Review
Biochemistry & Molecular Biology
Jiri Bonaventura, Eva Polakova, Veronika Vejtasova, Josef Veselka
Summary: Hypertrophic cardiomyopathy (HCM) is a common inherited heart disease with complex genetic basis involving mutations in multiple genes. Patients without pathogenic variants are now believed to have non-Mendelian HCM and may have a better prognosis. Identifying the genetic basis of HCM provides opportunities for understanding disease development and potential interventions.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
(2021)
Article
Cardiac & Cardiovascular Systems
Leon Dinshaw, Paula Muenkler, Benjamin Schaeffer, Niklas Klatt, Christiane Jungen, Jannis Dickow, Annika Tamenang, Ruben Schleberger, Simon Pecha, Hans Pinnschmidt, Monica Patten, Hermann Reichenspurner, Stephan Willems, Christian Meyer
Summary: Ablation of atrial fibrillation in patients with hypertrophic cardiomyopathy is effective for long-term rhythm control, especially in those with paroxysmal AF undergoing pulmonary vein isolation. Despite a high proportion of patients requiring antiarrhythmic drug therapy post-ablation, a reasonable number of patients achieve freedom from atrial arrhythmias, particularly after persistent AF ablation.
JOURNAL OF THE AMERICAN HEART ASSOCIATION
(2021)
Article
Medicine, General & Internal
Francesca Girolami, Alessia Gozzini, Eszter Dalma Palinkas, Adelaide Ballerini, Alessia Tomberli, Katia Baldini, Alberto Marchi, Mattia Zampieri, Silvia Passantino, Giulio Porcedda, Giovanni Battista Calabri, Elena Bennati, Gaia Spaziani, Lia Crotti, Franco Cecchi, Silvia Favilli, Iacopo Olivotto
Summary: Genetic counselling and testing are crucial in diagnosing and managing hypertrophic cardiomyopathy (HCM), enabling personalized treatment strategies and family cascade testing. The complexity of interpreting genetic data, especially with Next Generation Sequencing technologies, necessitates collaboration between cardiologists and geneticists to accurately evaluate the pathogenicity of identified genetic alterations. Effective communication between the team and families is essential for delivering the full potential of genetic testing in HCM patients.
JOURNAL OF CLINICAL MEDICINE
(2023)
Article
Cardiac & Cardiovascular Systems
Elisabetta Lapenna, Teodora Nisi, Davide Carino, Benedetto Del Forno, Stefania Ruggeri, Davide Schiavi, Roberta Meneghin, Roberto Macri Demartino, Alessandro Castiglioni, Francesco Maisano, Ottavio Alfieri, Michele De Bonis
Summary: The short- and long-term outcomes of surgical treatment for hypertrophic obstructive cardiomyopathy were compared between patients aged 65 years and older and patients younger than 65 years. Older patients had higher surgical risk scores, higher pulmonary artery pressure, and more mitral annulus calcifications. However, they had comparable long-term survival rates to the general population and lower hospital mortality and morbidity rates.
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY
(2022)
Article
Biochemistry & Molecular Biology
Giovanna Gallo, Vittoria Mastromarino, Giuseppe Limongelli, Giulio Calcagni, Antonello Maruotti, Luca Ragni, Fabio Valente, Maria Beatrice Musumeci, Rachele Adorisio, Marta Rubino, Camillo Autore, Damiano Magri
Summary: The CPET assessment in pediatric HCM patients provides a true estimation of functional capacity and may be helpful in early identification of high-risk patients. Patients with worse CPET profiles were more likely to experience composite endpoint events, with peak oxygen uptake being strongly associated with adverse events during follow-up.
Article
Cardiac & Cardiovascular Systems
Simon Greulich, Andreas Seitz, Diana Herter, Fabian Guenther, Sabine Probst, Raffi Bekeredjian, Meinrad Gawaz, Udo Sechtem, Heiko Mahrholdt
Summary: The study evaluated the prognostic value of LGE-CMR for SCD risk stratification in patients with hypertrophic cardiomyopathy (HCM) over a 10-year follow-up period, suggesting that LGE amount may enhance the discriminatory power of established risk models.
EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING
(2021)
Review
Cardiac & Cardiovascular Systems
Katherine Chiswell, Louisa Zaininger, Christopher Semsarian
Summary: Studies in the past 30 years have revealed the genetic basis of hypertrophic cardiomyopathy (HCM), leading to advancements in precision medicine through genetic testing and therapy. These advancements have improved diagnosis, risk stratification, and prognosis. Recent research has also provided insights into non-Mendelian inheritance and the development of polygenic risk scores, paving the way for future gene therapy research.
PROGRESS IN CARDIOVASCULAR DISEASES
(2023)
Review
Cardiac & Cardiovascular Systems
Fergus Stafford, Kate Thomson, Alexandra Butters, Jodie Ingles
Summary: Our understanding of the genetic basis and molecular pathogenesis of hypertrophic cardiomyopathy (HCM) is continuously evolving, with recent advances in genetic testing showing the presence of important HCM sub-groups. Genetic testing has emerged as a valuable tool for cascade genetic testing and may play a significant role in prognosis and patient management in the future. Genotype may potentially enhance risk stratification, management, treatment, and prognosis in HCM, leading to improved outcomes for patients and their families.
CURRENT CARDIOLOGY REPORTS
(2021)
Article
Cardiac & Cardiovascular Systems
Atsuko Imai-Okazaki, Ayako Matsunaga, Yukiko Yatsuka, Kazuhiro R. Nitta, Yoshihito Kishita, Ayumu Sugiura, Yohei Sugiyama, Takuya Fushimi, Masaru Shimura, Keiko Ichimoto, Makiko Tajika, Minako Ogawa-Tominaga, Tomohiro Ebihara, Tetsuro Matsuhashi, Tomoko Tsuruoka, Masakazu Kohda, Tomoko Hirata, Hiroko Harashima, Shuko Nojiri, Atsuhito Takeda, Akihiro Nakaya, Shigetoyo Kogaki, Yasushi Sakata, Akira Ohtake, Kei Murayama, Yasushi Okazaki
Summary: In pediatric patients with mitochondrial disease, cardiomyopathy is common and associated with increased mortality. Left ventricular hypertrophy, neonatal onset, and chromosomal aberrations are independent predictors of all-cause mortality, especially unfavorable when combined together.
INTERNATIONAL JOURNAL OF CARDIOLOGY
(2021)
Article
Cardiac & Cardiovascular Systems
Soren K. Nielsen, Frederikke G. Hansen, Torsten B. Rasmussen, Thomas Fischer, Jens F. Lassen, Trine Madsen, Dorthe S. Moller, Ib C. Klausen, John B. Brodersen, Morten S. K. Jensen, Jens Mogensen
Summary: Family screening of relatives of HCM index patients with a normal genetic investigation revealed a small number of affected relatives with a favorable prognosis.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
(2023)
Article
Cardiac & Cardiovascular Systems
Emrah Kaya, Martijn Otten, Dominic A. M. J. Theuns, Kevin Veen, Sing-Chien Yap, Arend F. L. Schinkel, Alina A. Constantinescu, Michelle Michels, Olivier C. Manintveld, Tamas Szili-Torok, Kadir Caliskan
Summary: This study compared the long-term outcome of ICD therapy in patients with noncompaction cardiomyopathy (NCCM) with those with dilated cardiomyopathy (DCM) or hypertrophic cardiomyopathy (HCM). The results showed that the rate of appropriate and inappropriate ICD interventions in NCCM was comparable to that in DCM or HCM, and there was no difference in survival between the cardiomyopathy groups in multivariable analysis.
JACC-CLINICAL ELECTROPHYSIOLOGY
(2023)
Article
Biochemistry & Molecular Biology
Felicitas Escher, Ganna Aleshcheva, Heiko Pietsch, Christian Baumeier, Ulrich M. Gross, Benedikt Norbert Schrage, Dirk Westermann, Claus-Thomas Bock, Heinz-Peter Schultheiss
Summary: This study analyzed the impact of transcriptionally active cardiotropic B19V infection on long-term outcomes in adult patients with non-ischemic cardiomyopathy. The results showed that transcriptionally active B19V infection combined with inflammation was the strongest predictor of impaired survival. The findings suggest that advanced diagnostic differentiation of B19V-positive patients is of high prognostic importance and transcriptionally active B19V infection is an unfavorable prognostic trigger of adverse outcome.
Article
Cardiac & Cardiovascular Systems
Kenta Sugiura, Toru Kubo, Yuri Ochi, Kazuya Miyagawa, Yuichi Baba, Tatsuya Noguchi, Takayoshi Hirota, Naohito Yamasaki, Yoshinori L. Doi, Hiroaki Kitaoka
Summary: The study aimed to clarify the prognosis for patients with hypertrophic cardiomyopathy (HCM) over a follow-up period of more than 10 years. The results showed relatively favorable HCM-related mortality, but approximately half of the patients experienced HCM-related adverse events during the 20-year follow-up period, indicating the importance of long-term careful follow-up for HCM patients.
Review
Medicine, General & Internal
Amir Aziz, Szymon K. Musiol, William E. Moody, Luke Pickup, Rob Cooper, Gregory Y. H. Lip
Summary: The main predictors of informative genetic testing for hypertrophic cardiomyopathy include age, septal thickness, family history, and absence of hypertension. Using clinical predictors to decide whom to test is a feasible alternative to investigating all comers, but further validation is needed to make a concrete recommendation.
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
(2021)
Article
Cardiac & Cardiovascular Systems
Gabrielle Norrish, Gali Kolt, Elena Cervi, Ella Field, Kathleen Dady, Lidia Ziolkowska, 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
Summary: This study on infantile HCM aimed to characterize the etiology, phenotype, and outcomes in a multicentre European cohort. The cohort showed a diverse range of phenotypes and clinical courses, with poor overall outcomes largely related to underlying etiology. Comprehensive etiological investigations, including genetic testing, were highlighted as important in infantile HCM.
Review
Cardiac & Cardiovascular Systems
Sjoerd M. Verwijs, Yigal M. Pinto, Diederik W. D. Kuster, Jolanda van der Velden, Jacqueline Limpens, Juliette C. van Hattum, Saskia N. van der Crabben, Ronald H. Lekanne Deprez, Arthur A. M. Wilde, Harald T. Jorstad
Summary: Studies have shown that genetic variants associated with cardiomyopathies may be related to improved physical performance. This may explain the prevalence of such variants in athletes and the general population.
Review
Cardiac & Cardiovascular Systems
Jolanda van der Velden, Folkert W. Asselbergs, Jeroen Bakkers, Sandor Batkai, Luc Bertrand, Connie R. Bezzina, Ilze Bot, Bianca J. J. M. Brundel, Lucie Carrier, Steven Chamuleau, Michele Ciccarelli Dana Dawson, Sean M. Davidson, Andreas Dendorfer, Dirk J. Duncker, Thomas Eschenhagen, Larissa Fabritz, Ines Falcao-Pires, Peter Ferdinandy, Mauro Giacca, Henrique Girao, Can Gollmann-Tepekoeylue, Mariann Gyongyosi, Tomasz J. Guzik, Nazha Hamdani, Stephane Heymans, Andres Hilfiker, Denise Hilfiker-Kleiner, Alfons G. Hoekstra, Jean-Sebastien Hulot, Diederik W. D. Kuster, Linda W. van Laake, Sandrine Lecour, Tim Leiner, Wolfgang A. Linke, Joost Lumens, Esther Lutgens, Rosalinda Madonna, Lars Maegdefessel, Manuel Mayr, Peter van der Meer, Robert Passier, Filippo Perbellini, Cinzia Perrino, Maurizio Pesce, Silvia Priori, Carol Ann Remme, Bodo Rosenhahn, Ulrich Schotten, Rainer Schulz, Karin R. Sipido, Joost P. G. Sluijter, Frank van Steenbeek, Sabine Steffens, Cesare M. Terracciano, Carlo Gabriele Tocchetti, Patricia Vlasman, Kak Khee Yeung, Serena Zacchigna, Dayenne Zwaagman, Thomas Thum, Michele Ciccarelli
Summary: Cardiovascular diseases are a major cause of illness and death, and research is needed to improve diagnostics and discover new preventive and curative therapies. Translating basic science to clinical practice is challenging for complex conditions like cardiovascular diseases, which are often caused by multiple risk factors and comorbidities. Animal models play a vital role in providing important pathophysiological insights into disease mechanisms, particularly on an organ and systemic level.
CARDIOVASCULAR RESEARCH
(2022)
Review
Medicine, General & Internal
Karlijn B. Rombouts, Tara A. R. van Merrienboer, Johannes C. F. Ket, Natalija Bogunovic, Jolanda van der Velden, Kak Khee Yeung
Summary: This review highlights the crucial role of vSMC dysfunction in the development and progression of abdominal and thoracic Aortic Aneurysms (AA) and Aortic Dissections (AD). The study summarizes how stressors within the aortic wall modulate vSMC functions, leading to changes in processes such as TGF-beta signaling and regulatory RNA expression. Further research focusing on vSMC dysfunction is crucial in identifying potential noninvasive treatment options for AA and AD.
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
(2022)
Article
Cardiac & Cardiovascular Systems
Elmir Omerovic, Rodolfo Citro, Eduardo Bossone, Bjorn Redfors, Johannes Backs, Bastian Bruns, Michele Ciccarelli, Liam S. Couch, Dana Dawson, Guido Grassi, Massimo Iacoviello, Guido Parodi, Birke Schneider, Christian Templin, Jelena R. Ghadri, Thomas Thum, Ovidiu Chioncel, C. Gabriele Tocchetti, Jolanda van der Velden, Stephane Heymans, Alexander R. Lyon
Summary: The scientific statement on the pathophysiology of Takotsubo syndrome discusses various aspects including catecholamines, the sympathetic nervous system, vascular responses, the role of the nervous systems, gender differences, sex hormones, genetics, and chronic abnormalities of cardiovascular physiology in survivors. The limitations of current clinical and preclinical studies, implications for clinical management, and future research perspectives are also highlighted.
EUROPEAN JOURNAL OF HEART FAILURE
(2022)
Editorial Material
Cardiac & Cardiovascular Systems
P. Vlasman, J. van der Velden
NETHERLANDS HEART JOURNAL
(2022)
Review
Biophysics
Amy Li, K. Campbell, S. Lal, Y. Ge, A. Keogh, P. S. Macdonald, P. Lau, John Lai, W. A. Linke, J. van der Velden, A. Field, B. Martinac, M. Grosser, Cristobal dos Remedios
Summary: This review presents the current understanding of peripartum cardiomyopathy (PPCM) in terms of incidence, diagnosis, and treatment options. It discusses the potential vascular and/or hormonal causes of PPCM and examines the influence of comorbidities such as preeclampsia. Recent studies support the hypothesis that PPCM may have a familial component. While predominantly affecting the left ventricle, there is evidence to suggest that PPCM can also involve right ventricular failure. The review concludes that an RNAseq investigation at the cardiomyocyte level would provide valuable insights, and international collaborations are being sought to expand the available research samples.
BIOPHYSICAL REVIEWS
(2022)
Article
Cell Biology
Martijn Wehrens, Anne E. de Leeuw, Maya Wright-Clark, Joep E. C. Eding, Cornelis J. Boogerd, Bas Molenaar, Petra H. van der Kraak, Diederik W. D. Kuster, Jolanda van der Velden, Michelle Michels, Aryan Vink, Eva van Rooij
Summary: Functional links between genes and cell size relevant for HCM were identified using scRNA-seq on patients' samples. The study provides valuable insights into molecular events involved in HCM and may contribute to the development of enhanced therapies.
Article
Cardiac & Cardiovascular Systems
Roy Huurman, Nikki van der Velde, Arend F. L. Schinkel, H. Carlijne Hassing, Ricardo P. J. Budde, Marjon A. van Slegtenhorst, Judith Ma Verhagen, Alexander Hirsch, Michelle Michels
Summary: This study investigated the value of cardiovascular magnetic resonance (CMR) in phenotyping of relatives of hypertrophic cardiomyopathy (HCM) patients. The results showed that CMR reclassified 27% of the subjects, while normal electrocardiography (ECG) and transthoracic echocardiography (TTE) results almost excluded reclassifications by CMR.
EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING
(2022)
Article
Cardiac & Cardiovascular Systems
Edgar E. Nollet, Inez Duursma, Anastasiya Rozenbaum, Moritz Eggelbusch, Rob C. Wuest, Stephan A. C. Schoonvelde, Michelle Michels, Mark Jansen, Nicole N. van der Wel, Kenneth C. Bedi, Kenneth B. Margulies Jr, Jeff Nirschl, Diederik W. D. Kuster, Jolanda van der Velden
Summary: This study found that mitochondrial dysfunction is related to pathological remodelling in hypertrophic cardiomyopathy (HCM). In patients without genetic mutations, there is a stronger association between mitochondrial dysfunction and septal hypertrophy. The study also suggests that targeting mitochondria with specific drugs can restore mitochondrial function in HCM patients.
EUROPEAN HEART JOURNAL
(2023)
Editorial Material
Cardiac & Cardiovascular Systems
Monika M. Gladka, Jolanda van der Velden
CARDIOVASCULAR RESEARCH
(2023)
Article
Cardiac & Cardiovascular Systems
Sarah Abou Alaiwi, Thomas M. Roston, Peter Marstrand, Brian Lee Claggett, Victoria N. Parikh, Adam S. Helms, Jodie Ingles, Rachel Lampert, Neal K. Lakdawala, Michelle Michels, Anjali T. Owens, Joseph W. Rossano, Sara Saberi, Dominic J. Abrams, Euan A. Ashley, Christopher Semsarian, John C. Stendahl, James S. Ware, Erin Miller, Thomas D. Ryan, Mark W. Russell, Sharlene M. Day, Iacopo Olivotto, Christoffer R. Vissing, Carolyn Y. Y. Ho
Summary: A study on children diagnosed with hypertrophic cardiomyopathy (HCM) found that they have a higher risk of developing left ventricular systolic dysfunction (LVSD) compared to adult patients. This study highlights the importance of careful surveillance for LVSD in children with HCM, especially during their transition to adult care.
Review
Developmental Biology
Renee G. C. Maas, Floor W. van den Dolder, Qianliang Yuan, Jolanda van der Velden, Sean M. Wu, Joost P. G. Sluijter, Jan W. Buikema
Summary: Developmental research has revealed the key roles of Wnt and Hippo signaling in heart growth, but there are currently no clinically relevant therapies for cardiomyopathies. Understanding the decline in proliferation in adult hearts and finding new strategies for cardiac regeneration remain important. Multiple signaling pathways that regulate cardiomyocyte proliferation have been identified and upregulated in injured hearts. This review highlights the interaction of signaling pathways in heart development and their translation into current technologies for cardiomyocyte production.
Article
Cardiac & Cardiovascular Systems
Isabell Wiethoff, Maurits Sikking, Silvia Evers, Andrea Gabrio, Michiel Henkens, Michelle Michels, Job Verdonschot, Stephane Heymans, Mickael Hiligsmann
Summary: Dilated cardiomyopathy (DCM) is a major cause of heart failure, leading to low quality of life and high societal costs for patients, especially those with severe symptoms.
EUROPEAN HEART JOURNAL-QUALITY OF CARE AND CLINICAL OUTCOMES
(2023)
Article
Radiology, Nuclear Medicine & Medical Imaging
Stephan A. C. Schoonvelde, Claudine W. B. Ruijmbeek, Judith M. A. Verhagen, Debby M. E. I. Hellebrekers, Marcel J. M. Kofflard, Michelle Michels, Alexander Hirsch
Summary: This case report presents three siblings with a pathogenic variant of the mitochondrially encoded tRNA isoleucine (MT-TI) gene, causing left ventricular hypertrophy (LVH). Cardiac MRI revealed a distinctive cardiac phenotype, including extensive LVH and decreased ejection fraction.
RADIOLOGY-CARDIOTHORACIC IMAGING
(2023)
Article
Cardiac & Cardiovascular Systems
Qianliang Yuan, Renee G. C. Maas, Ellen C. J. Brouwer, Jiayi Pei, Christian Snijders Blok, Marko A. Popovic, Nanne J. Paauw, Niels Bovenschen, Jesper Hjortnaes, Magdalena Harakalova, Pieter A. Doevendans, Joost P. G. Sluijter, Jolanda van der Velden, Jan W. Buikema
Summary: This study investigates the disassembly of sarcomeres during mitosis in cardiomyocytes and the effects of CHIR99021 on hiPSC-CMs. The study reveals the activation of Wnt and Hippo signaling in proliferative hiPSC-CMs and the increased efficiency of non-viral vector incorporation by CHIR99021. The findings provide a valuable tool for gene manipulation studies in hiPSC-CMs and engineered cardiac tissue.
JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE
(2022)
Editorial Material
Cardiac & Cardiovascular Systems
Jose E. Exaire, Timothy A. Mixon
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Giuseppe Di Gioia, Federica Coletti, Lorenzo Buzzelli, Viviana Maestrini, Sara Monosilio, Andrea Segreti, Maria Rosaria Squeo, Erika Lemme, Antonio Nenna, Antonio Pelliccia
Summary: Dyslipidemia is common in Paralympic athletes, with lipid levels influenced by the type of disability and sporting discipline.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Esra Donmez, Sevgi Ozcan, Irfan Sahin, Murat Ziyrek, Ertugrul Okuyan
Summary: This study aimed to evaluate the predictive value of the GRACE risk score in acute pulmonary embolism (PE) patients for 30-day mortality and the need for thrombolytic treatment. The study found that the GRACE risk score, along with the PESI score, were independent risk factors associated with 30-day mortality and the need for thrombolytic treatment. The GRACE risk score showed high sensitivity and specificity in predicting mortality, and its combination with the PESI score helped define high-risk PE patients and predict poor prognosis.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Tom Kai Ming Wang, Reza Reyaldeen, Kevser Akyuz, Zoran B. Popovic, A. Marc Gillinov, Bo Xu, Brian P. Griffin, Milind Y. Desai
Summary: Transthoracic echocardiography (TTE) is commonly used to evaluate isolated tricuspid regurgitation (TR), but there is limited research comparing its quantification with magnetic resonance imaging (MRI). In this study, a novel TTE algorithm was developed to identify severe TR based on TTE parameters. The algorithm had a higher accuracy than the current guidelines' criteria in detecting severe TR by MRI.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Editorial Material
Cardiac & Cardiovascular Systems
Enkhtsogt Sainbayar, Ramzi Ibrahim, Hoang Nhat Pham, Wisam Beauti, Mahek Shahid, Natalie Hickerson, Mohammed Salih, Joao Paulo Ferreira, Mamas A. Mamas
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Richard E. Casazza, Hymie Chera, Carlos Adolfo Rodriguez, Sergey Ayzenberg
Summary: This article presents a case of a patient with known situs inversus who underwent cardiac catheterization and was found to have chronic total occlusion in the right coronary artery. Situs inversus is a rare congenital abnormality characterized by the inverted position of chest and abdominal organs. Cardiac catheterization is uncommon in patients with this particular abnormality, highlighting the importance of customizing techniques to engage coronary arteries and optimize guide support for percutaneous coronary intervention if needed.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Editorial Material
Cardiac & Cardiovascular Systems
Georgiana Pintea Bentea, Brahim Berdaoui, Sophie Samyn, Marielle Morissens, Philippe van de Borne, Jose Castro Rodriguez
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Bulbul Ahmed, Melissa G. Farb, Shakun Karki, Sophia D'Alessandro, Niloo M. Edwards, Noyan Gokce
Summary: This study evaluated the angiogenic capacity of adipose tissue in patients undergoing cardiac surgeries and found that patients with coronary artery disease (CAD) had reduced angiogenic capacity in their pericardial adipose tissue. Gene expression analysis revealed upregulated expression of the anti-angiogenic gene TSP-1 in CAD patients, with no significant differences in other angiogenic factors. Additionally, inhibiting TSP-1 expression significantly improved angiogenic deficiency in CAD patients.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Moshe Rav-Acha, Orli Wube, Oholi Tovia Brodie, Yoav Michowitz, Michael Ilan, Tal Ovdat, Robert Klempfner, Mahmud Suleiman, Ilan Goldenberg, Michael Glikson
Summary: The current guidelines recommend prophylactic implantable cardioverter-defibrillator (ICD) for patients with symptomatic heart failure (HF) and low left ventricular ejection fraction. However, not all patients will benefit from ICD treatment. This study evaluated the feasibility of using the MADIT-II-based Risk Stratification Score (MRSS) to predict the survival benefit of prophylactic ICDs in patients with HF. The results showed that different risk subgroups had varying levels of ICD survival benefit.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Ariel Banai, Rachel Retsky, Lior Lupu, Erez Levi, David Zahler, Omri Feder, Roei Merin, Yan Topilsky, Raphael Rosso, Shmuel Banai, Sami Viskin, Ehud Chorin
Summary: This study aims to evaluate the association between electromechanical window (EMW) and ventricular tachyarrhythmias in patients with Takotsubo syndrome (TTS). The study found that TTS patients had a lower EMW value, which was associated with an increased risk of ventricular tachyarrhythmias.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Harun Kundi, Kobina Hagan, Tamer Yahya, Garima Sharma, Sadeer Al-Kindi, Zulqarnain Javed, Khurram Nasir
Summary: Using latent class analysis (LCA), the study identified clinical, demographic, and social subphenotypes in ASCVD population and assessed the risk of all-cause and cardiovascular mortality across different socioclinical classes. The results showed that the younger, female, non-Hispanic Black or Hispanic individuals with a high burden of co-morbidities and unfavorable social determinants of health had the highest risk of mortality in the identified latent classes.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Moises A. Vasquez, Mina Iskander, Mohammed Mustafa, Juan A. Quintero-Martinez, Antonio Luna, Joel Mintz, Jose Noy, Juan Uribe, Ivan Mijares, Eduardo de Marchena, Yiannis S. Chatzizisis
Summary: The benefits of pericardiocentesis (PC) in patients with pulmonary hypertension (PH) and pericardial effusions are unclear. The study found that PC in PH patients is associated with higher in-hospital mortality and rates of cardiovascular complications.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Ken Kuwajima, Mana Ogawa, Irving Ruiz, Hiroko Hasegawa, Nobuichiro Yagi, Florian Rader, Robert J. Siegel, Takahiro Shiota
Summary: After cardiac surgery, the longitudinal function of the right ventricle and left ventricle is reduced, despite preserved global functions. In particular, tricuspid annular plane systolic excursion (TAPSE) remains decreased after surgery.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Min -Jung Kim, Robert H. Aseltine Jr, Sara R. Tabtabai
Summary: This study evaluated the rates and causes of 30-day readmissions after discharge for heart failure (HF) as a primary and secondary diagnosis. The findings indicate that efforts to reduce readmission rates should include patients with secondary HF diagnosis, and surveillance should extend to 2 weeks postdischarge to identify at-risk patients.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)
Article
Cardiac & Cardiovascular Systems
Ya He, Jianzhong Zhou
Summary: This study aimed to examine the relation between reverse septal curvature (RSC) and nonsustained ventricular tachycardia (NSVT) in patients with hypertrophic cardiomyopathy (HCM). The study found that patients with RSC were younger and had a higher incidence of NSVT, and RSC was identified as a strong independent risk factor for NSVT.
AMERICAN JOURNAL OF CARDIOLOGY
(2024)