Ankle-brachial index, arterial stiffness, and biomarkers in the prediction of mortality and outcomes in patients with end-stage kidney disease.


Journal

Clinical cardiology
ISSN: 1932-8737
Titre abrégé: Clin Cardiol
Pays: United States
ID NLM: 7903272

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 03 03 2019
revised: 22 04 2019
accepted: 24 04 2019
pubmed: 26 4 2019
medline: 24 12 2019
entrez: 26 4 2019
Statut: ppublish

Résumé

Although ankle-brachial index (ABI) and brachial-ankle pulse wave velocity (baPWV) are significant predictors of major adverse cardiovascular event (MACE), their prognostic value in association with biomarkers has not been fully evaluated in patients with end-stage kidney disease (ESKD). We hypothesized that ABI/baPWV would provide better prognostic value independent of biomarkers in ESKD patients. This study included 104 ESKD patients treated with maintenance hemodialysis who underwent ABI and baPWV examinations and laboratory tests, including brain-natriuretic peptide, high-sensitive cardiac troponin T (hs-cTnT), and high-sensitive C-reactive protein (hs-CRP). MACE was defined as a composite event of all-cause death, acute coronary syndrome, and stroke. During a mean follow-up of 3.6 ± 1.7 years, a total of 51 MACE were observed. The independent factors associated with MACE were age >75 years (adjusted hazard ratio [HR], 2.15; P < .05), abnormal ABI (adjusted HR, 2.01; P < .05), left ventricular ejection fraction (LVEF) <50% (adjusted HR, 3.33; P < .001), the upper tertile of hs-cTnT (adjusted HR, 2.77; P < .05), and hs-CRP (HR, 1.96; P < .05). However, baPWV did not remain as an independent predictor of MACE in the entire cohort and also in patients without abnormal ABI. The combination of predictors improves the predictive value of MACE, providing increased HR with 4.00 for abnormal ABI + hs-CRP, 4.42 for abnormal ABI + hs-cTnT, and 7.04 for abnormal ABI + LVEF <50% (all P < .001). Abnormal ABI is a robust predictor of MACE independent of biomarkers and their combination provides better risk stratification compared with a single predictor in ESKD patients.

Sections du résumé

BACKGROUND BACKGROUND
Although ankle-brachial index (ABI) and brachial-ankle pulse wave velocity (baPWV) are significant predictors of major adverse cardiovascular event (MACE), their prognostic value in association with biomarkers has not been fully evaluated in patients with end-stage kidney disease (ESKD).
HYPOTHESIS OBJECTIVE
We hypothesized that ABI/baPWV would provide better prognostic value independent of biomarkers in ESKD patients.
METHODS METHODS
This study included 104 ESKD patients treated with maintenance hemodialysis who underwent ABI and baPWV examinations and laboratory tests, including brain-natriuretic peptide, high-sensitive cardiac troponin T (hs-cTnT), and high-sensitive C-reactive protein (hs-CRP). MACE was defined as a composite event of all-cause death, acute coronary syndrome, and stroke.
RESULTS RESULTS
During a mean follow-up of 3.6 ± 1.7 years, a total of 51 MACE were observed. The independent factors associated with MACE were age >75 years (adjusted hazard ratio [HR], 2.15; P < .05), abnormal ABI (adjusted HR, 2.01; P < .05), left ventricular ejection fraction (LVEF) <50% (adjusted HR, 3.33; P < .001), the upper tertile of hs-cTnT (adjusted HR, 2.77; P < .05), and hs-CRP (HR, 1.96; P < .05). However, baPWV did not remain as an independent predictor of MACE in the entire cohort and also in patients without abnormal ABI. The combination of predictors improves the predictive value of MACE, providing increased HR with 4.00 for abnormal ABI + hs-CRP, 4.42 for abnormal ABI + hs-cTnT, and 7.04 for abnormal ABI + LVEF <50% (all P < .001).
CONCLUSION CONCLUSIONS
Abnormal ABI is a robust predictor of MACE independent of biomarkers and their combination provides better risk stratification compared with a single predictor in ESKD patients.

Identifiants

pubmed: 31020665
doi: 10.1002/clc.23188
pmc: PMC6605000
doi:

Substances chimiques

Biomarkers 0
Troponin T 0
Natriuretic Peptide, Brain 114471-18-0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

656-662

Informations de copyright

© 2019 The Authors. Clinical Cardiology published by Wiley Periodicals, Inc.

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Auteurs

Kenichiro Otsuka (K)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Koki Nakanishi (K)

Department of Cardiovascular Medicine, Baba Memorial Hospital, Sakai, Japan.

Kenei Shimada (K)

Department of Cardiovascular Medicine, Kashiba-seiki Hospital, Kashiba, Japan.

Haruo Nakamura (H)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Hitoshi Inanami (H)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Hiroki Nishioka (H)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Kohei Fujimoto (K)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Noriaki Kasayuki (N)

Department of Cardiovascular Medicine, Ishikiri-seiki Hospital, Higashi-osaka, Japan.

Minoru Yoshiyama (M)

Department of Cardiovascular Medicine, Osaka City University Graduate School of Medicine, Osaka, Japan.

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Classifications MeSH