Evidence map›Paper›PMID 25201307›Full record

ArticleThe British journal of nutrition2014

Gene polymorphisms and gene scores linked to low serum carotenoid status and their associations with metabolic disturbance and depressive symptoms in African-American adults.

May A Beydoun, Michael A Nalls, J Atilio Canas, Michele K Evans, Alan B Zonderman

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of nutrition, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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  5. Enzymology of vertebrate carotenoid oxygenases.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
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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

5 authors at 1 institution in 1 country.

May A BeydounLaboratory of Epidemiology and Population Sciences, National Institute on Aging, NIH Biomedical Research Center,IRP 251, Bayview Boulevard, Suite 100, Room 04B118,Baltimore,MD21224,USA.
Michael A NallsLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health,Bethesda,MD,USA.
J Atilio CanasPediatric Endocrinology, Diabetes and Metabolism, Nemours Children's Clinic,Jacksonville,FL,USA.
Michele K EvansLaboratory of Epidemiology and Population Sciences, National Institute on Aging, NIH Biomedical Research Center,IRP 251, Bayview Boulevard, Suite 100, Room 04B118,Baltimore,MD21224,USA.
Alan B ZondermanLaboratory of Epidemiology and Population Sciences, National Institute on Aging, NIH Biomedical Research Center,IRP 251, Bayview Boulevard, Suite 100, Room 04B118,Baltimore,MD21224,USA.
National Institutes of Health · US

Funding

Healthy Aging In Neighborhoods of Diversity Across the Life Span (HANDLS)ZIAAG000513 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2009 to 2025
$70.9M
Intramural NIH HHS Z99 AG999999
6 · The paper itself

Abstract

Gene polymorphisms provide a means to obtain unconfounded associations between carotenoids and various health outcomes. In the present study, we tested whether gene polymorphisms and gene scores linked to low serum carotenoid status are related to metabolic disturbance and depressive symptoms in African-American adults residing in Baltimore city, MD, using cross-sectional data from the Healthy Aging in Neighborhoods of Diversity across the Life Span study (age range 30-64 years, n 873-994). We examined twenty-four SNP of various gene loci that were previously shown to be associated with low serum carotenoid status (SNPlcar). Gene risk scores were created: five low specific-carotenoid risk scores (LSCRS: α-carotene, β-carotene, lutein+zeaxanthin, β-cryptoxanthin and lycopene) and one low total-carotenoid risk score (LTCRS: total carotenoids). SNPlcar, LSCRS and LTCRS were entered as predictors for a number of health outcomes. These included obesity, National Cholesterol Education Program Adult Treatment Panel III metabolic syndrome and its components, elevated homeostatic model assessment of insulin resistance, C-reactive protein, hyperuricaemia and elevated depressive symptoms (EDS, Center for Epidemiologic Studies-Depression score ≥ 16). Among the key findings, SNPlcar were not associated with the main outcomes after correction for multiple testing. However, an inverse association was found between the LTCRS and HDL-cholesterol (HDL-C) dyslipidaemia. Specifically, the α-carotene and β-cryptoxanthin LSCRS were associated with a lower odds of HDL-C dyslipidaemia. However, the β-cryptoxanthin LSCRS was linked to a higher odds of EDS, with a linear dose-response relationship. In summary, gene risk scores linked to low serum carotenoids had mixed effects on HDL-C dyslipidaemia and EDS. Further studies using larger African-American population samples are needed.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAdultBaltimoreBlack or African AmericanCarotenoidsCohort StudiesCross-Sectional StudiesCryptoxanthinsDepressionDyslipidemiasFemaleGenetic LociGenome-Wide Association StudyHealth SurveysHumansalpha-caroteneCarotenoidsCryptoxanthins

Identifiers

PMID25201307
PMCPMC4887136
OpenAlexW2138214411

What OpenQuestion holds

Textmetadata
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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.