Taste receptors, innate immunity and longevity: the case of TAS2R16 gene.

Bitter taste receptors Case control study GWAS Innate immunity Longevity TAS2R16 gene

Journal

Immunity & ageing : I & A
ISSN: 1742-4933
Titre abrégé: Immun Ageing
Pays: England
ID NLM: 101235427

Informations de publication

Date de publication:
2019
Historique:
received: 26 12 2018
accepted: 18 02 2019
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 6 3 2019
Statut: epublish

Résumé

Innate immunity utilizes components of sensory signal transduction such as bitter and sweet taste receptors. In fact, empirical evidence has shown bitter and sweet taste receptors to be an integral component of antimicrobial immune response in upper respiratory tract infections. Since an efficient immune response plays a key role in the attainment of longevity, it is not surprising that the rs978739 polymorphism of the bitter taste receptor TAS2R16 gene has been shown to be associated with longevity in a population of 941 individuals ranging in age from 20 to 106 years from Calabria (Italy). There are many possible candidate genes for human longevity, however of the many genes tested, only APOE and FOXO3 survived to association in replication studies. So, it is necessary to validate in other studies genes proposed to be associated with longevity. Thus, we analysed the association of the quoted polymorphism in a population of long lived individuals (LLIs) and controls from another Italian population from Cilento. The analysis has been performed on data previously obtained with genome-wide association study on a population of LLIs (age range 90-109 years) and young controls (age range 18-45 years) from Cilento (Italy). Statistical power calculations showed that the analysed cohort represented by 410 LLIs and 553 young controls was sufficiently powered to replicate the association between rs978739 and the longevity phenotype according to the effect size and frequencies described in the previous paper, under a dominant and additive genetic model. However, no evidence of association between rs978739 and the longevity phenotype was observed according to the additive or dominant model. There are several reasons for the failure of the confirmation of a previous study. However, the differences between the two studies in terms of environment of the population adopted and of the criteria of inclusion have made difficult the replication of the findings.

Sections du résumé

BACKGROUND BACKGROUND
Innate immunity utilizes components of sensory signal transduction such as bitter and sweet taste receptors. In fact, empirical evidence has shown bitter and sweet taste receptors to be an integral component of antimicrobial immune response in upper respiratory tract infections. Since an efficient immune response plays a key role in the attainment of longevity, it is not surprising that the rs978739 polymorphism of the bitter taste receptor TAS2R16 gene has been shown to be associated with longevity in a population of 941 individuals ranging in age from 20 to 106 years from Calabria (Italy). There are many possible candidate genes for human longevity, however of the many genes tested, only APOE and FOXO3 survived to association in replication studies. So, it is necessary to validate in other studies genes proposed to be associated with longevity. Thus, we analysed the association of the quoted polymorphism in a population of long lived individuals (LLIs) and controls from another Italian population from Cilento.
METHODS METHODS
The analysis has been performed on data previously obtained with genome-wide association study on a population of LLIs (age range 90-109 years) and young controls (age range 18-45 years) from Cilento (Italy).
RESULTS RESULTS
Statistical power calculations showed that the analysed cohort represented by 410 LLIs and 553 young controls was sufficiently powered to replicate the association between rs978739 and the longevity phenotype according to the effect size and frequencies described in the previous paper, under a dominant and additive genetic model. However, no evidence of association between rs978739 and the longevity phenotype was observed according to the additive or dominant model.
CONCLUSION CONCLUSIONS
There are several reasons for the failure of the confirmation of a previous study. However, the differences between the two studies in terms of environment of the population adopted and of the criteria of inclusion have made difficult the replication of the findings.

Identifiants

pubmed: 30833980
doi: 10.1186/s12979-019-0146-y
pii: 146
pmc: PMC6387736
doi:

Types de publication

Journal Article

Langues

eng

Pagination

5

Déclaration de conflit d'intérêts

The study was approved by the Multimedica Hospital ethics committee. The study was conducted in accordance with the ethical principles that have their origins in the Declaration of Helsinki. Written informed consent was obtained from each study participant.Not applicable.At the time of the submission, Prof. Caruso was the Editor in Chief of Immunity & Ageing. Dr. Accardi was member of the Editorial Board. The other authors declare that they have no competing interests.Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Auteurs

Alberto Malovini (A)

Laboratory of Informatics and Systems Engineering for Clinical Research, Istituti Clinici Scientifici Maugeri, 27100 Pavia, Italy.

Giulia Accardi (G)

2Section of General Pathology, Department of Biomedicine, Neurosciences and Advanced Technologies, University of Palermo, Corso Tukory 211, 90134 Palermo, Italy.

Anna Aiello (A)

2Section of General Pathology, Department of Biomedicine, Neurosciences and Advanced Technologies, University of Palermo, Corso Tukory 211, 90134 Palermo, Italy.

Riccardo Bellazzi (R)

3Department of Electrical, Computer and Biomedical Engineering, University of Pavia, 27100 Pavia, Italy.

Giuseppina Candore (G)

2Section of General Pathology, Department of Biomedicine, Neurosciences and Advanced Technologies, University of Palermo, Corso Tukory 211, 90134 Palermo, Italy.

Calogero Caruso (C)

2Section of General Pathology, Department of Biomedicine, Neurosciences and Advanced Technologies, University of Palermo, Corso Tukory 211, 90134 Palermo, Italy.

Mattia Emanuela Ligotti (ME)

2Section of General Pathology, Department of Biomedicine, Neurosciences and Advanced Technologies, University of Palermo, Corso Tukory 211, 90134 Palermo, Italy.

Anna Maciag (A)

4Cardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.

Francesco Villa (F)

4Cardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.

Annibale A Puca (AA)

4Cardiovascular Research Unit, IRCCS MultiMedica, 20138 Milan, Italy.
5Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi, SA Italy.

Classifications MeSH