University of Iceland

About: University of Iceland is a education organization based out in Reykjavik, Suðurnes, Iceland. It is known for research contribution in the topics: Population & Genome-wide association study. The organization has 5423 authors who have published 16199 publications receiving 694762 citations. The organization is also known as: Háskóli Íslands.

High-resolution climate records from the North Atlantic during the last interglacial

Abstract: THE two deep ice cores recovered by the GRIP1 and GISP22 projects at Summit, Greenland, agree in detail over the past 100,000 years3 and demonstrate dramatic climate variability in the North Atlantic region during the last glacial, before the current period of Holocene stability. This glacial climate instability has subsequently been documented in the marine sedimentary record of surface-ocean conditions in the North Atlantic4. Before 100 kyr ago the two ice core records are discrepant, however, casting doubt on whether the oxygen isotope fluctuations during the last interglacial (Eemian) seen in the GRIP core1,5 represent a true climate signal. Here we present high-resolution records of foraminiferal assemblages and ice-rafted detritus from two North Atlantic cores for the interval 65 kyr to 135 kyr ago, extending the surface-ocean record back to the Eemian. The correlation between our records and the Greenland ice-core records is good throughout the period in which the two ice cores agree, suggesting a regionally coherent climate response. During the Eemian, our marine records show a more stable climate than that implied by the GRIP ice core, suggesting that localized phenomena may be responsible for the variability in the latter record during the Eemian.

FERMI-LAT OBSERVATIONS of HIGH-ENERGY γ-RAY EMISSION TOWARD the GALACTIC CENTER

Abstract: The Fermi Large Area Telescope (LAT) has provided the most detailed view to date of the emission toward the Galactic center (GC) in high-energy gamma-rays. This paper describes the analysis of data ...

Physical activity attenuates the influence of FTO variants on obesity risk: A meta-analysis of 218,166 adults and 19,268 children

Abstract: Background: The FTO gene harbors the strongest known susceptibility locus for obesity. While many individual studies have suggested that physical activity (PA) may attenuate the effect of FTO on obesity risk, other studies have not been able to confirm this interaction. To confirm or refute unambiguously whether PA attenuates the association of FTO with obesity risk, we meta-analyzed data from 45 studies of adults (n=218,166) and nine studies of children and adolescents (n=19,268). Methods and Findings: All studies identified to have data on the FTO rs9939609 variant (or any proxy [r(2)>0.8]) and PA were invited to participate, regardless of ethnicity or age of the participants. PA was standardized by categorizing it into a dichotomous variable (physically inactive versus active) in each study. Overall, 25% of adults and 13% of children were categorized as inactive. Interaction analyses were performed within each study by including the FTOxPA interaction term in an additive model, adjusting for age and sex. Subsequently, random effects meta-analysis was used to pool the interaction terms. In adults, the minor (A-) allele of rs9939609 increased the odds of obesity by 1.23-fold/allele (95% CI 1.20-1.26), but PA attenuated this effect (p(interaction) = 0.001). More specifically, the minor allele of rs9939609 increased the odds of obesity less in the physically active group (odds ratio = 1.22/allele, 95% CI 1.19-1.25) than in the inactive group (odds ratio = 1.30/allele, 95% CI 1.24-1.36). No such interaction was found in children and adolescents. Conclusions: The association of the FTO risk allele with the odds of obesity is attenuated by 27% in physically active adults, highlighting the importance of PA in particular in those genetically predisposed to obesity.

Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

Abstract: To identify genetic variation underlying atrial fibrillation, the most common cardiac arrhythmia, we performed a genome-wide association study of >1,000,000 people, including 60,620 atrial fibrillation cases and 970,216 controls. We identified 142 independent risk variants at 111 loci and prioritized 151 functional candidate genes likely to be involved in atrial fibrillation. Many of the identified risk variants fall near genes where more deleterious mutations have been reported to cause serious heart defects in humans (GATA4, MYH6, NKX2-5, PITX2, TBX5)1, or near genes important for striated muscle function and integrity (for example, CFL2, MYH7, PKP2, RBM20, SGCG, SSPN). Pathway and functional enrichment analyses also suggested that many of the putative atrial fibrillation genes act via cardiac structural remodeling, potentially in the form of an 'atrial cardiomyopathy'2, either during fetal heart development or as a response to stress in the adult heart.