Taste Preference-Related Genetic Polymorphisms Modify Alcohol Consumption Behavior of the Hungarian General and Roma Populations

Author:

Kurshed Ali Abbas Mohammad123,Vincze Ferenc1ORCID,Pikó Péter4ORCID,Kósa Zsigmond5,Sándor János14,Ádány Róza146ORCID,Diószegi Judit1

Affiliation:

1. Department of Public Health and Epidemiology, Faculty of Medicine, University of Debrecen, 4028 Debrecen, Hungary

2. Doctoral School of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary

3. Institute of Nutrition and Food Science, University of Dhaka, Dhaka 1000, Bangladesh

4. ELKH-DE Public Health Research Group, University of Debrecen, 4028 Debrecen, Hungary

5. Department of Health Methodology and Public Health, Faculty of Health Sciences, University of Debrecen, 4400 Nyíregyháza, Hungary

6. Department of Public Health, Semmelweis University, 1089 Budapest, Hungary

Abstract

Harmful alcohol consumption has been considered a major public health issue globally, with the amounts of alcohol drunk being highest in the WHO European Region including Hungary. Alcohol consumption behaviors are complex human traits influenced by environmental factors and numerous genes. Beyond alcohol metabolization and neurotransmitter gene polymorphisms, taste preference-related genetic variants may also mediate alcohol consumption behaviors. Applying the Alcohol Use Disorders Identification Test (AUDIT) we aimed to elucidate the underlying genetic determinants of alcohol consumption patterns considering taste preference gene polymorphisms (TAS1R3 rs307355, TAS2R38 rs713598, TAS2R19 rs10772420 and CA6 rs2274333) in the Hungarian general (HG) and Roma (HR) populations. Alcohol consumption assessment was available for 410 HG and 387 HR individuals with 405 HG and 364 HR DNA samples being obtained for genotyping. No significant associations were found between TAS1R3 rs307355, TAS2R19 rs10772420, and CA6 rs2274333 polymorphisms and alcohol consumption phenotypes. Significant associations were identified between TAS2R38 rs713598 and the number of standard drinks consumed in the HG sample (genotype GG negatively correlated with the number of standard drinks; coef: −0.136, p = 0.028) and the prevalence of having six or more drinks among Roma (a negative correlation was identified in the recessive model; genotype GG, coef: −0.170, p = 0.049), although, none of these findings passed the Bonferroni-corrected probability criterion (p > 0.05). Nevertheless, our findings may suggest that alcohol consumption is partially driven by genetically determined taste preferences in our study populations. Further studies are required to strengthen the findings and to understand the drivers of alcohol consumption behavior in more depth.

Funder

European Union under the European Social Fund and European Regional Development Fund

Hungarian Academy of Sciences

Eötvös Loránd Research Network

K_20 funding

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference142 articles.

1. World Health Organization (2014). Global Status Report on Alcohol and Health, WHO.

2. GBD Alcohol Collaborators (2022). Population-level risks of alcohol consumption by amount, geography, age, sex, and year: A systematic analysis for the Global Burden of Disease Study 2020. Lancet, 400, 185–235.

3. GBD 2019 Risk Factors Collaborators (2020). Global burden of 87 risk factors in 204 countries and territories, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet, 396, 1223–1249.

4. Alcohol-related deathsduring the COVID-19 pandemic;White;JAMA,2022

5. World Health Organization (2018). Global Status Report on Alcohol and Health 2018, WHO. Licence: CC BY-NC-SA 3.0IGO.

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