Arrhythmic Risk Stratification in Non-ischemic Cardiomyopathy Based on Cardiovascular Magnetic Resonance Measures of Myocardial Fibrosis and Gray Zone Fibrosis

Autor: Daniel Hammersley, MD, Abbasin Zegard, MD, Emmanuel Androulakis, MD, Richard Jones, MD, PhD, Osita Okafor, MD, Suzan Hatipoglu, MD, Lukas Mach, MD, Amrit Lota, MD, PhD, Zohya Khalique, MD, PhD, Antonio De Marvao, MD, PhD, Resham Baruah, MD, PhD, Kaushik Guha, James Ware, PhD, Upasana Tayal, MD, PhD, Dudley Pennell, MD, FSCMR, Brian Halliday, MD, PhD, BSc, Tian Qiu, Sanjay Prasad, MD, PhD, Francisco Leyva, MD, PhD

Publikováno v: Journal of Cardiovascular Magnetic Resonance, Vol 26, Iss , Pp 100353- (2024)

Externí odkaz: https://doaj.org/article/795b5b5fcf294715bb7ec9fe9b895462

Clinical presentation and long‐term outcomes of infantile hypertrophic cardiomyopathy: a European multicentre study

Autor: Gabrielle Norrish, Gali Kolt, Elena Cervi, Ella Field, Kathleen Dady, Lidia Ziółkowska, Iacopo Olivotto, Silvia Favilli, Silvia Passantino, Giuseppe Limongelli, Martina Caiazza, Marta Rubino, Anwar Baban, Fabrizio Drago, Karen Mcleod, Maria Ilina, Ruth McGowan, Graham Stuart, Vinay Bhole, Orhan Uzun, Amos Wong, Laz Lazarou, Elspeth Brown, Piers E.F. Daubeney, Amrit Lota, Grazia Delle Donne, Katie Linter, Sujeev Mathur, Tara Bharucha, Satish Adwani, Jon Searle, Anca Popoiu, Caroline B. Jones, Zdenka Reinhardt, Juan Pablo Kaski

Publikováno v: ESC Heart Failure, Vol 8, Iss 6, Pp 5057-5067 (2021)

Abstract Aims Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a poor prognosis, but this heterogeneous group has not been systematically characterized. This study aimed to describe the aetiology, phenotype,

Externí odkaz: https://doaj.org/article/606e02324a3e411484c1c9f074115236

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

Autor: Edgar T. Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N. Parikh, Gerard J. te Meerman, Belinda Gray, Ahmet Adiyaman, Richard D. Bagnall, Daniela Q.C.M. Barge-Schaapveld, Maarten P. van den Berg, Marianne Bootsma, Laurens P. Bosman, Gemma Correnti, Johan Duflou, Ruben N. Eppinga, Diane Fatkin, Michael Fietz, Eric Haan, Jan D.H. Jongbloed, Arnaud D. Hauer, Lien Lam, Freyja H.M. van Lint, Amrit Lota, Carlo Marcelis, Hugh J. McCarthy, Anneke M. van Mil, Rogier A. Oldenburg, Nicholas Pachter, R. Nils Planken, Chloe Reuter, Christopher Semsarian, Jasper J. van der Smagt, Tina Thompson, Jitendra Vohra, Paul G.A. Volders, Jaap I. van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S. Amin, Arthur A.M. Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A. Ashley, Matthew T. Wheeler, James S. Ware, J. Peter van Tintelen, Jodie Ingles

Publikováno v: Circulation. Genomic and Precision Medicine, 16, 1
Circulation: Genomic and Precision Medicine, 16(1):E003672. LIPPINCOTT WILLIAMS & WILKINS
Circulation. Genomic and precision medicine, 16(1). Lippincott Williams and Wilkins Ltd.
Circulation: Genomic and Precision Medicine, 16(1), 69-79. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and Precision Medicine, 16
Circulation: Genomic and Precision Medicine, 16(1). Lippincott Williams & Wilkins

Background: Truncating variants in desmoplakin ( DSP tv) are an important cause of arrhythmogenic cardiomyopathy; however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors fo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168e6f2d791aa1fd96556c202c710360

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (

Autor: Edgar T, Hoorntje, Charlotte, Burns, Luisa, Marsili, Ben, Corden, Victoria N, Parikh, Gerard J, Te Meerman, Belinda, Gray, Ahmet, Adiyaman, Richard D, Bagnall, Daniela Q C M, Barge-Schaapveld, Maarten P, van den Berg, Marianne, Bootsma, Laurens P, Bosman, Gemma, Correnti, Johan, Duflou, Ruben N, Eppinga, Diane, Fatkin, Michael, Fietz, Eric, Haan, Jan D H, Jongbloed, Arnaud D, Hauer, Lien, Lam, Freyja H M, van Lint, Amrit, Lota, Carlo, Marcelis, Hugh J, McCarthy, Anneke M, van Mil, Rogier A, Oldenburg, Nicholas, Pachter, R Nils, Planken, Chloe, Reuter, Christopher, Semsarian, Jasper J, van der Smagt, Tina, Thompson, Jitendra, Vohra, Paul G A, Volders, Jaap I, van Waning, Nicola, Whiffin, Arthur, van den Wijngaard, Ahmad S, Amin, Arthur A M, Wilde, Gijs, van Woerden, Laura, Yeates, Dominica, Zentner, Euan A, Ashley, Matthew T, Wheeler, James S, Ware, J Peter, van Tintelen, Jodie, Ingles

Publikováno v: Circulation. Genomic and precision medicine.

Truncating variants in desmoplakin (Individuals withThere were 98 probands and 72 family members (mean age at diagnosis 43±8 years, 59% women) with aIn the largest series of individuals with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7142023d0a2271d92d9519c93025ddd3
https://pubmed.ncbi.nlm.nih.gov/36580316

Predictors of left ventricular remodelling in patients with dilated cardiomyopathy – a cardiovascular magnetic resonance study

Autor: Upasana Tayal, Amrit Lota, John G.F. Cleland, Amal Muthumala, Michael P. Frenneaux, John Gregson, Sanjay K Prasad, Suzan Hatipoglu, Ramasamy Manivarmane, Ravi Assomull, Stuart A. Cook, Ricardo Wage, James S. Ware, Cemil Izgi, Andrew D Scott, Dudley J. Pennell, Jason Dungu, Brian P Halliday, Simon Newsome

Publikováno v: European Journal of Heart Failure. 22:1160-1170

Aims:\ud There is an important need for better biomarkers to predict left ventricular (LV) remodelling in dilated cardiomyopathy (DCM). We undertook a comprehensive assessment of cardiac structure and myocardial composition to determine predictors of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02989882121b6ee83d604f3f64c6f92
https://doi.org/10.1002/ejhf.1734