Evidence map›Paper›PMID 21810599›Full record

SynthesisDiabetes2011

Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis.

Stavroula Kanoni, Jennifer A Nettleton, Marie-France Hivert, Zheng Ye, Frank J A van Rooij, Dmitry Shungin, Emily Sonestedt, Julius S Ngwa, Mary K Wojczynski, Rozenn N Lemaitre and 47 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Diabetes, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 5 pooled it
8.6field-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

59 citing papers in PubMed, 5 syntheses or guidelines pooled it, 99 citations in OpenAlex.

  1. Pooled it
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  6. A loss of function variant inmedRxiv : the preprint server for health sciences · 2026
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  9. Type 2 diabetes mellitus and zinc dysregulation: From basic and epidemiological evidence to interventions.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

57 authors at 20 institutions in 7 countries.

Stavroula KanoniDepartment of Nutrition-Dietetics, Harokopio University, Athens, Greece. stavroula.kanoni@sanger.ac.uk
Jennifer A Nettleton
Marie-France Hivert
Zheng Ye
Frank J A van Rooij
Dmitry Shungin
Emily Sonestedt
Julius S Ngwa
Mary K Wojczynski
Rozenn N Lemaitre
Stefan Gustafsson
Jennifer S Anderson
Toshiko Tanaka
George Hindy
Georgia Saylor
Frida Renstrom
Amanda J Bennett
Cornelia M van Duijn
Jose C Florez
Caroline S Fox
Albert Hofman
Ron C Hoogeveen
Denise K Houston
Frank B Hu
Paul F Jacques
Ingegerd Johansson
Lars Lind
Yongmei Liu
Nicola McKeown
Jose Ordovas
James S Pankow
Eric J G Sijbrands
Ann-Christine Syvänen
André G Uitterlinden
Mary Yannakoulia
M Carola Zillikens
MAGIC Investigators
Nick J Wareham
Inga Prokopenko
Stefania Bandinelli
Nita G Forouhi
L Adrienne Cupples
Ruth J Loos
Goran Hallmans
Josée Dupuis
Claudia Langenberg
Luigi Ferrucci
Stephen B Kritchevsky
Mark I McCarthy
Erik Ingelsson
Ingrid B Borecki
Jacqueline C M Witteman
Marju Orho-Melander
David S Siscovick
James B Meigs
Paul W Franks
George V Dedoussis
Lund University · SEErasmus MC · NLBoston University · USCentre for Human Genetics · GBNational Institute on Aging · USTufts University · USWashington University in St. Louis · USAddenbrooke's Hospital · GBAtrium Health Wake Forest Baptist · USHarokopio University of Athens · GRUniversity of Washington · USUppsala University · SEWake Forest University · USAzienda Sanitaria di Firenze · ITBrigham and Women's Hospital · USBroad Institute · USHouston Methodist · USKarolinska Institutet · SEMRC Epidemiology Unit · GBOxford Centre for Diabetes, Endocrinology and Metabolism · GB

Funding

Framingham Heart Study/FoxZIAHL006094 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI FOX, CAROLINE · 2010 to 2015
$6.9M
FHS-SCAN Genome Wide Association Scan for Atherosclerosis Pathway GenesR01HL087700 · NHLBI · WASHINGTON UNIVERSITY · PI PROVINCE, MICHAEL A. · 2006 to 2008
$5.4M
The InChianti StudyZIAAG001050 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2025
$2.1M
Medical Research Council G0701863Medical Research Council MC_U106179471Medical Research Council MC_U106188470Medical Research Council MC_UP_A100_1003NHLBI NIH HHS R01 HL087700Wellcome Trust 090532
6 · The paper itself

Abstract

objectiveMany genetic variants have been associated with glucose homeostasis and type 2 diabetes in genome-wide association studies. Zinc is an essential micronutrient that is important for β-cell function and glucose homeostasis. We tested the hypothesis that zinc intake could influence the glucose-raising effect of specific variants. RESEARCH DESIGN AND

methodsWe conducted a 14-cohort meta-analysis to assess the interaction of 20 genetic variants known to be related to glycemic traits and zinc metabolism with dietary zinc intake (food sources) and a 5-cohort meta-analysis to assess the interaction with total zinc intake (food sources and supplements) on fasting glucose levels among individuals of European ancestry without diabetes.

resultsWe observed a significant association of total zinc intake with lower fasting glucose levels (β-coefficient ± SE per 1 mg/day of zinc intake: -0.0012 ± 0.0003 mmol/L, summary P value = 0.0003), while the association of dietary zinc intake was not significant. We identified a nominally significant interaction between total zinc intake and the SLC30A8 rs11558471 variant on fasting glucose levels (β-coefficient ± SE per A allele for 1 mg/day of greater total zinc intake: -0.0017 ± 0.0006 mmol/L, summary interaction P value = 0.005); this result suggests a stronger inverse association between total zinc intake and fasting glucose in individuals carrying the glucose-raising A allele compared with individuals who do not carry it. None of the other interaction tests were statistically significant.

conclusionsOur results suggest that higher total zinc intake may attenuate the glucose-raising effect of the rs11558471 SLC30A8 (zinc transporter) variant. Our findings also support evidence for the association of higher total zinc intake with lower fasting glucose levels.

Indexed as

Blood GlucoseCation Transport ProteinsCohort StudiesHumansPolymorphism, Single NucleotideZincZinc Transporter 8Blood GlucoseCation Transport ProteinsSLC30A8 protein, humanZincZinc Transporter 8

Identifiers

PMID21810599
PMCPMC3161318
OpenAlexW2117706536

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.