997, Nov 12, 2009. Correspondence

This article has been cited by other articles:

• Chuang, J.-Y., Ma, L., Zhao, G., Xia, F., Caselli, R. J., Dueck, A. C., Reiman, E. M. (2009). Age-related memory decline and the APOE epsilon4 effect.. NEJM 361: 1996-1996 [Full Text]  
• Kane, R. A., Kane, R. L. (2009). Effect of Genetic Testing for Risk of Alzheimer's Disease. NEJM 361: 298-299 [Full Text]