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DOI 10.1016/j.rec.2020.03.026

Медицинская библиотека · Revista espanola de cardiologia (English ed.) · 2020

Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry.

Barriales-Villa Roberto, Ochoa Juan P, Larrañaga-Moreira José M, Salazar-Mendiguchía Joel, Díez-López Carles, Restrepo-Córdoba María Alejandra, Álvarez-Rubio Jorge, Robles-Mezcua Ainhoa, Olmo-Conesa María C, Nicolás-Rocamora Elisa, Sanz Jorge, Villacorta Eduardo, Gallego-Delgado María, Yotti Raquel, Espinosa María Ángeles, Manovel Ana, Rincón-Díaz Luis M, Jiménez-Jaimez Juan, Bermúdez-Jiménez Francisco J, Basurte-Elorz M Teresa, Climent-Payá Vicente, García-Álvarez María I, Rodríguez-Palomares José Fernando, Limeres-Freire Javier, Pérez-Guerrero Ainhoa, Cantero-Pérez Eva M, Peña-Peña María L, Palomino-Doza Julián, Crespo-Leiro María G, García-Pinilla José M, Zorio Esther, Ripoll-Vera Tomás, García-Pavía Pablo, Ortiz-Genga Martín, Monserrat Lorenzo

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Аннотация

INTRODUCTION AND

OBJECTIVES

According to sudden cardiac death guidelines, an implantable cardioverter-defibrillator (ICD) should be considered in patients with LMNA-related dilated cardiomyopathy (DCM) and ≥ 2 risk factors: male sex, left ventricular ejection fraction (LVEF) <45%, nonsustained ventricular tachycardia (NSVT), and nonmissense genetic variants. In this study we aimed to describe the clinical characteristics of carriers of LMNA genetic variants among individuals from a Spanish cardiac-laminopathies cohort (REDLAMINA registry) and to assess previously reported risk criteria.

METHODS

The relationship between risk factors and cardiovascular events was evaluated in a cohort of 140 carriers (age ≥ 16 years) of pathogenic LMNA variants (54 probands, 86 relatives). We considered: a) major arrhythmic events (MAE) if there was appropriate ICD discharge or sudden cardiac death; b) heart failure death if there was heart transplant or death due to heart failure.

RESULTS

We identified 11 novel and 21 previously reported LMNA-related DCM variants. LVEF <45% (P=.001) and NSVT (P <.001) were related to MAE, but not sex or type of genetic variant. The only factor independently related to heart failure death was LVEF <45% (P <.001).

CONCLUSIONS

In the REDLAMINA registry cohort, the only predictors independently associated with MAE were NSVT and LVEF <45%. Therefore, female carriers of missense variants with either NSVT or LVEF <45% should not be considered a low-risk group. It is important to individualize risk stratification in carriers of LMNA missense variants, because not all have the same prognosis.

Для цитирования: Barriales-Villa Roberto, Ochoa Juan P, Larrañaga-Moreira José M, Salazar-Mendiguchía Joel, Díez-López Carles, Restrepo-Córdoba María Alejandra, Álvarez-Rubio Jorge, Robles-Mezcua Ainhoa, Olmo-Conesa María C, Nicolás-Rocamora Elisa, Sanz Jorge, Villacorta Eduardo, Gallego-Delgado María, Yotti Raquel, Espinosa María Ángeles, Manovel Ana, Rincón-Díaz Luis M, Jiménez-Jaimez Juan, Bermúdez-Jiménez Francisco J, Basurte-Elorz M Teresa, Climent-Payá Vicente, García-Álvarez María I, Rodríguez-Palomares José Fernando, Limeres-Freire Javier, Pérez-Guerrero Ainhoa, Cantero-Pérez Eva M, Peña-Peña María L, Palomino-Doza Julián, Crespo-Leiro María G, García-Pinilla José M, Zorio Esther, Ripoll-Vera Tomás, García-Pavía Pablo, Ortiz-Genga Martín, Monserrat Lorenzo. Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry.. Revista espanola de cardiologia (English ed.). 2020. DOI: 10.1016/j.rec.2020.03.026.

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