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Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women

OBJECTIVE: Pro-inflammatory interleukin 6 (IL6) trans-signalling is associated with increased risk of cardiovascular events (CVEs). Whether this association exists for both sexes is, however, uncertain. Hence, we analysed the risk of CVE associated with IL6 trans-signalling in men and women and inve...

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Autores principales: Miri, Yasmin, Leander, Karin, Eriksson, Per, Gigante, Bruna, Ziegler, Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506880/
https://www.ncbi.nlm.nih.gov/pubmed/34635574
http://dx.doi.org/10.1136/openhrt-2021-001694
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author Miri, Yasmin
Leander, Karin
Eriksson, Per
Gigante, Bruna
Ziegler, Louise
author_facet Miri, Yasmin
Leander, Karin
Eriksson, Per
Gigante, Bruna
Ziegler, Louise
author_sort Miri, Yasmin
collection PubMed
description OBJECTIVE: Pro-inflammatory interleukin 6 (IL6) trans-signalling is associated with increased risk of cardiovascular events (CVEs). Whether this association exists for both sexes is, however, uncertain. Hence, we analysed the risk of CVE associated with IL6 trans-signalling in men and women and investigated if potential interaction between IL6 trans-signalling and sex affects the risk. METHODS: In a prospective cohort of 60-year-old men and women without cardiovascular disease (men=2039, women=2193), subjects were followed for 20 years. To assess the IL6 trans-signalling activity, the proportion between the active binary and inactive ternary IL6 complexes, the binary/ternary ratio (B/T ratio), was estimated. CVE (myocardial infarction, angina pectoris and ischaemic stroke, n=629) risk was analysed with Cox regression, presented as HRs with 95% CIs. B/T ratio was dichotomised, with levels >median representing IL6 trans-signalling. Interaction was analysed on the additive scale and expressed as the synergy index (S). Analyses were adjusted for cardiovascular risk factors. RESULTS: B/T ratio >median was associated with increased CVE risk in men (HR 1.63; 95% CI 1.32 to 2.01), but not in women (HR 1.21; 95% CI 0.93 to 1.57). There was a significant synergistic interaction (S=1.98; 95% CI 1.15 to 3.42) between the B/T ratio and male sex, the combination increasing the risk by 88%. CONCLUSIONS: Our results suggest differential susceptibility to inflammation mediated by IL6 trans-signalling and subsequent CVE in men and women. The B/T ratio could be considered as a novel biomarker for cardiovascular risk in men, but not in women.
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spelling pubmed-85068802021-10-22 Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women Miri, Yasmin Leander, Karin Eriksson, Per Gigante, Bruna Ziegler, Louise Open Heart Cardiac Risk Factors and Prevention OBJECTIVE: Pro-inflammatory interleukin 6 (IL6) trans-signalling is associated with increased risk of cardiovascular events (CVEs). Whether this association exists for both sexes is, however, uncertain. Hence, we analysed the risk of CVE associated with IL6 trans-signalling in men and women and investigated if potential interaction between IL6 trans-signalling and sex affects the risk. METHODS: In a prospective cohort of 60-year-old men and women without cardiovascular disease (men=2039, women=2193), subjects were followed for 20 years. To assess the IL6 trans-signalling activity, the proportion between the active binary and inactive ternary IL6 complexes, the binary/ternary ratio (B/T ratio), was estimated. CVE (myocardial infarction, angina pectoris and ischaemic stroke, n=629) risk was analysed with Cox regression, presented as HRs with 95% CIs. B/T ratio was dichotomised, with levels >median representing IL6 trans-signalling. Interaction was analysed on the additive scale and expressed as the synergy index (S). Analyses were adjusted for cardiovascular risk factors. RESULTS: B/T ratio >median was associated with increased CVE risk in men (HR 1.63; 95% CI 1.32 to 2.01), but not in women (HR 1.21; 95% CI 0.93 to 1.57). There was a significant synergistic interaction (S=1.98; 95% CI 1.15 to 3.42) between the B/T ratio and male sex, the combination increasing the risk by 88%. CONCLUSIONS: Our results suggest differential susceptibility to inflammation mediated by IL6 trans-signalling and subsequent CVE in men and women. The B/T ratio could be considered as a novel biomarker for cardiovascular risk in men, but not in women. BMJ Publishing Group 2021-10-11 /pmc/articles/PMC8506880/ /pubmed/34635574 http://dx.doi.org/10.1136/openhrt-2021-001694 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Cardiac Risk Factors and Prevention
Miri, Yasmin
Leander, Karin
Eriksson, Per
Gigante, Bruna
Ziegler, Louise
Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title_full Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title_fullStr Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title_full_unstemmed Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title_short Interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
title_sort interleukin 6 trans-signalling and the risk of future cardiovascular events in men and women
topic Cardiac Risk Factors and Prevention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506880/
https://www.ncbi.nlm.nih.gov/pubmed/34635574
http://dx.doi.org/10.1136/openhrt-2021-001694
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