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Epigenome-Wide Association Study of Dietary Fiber Intake in African American Adolescents

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Scope: Low fiber intake is associated with increased risk for cardiovascular disease (CVD) and cancer. However, the underlying mechanisms are not well understood. Two hypotheses are tested: 1) dietary fiber would be associated with DNA methylation levels; 2) those DNA methylation changes would be associated with visceral adiposity and inflammation. Also the possibility that the associations between fiber and DNA methylation levels might be confounded with folic acid intake as sensitivity analysis are explored. Methods and results: An epigenome-wide association study is conducted using Illumina 450K Bead-Chip on leukocyte DNA in 284 African American adolescents. Linear regression is performed to identify differentially methylated CpG sites associated with fiber. The methylation levels of 3 CpG sites (cg15200711, cg19462022, and cg07035602) in LPCAT1 and RASA3 genes are associated with fiber (false discovery rate [FDR] < 0.05) after adjustment for covariates including folic acid. The methylation levels of cg07035602 and cg19462022 are also associated with visceral adiposity and inflammation. Conclusions: The data show that DNA methylation levels at LPCAT1 and RASA3 genes are associated with dietary fiber intake as well as with adiposity and inflammation. Future studies are warranted to determine whether epigenetic regulation may underlie the beneficial effects of fiber intake on adiposity and inflammation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

1800155

Journal (Volume, Issue Number)

Molecular Nutrition and Food Research (Volume 62, Issue 12)

Publication milestones

  • Accepted/In press - 01/01/2018
  • Published - 06/2018

Publication status

Published - 06/2018

ISSN

1613-4125

Publication IDs

  • Scopus: 85047658434
  • PubMed: 29644791
  • ORCID: /0000-0003-2454-4849/work/105758342

Publication metrics

Metrics

Scopus
citations
SciVal
citations
2
Fractional count
4
Fractional count
0.57
Fractional count
3
Fractional count
0.43
Fractional count
4
Fractional count
1
SciVal
FWCI
0.22
SciVal
Author count
7
SciVal
Paper percentile
49

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Citation count
11
Captures
35

Funding Details

L.C. and H.Z. conceptualized and designed the study, drafted the initial manuscript, critically reviewed and revised the manuscript. Y.H., B.G., and Y.D. collected the data, critically reviewed and revised the manuscript. X.W. and G.H. critically reviewed the manuscript. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work. Study was funded by National Heart, Lung and Blood Institute (HL105689), and American Heart Association (14GRNT20480211).
FundersFunding numbers
NHLBI
HL105689, R01HL104125
AHA
14GRNT20480211