Cargando…
Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review
OBJECTIVE: Cardiac resynchronisation therapy (CRT) is an effective therapy for selected patients with heart failure (HF); however, a significant non-response rate exists. We examined current evidence on extracellular cardiac matrix (ECM) biomarkers in predicting response following CRT. METHODS: Comp...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574440/ https://www.ncbi.nlm.nih.gov/pubmed/28878953 http://dx.doi.org/10.1136/openhrt-2017-000639 |
_version_ | 1783259838063575040 |
---|---|
author | McAloon, Christopher J Ali, Danish Hamborg, Thomas Banerjee, Prithwish O'Hare, Paul Randeva, Harpal Osman, Faizel |
author_facet | McAloon, Christopher J Ali, Danish Hamborg, Thomas Banerjee, Prithwish O'Hare, Paul Randeva, Harpal Osman, Faizel |
author_sort | McAloon, Christopher J |
collection | PubMed |
description | OBJECTIVE: Cardiac resynchronisation therapy (CRT) is an effective therapy for selected patients with heart failure (HF); however, a significant non-response rate exists. We examined current evidence on extracellular cardiac matrix (ECM) biomarkers in predicting response following CRT. METHODS: Complete literature review of PubMed, Ovid SP MEDLINE, Cochrane Library and TRIP, reference lists, international cardiology conferences and ongoing studies between December 1999 and December 2015 conducted according to prospectively registered study selection and analysis criteria (PROSPERO:CRD42016025864) was performed. All observational and randomised control trials (RCT) were included if they tested prespecified ECM biomarkers’ ability to predict CRT response. Risk of bias assessment and data extraction determined pooling of included studies was not feasible due to heterogeneity of the selected studies. RESULTS: A total of 217 studies were screened; six (five prospective cohort and one RCT substudy) were included in analysis with 415 participants in total. Study sizes varied (n=55–260), cohort characteristics contrasted (male: 67.8%–83.6%, ischaemic aetiology: 40.2%–70.3%) and CRT response definitions differed (three clinical/functional, three echocardiographic). Consistent observation in all ECM biomarker behaviour before and after CRT implantation was not observed between studies. Lower type I and type III collagen synthesis biomarkers (N-terminal propeptides of type I and III procollagens) expression demonstrated replicated ability to predict reverse left ventricular remodelling. CONCLUSION: Collagen synthesis biomarkers offer the most potential as ECM biomarkers for predicting CRT response. Heterogeneity between these studies was large and limited the ability to pool and compare results numerically. Use of different response definitions was one of the biggest challenges. |
format | Online Article Text |
id | pubmed-5574440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55744402017-09-06 Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review McAloon, Christopher J Ali, Danish Hamborg, Thomas Banerjee, Prithwish O'Hare, Paul Randeva, Harpal Osman, Faizel Open Heart Heart Failure and Cardiomyopathies OBJECTIVE: Cardiac resynchronisation therapy (CRT) is an effective therapy for selected patients with heart failure (HF); however, a significant non-response rate exists. We examined current evidence on extracellular cardiac matrix (ECM) biomarkers in predicting response following CRT. METHODS: Complete literature review of PubMed, Ovid SP MEDLINE, Cochrane Library and TRIP, reference lists, international cardiology conferences and ongoing studies between December 1999 and December 2015 conducted according to prospectively registered study selection and analysis criteria (PROSPERO:CRD42016025864) was performed. All observational and randomised control trials (RCT) were included if they tested prespecified ECM biomarkers’ ability to predict CRT response. Risk of bias assessment and data extraction determined pooling of included studies was not feasible due to heterogeneity of the selected studies. RESULTS: A total of 217 studies were screened; six (five prospective cohort and one RCT substudy) were included in analysis with 415 participants in total. Study sizes varied (n=55–260), cohort characteristics contrasted (male: 67.8%–83.6%, ischaemic aetiology: 40.2%–70.3%) and CRT response definitions differed (three clinical/functional, three echocardiographic). Consistent observation in all ECM biomarker behaviour before and after CRT implantation was not observed between studies. Lower type I and type III collagen synthesis biomarkers (N-terminal propeptides of type I and III procollagens) expression demonstrated replicated ability to predict reverse left ventricular remodelling. CONCLUSION: Collagen synthesis biomarkers offer the most potential as ECM biomarkers for predicting CRT response. Heterogeneity between these studies was large and limited the ability to pool and compare results numerically. Use of different response definitions was one of the biggest challenges. BMJ Publishing Group 2017-08-21 /pmc/articles/PMC5574440/ /pubmed/28878953 http://dx.doi.org/10.1136/openhrt-2017-000639 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Heart Failure and Cardiomyopathies McAloon, Christopher J Ali, Danish Hamborg, Thomas Banerjee, Prithwish O'Hare, Paul Randeva, Harpal Osman, Faizel Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title | Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title_full | Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title_fullStr | Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title_full_unstemmed | Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title_short | Extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
title_sort | extracellular cardiac matrix biomarkers in patients with reduced ejection fraction heart failure as predictors of response to cardiac resynchronisation therapy: a systematic review |
topic | Heart Failure and Cardiomyopathies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574440/ https://www.ncbi.nlm.nih.gov/pubmed/28878953 http://dx.doi.org/10.1136/openhrt-2017-000639 |
work_keys_str_mv | AT mcaloonchristopherj extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT alidanish extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT hamborgthomas extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT banerjeeprithwish extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT oharepaul extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT randevaharpal extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview AT osmanfaizel extracellularcardiacmatrixbiomarkersinpatientswithreducedejectionfractionheartfailureaspredictorsofresponsetocardiacresynchronisationtherapyasystematicreview |