Abstract

BackgroundThe aim of the study was to assess the relationship between the occurrence of rheumatoid arthritis (RA) and ankylosing spondylitis (AS) and the cardiac magnetic resonance (CMR) changes in people without clinically overt heart disease.MethodsThe study group consisted of 74 people (48.81 ± 11.35 years): 29 patients with RA, 23 patients with AS and 22 people from control group. Blood samples were taken to assess laboratory parameters, disease activity was determined using activity scales, and CMR was performed.ResultsIt was shown that the factors independently related to higher left ventricular mass index are AS occurrence, human B27 leukocyte antigen occurrence, higher neutrophil gelatinase–associated lipocalin concentration (NGAL) and higher body mass index (BMI). The lower right ventricular ejection fraction is result of an independent effect of RA, AS and higher NGAL. RA presence, methotrexate use, higher rheumatoid factor titer, higher NGAL, older age and higher BMI should be considered independent risk factors for greater left ventricular myocardium water content. RA occurrence, AS occurrence, type 2 diabetes occurrence and a higher C-reactive protein concentration can be independently associated with a higher probability of non-ischemic left ventricular myocardium injury. Larger pericardial fluid volume is result of an independent effect of higher NGAL, higher anti-cyclic citrullinated peptide antibodies titer and higher DAS28 disease activity index. Use of steroids is protective factor against larger volume of pericardial fluid.ConclusionsRA and AS in people without clinically apparent heart disease are associated with the occurrence of adverse changes in CMR.Key Points•RA and AS in people without clinically apparent heart disease are associated with the occurrence of adverse changes in CMR..•The independent risk factors for higher LVEF are AS occurrence, human B27 leukocyte antigen occurrence, higher NGAL concentration and higher BMI..•RA presence, methotrexate use, higher RF, higher NGAL, older age and higher BMI are independent risk factors for higher LV T2 ratio..•RA occurrence, AS occurrence, type 2 diabetes occurrence and a higher CRP are independently associated with a higher risk of non-ischemic LV myocardium injury..

Highlights

  • Cardiovascular diseases are the leading cause of death in the world [1]

  • In terms of heart cavity dimensions, the group with rheumatoid arthritis (RA) was characterized by significantly higher posterior wall diastolic diameter (PWDD) compared to the control group (8.50 ± 1.53 mm vs. 7.18 ± 1.23 mm), while the group with ankylosing spondylitis (AS) has a significantly higher Left ventricular mass index (LVMI) than the control group (68.40 ± 24.94 g/m2 vs. 61.12 ± 15.26 g/m2)

  • Both examined groups of patients in relation to the control group had worse right ventricular systolic function expressed in significantly lower RV Ejection fraction (EF) (RA: 55.80 ± 2.05%, AS: 55.31 ± 1.81%, CON: 62.15 ± 7.00%)

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Summary

Introduction

Cardiovascular diseases are the leading cause of death in the world [1]. The problem of the prevalence of cardiovascular diseases is more applicable to areas with high gross domestic product [2, 3]. The aim of the study was to assess the relationship between the occurrence of rheumatoid arthritis (RA) and ankylosing spondylitis (AS) and the cardiac magnetic resonance (CMR) changes in people without clinically overt heart disease. Results It was shown that the factors independently related to higher left ventricular mass index are AS occurrence, human B27 leukocyte antigen occurrence, higher neutrophil gelatinase–associated lipocalin concentration (NGAL) and higher body mass index (BMI). RA presence, methotrexate use, higher rheumatoid factor titer, higher NGAL, older age and higher BMI should be considered independent risk factors for greater left ventricular myocardium water content. Larger pericardial fluid volume is result of an independent effect of higher NGAL, higher anti-cyclic citrullinated peptide antibodies titer and higher DAS28 disease activity index.

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