Evidence map›Paper›PMID 23292069›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Genetic signatures in choline and 1-carbon metabolism are associated with the severity of hepatic steatosis.

Karen D Corbin, Manal F Abdelmalek, Melanie D Spencer, Kerry-Ann da Costa, Joseph A Galanko, Wei Sha, Ayako Suzuki, Cynthia D Guy, Diana M Cardona, Alfonso Torquati and 2 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02837367 (Use of Nutrigenomic Models for the Personalized Treatment With Medical Foods in Obese People), which is not on this map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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.

NCT02837367 naunknown statusnot on this mapstarted 2016, after this paper: background citation

Use of Nutrigenomic Models for the Personalized Treatment With Medical Foods in Obese People

TypeinterventionalSponsorUniversity of Medicine and Pharmacy "Victor Babes" TimisoaraRan2016 to 2019Enrolled600ConditionsObesity, DyslipidemiaArmsAdministration of supplements containing methyl-donors
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Racial and Ethnic Disparities in Nonalcoholic Fatty Liver Disease Prevalence, Severity, and Outcomes in the United States: A Systematic Review and Meta-analysis.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2018
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. NAFLD in normal weight individuals.Diabetology & metabolic syndrome · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Diabetes, metabolic syndrome and obesity : targets and therapy · 2020
    Article
  13. Article
  14. Article
  15. Plasma 1-carbon metabolites and academic achievement in 15-yr-old adolescents.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  16. Article
  17. Evidence for negative selection of gene variants that increase dependence on dietary choline in a Gambian cohort.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  18. Article
  19. Article
  20. Identification of new genetic polymorphisms that alter the dietary requirement for choline and vary in their distribution across ethnic and racial groups.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
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

12 authors at 6 institutions in 1 country.

Karen D CorbinUniversity of North Carolina at Chapel Hill Nutrition Research Institute, Kannapolis, NorthCarolina 28081, USA.
Manal F Abdelmalek
Melanie D Spencer
Kerry-Ann da Costa
Joseph A Galanko
Wei Sha
Ayako Suzuki
Cynthia D Guy
Diana M Cardona
Alfonso Torquati
Anna Mae Diehl
Steven H Zeisel
University of North Carolina at Chapel Hill · USDuke Medical Center · USDuke University · USDavid H. Murdock Research Institute · USDuke University Hospital · USUniversity of North Carolina at Charlotte · US

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUSAN M. SMITH · 1999 to 2026
$31.6M
PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBERT S. SANDLER · 1985 to 2026
$30.5M
GASTROENTEROLOGY RESEARCH TRAININGT32DK007737 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHEHZAD Z. SHEIKH · 1996 to 2026
$7.8M
HUMAN REQUIREMENTS FOR THE NUTRIENT CHOLINER01DK055865 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZEISEL, STEVEN H · 2000 to 2011
$7.6M
Hyperinsulinemia and Insulin Resistance in Fatty LiverK23DK062116 · NIDDK · UNIVERSITY OF FLORIDA · PI ABDELMALEK, MANAL F. · 2005 to 2009
$618k
NIDDK NIH HHS DK034987NIDDK NIH HHS K23 DK062116NIDDK NIH HHS K23-DK062116NIDDK NIH HHS P30 DK034987NIDDK NIH HHS P30 DK056350NIDDK NIH HHS P30DK056350NIDDK NIH HHS R01 DK055865NIDDK NIH HHS R01DK055865NIDDK NIH HHS T32 DK007737NIEHS NIH HHS P30 ES010126
6 · The paper itself

Abstract

Choline metabolism is important for very low-density lipoprotein secretion, making this nutritional pathway an important contributor to hepatic lipid balance. The purpose of this study was to assess whether the cumulative effects of multiple single nucleotide polymorphisms (SNPs) across genes of choline/1-carbon metabolism and functionally related pathways increase susceptibility to developing hepatic steatosis. In biopsy-characterized cases of nonalcoholic fatty liver disease and controls, we assessed 260 SNPs across 21 genes in choline/1-carbon metabolism. When SNPs were examined individually, using logistic regression, we only identified a single SNP (PNPLA3 rs738409) that was significantly associated with severity of hepatic steatosis after adjusting for confounders and multiple comparisons (P=0.02). However, when groupings of SNPs in similar metabolic pathways were defined using unsupervised hierarchical clustering, we identified groups of subjects with shared SNP signatures that were significantly correlated with steatosis burden (P=0.0002). The lowest and highest steatosis clusters could also be differentiated by ethnicity. However, unique SNP patterns defined steatosis burden irrespective of ethnicity. Our results suggest that analysis of SNP patterns in genes of choline/1-carbon metabolism may be useful for prediction of severity of steatosis in specific subsets of people, and the metabolic inefficiencies caused by these SNPs should be examined further.

Indexed as

AdolescentAdultAgedAged, 80 and overBiopsyCarbonCholineFatty LiverGenotypeHumansLiverMiddle AgedPolymorphism, Single NucleotideYoung AdultCarbonCholine

Identifiers

PMID23292069
PMCPMC3606533
OpenAlexW2152115036

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.