Nho, KwangsikSaykin, Andrew J.Nelson, Peter T.2017-06-082017-06-082016Nho, K., Saykin, A. J., Alzheimer’s Disease Neuroimaging Initiative, & Nelson, P. T. (2016). Hippocampal Sclerosis of Aging, a Common Alzheimer’s Disease “Mimic”: Risk Genotypes are Associated with Brain Atrophy Outside the Temporal Lobe. Journal of Alzheimer’s Disease : JAD, 52(1), 373–383. http://doi.org/10.3233/JAD-160077https://hdl.handle.net/1805/12916Hippocampal sclerosis of aging (HS-Aging) is a common brain disease in older adults with a clinical course that is similar to Alzheimer's disease. Four single-nucleotide polymorphisms (SNPs) have previously shown association with HS-Aging. The present study investigated structural brain changes associated with these SNPs using surface-based analysis. Participants from the Alzheimer's Disease Neuroimaging Initiative cohort (ADNI; n = 1,239), with both MRI scans and genotype data, were used to assess the association between brain atrophy and previously identified HS-Aging risk SNPs in the following genes: GRN, TMEM106B, ABCC9, and KCNMB2 (minor allele frequency for each is >30%). A fifth SNP (near the ABCC9 gene) was evaluated in post-hoc analysis. The GRN risk SNP (rs5848_T) was associated with a pattern of atrophy in the dorsomedial frontal lobes bilaterally, remarkable since GRN is a risk factor for frontotemporal dementia. The ABCC9 risk SNP (rs704180_A) was associated with multifocal atrophy whereas a SNP (rs7488080_A) nearby (∼50 kb upstream) ABCC9 was associated with atrophy in the right entorhinal cortex. Neither TMEM106B (rs1990622_T), KCNMB2 (rs9637454_A), nor any of the non-risk alleles were associated with brain atrophy. When all four previously identified HS-Aging risk SNPs were summed into a polygenic risk score, there was a pattern of associated multifocal brain atrophy in a predominately frontal pattern. We conclude that common SNPs previously linked to HS-Aging pathology were associated with a distinct pattern of anterior cortical atrophy. Genetic variation associated with HS-Aging pathology may represent a non-Alzheimer's disease contribution to atrophy outside of the hippocampus in older adults.en-USPublisher PolicyArteriolosclerosisDementiaKATPProgranulinrs5848rs704180rs1990622rs9637454SUR2TDP-43Article