Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations

被引:9
|
作者
Pioner, Jose Manuel
Vitale, Giulia
Gentile, Francesca
Scellini, Beatrice
Piroddi, Nicoletta
Cerbai, Elisabetta
Olivotto, Iacopo
Tardiff, Jil
Coppini, Raffaele
Tesi, Chiara
Poggesi, Corrado
Ferrantini, Cecilia
机构
[1] Department of Biology, University of Florence, Florence
[2] Department of Experimental and Clinical Medicine, University of Florence, Florence
[3] Department NeuroFarBa, University of Florence, Florence
[4] Department of Medicine and Biomedical Engineering, University of Arizona, Tucson, AZ
关键词
hypertrophic cardiomyopathy; atrial myopathy; atrial fibrillation; sarcomere mechanics; sarcomere energetics; excitation-contraction coupling; cardiac troponin T; CARDIAC TROPONIN-T; MURINE HEARTS; MOUSE MODEL; DYSFUNCTION; BINDING; ACTIVATION; GENERATION; IMPACT;
D O I
10.3389/fphys.2022.864547
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Atrial dilation and atrial fibrillation (AF) are common in Hypertrophic CardioMyopathy (HCM) patients and associated with a worsening of prognosis. The pathogenesis of atrial myopathy in HCM remains poorly investigated and no specific association with genotype has been identified. By re-analysis of our cohort of thin-filament HCM patients (Coppini et al. 2014) AF was identified in 10% of patients with sporadic mutations in the cardiac Troponin T gene (TNNT2), while AF occurrence was much higher (25-75%) in patients carrying specific "hot-spot" TNNT2 mutations. To determine the molecular basis of arrhythmia occurrence, two HCM mouse models expressing human TNNT2 variants (a "hot-spot" one, R92Q, and a "sporadic" one, E163R) were selected according to the different pathophysiological pathways previously demonstrated in ventricular tissue. Echocardiography studies showed a significant left atrial dilation in both models, but more pronounced in the R92Q. In E163R atrial trabeculae, in line with what previously observed in ventricular preparations, the energy cost of tension generation was markedly increased. However, no changes of twitch amplitude and kinetics were observed, and there was no atrial arrhythmic propensity. R92Q atrial trabeculae, instead, displayed normal ATP consumption but markedly increased myofilament calcium sensitivity, as previously observed in ventricular preparations. This was associated with reduced inotropic reserve and slower kinetics of twitch contractions and, importantly, with an increased occurrence of spontaneous beats and triggered contractions that represent an intrinsic arrhythmogenic mechanism promoting AF. The association of specific TNNT2 mutations with AF occurrence depends on the mutation-driven pathomechanism (i.e., increased atrial myofilament calcium sensitivity rather than increased myofilament tension cost) and may influence the individual response to treatment.
引用
收藏
页数:13
相关论文
共 50 条
  • [31] Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study
    Piva e Mattos, Beatriz
    Scolari, Fernando Luis
    Rodrigues Torres, Marco Antonio
    Simon, Laura
    de Freitas, Valeria Centeno
    Giugliani, Roberto
    Matte, Ursula
    ARQUIVOS BRASILEIROS DE CARDIOLOGIA, 2016, 107 (03) : 257 - 265
  • [32] Dofetilide for suppression of atrial fibrillation in hypertrophic cardiomyopathy: A case series and literature review
    Moore, JoEllyn C.
    Trager, Lena
    Anzia, Lucille E.
    Saliba, Walid
    Bassiouny, Mohamed
    Bhargava, Mandeep
    Chung, Mina
    Desai, Milind
    Garberich, Ross
    Lever, Harry
    Lindsay, Bruce D.
    Sengupta, Jay
    Tchou, Patrick
    Wazni, Oussama
    Wilkoff, Bruce L.
    PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2018, 41 (04): : 396 - 401
  • [33] Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activity
    Ruggiero, Alessandra
    Chen, Suet Nee
    Lombardi, Raffaella
    Rodriguez, Gabriela
    Marian, Ali J.
    CARDIOVASCULAR RESEARCH, 2013, 97 (01) : 44 - 54
  • [34] A new mutation (Arg-278-Pro) in the cardiac troponin T gene (TNNT2) was identified in one patient with typical hypertrophic cardiomyopathy (HCM)
    Erdmann, FJ
    Wischke, S
    Riedel, K
    Kallisch, H
    Fleck, ME
    Regitz-Zagrosek, FV
    CIRCULATION, 1998, 98 (17) : 245 - 245
  • [35] Atrial fibrillation develops more frequently in patients with hypertrophic cardiomyopathy with mutations of troponin thin filament genes
    Ino, Hidekazu
    Fujino, Noboru
    Hayashi, Kenshi
    Konno, Tetsuo
    Uchiyama, Katsuharu
    Tsubokawa, Toshinari
    Katoh, Hiromasa
    Yamagishi, Masakazu
    CIRCULATION, 2006, 114 (18) : 769 - 769
  • [36] Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy
    Petropoulou, Evmorfia
    Soltani, Mohammadhossein
    Firoozabadi, Ali Dehghani
    Namayandeh, Seyedeh Mahdieh
    Crockford, Jade
    Maroofian, Reza
    Jamshidi, Yalda
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2017, 60 (09) : 485 - 488
  • [37] Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathy
    Ogimoto, A
    Hamada, M
    Nakura, J
    Miki, T
    Hiwada, K
    JOURNAL OF HUMAN GENETICS, 2002, 47 (04) : 184 - 189
  • [38] Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathy
    A. Ogimoto
    M. Hamada
    J. Nakura
    T. Miki
    K. Hiwada
    Journal of Human Genetics, 2002, 47 : 184 - 189
  • [39] Atrial remodeling in hypertrophic cardiomyopathy: insights from mouse models carrying different mutations in cTnT
    Gentile, F.
    Pioner, J. M.
    Coppini, R.
    Scellini, B.
    Tardiff, J.
    Tesi, C.
    Poggesi, C.
    Ferrantini, C.
    CARDIOVASCULAR RESEARCH, 2016, 111 : S35 - S36
  • [40] HIGH RISK FOR ISCHEMIC STROKE: A CASE OF APICAL HYPERTROPHIC CARDIOMYOPATHY WITH PREVIOUSLY UNDIAGNOSED ATRIAL FIBRILLATION
    Mishra, Shiwangi
    Yuvaraj, Yaswanraj
    Alvarez, Gustavo A. Rivera
    Khan, Hassan
    Perez, Vianka
    Alonso, Raul
    Cintron, Daniel
    CHEST, 2024, 166 (04) : 356A - 356A