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A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection

Overview of attention for article published in PLoS Genetics, September 2011
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (92nd percentile)
  • High Attention Score compared to outputs of the same age and source (86th percentile)

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2 blogs
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2 X users
facebook
1 Facebook page
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2 Wikipedia pages

Readers on

mendeley
203 Mendeley
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4 CiteULike
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Article details
Title
A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection
Published in
PLoS Genetics, September 2011
DOI 10.1371/journal.pgen.1002270
Pubmed ID
Authors
Abstract

We have performed a metabolite quantitative trait locus (mQTL) study of the (1)H nuclear magnetic resonance spectroscopy ((1)H NMR) metabolome in humans, building on recent targeted knowledge of genetic drivers of metabolic regulation. Urine and plasma samples were collected from two cohorts of individuals of European descent, with one cohort comprised of female twins donating samples longitudinally. Sample metabolite concentrations were quantified by (1)H NMR and tested for association with genome-wide single-nucleotide polymorphisms (SNPs). Four metabolites' concentrations exhibited significant, replicable association with SNP variation (8.6×10(-11)<p<2.8×10(-23)). Three of these-trimethylamine, 3-amino-isobutyrate, and an N-acetylated compound-were measured in urine. The other-dimethylamine-was measured in plasma. Trimethylamine and dimethylamine mapped to a single genetic region (hence we report a total of three implicated genomic regions). Two of the three hit regions lie within haplotype blocks (at 2p13.1 and 10q24.2) that carry the genetic signature of strong, recent, positive selection in European populations. Genes NAT8 and PYROXD2, both with relatively uncharacterized functional roles, are good candidates for mediating the corresponding mQTL associations. The study's longitudinal twin design allowed detailed variance-components analysis of the sources of population variation in metabolite levels. The mQTLs explained 40%-64% of biological population variation in the corresponding metabolites' concentrations. These effect sizes are stronger than those reported in a recent, targeted mQTL study of metabolites in serum using the targeted-metabolomics Biocrates platform. By re-analysing our plasma samples using the Biocrates platform, we replicated the mQTL findings of the previous study and discovered a previously uncharacterized yet substantial familial component of variation in metabolite levels in addition to the heritability contribution from the corresponding mQTL effects.

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X Demographics

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Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 203 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
United States 3 1%
Denmark 2 <1%
Germany 2 <1%
Switzerland 2 <1%
Qatar 1 <1%
Netherlands 1 <1%
Italy 1 <1%
United Kingdom 1 <1%
France 1 <1%
Other 1 <1%
Unknown 188 93%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 58 29%
Student > Ph. D. Student 53 26%
Student > Master 15 7%
Professor 14 7%
Professor > Associate Professor 13 6%
Other 29 14%
Unknown 21 10%
Readers by discipline
Readers by discipline Count As %
Agricultural and Biological Sciences 82 40%
Biochemistry, Genetics and Molecular Biology 32 16%
Medicine and Dentistry 22 11%
Computer Science 9 4%
Chemistry 8 4%
Other 19 9%
Unknown 31 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 17. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 August 2023.
All research outputs
#2,471,120
of 28,649,717 outputs
Outputs from PLoS Genetics
#1,724
of 9,236 outputs
Outputs of similar age
#11,432
of 145,720 outputs
Outputs of similar age from PLoS Genetics
#20
of 151 outputs
Altmetric has tracked 28,649,717 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 91st percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 9,236 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 17.2. This one has done well, scoring higher than 81% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 145,720 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 92% of its contemporaries.
We're also able to compare this research output to 151 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 86% of its contemporaries.