10 research outputs found

    Cerebral small vessel disease genomics and its implications across the lifespan

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    White matter hyperintensities (WMH) are the most common brain-imaging feature of cerebral small vessel disease (SVD), hypertension being the main known risk factor. Here, we identify 27 genome-wide loci for WMH-volume in a cohort of 50,970 older individuals, accounting for modification/confounding by hypertension. Aggregated WMH risk variants were associated with altered white matter integrity (p = 2.5×10-7) in brain images from 1,738 young healthy adults, providing insight into the lifetime impact of SVD genetic risk. Mendelian randomization suggested causal association of increasing WMH-volume with stroke, Alzheimer-type dementia, and of increasing blood pressure (BP) with larger WMH-volume, notably also in persons without clinical hypertension. Transcriptome-wide colocalization analyses showed association of WMH-volume with expression of 39 genes, of which four encode known drug targets. Finally, we provide insight into BP-independent biological pathways underlying SVD and suggest potential for genetic stratification of high-risk individuals and for genetically-informed prioritization of drug targets for prevention trials.Peer reviewe

    The genetic architecture of the human cerebral cortex

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    The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder

    Self-Reported High-Risk Locations of Drug Use among Drug Offenders: Ethnic and Gender Differences

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    This study provides a detailed multiple-choice self-report analysis of home, work, and other public locations where drug offenders report using drugs. Specific settings were examined as a function of gender and Latino versus Anglo ethnicity. The participants for this study were 391 individuals attending drug diversion programs in Southern California. The single most frequently reported location of use was the participants’living rooms with a small group of friends. There was no evidence that Latinos were relatively likely to use at home, which had been suggested in previous work. Rather, Latinos differed from Anglos most by showing a relative preference for outdoor locations of use at home or work contexts. These results could reflect a lifestyle difference between Anglos and Latinos

    Losers: Recovering Lost Property in Japan and the United States

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    Detecting and Managing Adverse Effects of Antipsychotic Medications

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    Contested Cultural Heritage: A Selective Historiography

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    Subretinal Hyperreflective Material in the Comparison of Age-Related Macular Degeneration Treatments Trials

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