Evidence map›Paper›PMID 38683826›Full record

ArticlePloS one2024

Understanding the determinants of sweet taste liking in the African and East Asian ancestry groups in the U.S.-A study protocol.

May M Cheung, Patrice A Hubert, Danielle R Reed, Enrique R Pouget, Xinyin Jiang, Liang-Dar Hwang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

May M CheungCity University of New York, Brooklyn College, Brooklyn, New York, United States of America.ORCID 0000-0003-0754-5882
Patrice A HubertMonell Chemical Senses Center, Philadelphia, Pennsylvania, United States of America.
Danielle R ReedMonell Chemical Senses Center, Philadelphia, Pennsylvania, United States of America.
Enrique R PougetCity University of New York, Brooklyn College, Brooklyn, New York, United States of America.ORCID 0000-0002-5907-1909
Xinyin JiangCity University of New York, Brooklyn College, Brooklyn, New York, United States of America.
Liang-Dar HwangInstitute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
Brooklyn College · USMonell Chemical Senses Center · USThe University of Queensland · AU

Funding

INTERDISCIPLINARY TRAINING IN THE CHEMICAL SENSEST32DC000014 · NIDCD · MONELL CHEMICAL SENSES CENTER · PI PAMELA HELEN DALTON, Joel D Mainland · 1989 to 2026
$6.2M
Genetic and Environmental Influences on Individual Sweet Preference Across Ancestry Groups in the U.S.R16GM150411 · NIGMS · BROOKLYN COLLEGE · PI May Meiyu Cheung · 2023 to 2026
$785k
NIDCD NIH HHS T32 DC000014NIGMS NIH HHS R16 GM150411
6 · The paper itself

Abstract

backgroundThe liking for sweet taste is a powerful driver for consuming added sugars, and therefore, understanding how sweet liking is formed is a critical step in devising strategies to lower added sugars consumption. However, current research on the influence of genetic and environmental factors on sweet liking is mostly based on research conducted with individuals of European ancestry. Whether these results can be generalized to people of other ancestry groups warrants investigation.

methodsWe will determine the differences in allele frequencies in sweet-related genetic variants and their effects on sweet liking in 426 adults of either African or East Asian ancestry, who have the highest and lowest average added sugars intake, respectively, among ancestry groups in the U.S. We will collect information on participants' sweet-liking phenotype, added sugars intake (sweetness exposure), anthropometric measures, place-of-birth, and for immigrants, duration of time living in the U.S. and age when immigrated. Ancestry-specific polygenic scores of sweet liking will be computed based on the effect sizes of the sweet-related genetic variants on the sweet-liking phenotype for each ancestry group. The predictive validity of the polygenic scores will be tested using individuals of African and East Asian ancestry from the UK Biobank. We will also compare sweet liking between U.S.-born individuals and immigrants within each ancestry group to test whether differences in environmental sweetness exposure during childhood affect sweet liking in adulthood. DISCUSSION: Expanding genetic research on taste to individuals from ancestry groups traditionally underrepresented in such research is consistent with equity goals in sensory and nutrition science. Findings from this study will help in the development of a more personalized nutrition approach for diverse populations.

trial registrationThis protocol has been preregistered with the Center for Open Science (https://doi.org/10.17605/OSF.IO/WPR9E).

Indexed as

AsianBlack or African AmericanFood PreferencesTasteAdultFemaleGene FrequencyHumansMaleMiddle AgedPolymorphism, Single NucleotideResearch DesignUnited StatesYoung Adult

Identifiers

PMID38683826
PMCPMC11057733
OpenAlexW4396239853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.