Genetics, cardiac phenotype and cardiovascular outcomes in Fabry disease patients in Finland

dc.contributor.authorValtola, Kati
dc.contributor.authorPietilä‐Effati, Päivi
dc.contributor.authorMännistö, Jonna M. E.
dc.contributor.authorWalls, Susanne
dc.contributor.authorKantola, Ilkka
dc.contributor.authorKuusisto, Johanna
dc.contributor.organizationfi=lääketieteellinen tiedekunta|en=Faculty of Medicine|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.13290506867
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id499717310
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/499717310
dc.date.accessioned2026-01-21T12:07:02Z
dc.date.available2026-01-21T12:07:02Z
dc.description.abstract<p><b>Aims</b><br></p><p>To investigate the genetics, cardiac phenotype and cardiovascular outcomes of Finnish Fabry patients.<br></p><p><b>Methods and results</b><br></p><p>Among the 109 patients with Fabry disease (FD) diagnosed in Finland by 2018, 97 (89%; 32 males and 65 females, mean ages 42 and 52 years) were followed for a mean of 12 years. Data on genetics, phenotypes, cardiac imaging and cardiovascular outcomes were collected from the Fabry Registry and medical records. The 26 families with FD harboured 22 different hemi-/heterozygous GLA variants, most commonly p.R227X, p.A143T or p.P409A. The Fabry phenotype in males was classic in 19 (59%), late-onset in 10 (31%) and intermediate in 3 (9%) patients. Among the females, 62 (95%) were symptomatic. Fabry cardiomyopathy (FC, maximal left ventricular wall thickness >= 13 mm, or an increased cardiac mass and decreased T1 time, or typical late gadolinium enhancement (LGE) in CMR) was present in 21 (66%) males manifesting since their 20s, and in 32 (49%) females since their 40s. LGE in CMR was detected in most subjects with cardiomyopathy, particularly in females. Among the 53 patients with FC, 16 (30%) developed atrial fibrillation, 17 (32%) stroke, 14 (26%) heart failure (HF) and 3 (6%) end-stage renal disease. Nine patients died during the follow-up at mean ages of 48 (males) and 75 years (females), three of whom died from HF and three from stroke. Eight of those who died had cardiomyopathy.<br></p><p><b>Conclusions</b><br></p><p>In Finland, FD is caused by multiple GLA variants. Classic phenotype is more common. Contrasting previous studies, most women are symptomatic. Cardiomyopathy is very common also in women since their 40s and associates with atrial fibrillation, HF, stroke and death, emphasizing the malignant natural course of FC. Our findings highlight the need for even more diligent monitoring of cardiac manifestations also in females with FD by regular cardiac imaging with CMR.</p>
dc.identifier.eissn2055-5822
dc.identifier.jour-issn2055-5822
dc.identifier.olddbid212129
dc.identifier.oldhandle10024/195147
dc.identifier.urihttps://www.utupub.fi/handle/11111/37882
dc.identifier.urlhttps://doi.org/10.1002/ehf2.15387
dc.identifier.urnURN:NBN:fi-fe202601216552
dc.language.isoen
dc.okm.affiliatedauthorPietilä-Effati, Päivi
dc.okm.affiliatedauthorKantola, Ilkka
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWiley
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.publisher.placeSAN FRANCISCO
dc.relation.articlenumberehf2.15387
dc.relation.doi10.1002/ehf2.15387
dc.relation.ispartofjournalESC Heart Failure
dc.source.identifierhttps://www.utupub.fi/handle/10024/195147
dc.titleGenetics, cardiac phenotype and cardiovascular outcomes in Fabry disease patients in Finland
dc.year.issued2025

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