A gene and ε4 interaction is associated with apathy and structural brain changes in mild cognitive impairment and Alzheimer's disease.

BACKGROUND

Apathy in patients with Alzheimer's disease (AD) is associated with significant morbidity and is often one of the first neuropsychiatric symptoms to present in mild cognitive impairment (MCI). Apathy is associated with accelerated cognitive decline and atrophy in fronto-striatal regions of the brain. Previous work has shown a link between apathy and the gene in the context of AD, as the 4 allele is already known to be associated with the onset of AD. However, other genetic associations with apathy are largely unexplored.

OBJECTIVE

To examine whether interactions between genetic variants related to neurotransmitter systems and regional brain atrophy are associated with apathy in patients with MCI and AD.

METHODS

In a sample of individuals with AD (n = 266), MCI (n = 518), and cognitively normal controls (n = 378), a partial least squares correspondence analysis modeled interactions between single nucleotide polymorphisms, structural whole-brain imaging variables, and apathy.

RESULTS

An interaction was found between apathy, the possession of an ε4 allele combined with minor homozygosity for the (dopamine transporter 1) gene, and regional brain atrophy. This interaction was closely linked to the MCI and AD groups.

CONCLUSIONS

The results point to an association of a dopaminergic genetic marker and apathy in the AD continuum and may inform future design of clinical trials of apathy, as well as new treatment targets.