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Less functional variants of TLR-1/-6/-10 genes are associated with age
BACKGROUND: Determining the prerequisites for healthy aging is a major task in the modern world characterized by a longer lifespan of the individuals. Besides lifestyle and environmental influences genetic factors are involved as shown by several genome-wide association studies. Older individuals ar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495943/ https://www.ncbi.nlm.nih.gov/pubmed/26157469 http://dx.doi.org/10.1186/s12979-015-0034-z |
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author | Hamann, Lutz Kupcinskas, Juozas Almanza, Berrocal Skieceviciene, Jurgita Franke, Andre Nöthlings, Ute Schumann, Ralf R. |
author_facet | Hamann, Lutz Kupcinskas, Juozas Almanza, Berrocal Skieceviciene, Jurgita Franke, Andre Nöthlings, Ute Schumann, Ralf R. |
author_sort | Hamann, Lutz |
collection | PubMed |
description | BACKGROUND: Determining the prerequisites for healthy aging is a major task in the modern world characterized by a longer lifespan of the individuals. Besides lifestyle and environmental influences genetic factors are involved as shown by several genome-wide association studies. Older individuals are known to have an impaired immune response, a condition recently termed “inflamm-aging”. We hypothesize that the induction of this condition in the elderly is influenced by the sensitivity of the innate immune system. Therefore, we investigated genetic variants of the Toll-like receptor (TLR) family, one of the major family of innate immune receptors, for association with age in two cohorts of healthy, disease-free subjects. RESULTS: According to sex we found a positive association of loss-of-function variants of TLR-1 and −6 with healthy aging with odds ratios of 1.54 in males for TLR-6 (249 S/S), and 1.41, 1.66, and 1.64 in females for TLR-1 prom., TLR-1 (248 S/S), and TLR-1 (602 S/S), respectively. Thus, the presence of these variants increases the probability of achieving healthy old age and indicates that a reduced TLR activity may be beneficial in the elderly. CONCLUSIONS: This is the first report showing an association of TLR variants with age. While a loss of function of an important immune receptor may be a risk factor for acute infections as has been shown previously, in the setting of healthy ageing it appears to be protective, which may relate to “inflamm-aging”. These first results should be reproduced in larger trials to confirm this hypothesis. |
format | Online Article Text |
id | pubmed-4495943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44959432015-07-09 Less functional variants of TLR-1/-6/-10 genes are associated with age Hamann, Lutz Kupcinskas, Juozas Almanza, Berrocal Skieceviciene, Jurgita Franke, Andre Nöthlings, Ute Schumann, Ralf R. Immun Ageing Research BACKGROUND: Determining the prerequisites for healthy aging is a major task in the modern world characterized by a longer lifespan of the individuals. Besides lifestyle and environmental influences genetic factors are involved as shown by several genome-wide association studies. Older individuals are known to have an impaired immune response, a condition recently termed “inflamm-aging”. We hypothesize that the induction of this condition in the elderly is influenced by the sensitivity of the innate immune system. Therefore, we investigated genetic variants of the Toll-like receptor (TLR) family, one of the major family of innate immune receptors, for association with age in two cohorts of healthy, disease-free subjects. RESULTS: According to sex we found a positive association of loss-of-function variants of TLR-1 and −6 with healthy aging with odds ratios of 1.54 in males for TLR-6 (249 S/S), and 1.41, 1.66, and 1.64 in females for TLR-1 prom., TLR-1 (248 S/S), and TLR-1 (602 S/S), respectively. Thus, the presence of these variants increases the probability of achieving healthy old age and indicates that a reduced TLR activity may be beneficial in the elderly. CONCLUSIONS: This is the first report showing an association of TLR variants with age. While a loss of function of an important immune receptor may be a risk factor for acute infections as has been shown previously, in the setting of healthy ageing it appears to be protective, which may relate to “inflamm-aging”. These first results should be reproduced in larger trials to confirm this hypothesis. BioMed Central 2015-07-08 /pmc/articles/PMC4495943/ /pubmed/26157469 http://dx.doi.org/10.1186/s12979-015-0034-z Text en © Hamann et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hamann, Lutz Kupcinskas, Juozas Almanza, Berrocal Skieceviciene, Jurgita Franke, Andre Nöthlings, Ute Schumann, Ralf R. Less functional variants of TLR-1/-6/-10 genes are associated with age |
title | Less functional variants of TLR-1/-6/-10 genes are associated with age |
title_full | Less functional variants of TLR-1/-6/-10 genes are associated with age |
title_fullStr | Less functional variants of TLR-1/-6/-10 genes are associated with age |
title_full_unstemmed | Less functional variants of TLR-1/-6/-10 genes are associated with age |
title_short | Less functional variants of TLR-1/-6/-10 genes are associated with age |
title_sort | less functional variants of tlr-1/-6/-10 genes are associated with age |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495943/ https://www.ncbi.nlm.nih.gov/pubmed/26157469 http://dx.doi.org/10.1186/s12979-015-0034-z |
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