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Dive into the research topics where Thor Aspelund is active.

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Featured researches published by Thor Aspelund.


Nature Genetics | 2009

Genome-wide association study of blood pressure and hypertension

Daniel Levy; Georg B. Ehret; Kenneth Rice; Germaine C. Verwoert; Lenore J. Launer; Abbas Dehghan; Nicole L. Glazer; Alanna C. Morrison; Andrew D. Johnson; Thor Aspelund; Yurii S. Aulchenko; Thomas Lumley; Anna Köttgen; Fernando Rivadeneira; Gudny Eiriksdottir; Xiuqing Guo; Dan E. Arking; Gary F. Mitchell; Francesco Mattace-Raso; Albert V. Smith; Kent D. Taylor; Robert B. Scharpf; Shih Jen Hwang; Eric J.G. Sijbrands; Joshua C. Bis; Tamara B. Harris; Santhi K. Ganesh; Christopher J. O'Donnell; Albert Hofman; Jerome I. Rotter

Blood pressure is a major cardiovascular disease risk factor. To date, few variants associated with interindividual blood pressure variation have been identified and replicated. Here we report results of a genome-wide association study of systolic (SBP) and diastolic (DBP) blood pressure and hypertension in the CHARGE Consortium (n = 29,136), identifying 13 SNPs for SBP, 20 for DBP and 10 for hypertension at P < 4 × 10−7. The top ten loci for SBP and DBP were incorporated into a risk score; mean BP and prevalence of hypertension increased in relation to the number of risk alleles carried. When ten CHARGE SNPs for each trait were included in a joint meta-analysis with the Global BPgen Consortium (n = 34,433), four CHARGE loci attained genome-wide significance (P < 5 × 10−8) for SBP (ATP2B1, CYP17A1, PLEKHA7, SH2B3), six for DBP (ATP2B1, CACNB2, CSK-ULK3, SH2B3, TBX3-TBX5, ULK4) and one for hypertension (ATP2B1). Identifying genes associated with blood pressure advances our understanding of blood pressure regulation and highlights potential drug targets for the prevention or treatment of hypertension.


JAMA | 2010

Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease

Sudha Seshadri; Annette L. Fitzpatrick; M. Arfan Ikram; Anita L. DeStefano; Vilmundur Gudnason; Mercè Boada; Joshua C. Bis; Albert V. Smith; Minerva M. Carassquillo; Jean Charles Lambert; Denise Harold; Elisabeth M.C. Schrijvers; Reposo Ramírez-Lorca; Stéphanie Debette; W. T. Longstreth; A. Cecile J. W. Janssens; V. Shane Pankratz; Jean-François Dartigues; Paul Hollingworth; Thor Aspelund; Isabel Hernández; Alexa Beiser; Lewis H. Kuller; Peter J. Koudstaal; Dennis W. Dickson; Christophe Tzourio; Richard Abraham; Carmen Antúnez; Yangchun Du; Jerome I. Rotter

CONTEXT Genome-wide association studies (GWAS) have recently identified CLU, PICALM, and CR1 as novel genes for late-onset Alzheimer disease (AD). OBJECTIVES To identify and strengthen additional loci associated with AD and confirm these in an independent sample and to examine the contribution of recently identified genes to AD risk prediction in a 3-stage analysis of new and previously published GWAS on more than 35,000 persons (8371 AD cases). DESIGN, SETTING, AND PARTICIPANTS In stage 1, we identified strong genetic associations (P < 10(-3)) in a sample of 3006 AD cases and 14,642 controls by combining new data from the population-based Cohorts for Heart and Aging Research in Genomic Epidemiology consortium (1367 AD cases [973 incident]) with previously reported results from the Translational Genomics Research Institute and the Mayo AD GWAS. We identified 2708 single-nucleotide polymorphisms (SNPs) with P < 10(-3). In stage 2, we pooled results for these SNPs with the European AD Initiative (2032 cases and 5328 controls) to identify 38 SNPs (10 loci) with P < 10(-5). In stage 3, we combined data for these 10 loci with data from the Genetic and Environmental Risk in AD consortium (3333 cases and 6995 controls) to identify 4 SNPs with P < 1.7x10(-8). These 4 SNPs were replicated in an independent Spanish sample (1140 AD cases and 1209 controls). Genome-wide association analyses were completed in 2007-2008 and the meta-analyses and replication in 2009. MAIN OUTCOME MEASURE Presence of Alzheimer disease. RESULTS Two loci were identified to have genome-wide significance for the first time: rs744373 near BIN1 (odds ratio [OR],1.13; 95% confidence interval [CI],1.06-1.21 per copy of the minor allele; P = 1.59x10(-11)) and rs597668 near EXOC3L2/BLOC1S3/MARK4 (OR, 1.18; 95% CI, 1.07-1.29; P = 6.45x10(-9)). Associations of these 2 loci plus the previously identified loci CLU and PICALM with AD were confirmed in the Spanish sample (P < .05). However, although CLU and PICALM were confirmed to be associated with AD in this independent sample, they did not improve the ability of a model that included age, sex, and APOE to predict incident AD (improvement in area under the receiver operating characteristic curve from 0.847 to 0.849 in the Rotterdam Study and 0.702 to 0.705 in the Cardiovascular Health Study). CONCLUSIONS Two genetic loci for AD were found for the first time to reach genome-wide statistical significance. These findings were replicated in an independent population. Two recently reported associations were also confirmed. These loci did not improve AD risk prediction. While not clinically useful, they may implicate biological pathways useful for future research.


JAMA | 2008

Intra-individual change over time in DNA methylation with familial clustering.

Hans T. Bjornsson; Martin I. Sigurdsson; M. Daniele Fallin; Rafael A. Irizarry; Thor Aspelund; Hengmi Cui; Wenqiang Yu; Michael Rongione; Tomas J. Ekström; Tamara B. Harris; Lenore J. Launer; Gudny Eiriksdottir; M. Leppert; Carmen Sapienza; Vilmundur Gudnason; Andrew P. Feinberg

CONTEXT Changes over time in epigenetic marks, which are modifications of DNA such as by DNA methylation, may help explain the late onset of common human diseases. However, changes in methylation or other epigenetic marks over time in a given individual have not yet been investigated. OBJECTIVES To determine whether there are longitudinal changes in global DNA methylation in individuals and to evaluate whether methylation maintenance demonstrates familial clustering. DESIGN, SETTING, AND PARTICIPANTS We measured global DNA methylation by luminometric methylation assay, a quantitative measurement of genome-wide DNA methylation, on DNA sampled at 2 visits on average 11 years apart in 111 individuals from an Icelandic cohort (1991 and 2002-2005) and on average 16 years apart in 126 individuals from a Utah sample (1982-1985 and 1997-2005). MAIN OUTCOME MEASURE Global methylation changes over time. RESULTS Twenty-nine percent of Icelandic individuals showed greater than 10% methylation change over time (P < .001). The family-based Utah sample also showed intra-individual changes over time, and further demonstrated familial clustering of methylation change (P = .003). The family showing the greatest global methylation loss also demonstrated the greatest loss of gene-specific methylation by a separate methylation assay. CONCLUSION These data indicate that methylation changes over time and suggest that methylation maintenance may be under genetic control.


PLOS ONE | 2013

Genetic loci for retinal arteriolar microcirculation

Xueling Sim; Richard Jensen; M. Kamran Ikram; Mary Frances Cotch; Xiaohui Li; Stuart MacGregor; Jing Xie; Albert V. Smith; Eric Boerwinkle; Paul Mitchell; Ronald Klein; Barbara Ek Klein; Nicole L. Glazer; Thomas Lumley; Barbara McKnight; Bruce M. Psaty; Paulus T. V. M. de Jong; Albert Hofman; Fernando Rivadeneira; André G. Uitterlinden; Cornelia M. van Duijn; Thor Aspelund; Gudny Eiriksdottir; Tamara B. Harris; Fridbert Jonasson; Lenore J. Launer; John Attia; Paul N. Baird; Stephen B. Harrap; Elizabeth G. Holliday

Narrow arterioles in the retina have been shown to predict hypertension as well as other vascular diseases, likely through an increase in the peripheral resistance of the microcirculatory flow. In this study, we performed a genome-wide association study in 18,722 unrelated individuals of European ancestry from the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium and the Blue Mountain Eye Study, to identify genetic determinants associated with variations in retinal arteriolar caliber. Retinal vascular calibers were measured on digitized retinal photographs using a standardized protocol. One variant (rs2194025 on chromosome 5q14 near the myocyte enhancer factor 2C MEF2C gene) was associated with retinal arteriolar caliber in the meta-analysis of the discovery cohorts at genome-wide significance of P-value <5×10−8. This variant was replicated in an additional 3,939 individuals of European ancestry from the Australian Twins Study and Multi-Ethnic Study of Atherosclerosis (rs2194025, P-value = 2.11×10−12 in combined meta-analysis of discovery and replication cohorts). In independent studies of modest sample sizes, no significant association was found between this variant and clinical outcomes including coronary artery disease, stroke, myocardial infarction or hypertension. In conclusion, we found one novel loci which underlie genetic variation in microvasculature which may be relevant to vascular disease. The relevance of these findings to clinical outcomes remains to be determined.


Brain | 2011

Arterial stiffness, pressure and flow pulsatility and brain structure and function: the Age, Gene/Environment Susceptibility – Reykjavik Study

Gary F. Mitchell; Mark A. van Buchem; Sigurdur Sigurdsson; John D. Gotal; Maria K. Jonsdottir; Olafur Kjartansson; Melissa Garcia; Thor Aspelund; Tamara B. Harris; Vilmundur Gudnason; Lenore J. Launer

Aortic stiffness increases with age and vascular risk factor exposure and is associated with increased risk for structural and functional abnormalities in the brain. High ambient flow and low impedance are thought to sensitize the cerebral microcirculation to harmful effects of excessive pressure and flow pulsatility. However, haemodynamic mechanisms contributing to structural brain lesions and cognitive impairment in the presence of high aortic stiffness remain unclear. We hypothesized that disproportionate stiffening of the proximal aorta as compared with the carotid arteries reduces wave reflection at this important interface and thereby facilitates transmission of excessive pulsatile energy into the cerebral microcirculation, leading to microvascular damage and impaired function. To assess this hypothesis, we evaluated carotid pressure and flow, carotid-femoral pulse wave velocity, brain magnetic resonance images and cognitive scores in participants in the community-based Age, Gene/Environment Susceptibility--Reykjavik study who had no history of stroke, transient ischaemic attack or dementia (n = 668, 378 females, 69-93 years of age). Aortic characteristic impedance was assessed in a random subset (n = 422) and the reflection coefficient at the aorta-carotid interface was computed. Carotid flow pulsatility index was negatively related to the aorta-carotid reflection coefficient (R = -0.66, P<0.001). Carotid pulse pressure, pulsatility index and carotid-femoral pulse wave velocity were each associated with increased risk for silent subcortical infarcts (hazard ratios of 1.62-1.71 per standard deviation, P<0.002). Carotid-femoral pulse wave velocity was associated with higher white matter hyperintensity volume (0.108 ± 0.045 SD/SD, P = 0.018). Pulsatility index was associated with lower whole brain (-0.127 ± 0.037 SD/SD, P<0.001), grey matter (-0.079 ± 0.038 SD/SD, P = 0.038) and white matter (-0.128 ± 0.039 SD/SD, P<0.001) volumes. Carotid-femoral pulse wave velocity (-0.095 ± 0.043 SD/SD, P = 0.028) and carotid pulse pressure (-0.114 ± 0.045 SD/SD, P = 0.013) were associated with lower memory scores. Pulsatility index was associated with lower memory scores (-0.165 ± 0.039 SD/SD, P<0.001), slower processing speed (-0.118 ± 0.033 SD/SD, P<0.001) and worse performance on tests assessing executive function (-0.155 ± 0.041 SD/SD, P<0.001). When magnetic resonance imaging measures (grey and white matter volumes, white matter hyperintensity volumes and prevalent subcortical infarcts) were included in cognitive models, haemodynamic associations were attenuated or no longer significant, consistent with the hypothesis that increased aortic stiffness and excessive flow pulsatility damage the microcirculation, leading to quantifiable tissue damage and reduced cognitive performance. Marked stiffening of the aorta is associated with reduced wave reflection at the interface between carotid and aorta, transmission of excessive flow pulsatility into the brain, microvascular structural brain damage and lower scores in various cognitive domains.


The New England Journal of Medicine | 2013

Genetic Associations with Valvular Calcification and Aortic Stenosis

George Thanassoulis; Catherine Y. Campbell; David S. Owens; J. Gustav Smith; Albert V. Smith; Gina M. Peloso; Kathleen F. Kerr; Sonali Pechlivanis; Matthew J. Budoff; Tamara B. Harris; Rajeev Malhotra; Kevin D. O'Brien; Pia R. Kamstrup; Børge G. Nordestgaard; Anne Tybjærg-Hansen; Matthew A. Allison; Thor Aspelund; Michael H. Criqui; Susan R. Heckbert; Shih Jen Hwang; Yongmei Liu; Marketa Sjögren; Jesper van der Pals; Hagen Kälsch; Thomas W. Mühleisen; Markus M. Nöthen; L. Adrienne Cupples; Muriel J. Caslake; Emanuele Di Angelantonio; John Danesh

BACKGROUND Limited information is available regarding genetic contributions to valvular calcification, which is an important precursor of clinical valve disease. METHODS We determined genomewide associations with the presence of aortic-valve calcification (among 6942 participants) and mitral annular calcification (among 3795 participants), as detected by computed tomographic (CT) scanning; the study population for this analysis included persons of white European ancestry from three cohorts participating in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium (discovery population). Findings were replicated in independent cohorts of persons with either CT-detected valvular calcification or clinical aortic stenosis. RESULTS One SNP in the lipoprotein(a) (LPA) locus (rs10455872) reached genomewide significance for the presence of aortic-valve calcification (odds ratio per allele, 2.05; P=9.0×10(-10)), a finding that was replicated in additional white European, African-American, and Hispanic-American cohorts (P<0.05 for all comparisons). Genetically determined Lp(a) levels, as predicted by LPA genotype, were also associated with aortic-valve calcification, supporting a causal role for Lp(a). In prospective analyses, LPA genotype was associated with incident aortic stenosis (hazard ratio per allele, 1.68; 95% confidence interval [CI], 1.32 to 2.15) and aortic-valve replacement (hazard ratio, 1.54; 95% CI, 1.05 to 2.27) in a large Swedish cohort; the association with incident aortic stenosis was also replicated in an independent Danish cohort. Two SNPs (rs17659543 and rs13415097) near the proinflammatory gene IL1F9 achieved genomewide significance for mitral annular calcification (P=1.5×10(-8) and P=1.8×10(-8), respectively), but the findings were not replicated consistently. CONCLUSIONS Genetic variation in the LPA locus, mediated by Lp(a) levels, is associated with aortic-valve calcification across multiple ethnic groups and with incident clinical aortic stenosis. (Funded by the National Heart, Lung, and Blood Institute and others.).


Nature Genetics | 2010

Genome-wide association study of PR interval

Arne Pfeufer; Charlotte van Noord; Kristin D. Marciante; Dan E. Arking; Martin G. Larson; Albert V. Smith; Kirill V. Tarasov; Martina Müller; Nona Sotoodehnia; Moritz F. Sinner; Germaine C. Verwoert; Man Li; W.H. Linda Kao; Anna Köttgen; Josef Coresh; Joshua C. Bis; Bruce M. Psaty; Kenneth Rice; Jerome I. Rotter; Fernando Rivadeneira; Albert Hofman; Jan A. Kors; Bruno H. Stricker; André G. Uitterlinden; Cornelia M. van Duijn; Britt M. Beckmann; Wiebke Sauter; Christian Gieger; Steven A. Lubitz; Christopher Newton-Cheh

The electrocardiographic PR interval (or PQ interval) reflects atrial and atrioventricular nodal conduction, disturbances of which increase risk of atrial fibrillation. We report a meta-analysis of genome-wide association studies for PR interval from seven population-based European studies in the CHARGE Consortium: AGES, ARIC, CHS, FHS, KORA, Rotterdam Study, and SardiNIA (N = 28,517). We identified nine loci associated with PR interval at P < 5 × 10−8. At the 3p22.2 locus, we observed two independent associations in voltage-gated sodium channel genes, SCN10A and SCN5A. Six of the loci were near cardiac developmental genes, including CAV1-CAV2, NKX2-5 (CSX1), SOX5, WNT11, MEIS1, and TBX5-TBX3, providing pathophysiologically interesting candidate genes. Five of the loci, SCN5A, SCN10A, NKX2-5, CAV1-CAV2, and SOX5, were also associated with atrial fibrillation (N = 5,741 cases, P < 0.0056). This suggests a role for common variation in ion channel and developmental genes in atrial and atrioventricular conduction as well as in susceptibility to atrial fibrillation.


Nature Genetics | 2009

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

Emelia J. Benjamin; Kenneth Rice; Dan E. Arking; Arne Pfeufer; Charlotte van Noord; Albert V. Smith; Renate B. Schnabel; Joshua C. Bis; Eric Boerwinkle; Moritz F. Sinner; Abbas Dehghan; Steven A. Lubitz; Ralph B. D'Agostino; Thomas Lumley; Georg B. Ehret; Jan Heeringa; Thor Aspelund; Christopher Newton-Cheh; Martin G. Larson; Kristin D. Marciante; Elsayed Z. Soliman; Fernando Rivadeneira; Thomas J. Wang; Gudny Eiriksdottir; Daniel Levy; Bruce M. Psaty; Man Li; Alanna M. Chamberlain; Albert Hofman; Tamara B. Harris

We conducted meta-analyses of genome-wide association studies for atrial fibrillation (AF) in participants from five community-based cohorts. Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 × 10−7). We replicated this association in an independent cohort from the German AF Network (odds ratio = 1.44; P = 1.6 × 10−11; combined RR = 1.25; combined P = 1.8 × 10−15).


Nature Genetics | 2009

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

Santhi K. Ganesh; Neil A. Zakai; Frank J. A. van Rooij; Nicole Soranzo; Albert V. Smith; Michael A. Nalls; Ming-Huei Chen; Anna Köttgen; Nicole L. Glazer; Abbas Dehghan; Brigitte Kühnel; Thor Aspelund; Qiong Yang; Toshiko Tanaka; Andrew E. Jaffe; Joshua C. Bis; Germaine C. Verwoert; Alexander Teumer; Caroline S. Fox; Jack M. Guralnik; Georg B. Ehret; Kenneth Rice; Janine F. Felix; Augusto Rendon; Gudny Eiriksdottir; Daniel Levy; Kushang V. Patel; Eric Boerwinkle; Jerome I. Rotter; Albert Hofman

Measurements of erythrocytes within the blood are important clinical traits and can indicate various hematological disorders. We report here genome-wide association studies (GWAS) for six erythrocyte traits, including hemoglobin concentration (Hb), hematocrit (Hct), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC) and red blood cell count (RBC). We performed an initial GWAS in cohorts of the CHARGE Consortium totaling 24,167 individuals of European ancestry and replication in additional independent cohorts of the HaemGen Consortium totaling 9,456 individuals. We identified 23 loci significantly associated with these traits in a meta-analysis of the discovery and replication cohorts (combined P values ranging from 5 × 10−8 to 7 × 10−86). Our findings include loci previously associated with these traits (HBS1L-MYB, HFE, TMPRSS6, TFR2, SPTA1) as well as new associations (EPO, TFRC, SH2B3 and 15 other loci). This study has identified new determinants of erythrocyte traits, offering insight into common variants underlying variation in erythrocyte measures.


Science Translational Medicine | 2010

Personalized Epigenomic Signatures That Are Stable Over Time and Covary with Body Mass Index

Andrew P. Feinberg; Rafael A. Irizarry; Delphine Fradin; Martin J. Aryee; Peter Murakami; Thor Aspelund; Gudny Eiriksdottir; Tamara B. Harris; Lenore J. Launer; Vilmundur Gudnason; M. Daniele Fallin

A genome-scale, gene-specific analysis of DNA methylation in the same individuals over a decade apart identifies a personalized epigenomic signature that may correlate with a common genetic trait. The Writing is on the Genes: Can Epigenomics Predict Disease Risk? In the nature versus nurture debate about human traits, epigenomics holds a special place. Epigenetic changes are physical changes that happen to genes but do not change the gene (DNA) sequence itself—such as DNA methylation. The regulation of these changes is not yet well-understood, providing new ammunition to the age-old argument. It is possible that the methylation pattern is all “nature”, predetermined by a person’s genetic makeup, or alternatively methylation could be a result of “nurture”, reflecting the influence of regulatory signals outside the cell, that is, the environment. Having analyzed the detailed methylation patterns in several dozen individuals at two different time points, over a decade apart, Feinberg et al. present evidence that the answer may actually be both—a combination of genetic determinants and environmental regulation. In this study, the authors analyzed the full methylation pattern at 4.5 million sites genome-wide in 74 volunteers. The participants, who were on average 74 years old at the time of the first visit, provided blood samples again 11 to 14 years later, allowing for comparison of methylation patterns both between individuals, and in the same individuals across time. In doing this, the authors found 227 variably methylated regions (VMRs), which varied widely between the study participants. Of these, 119 VMRs remained stable within each individual over time, constituting an epigenetic fingerprint that may be genetically predetermined and differed between pairs of individual participants. The remaining VMRs were highly variable over time, suggesting that their pattern is affected by environmental influences. Four of the stable VMRs consistently correlated with study subjects’ body mass index in both visits. All four of these sites were located at or near genes that are known to be involved in the pathogenesis of diabetes or obesity, lending biological plausibility to the correlation between the methylation pattern and obesity risk. Through their analysis of the epigenome in a large pool of volunteer subjects, Feinberg et al. have demonstrated a unique signature of stable epigenetic changes within each individual. Several of these stable methylation sites were correlated with the patients’ body mass index. If these results are confirmed in younger individuals and consistent throughout the life span, tests for methylation might be used to screen patients in childhood and identify those at risk for obesity, allowing preventative treatment. In theory, similar testing for other common diseases that may have a stable epigenetic component, such as diabetes or asthma, could allow early intervention and prevention. The epigenome consists of non–sequence-based modifications, such as DNA methylation, that are heritable during cell division and that may affect normal phenotypes and predisposition to disease. Here, we have performed an unbiased genome-scale analysis of ~4 million CpG sites in 74 individuals with comprehensive array-based relative methylation (CHARM) analysis. We found 227 regions that showed extreme interindividual variability [variably methylated regions (VMRs)] across the genome, which are enriched for developmental genes based on Gene Ontology analysis. Furthermore, half of these VMRs were stable within individuals over an average of 11 years, and these VMRs defined a personalized epigenomic signature. Four of these VMRs showed covariation with body mass index consistently at two study visits and were located in or near genes previously implicated in regulating body weight or diabetes. This work suggests an epigenetic strategy for identifying patients at risk of common disease.

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Tamara B. Harris

National Institutes of Health

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Lenore J. Launer

National Institutes of Health

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Sigurdur Sigurdsson

University of Texas Health Science Center at Houston

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