Structural Progression in Patients with Definite and Non-Definite Arrhythmogenic Right Ventricular Cardiomyopathy and Risk of Major Adverse Cardiac Events

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Structural Progression in Patients with Definite and Non-Definite Arrhythmogenic Right Ventricular Cardiomyopathy and Risk of Major Adverse Cardiac Events. / Aljehani, Areej; Baig, Shanat; Kew, Tania; Kalla, Manish; Sommerfeld, Laura C; Murukutla, Vaishnavi Ameya; Fabritz, Larissa; Steeds, Richard P.

In: BIOMEDICINES, Vol. 12, No. 2, 328, 31.01.2024.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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@article{1ca5c999649249878897421202b6d230,
title = "Structural Progression in Patients with Definite and Non-Definite Arrhythmogenic Right Ventricular Cardiomyopathy and Risk of Major Adverse Cardiac Events",
abstract = "Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disease characterised by early arrhythmias and structural changes. Still, there are limited echocardiography data on its structural progression. We studied structural progression and its impact on the occurrence of major adverse cardiovascular events (MACE). In this single-centre observational cohort study, structural progression was defined as the development of new major or minor imaging 2010 Task Force Criteria during follow-up. Of 101 patients, a definite diagnosis of ARVC was made in 51 patients, while non-definite 'early' disease was diagnosed in 50 patients. During 4 years of follow-up (IQR: 2-6), 23 (45%) patients with a definite diagnosis developed structural progression while only 1 patient in the non-definite (early) group gained minor imaging Task Force Criteria. Male gender was strongly associated with structural progression (62% of males progressed structurally, while 88% of females remained stable). Patients with structural progression were at higher risk of MACE (64% of patients with MACE had structural progression). Therefore, the rate of structural progression is an essential factor to be considered in ARVC studies.",
author = "Areej Aljehani and Shanat Baig and Tania Kew and Manish Kalla and Sommerfeld, {Laura C} and Murukutla, {Vaishnavi Ameya} and Larissa Fabritz and Steeds, {Richard P}",
year = "2024",
month = jan,
day = "31",
doi = "10.3390/biomedicines12020328",
language = "English",
volume = "12",
journal = "BIOMEDICINES",
issn = "2227-9059",
publisher = "MDPI AG",
number = "2",

}

RIS

TY - JOUR

T1 - Structural Progression in Patients with Definite and Non-Definite Arrhythmogenic Right Ventricular Cardiomyopathy and Risk of Major Adverse Cardiac Events

AU - Aljehani, Areej

AU - Baig, Shanat

AU - Kew, Tania

AU - Kalla, Manish

AU - Sommerfeld, Laura C

AU - Murukutla, Vaishnavi Ameya

AU - Fabritz, Larissa

AU - Steeds, Richard P

PY - 2024/1/31

Y1 - 2024/1/31

N2 - Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disease characterised by early arrhythmias and structural changes. Still, there are limited echocardiography data on its structural progression. We studied structural progression and its impact on the occurrence of major adverse cardiovascular events (MACE). In this single-centre observational cohort study, structural progression was defined as the development of new major or minor imaging 2010 Task Force Criteria during follow-up. Of 101 patients, a definite diagnosis of ARVC was made in 51 patients, while non-definite 'early' disease was diagnosed in 50 patients. During 4 years of follow-up (IQR: 2-6), 23 (45%) patients with a definite diagnosis developed structural progression while only 1 patient in the non-definite (early) group gained minor imaging Task Force Criteria. Male gender was strongly associated with structural progression (62% of males progressed structurally, while 88% of females remained stable). Patients with structural progression were at higher risk of MACE (64% of patients with MACE had structural progression). Therefore, the rate of structural progression is an essential factor to be considered in ARVC studies.

AB - Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disease characterised by early arrhythmias and structural changes. Still, there are limited echocardiography data on its structural progression. We studied structural progression and its impact on the occurrence of major adverse cardiovascular events (MACE). In this single-centre observational cohort study, structural progression was defined as the development of new major or minor imaging 2010 Task Force Criteria during follow-up. Of 101 patients, a definite diagnosis of ARVC was made in 51 patients, while non-definite 'early' disease was diagnosed in 50 patients. During 4 years of follow-up (IQR: 2-6), 23 (45%) patients with a definite diagnosis developed structural progression while only 1 patient in the non-definite (early) group gained minor imaging Task Force Criteria. Male gender was strongly associated with structural progression (62% of males progressed structurally, while 88% of females remained stable). Patients with structural progression were at higher risk of MACE (64% of patients with MACE had structural progression). Therefore, the rate of structural progression is an essential factor to be considered in ARVC studies.

U2 - 10.3390/biomedicines12020328

DO - 10.3390/biomedicines12020328

M3 - SCORING: Journal article

C2 - 38397930

VL - 12

JO - BIOMEDICINES

JF - BIOMEDICINES

SN - 2227-9059

IS - 2

M1 - 328

ER -