Cardiac Biomarkers and Left Ventricular Hypertrophy in Relation to Outcomes in Patients With Atrial Fibrillation: Experiences From the RE - LY Trial.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
22 01 2019
Historique:
entrez: 18 1 2019
pubmed: 18 1 2019
medline: 4 1 2020
Statut: ppublish

Résumé

Background Cardiac biomarkers and left ventricular hypertrophy ( LVH ) are related to the risk of stroke and death in patients with atrial fibrillation. We investigated the interrelationship between LVH and cardiac biomarkers and their independent associations with outcomes. Methods and Results Plasma samples were obtained at baseline in 5275 patients with atrial fibrillation in the RE - LY (Randomized Evaluation of Long-Term Anticoagulation Therapy) trial. NT -proBNP (N-terminal pro-B-type natriuretic peptide), cardiac troponin I and T, and growth differentiation factor-15 were determined using high-sensitivity (hs) assays. LVH was defined by ECG . Cox models were adjusted for baseline characteristics, LVH , and biomarkers. LVH was present in 1257 patients. During a median follow-up of 2.0 years, 165 patients developed a stroke and 370 died. LVH was significantly ( P<0.0001) associated with higher levels of all biomarkers in linear regression analyses adjusting for baseline characteristics. Geometric mean ratios (95% CIs) were as follows: NT -pro BNP , 1.32 (1.25-1.38); hs cardiac troponin I, 1.67 (1.57-1.78); hs troponin T, 1.38 (1.32-1.44); and growth differentiation factor-15, 1.09 (1.05-1.12). For stroke, the hazard ratios (95% CIs) per 50% increase were as follows: NT -pro BNP, 1.09 (1.00-1.19); hs cardiac troponin I, 1.09 (1.03-1.15); hs troponin T, 1.14 (1.06-1.24); and growth differentiation factor-15, 1.22 (1.08-1.38) (all P<0.05). For death, hazard ratios (95% CIs) were as follows: NT -pro BNP , 1.24 (1.17-1.31); hs cardiac troponin I, 1.13 (1.10-1.17); hs troponin T, 1.28 (1.23-1.34); and growth differentiation factor-15, 1.31 (1.22-1.42) (all P<0.0001). LVH was not significantly associated with stroke or death after adjustment for biomarkers. Conclusions Cardiac biomarkers are significantly associated with LVH . The prognostic value of biomarkers for stroke and death is not affected by LVH . The prognostic information of LVH is attenuated in the presence of cardiac biomarkers. Clinical Trial Registration URL : http://www.clinicaltrials.gov . Unique identifier: NCT 00262600.

Identifiants

pubmed: 30651032
doi: 10.1161/JAHA.118.010107
pmc: PMC6497355
doi:

Substances chimiques

Anticoagulants 0
Biomarkers 0
Troponin I 0
Troponin T 0

Banques de données

ClinicalTrials.gov
['NCT00262600']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010107

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Auteurs

Ziad Hijazi (Z)

1 Department of Medical Sciences Cardiology Uppsala University Uppsala Sweden.
2 Uppsala Clinical Research Center Uppsala University Uppsala Sweden.

Paolo Verdecchia (P)

3 Department of Medicine Hospital of Assisi Italy.

Jonas Oldgren (J)

1 Department of Medical Sciences Cardiology Uppsala University Uppsala Sweden.
2 Uppsala Clinical Research Center Uppsala University Uppsala Sweden.

Ulrika Andersson (U)

2 Uppsala Clinical Research Center Uppsala University Uppsala Sweden.

Gianpaolo Reboldi (G)

4 Department of Medicine University of Perugia Italy.

Giuseppe Di Pasquale (G)

5 Department of Cardiology Maggiore Hospital Bologna Italy.

Giovanni Mazzotta (G)

3 Department of Medicine Hospital of Assisi Italy.

Fabio Angeli (F)

6 Department of Cardiology and Cardiovascular Pathophysiology University of Perugia Perugia Italy.

John W Eikelboom (JW)

8 Population Health Research Institute Hamilton Ontario Canada.

Michael D Ezekowitz (MD)

7 Thomas Jefferson Medical College and the Heart Center Wynnewood PA.

Stuart J Connolly (SJ)

8 Population Health Research Institute Hamilton Ontario Canada.

Salim Yusuf (S)

8 Population Health Research Institute Hamilton Ontario Canada.

Lars Wallentin (L)

1 Department of Medical Sciences Cardiology Uppsala University Uppsala Sweden.
2 Uppsala Clinical Research Center Uppsala University Uppsala Sweden.

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Classifications MeSH