Testosterone modifies the effect of APOE genotype on hippocampal volume in middle-aged men

• Published in: Neurology Vol. 75; no. 10; pp. 874 - 880
• Main Authors: PANIZZON, M. S, HAUGER, R, JACOBSON, K. C, LYONS, M. J, MENDOZA, S. P, NEALE, M. C, PROM-WORMLEY, E. C, SEIDMAN, L. J, TSUANG, M. T, XIAN, H, KREMEN, W. S, DALE, A. M, EAVES, L. J, EYLER, L. T, FISCHL, B, FENNEMA-NOTESTINE, C, FRANZ, C. E, GRANT, M. D, JAK, A. J
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 07-09-2010; American Academy of Neurology
• Subjects: Aging - genetics; Alleles; Apolipoproteins E - genetics; Apolipoproteins E - metabolism; Biological and medical sciences; Genotype; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Hippocampus - anatomy & histology; Hippocampus - metabolism; Humans; Magnetic Resonance Imaging; Male; Medical sciences; Middle Aged; Nervous system (semeiology, syndromes); Neurology; Organ Size; Polymorphism, Genetic; Testosterone - blood; United States; Veterans; Vietnam Conflict; United States; Human; Testosterone; Nervous system diseases; Androgen; Central nervous system; Genotype; Testicular hormone; Sex steroid hormone; Hippocampus; Encephalon
• ISSN: 0028-3878; 1526-632X
• DOI: 10.1212/WNL.0b013e3181f11deb

The APOE epsilon4 allele is an established risk factor for Alzheimer disease (AD), yet findings are mixed for how early its effects are manifest. One reason for the mixed results could be the presence of interaction effects with other AD risk factors. Increasing evidence indicates that testosterone may play a significant role in the development of AD. The aim of the present study was to examine the potential interaction of testosterone and APOE genotype with respect to hippocampal volume in middle age.
Participants were men from the Vietnam Era Twin Study of Aging (n = 375). The mean age was 55.9 years (range 51-59). Between-group comparisons were performed utilizing a hierarchical linear mixed model that adjusted for the nonindependence of twin data.
A significant interaction was observed between testosterone and APOE genotype (epsilon4-negative vs epsilon4-positive). Those with both low testosterone (> or =1 SD below the mean) and an epsilon4-positive status had the smallest hippocampal volumes, although comparisons with normal testosterone groups were not significant. However, individuals with low testosterone and epsilon4-negative status had significantly larger hippocampal volumes relative to all other groups. A main effect of APOE genotype on hippocampal volume was observed, but only when the APOE-by-testosterone interaction was present.
These findings demonstrate an interaction effect between testosterone and the APOE epsilon4 allele on hippocampal volume in middle-aged men, and they may suggest 2 low testosterone subgroups. Furthermore, these results allude to potential gene-gene interactions between APOE and either androgen receptor polymorphisms or genes associated with testosterone production.