Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis Insights From THAOS

被引:41
作者
Caponetti, Angelo Giuseppe [1 ]
Rapezzi, Claudio [2 ,3 ]
Gagliardi, Christian [1 ]
Milandri, Agnese [4 ]
Dispenzieri, Angela [5 ]
Kristen, Arnt, V [6 ]
Wixner, Jonas [7 ]
Maurer, Mathew S. [8 ]
Garcia-Pavia, Pablo [9 ,10 ]
Tournev, Ivailo [11 ,12 ,13 ]
Plante-Bordeneuve, Violaine [14 ]
Chapman, Douglass [15 ]
Amass, Leslie [15 ]
机构
[1] Univ Bologna, Cardiol, Dept Expt Diagnost & Specialty Med, Bologna, Italy
[2] Univ Ferrara, Cardiol Ctr, Ferrara, Italy
[3] Maria Cecilia Hosp, GVM Care & Res, Cotignola, Emilia Romagna, Italy
[4] Bentivoglio Hosp, Dept Cardiol, Bologna, Italy
[5] Mayo Clin, Div Hematol, Rochester, MN USA
[6] Med Univ Heidelberg, Dept Cardiol Angiol Resp Med, Heidelberg, Germany
[7] Umea Univ, Dept Publ Hlth & Clin Med, Umea, Sweden
[8] Columbia Univ Coll Phys & Surg, 630 W 168th St, New York, NY 10032 USA
[9] Hosp Univ Puerta Hierro Majadahonda, Ctr Invest Biomed Red Enfermedades Cardiovasc, Dept Cardiol, Madrid, Spain
[10] Univ Francisco Vitoria, Madrid, Spain
[11] Univ Hosp Aleksandrovska, Clin Nervous Dis, Sofia, Bulgaria
[12] Med Univ, Dept Neurol, Sofia, Bulgaria
[13] New Bulgarian Univ, Dept Cognit Sci & Psychol, Sofia, Bulgaria
[14] Univ Hosp Henri Mondor, AP HP, Dept Neurol, Amyloid Network,IMRB,INSERM,U955,Team 10 Biol Neu, Creteil, France
[15] Pfizer, New York, NY USA
关键词
ATTRv amyloidosis; myocardial involvement; registry; sex; PRIMARY SYSTEMIC AMYLOIDOSIS; ATRIAL AMYLOIDOSIS; NATURAL-HISTORY; HEART-FAILURE; CARDIOMYOPATHY; DEPOSITION; FEATURES;
D O I
10.1016/j.jchf.2021.05.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES Because patients with ATTRv cardiomyopathy are more likely to be male, this analysis aimed to increase information on associations between sex and genotype, phenotype, and degree of myocardial involvement in ATTRv amyloidosis. BACKGROUND Transthyretin amyloid cardiomyopathy is a progressive, fatal disease that occurs due to accumulation of wild-type or variant (ATTRv) transthyretin amyloid fibrils in the myocardium. METHODS The Transthyretin Amyloidosis Outcomes Survey (THAOS) is an ongoing global longitudinal observational survey of patients with ATTR amyloidosis and asymptomatic carriers with TTR mutations. Data from THAOS (data cutoff: January 6, 2020) were analyzed to determine any sex-based differences in genotype, phenotype, and presence of cardiac and neurological symptoms in patients with ATTRv amyloidosis and in patients with ATTRv amyloidosis and cardiomyopathy. RESULTS There were 2,790 patients with ATTRv amyloidosis enrolled in THAOS, with male patients more likely to have symptoms of cardiac involvement and a cardiac phenotype. Male prevalence was greater in patients with more severe cardiac manifestations of disease, as assessed with N-terminal pro-B-type natriuretic peptide, left-ventricular (LV) ejection fraction, mean LV wall thickness divided by height, and LV mass index divided by height. Sex, age at disease onset, and genotype category were identified by multivariate analyses as risk factors for the development of cardiomyopathy (defined as increased LV septum thickness divided by height). CONCLUSIONS In this analysis, myocardial involvement was more frequent and pronounced in male patients with ATTRv amyloidosis, suggesting that there may be biological characteristics that inhibit myocardial amyloid infiltration in females or facilitate it in males. (J Am Coll Cardiol HF 2021;9:736-746) (c) 2021 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:736 / 746
页数:11
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