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      Prevalence and prognostic value of monoclonal gammopathy in heart failure patients with preserved ejection fraction: A prospective study

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          Abstract

          Background

          Heart failure (HF) with preserved ejection fraction (HFpEF) and monoclonal gammopathy of uncertain significance (MGUS) are two entities that share pathophysiological mechanisms. The aim herein, was to assess the prevalence of MGUS in patients with HFpEF and no left ventricular (LV) hypertrophy, as well as its association with a pre-specified clinical endpoint at 12 months.

          Methods

          The present study prospectively enrolled 69 patients admitted with HF, with ejection fraction ≥ 50%, and LV wall thickness < 12 mm. All patients were screened for MGUS. Clinical events were determined over a 12 month follow-up. The pre-specified composite clinical endpoint was readmission for HF or death.

          Results

          The prevalence of MGUS in this population was 13%. There were no differences in the incidence of the composite clinical endpoint between patients with and without MGUS. Multivariate analysis showed that treatment with angiotensin converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) was associated with fewer clinical events (HR: 0.153, 95% CI: 0.037–0.622, p = 0.009) and indicated a trend to lower risk of readmission for HF and death. Beta-blockers were associated with lower rates of the composite clinical endpoint (HR: 0.192, 95% CI: 0.05–0.736, p = = 0.016), readmission for HF (HR: 0.272, 95% CI: 0.087–0.851, p = 0.025) and indicated a trend to lower mortality. Moreover, potassium serum levels > 5 mEq/L were associated with higher rates of the composite endpoint (HR: 6.074, 95% CI: 1.6–22.65, p = 0.007).

          Conclusions

          The prevalence of MGUS in patients with HFpEF without hypertrophy was 3-fold that of the general population. There was no significant correlation between clinical outcomes and the presence of MGUS. Beta-blockers and ACEIs/ARBs reduced the composite of mortality and readmissions for HF in HFpEF patients. Hyperpotassemia was related to worse prognosis.

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          Most cited references29

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          2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC.

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            Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging.

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              International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma.

              This International Myeloma Working Group consensus updates the disease definition of multiple myeloma to include validated biomarkers in addition to existing requirements of attributable CRAB features (hypercalcaemia, renal failure, anaemia, and bone lesions). These changes are based on the identification of biomarkers associated with near inevitable development of CRAB features in patients who would otherwise be regarded as having smouldering multiple myeloma. A delay in application of the label of multiple myeloma and postponement of therapy could be detrimental to these patients. In addition to this change, we clarify and update the underlying laboratory and radiographic variables that fulfil the criteria for the presence of myeloma-defining CRAB features, and the histological and monoclonal protein requirements for the disease diagnosis. Finally, we provide specific metrics that new biomarkers should meet for inclusion in the disease definition. The International Myeloma Working Group recommends the implementation of these criteria in routine practice and in future clinical trials, and recommends that future studies analyse any differences in outcome that might occur as a result of the new disease definition.
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                Author and article information

                Journal
                Cardiol J
                Cardiol J
                Cardiology Journal
                Via Medica
                1897-5593
                1898-018X
                2022
                07 April 2022
                : 29
                : 2
                : 216-227
                Affiliations
                [1 ]Department of Cardiology, IIS-Hospital Universitario Fundación Jiménez Díaz — Quironsalud, Madrid, Spain
                [2 ]Department of Internal Medicine, Hospital Universitario Fundación Jiménez Díaz — Quironsalud, Madrid, Spain
                [3 ]School of Medicine and Surgery, University of Milan, Italy
                [4 ]Department of Hematology, Hospital Universitario Fundación Jiménez Díaz — Quironsalud, Madrid, Spain
                [5 ]Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain
                [6 ]Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain
                [7 ]Department of Nuclear Medicine, Hospital Universitario Fundación Jiménez Díaz — Quironsalud, Madrid, Spain
                Author notes
                Address for correspondence: Álvaro Aceña, MD, PhD, Department of Cardiology, Fundación Jiménez Díaz, Avenida Reyes Católicos, 2, Madrid, 28040, Spain, tel: (+34) 915504900, ext. 3702, fax: (+34) 915448014, e-mail: aacena@ 123456fjd.es
                Article
                cardj-29-2-216
                10.5603/CJ.a2020.0059
                9007484
                32329041
                f654d5c1-ce4b-48e7-887f-9211362157d8
                Copyright © 2022 Via Medica

                This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially

                History
                : 15 January 2020
                : 18 February 2020
                Categories
                Clinical Cardiology
                Original Article

                monoclonal gammopathy,heart failure,inflammation,acei,arb
                monoclonal gammopathy, heart failure, inflammation, acei, arb

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