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Genetic architecture of epigenetic and neuronal ageing rates in human brain regions
Identifying genes regulating the pace of epigenetic ageing represents a new frontier in genome-wide association studies (GWASs). Here using 1,796 brain samples from 1,163 individuals, we carry out a GWAS of two DNA methylation-based biomarkers of brain age: the epigenetic ageing rate and estimated p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454371/ https://www.ncbi.nlm.nih.gov/pubmed/28516910 http://dx.doi.org/10.1038/ncomms15353 |
Sumario: | Identifying genes regulating the pace of epigenetic ageing represents a new frontier in genome-wide association studies (GWASs). Here using 1,796 brain samples from 1,163 individuals, we carry out a GWAS of two DNA methylation-based biomarkers of brain age: the epigenetic ageing rate and estimated proportion of neurons. Locus 17q11.2 is significantly associated (P=4.5 × 10(−9)) with the ageing rate across five brain regions and harbours a cis-expression quantitative trait locus for EFCAB5 (P=3.4 × 10(−20)). Locus 1p36.12 is significantly associated (P=2.2 × 10(−8)) with epigenetic ageing of the prefrontal cortex, independent of the proportion of neurons. Our GWAS of the proportion of neurons identified two genome-wide significant loci (10q26 and 12p13.31) and resulted in a gene set that overlaps significantly with sets found by GWAS of age-related macular degeneration (P=1.4 × 10(−12)), ulcerative colitis (P<1.0 × 10(−20)), type 2 diabetes (P=2.8 × 10(−13)), hip/waist circumference in men (P=1.1 × 10(−9)), schizophrenia (P=1.6 × 10(−9)), cognitive decline (P=5.3 × 10(−4)) and Parkinson's disease (P=8.6 × 10(−3)). |
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