Distribution of functional polymorphic variants of inflammation-related genes RANTES and CCR5 in long-lived individuals

Author

Laplana Lafaja, Marina

Fibla Palazón, Joan

Publication date

2020-02-12T10:53:40Z

2020-02-12T10:53:40Z

2012

2020-02-12T10:53:41Z



Abstract

Although persistent inflammation has been related to unsuccessful aging, a pro-inflammatory status is the common phenotype in older people. To assess for a genetic component in the inflammatory status of the oldest we studied the distribution of two polymorphic chemokine pathway genes, RANTES and CCR5, in elderly. RANTES −403G/A and RANTES Int1.1T/C polymorphisms and CCR5Δ32 polymorphism were genotyped in 104 elderly and 110 controls. RANTES −403A and RANTES Int1.1C alleles have been associated with pro-inflammatory and anti-inflammatory status, respectively. CCR5Δ32 abrogates functional receptor expression of the pro-inflammatory CCR5-mediated action. Prevalence of RANTES −403G allele, associated in other studies with high RANTES production, was reduced in elderly males, compared with controls. In addition, RANTES pro-inflammatory haplotype −403A-Int1.1T was overrepresented in elderly males, while RANTES anti-inflammatory haplotype −403G-Int1.1C was overrepresented in elderly females. Our results suggest a sex-specific RANTES inflammatory genetic determinant that could contribute to the known sex-related differences in aging.


M.L. was recipient of a fellowship from the University of Lleida. This work was supported by grants to the University of Lleida (J.F., principal investigator) from Fondo de Investigación Sanitaria (FIS, PI051778) and Ministerio de Ciencia e Innovación (CGL 2007-62875).

Document Type

Article
Accepted version

Language

English

Subjects and keywords

Longevidad; Inflamación; Genética humana; SNP; Cytokines

Publisher

Elsevier

Related items

MIECI/PN2004-2007/CGL-2007-62875

Versió postprint del document publicat a: https://doi.org/10.1016/j.cyto.2011.12.021

Cytokine, 2012, vol. 58, num. 1, p. 10-13

Rights

cc-by-nc-nd, (c) Elsevier, 2012

http://creativecommons.org/licenses/by-nc-nd/4.0/

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