PLoS ONE (Jan 2012)

Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease.

  • Christiane Reitz,
  • Giuseppe Tosto,
  • Richard Mayeux,
  • Jose A Luchsinger,
  • NIA-LOAD/NCRAD Family Study Group,
  • Alzheimer's Disease Neuroimaging Initiative

DOI
https://doi.org/10.1371/journal.pone.0050354
Journal volume & issue
Vol. 7, no. 12
p. e50354

Abstract

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BACKGROUND:Recent studies showed that polymorphisms in the Fat and Obesity-Associated (FTO) gene have robust effects on obesity, obesity-related traits and endophenotypes associated with Alzheimer's disease (AD). METHODS:We used 1,877 Caucasian cases and controls from the NIA-LOAD study and 1,093 Caribbean Hispanics to further explore the association of FTO with AD. Using logistic regression, we assessed 42 SNPs in introns 1 and 2, the region previously reported to be associated with AD endophenotypes, which had been derived by genome-wide screenings. In addition, we performed gene expression analyses of neuropathologically confirmed AD cases and controls of two independent datasets (19 AD cases, 10 controls; 176 AD cases, 188 controls) using within- and between-group factors ANOVA of log(10) transformed rank invariant normalized expression data. RESULTS:In the NIALOAD study, one SNP was significantly associated with AD and three additional markers were close to significance (rs6499640, rs10852521, rs16945088, rs8044769, FDR p-value: 0.050.9) with the previously reported SNPs. In the Caribbean Hispanic dataset, we identified three SNPs (rs17219084, rs11075996, rs11075997, FDR p-value: 0.009<p<0.01) that were associated with AD. These results were confirmed by haplotype analyses and in a metaanalysis in which we included the ADNI dataset. FTO had a significantly lower expresssion in AD cases compared to controls in two independent datasets derived from human cortex and amygdala tissue, respectively (p = 2.18 × 10-5 and p<0.0001). CONCLUSIONS:Our data support the notion that genetic variation in Introns 1 and 2 of the FTO gene may contribute to AD risk.