Evaluation of left cardiac chamber function with cardiac magnetic resonance and association with outcome in patients with systemic sclerosis

dc.contributor.authorButcher Steele C
dc.contributor.authorVos Jaqueline L
dc.contributor.authorFortuni Federico
dc.contributor.authorGalloo Xavier
dc.contributor.authorLiem Sophie IE
dc.contributor.authorBax Jeroen J
dc.contributor.authorDelgado Victoria
dc.contributor.authorVonk Madelon C
dc.contributor.authorvan Leuven Sander I
dc.contributor.authorSnoeren Miranda
dc.contributor.authorEl Messaoudi Saloua
dc.contributor.authorde Vries-Bouwstra Jeska K
dc.contributor.authorNijveldt Robin
dc.contributor.authorMarsan Nina Ajmone
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.14646305228
dc.converis.publication-id175907618
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175907618
dc.date.accessioned2025-08-27T21:54:34Z
dc.date.available2025-08-27T21:54:34Z
dc.description.abstract<p>Objective <br></p><p>This study aimed to determine whether lower values of feature-tracking cardiovascular magnetic resonance (CMR)-derived left atrial reservoir strain (LARS) and impaired left ventricular (LV) global longitudinal strain (GLS) were associated with the presence of symptoms and long-term prognosis in patients with SSc. <br></p><p>Methods <br></p><p>A total of 100 patients {54 [interquartile range (IQR) 46-64] years, 42% male} with SSc who underwent CMR imaging at two tertiary referral centres were included. All patients underwent analysis of LARS and LV GLS using feature-tracking on CMR and were followed-up for the occurrence of all-cause mortality. <br></p><p>Results <br></p><p>The median LV GLS was -21.8% and the median LARS was 36%. On multivariable logistic regression, LARS [odds ratio (OR) 0.964 per %, 95% CI 0.929, 0.998, P = 0.049] was independently associated with New York Heart Association (NYHA) class II-IV heart failure symptoms. Over a median follow-up of 37 (21-62) months, a total of 24 (24%) patients died. Univariable Cox regression analysis demonstrated that LARS [hazard ratio (HR) 0.94 per 1%, 95% CI 0.91, 0.97, P < 0.0001) and LV GLS (HR 1.10 per %, 95% CI 1.03, 1.17, P = 0.005) were associated with all-cause mortality, while LV ejection fraction was not. Likelihood ratio tests demonstrated that LARS provided incremental value over prognostically important clinical and imaging parameters, including late gadolinium enhancement. <br></p><p>Conclusion <br></p><p>In patients with SSc, LARS was independently associated with the presence of NYHA class II-IV heart failure symptoms. Although both LARS and LV GLS were associated with all-cause mortality, only LARS provided incremental value over all evaluated variables known to be prognostically important in patients with SSc.</p>
dc.format.pagerangeS120
dc.format.pagerangeS131
dc.identifier.eissn1462-0332
dc.identifier.jour-issn1462-0324
dc.identifier.olddbid201385
dc.identifier.oldhandle10024/184412
dc.identifier.urihttps://www.utupub.fi/handle/11111/48215
dc.identifier.urlhttps://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/keac256/6575497
dc.identifier.urnURN:NBN:fi-fe2023040535083
dc.language.isoen
dc.okm.affiliatedauthorBax, Jeroen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherOxford Univ Press
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1093/rheumatology/keac256
dc.relation.ispartofjournalRheumatology
dc.relation.issueS1
dc.relation.volume62
dc.source.identifierhttps://www.utupub.fi/handle/10024/184412
dc.titleEvaluation of left cardiac chamber function with cardiac magnetic resonance and association with outcome in patients with systemic sclerosis
dc.year.issued2023

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