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Verheyen, N; Schmid, J; Kolesnik, E; Schwegel, N; Späth, J; Kattnig, L; Riepl, H; Zach, D; Santner, V; Höller, V; Pilz, S; Tomaschitz, A; Fuchsjäger, M; Fahrleitner-Pammer, A; Dimai, HP; Obermayer-Pietsch, B; Fruhwald, F; Scherr, D; Zirlik, A; von, Lewinski, D; Ablasser, K.
Prevalence and prognostic impact of bone disease in chronic heart failure with reduced ejection fraction.
ESC Heart Fail. 2024; 11(3):1730-1738 Doi: 10.1002/ehf2.14741 [OPEN ACCESS]
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Leading authors Med Uni Graz
Schmid Johannes
Verheyen Nicolas Dominik
von Lewinski Dirk
Co-authors Med Uni Graz
Ablasser Klemens
Dimai Hans Peter
Fahrleitner-Pammer Astrid
Fruhwald Friedrich
Fuchsjäger Michael
Höller Viktoria
Kolesnik Ewald
Obermayer-Pietsch Barbara
Pilz Stefan
Riepl Hermann Stefan
Santner Viktoria
Scherr Daniel
Schwegel Nora
Tomaschitz Andreas
Zach David
Zirlik Andreas
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Abstract:
AIMS: Chronic heart failure is associated with a bone-catabolic state and increases the risk of osteoporosis and fractures. Prospective studies investigating the clinical relevance of bone disease in heart failure are lacking. We aimed to assess the prevalence and prognostic impact of osteoporosis and vertebral fractures (VFs) in chronic heart failure with reduced ejection fraction (HFrEF). METHODS AND RESULTS: Symptomatic outpatients with chronic heart failure and a previous diagnosis of overtly reduced left ventricular ejection fraction < 40% on stable, optimal HFrEF therapy and left ventricular ejection fraction < 50% at enrolment were included into a prospective single-centre study. Osteoporosis was determined with dual-energy X-ray absorptiometry and defined as a T-score ≤ 2.5 at any site. VFs were assessed using X-ray of both thoracic and lumbar spine applying the semiquantitative Genant score. We enrolled 205 patients (22% women), with a median age of 66 (IQR 58-74) years. Median left ventricular ejection fraction was 37 (IQR 30-43) % and median N-terminal pro B-type natriuretic peptide was 964 (IQR 363-2173) pg/mL. Osteoporosis, as defined by bone mineral density, and at least one VF were prevalent in 31 (15%) and 29 patients (14%). Osteoporosis or VF were present in 55 patients (27%) and 5 patients (2%) had both osteoporosis and a VF. During a median follow-up of 4.7 (IQR 4.0-5.3) years, 18 patients (9%) died due to cardiovascular (CV) cause, and 46 patients (22%) had a worsening heart failure (WHF) hospitalization. In multivariate Cox regression analyses, presence of VF independently predicted CV death (HR 2.82, 95% CI 1.04-7.65, P = 0.042), WHF hospitalizations (HR 2.39, 95% CI 1.18-4.82, P = 0.015), and a composite endpoint of CV death and WHF hospitalizations (HR 2.44, 95% CI 1.23-4.82, P = 0.011). Osteoporosis was not significantly associated with CV events. CONCLUSIONS: In a prospective study, bone disease affected every fourth patient with HFrEF, and patients with VF at baseline had a two-fold risk of subsequent CV death or WHF hospitalization. Prevalent bone disease, particularly VF, should be considered as a clinically relevant comorbidity in HFrEF.
Find related publications in this database (using NLM MeSH Indexing)
Humans - administration & dosage
Female - administration & dosage
Male - administration & dosage
Heart Failure - physiopathology, epidemiology, complications
Stroke Volume - physiology
Prospective Studies - administration & dosage
Prevalence - administration & dosage
Aged - administration & dosage
Prognosis - administration & dosage
Middle Aged - administration & dosage
Osteoporosis - epidemiology, physiopathology
Bone Density - physiology
Ventricular Function, Left - physiology
Follow-Up Studies - administration & dosage
Absorptiometry, Photon - administration & dosage
Risk Factors - administration & dosage
Chronic Disease - administration & dosage

Find related publications in this database (Keywords)
Heart failure with reduced ejection fraction
Mortality
Osteoporosis
Prospective cohort study
Vertebral fractures
Worsening heart failure hospitalization
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