Telomere attrition in heart failure

Cross-sectional investigations report shorter telomeres in patients with heart failure (HF); however, no studies describe telomere length (TL) trajectory and its relationship with HF progression. Here we aimed to investigate telomere shortening over time and its relationship to outcomes. Our study c...

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Detalles Bibliográficos
Autores: Teubel, Iris, Elchinova, Elena Georgieva, Roura, Santiago|||0000-0003-4063-9661, Fernández, Marco A.|||0000-0002-3921-2209, Gálvez-Montón, Carolina|||0000-0003-2254-9371, Moliner, P.|||0000-0002-5511-8597, de Antonio Ferrer, Marta|||0000-0002-4319-797X, Lupón, Josep|||0000-0002-5601-9611, Bayés-Genís, Antoni|||0000-0002-3044-197X
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:187894
Acceso en línea:https://ddd.uab.cat/record/187894
https://dx.doi.org/urn:doi:10.1186/s12967-018-1412-z
Access Level:acceso abierto
Palabra clave:Heart failure
Monocyte subsets
Telomere attrition
Telomere length
Descripción
Sumario:Cross-sectional investigations report shorter telomeres in patients with heart failure (HF); however, no studies describe telomere length (TL) trajectory and its relationship with HF progression. Here we aimed to investigate telomere shortening over time and its relationship to outcomes. Our study cohort included 101 ambulatory patients with HF. Blood samples were collected at baseline (n = 101) and at the 1-year follow-up (n = 54). Using flow-FISH analysis of circulating monocytes, we simultaneously measured three monocyte subsets-classical (CD14 ++ CD16 -), intermediate (CD14 ++ CD16 +), and nonclassical (CD14 + CD16 ++)-and their respective TLs based on FITC-labeled PNA probe hybridization. The primary endpoints were all-cause death and the composite of all-cause death or HF-related hospitalization, assessed at 2.3 ± 0.6 years. All statistical analyses were executed by using the SPSS 15.0 software, and included Student's t test and ANOVA with post hoc Scheffe analysis, Pearson or Spearman rho correlation and univariate Cox regression when applicable. We found high correlations between TL values of different monocyte subsets: CD14 ++ CD16 + vs. CD14 ++ CD16 -, R = 0.95, p < 0.001; CD14 ++ CD16 + vs. CD14 + CD16 ++, R = 0.90, p < 0.001; and CD14 ++ CD16 - vs. CD14 + CD16 ++, R = 0.89, p < 0.001. Mean monocyte TL exhibited significant attrition from baseline to the 1-year follow-up (11.1 ± 3.3 vs. 8.3 ± 2.1, p < 0.001). TL did not significantly differ between monocyte subsets at either sampling time-point (all p values.