Evidence map›Paper›PMID 39284855›Full record

ArticleScientific reports2024

Genomic study of taste perception genes in African Americans reveals SNPs linked to Alzheimer's disease.

Paule Valery Joseph, Malak Abbas, Gabriel Goodney, Ana Diallo, Amadou Gaye

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Paule Valery JosephSensory Science and Metabolism Unit, Biobehavioral Branch, National Institute On Alcohol Abuse and Alcoholism, National Institue of Nursing Research, National Institutes of Health, Bethesda, MD, USA.
Malak AbbasNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Gabriel GoodneyNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Ana DialloDepartment of Pharmacotherapy & Outcomes Science, Virginia Commonwealth University, Richmond, VA, USA.
Amadou GayeDepartment of Integrative Genomics and Epidemiology, School of Graduate Studies, Meharry Medical College, Nashville, TN, USA. amadou.gaye@mmc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While previous research has shown the potential links between taste perception pathways and brain-related conditions, the area involving Alzheimer's disease remains incompletely understood. Taste perception involves neurotransmitter signaling, including serotonin, glutamate, and dopamine. Disruptions in these pathways are implicated in neurodegenerative diseases. The integration of olfactory and taste signals in flavor perception may impact brain health, evident in olfactory dysfunction as an early symptom in neurodegenerative conditions. Shared immune response and inflammatory pathways may contribute to the association between altered taste perception and conditions like neurodegeneration, present in Alzheimer's disease. This study consists of an exploration of expression-quantitative trait loci (eQTL), utilizing whole-blood transcriptome profiles, of 28 taste perception genes, from a combined cohort of 475 African American subjects. This comprehensive dataset was subsequently intersected with single-nucleotide polymorphisms (SNPs) identified in Genome-Wide Association Studies (GWAS) of Alzheimer's Disease (AD). Finally, the investigation delved into assessing the association between eQTLs reported in GWAS of AD and the profiles of 741 proteins from the Olink Neurological Panel. The eQTL analysis unveiled 3,547 statistically significant SNP-Gene associations, involving 412 distinct SNPs that spanned all 28 taste genes. In 17 GWAS studies encompassing various traits, a total of 14 SNPs associated with 12 genes were identified, with three SNPs consistently linked to Alzheimer's disease across four GWAS studies. All three SNPs demonstrated significant associations with the down-regulation of TAS2R41, and two of them were additionally associated with the down-regulation of TAS2R60. In the subsequent pQTL analysis, two of the SNPs linked to TAS2R41 and TAS2R60 genes (rs117771145 and rs10228407) were correlated with the upregulation of two proteins, namely EPHB6 and ADGRB3. Our investigation introduces a new perspective to the understanding of Alzheimer's disease, emphasizing the significance of bitter taste receptor genes in its pathogenesis. These discoveries set the stage for subsequent research to delve into these receptors as promising avenues for both intervention and diagnosis. Nevertheless, the translation of these genetic insights into clinical practice requires a more profound understanding of the implicated pathways and their pertinence to the disease's progression across diverse populations.

Indexed as

Alzheimer DiseaseBlack or African AmericanGenome-Wide Association StudyPolymorphism, Single NucleotideQuantitative Trait LociTaste PerceptionAgedFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedTranscriptomeAfrican AmericanAlzheimer’s diseaseGWASProteomeTaste genesTranscriptome

Identifiers

PMID39284855
PMCPMC11405524

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