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Gender in cardiac resynchronisation therapy

Introduction: Gender differences in cardiac resynchronisation therapy (CRT) response are not clear enough. This study aimed to assess gender influence on systemic inflammation, neurohormonal activation, fibrosis in patients with congestive heart failure (CHF) and CRT. Methods: We compared group I (6...

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Autores principales: Enina, Tatiana N., Kuznetsov, Vadim A., Soldatova, Anna M., Petelina, Tatiana I., Krinochkin, Dmitriy V., Rychkov, Alexander Yu., Nochrina, Olga Yu.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335983/
https://www.ncbi.nlm.nih.gov/pubmed/30680077
http://dx.doi.org/10.15171/jcvtr.2018.34
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author Enina, Tatiana N.
Kuznetsov, Vadim A.
Soldatova, Anna M.
Petelina, Tatiana I.
Krinochkin, Dmitriy V.
Rychkov, Alexander Yu.
Nochrina, Olga Yu.
author_facet Enina, Tatiana N.
Kuznetsov, Vadim A.
Soldatova, Anna M.
Petelina, Tatiana I.
Krinochkin, Dmitriy V.
Rychkov, Alexander Yu.
Nochrina, Olga Yu.
author_sort Enina, Tatiana N.
collection PubMed
description Introduction: Gender differences in cardiac resynchronisation therapy (CRT) response are not clear enough. This study aimed to assess gender influence on systemic inflammation, neurohormonal activation, fibrosis in patients with congestive heart failure (CHF) and CRT. Methods: We compared group I (61 men) and group II (16 women) of patients undergoing CRT. Plasma levels of Nt-proBNP, interleukin (IL)-1β, IL-6, IL-10, tumor necrosis factor alpha (TNF-α), C-reactive protein, galectin-3 (Gal-3), metalloproteinase-9 (MMP-9), tissue inhibitors of metalloproteinase 1 and 4 (TIMP-1, TIMP-4), ratio MMP-9/TIMP-1, MMP-9/TIMP-4 were measured. According to dynamics of left ventricular end-systolic volume patients were classified into non-responders, responders, super-responders. Results: Women more likely had left bundle branch block (81.3 vs 47.5%, P = 0.016), were more super-responders (66.7 vs 30.5%). Both groups showed decrease of IL-6 (P < 0.05), TNF-α (P < 0.001; P < 0.05), NT-proBNP (P = 0.001; P < 0.05), Gal-3 (P < 0.05). In women there was decrease of IL-6 by 44.4 vs 23.5% in men (PP = 0.029), TNF-α by 41.4 vs 30.9%, NT-proBNP by 73.3 vs 46% (P = 0.002), Gal-3 by 82.3 vs 64.9% (P < 0.05). Group I also showed decrease of IL-10 by 34.2% (P < 0.05). Group dynamics of TIMP-1 was opposite: men showed tendency to reduction of TIMP-1 (P = 0.054), women showed increase of TIMP-1 (P < 0.05). Besides, men showed decrease of MMP-9 (P < 0.05) and ratio MMP-9/TIMP-4 (P < 0.05). Conclusion: The best response to CRT is associated with female gender explained by greater decrease of neurohormonal activation, systemic inflammation and fibrosis. The revealed opposite dynamics of TIMP-1 in the groups can demonstrate the existence of gender features of matrix metalloproteinase system activity and their tissue inhibitors.
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spelling pubmed-63359832019-01-24 Gender in cardiac resynchronisation therapy Enina, Tatiana N. Kuznetsov, Vadim A. Soldatova, Anna M. Petelina, Tatiana I. Krinochkin, Dmitriy V. Rychkov, Alexander Yu. Nochrina, Olga Yu. J Cardiovasc Thorac Res Original Article Introduction: Gender differences in cardiac resynchronisation therapy (CRT) response are not clear enough. This study aimed to assess gender influence on systemic inflammation, neurohormonal activation, fibrosis in patients with congestive heart failure (CHF) and CRT. Methods: We compared group I (61 men) and group II (16 women) of patients undergoing CRT. Plasma levels of Nt-proBNP, interleukin (IL)-1β, IL-6, IL-10, tumor necrosis factor alpha (TNF-α), C-reactive protein, galectin-3 (Gal-3), metalloproteinase-9 (MMP-9), tissue inhibitors of metalloproteinase 1 and 4 (TIMP-1, TIMP-4), ratio MMP-9/TIMP-1, MMP-9/TIMP-4 were measured. According to dynamics of left ventricular end-systolic volume patients were classified into non-responders, responders, super-responders. Results: Women more likely had left bundle branch block (81.3 vs 47.5%, P = 0.016), were more super-responders (66.7 vs 30.5%). Both groups showed decrease of IL-6 (P < 0.05), TNF-α (P < 0.001; P < 0.05), NT-proBNP (P = 0.001; P < 0.05), Gal-3 (P < 0.05). In women there was decrease of IL-6 by 44.4 vs 23.5% in men (PP = 0.029), TNF-α by 41.4 vs 30.9%, NT-proBNP by 73.3 vs 46% (P = 0.002), Gal-3 by 82.3 vs 64.9% (P < 0.05). Group I also showed decrease of IL-10 by 34.2% (P < 0.05). Group dynamics of TIMP-1 was opposite: men showed tendency to reduction of TIMP-1 (P = 0.054), women showed increase of TIMP-1 (P < 0.05). Besides, men showed decrease of MMP-9 (P < 0.05) and ratio MMP-9/TIMP-4 (P < 0.05). Conclusion: The best response to CRT is associated with female gender explained by greater decrease of neurohormonal activation, systemic inflammation and fibrosis. The revealed opposite dynamics of TIMP-1 in the groups can demonstrate the existence of gender features of matrix metalloproteinase system activity and their tissue inhibitors. Tabriz University of Medical Sciences 2018 2018-11-10 /pmc/articles/PMC6335983/ /pubmed/30680077 http://dx.doi.org/10.15171/jcvtr.2018.34 Text en © 2018 The Author(s) 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 cited.
spellingShingle Original Article
Enina, Tatiana N.
Kuznetsov, Vadim A.
Soldatova, Anna M.
Petelina, Tatiana I.
Krinochkin, Dmitriy V.
Rychkov, Alexander Yu.
Nochrina, Olga Yu.
Gender in cardiac resynchronisation therapy
title Gender in cardiac resynchronisation therapy
title_full Gender in cardiac resynchronisation therapy
title_fullStr Gender in cardiac resynchronisation therapy
title_full_unstemmed Gender in cardiac resynchronisation therapy
title_short Gender in cardiac resynchronisation therapy
title_sort gender in cardiac resynchronisation therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335983/
https://www.ncbi.nlm.nih.gov/pubmed/30680077
http://dx.doi.org/10.15171/jcvtr.2018.34
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