Evidence map›Paper›PMID 20519558›Full record

SynthesisThe American journal of clinical nutrition2010

Genetic variation at the SLC23A1 locus is associated with circulating concentrations of L-ascorbic acid (vitamin C): evidence from 5 independent studies with >15,000 participants.

Nicholas J Timpson, Nita G Forouhi, Marie-Jo Brion, Roger M Harbord, Derek G Cook, Paul Johnson, Alex McConnachie, Richard W Morris, Santiago Rodriguez, Jian'an Luan and 10 more

Erratum issuedAbstract readMeta-Analysis
In one paragraph

Synthesis in The American journal of clinical nutrition, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 3 syntheses or guidelines pooled it, 107 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 1 institution in 1 country.

Nicholas J TimpsonMedical Research Council Centre for Causal Analyses in Translational Epidemiology, University of Bristol, Department of Social Medicine, Oakfield House, Oakfield Grove, Bristol, BS8 2BN, United Kingdom. n.j.timpson@bris.ac.uk
Nita G Forouhi
Marie-Jo Brion
Roger M Harbord
Derek G Cook
Paul Johnson
Alex McConnachie
Richard W Morris
Santiago Rodriguez
Jian'an Luan
Shah Ebrahim
Sandosh Padmanabhan
Graham Watt
K Richard Bruckdorfer
Nicholas J Wareham
Peter H Whincup
Steve Chanock
Naveed Sattar
Debbie A Lawlor
George Davey Smith
University of Bristol · GB

Funding

British Heart Foundation FS/05/095/19937British Heart Foundation FS05/125British Heart Foundation PG97012British Heart Foundation PG97027British Heart Foundation RG/08/013/25942Department of HealthMedical Research Council G0600705Medical Research Council G0601625Medical Research Council G9900686Medical Research Council MC_U106179471Medical Research Council MC_UP_A100_1003Wellcome Trust 051187/Z/97/AWellcome Trust 085515
6 · The paper itself

Abstract

backgroundL-ascorbic acid is an essential part of the human diet and has been associated with a wide range of chronic complex diseases, including cardiovascular outcomes. To date, there are no confirmed genetic correlates of circulating concentrations of L-ascorbic acid.

objectiveWe aimed to confirm the existence of an association between common variation at the SLC23A1 gene locus and circulating concentrations of L-ascorbic acid.

designWe used a 2-stage design, which included a discovery cohort (the British Women's Heart and Health Study), a series of follow-up cohorts, and meta-analysis (totaling 15,087 participants) to assess the relation between variation at SLC23A1 and circulating concentrations of L-ascorbic acid.

resultsIn the discovery cohort, variation at rs33972313 was associated with a reduction in circulating concentrations of L-ascorbic acid (-4.15 micromol/L; 95% CI: -0.49, -7.81 micromol/L; P = 0.03 reduction per minor allele). Pooled analysis of the relation between rs33972313 and circulating L-ascorbic acid across all studies confirmed this and showed that each additional rare allele was associated with a reduction in circulating concentrations of L-ascorbic acid of -5.98 micromol/L (95% CI: -8.23, -3.73 micromol/L; P = 2.0 x 10(-7) per minor allele).

conclusionsA genetic variant (rs33972313) in the SLC23A1 vitamin C active transporter locus was identified that is reliably associated with circulating concentrations of L-ascorbic acid in the general population. This finding has implications more generally for the epidemiologic investigation of relations between circulating L-ascorbic acid and health outcomes.

Indexed as

Polymorphism, Single NucleotideAdultAgedAscorbic AcidCohort StudiesFemaleGenetics, PopulationGenotypeHumansLinear ModelsMaleMiddle AgedOrganic Anion Transporters, Sodium-DependentSodium-Coupled Vitamin C TransportersSymportersAscorbic AcidOrganic Anion Transporters, Sodium-DependentSLC23A1 protein, humanSodium-Coupled Vitamin C TransportersSymporters

Identifiers

PMID20519558
PMCPMC3605792
OpenAlexW2161822077

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.