Evidence map›Paper›PMID 19819120›Full record

ArticleNutrition, metabolism, and cardiovascular diseases : NMCD2010

ADAM17_i33708A>G polymorphism interacts with dietary n-6 polyunsaturated fatty acids to modulate obesity risk in the Genetics of Lipid Lowering Drugs and Diet Network study.

M Junyent, L D Parnell, C-Q Lai, D K Arnett, M Y Tsai, E K Kabagambe, R J Straka, M Province, P An, C E Smith and 3 more

Abstract read
In one paragraph

Article in Nutrition, metabolism, and cardiovascular diseases : NMCD, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. SARS- CoV-2 infection and oxidative stress in early-onset preeclampsia.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Review
  6. Contribution of ADAM17 and related ADAMs in cardiovascular diseases.Cellular and molecular life sciences : CMLS · 2021
    Review
  7. Article
  8. Postprandial activation of leukocyte-endothelium interaction by fatty acids in the visceral adipose tissue microcirculation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Fatty acid-gene interactions, adipokines and obesity.European journal of clinical nutrition · 2011
    Review
  17. Article
  18. Adaptive genetic variation and heart disease risk.Current opinion in lipidology · 2010
    Review
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

13 authors at 5 institutions in 1 country.

M JunyentNutrition and Genomics Laboratory, JM-USDA-HNRCA at Tufts University, Boston, MA 02111, USA. mireia.junyent@tufts.edu
L D Parnell
C-Q Lai
D K Arnett
M Y Tsai
E K Kabagambe
R J Straka
M Province
P An
C E Smith
Y-C Lee
I Borecki
J M Ordovás
Jean Mayer Human Nutrition Research Center on Aging · USTufts University · USWashington University in St. Louis · USUniversity of Alabama at Birmingham · USUniversity of Minnesota · US

Funding

Genetic and Environmental Determinants of TriglyceridesU01HL072524 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARNETT, DONNA K · 2002 to 2008
$11.9M
Genomewide Association Study of Lipid Response to Fenofibrate and Dietary FatR01HL091357 · NHLBI · UNIVERSITY OF KENTUCKY · PI ARNETT, DONNA K · 2008 to 2018
$5.8M
GENE/DIET EFFECTS ON PLASMA LIPOPROTEIN LEVELSR01HL054776 · NHLBI · TUFTS UNIVERSITY BOSTON · PI ORDOVAS, JOSE M. · 1996 to 2010
$2.6M
TRAINING PROGRAM IN HUMAN NUTRITION AND METABOLISMT32DK007651 · NIDDK · TUFTS UNIVERSITY BOSTON · PI MASON, JOEL B · 1990 to 2009
$1.9M
PAT PROTEINS: GENE-DIET INTERACTIONS OBESITY RISK AND HEALTHR01DK075030 · NIDDK · TUFTS UNIVERSITY BOSTON · PI ORDOVAS, JOSE M. · 2007 to 2009
$989k
NHLBI NIH HHS HL-54776NHLBI NIH HHS R01 HL054776NHLBI NIH HHS R01 HL091357NHLBI NIH HHS U 01 HL72524NIDDK NIH HHS DK075030NIDDK NIH HHS R01 DK075030NIDDK NIH HHS T32 DK007651NIDDK NIH HHS T32 DK007651-19NIMHD NIH HHS L60 MD003562
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe disintegrin and metalloproteinase ADAM17, also known as tumor necrosis factor alpha converting enzyme, is expressed in adipocytes. Importantly, elevated levels of ADAM17 expression have been linked to obesity and insulin resistance. Therefore, the aim of this study was to evaluate the association of six ADAM17 single nucleotide polymorphisms (SNPs) (m1254A>G, i14121C>A, i33708A>G, i48827A>C, i53440C>T, and i62781G>T) with insulin-resistance phenotypes and obesity risk, and their potential interactions with dietary polyunsaturated fatty acids (PUFA). METHODS AND

resultsADAM17 SNPs were genotyped in 936 subjects (448 men/488 women) who participated in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study. Anthropometrical and biochemical measurements were determined by standard procedures. PUFA intake was estimated using a validated questionnaire. G allele carriers at the ADAM17_m1254A>G polymorphism exhibited significantly higher risk of obesity (P=0.003), were shorter (P=0.017), had higher insulin (P=0.016), and lower HDL-C concentrations (P=0.027) than AA subjects. For the ADAM17_i33708A>G SNP, homozygotes for the A allele displayed higher risk of obesity (P=0.001), were heavier (P=0.011), had higher BMI (P=0.005), and higher waist measurements (P=0.023) than GG subjects. A significant gene-diet interaction was found (P=0.030), in which the deleterious association of the i33708A allele with obesity was observed in subjects with low intakes from (n-6) PUFA (P<0.001), whereas no differences in obesity risk were seen among subjects with high (n-6) PUFA intake (P>0.5)

conclusionThese findings support that ADAM17 (m1254A>G and i33708A>G) SNPs may contribute to obesity risk. For the ADAM17_i33708A>G SNP, this risk may be further modulated by (n-6) PUFA intake.

Indexed as

Polymorphism, Single NucleotideADAM17 ProteinADAM ProteinsAdipocytesAdultAgedAllelesBody Mass IndexCholesterol, HDLDietDietary Fats, UnsaturatedFatty Acids, Omega-6FemaleGenetic Predisposition to DiseaseGenotypeHumansADAM17 ProteinADAM17 protein, humanADAM ProteinsCholesterol, HDLDietary Fats, UnsaturatedFatty Acids, Omega-6Insulin

Identifiers

PMID19819120
PMCPMC4361226
OpenAlexW1979595539

What OpenQuestion holds

Textmetadata
LicenceTDM
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.