Cardiovascular disease and breast cancer: where these entities intersect: a scientific statement from the American Heart Association

LS Mehta, KE Watson, A Barac, TM Beckie, V Bittner… - Circulation, 2018 - Am Heart Assoc
Cardiovascular disease (CVD) remains the leading cause of mortality in women, yet many
people perceive breast cancer to be the number one threat to women's health. CVD and …

Dilated cardiomyopathy

HP Schultheiss, DL Fairweather, ALP Caforio… - Nature reviews Disease …, 2019 - nature.com
Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or
biventricular dilation and impaired contraction that is not explained by abnormal loading …

Force generation via β-cardiac myosin, titin, and α-actinin drives cardiac sarcomere assembly from cell-matrix adhesions

A Chopra, ML Kutys, K Zhang, WJ Polacheck… - Developmental cell, 2018 - cell.com
Truncating mutations in the sarcomere protein titin cause dilated cardiomyopathy due to
sarcomere insufficiency. However, it remains mechanistically unclear how these mutations …

BET bromodomain inhibition suppresses innate inflammatory and profibrotic transcriptional networks in heart failure

Q Duan, S McMahon, P Anand, H Shah… - Science translational …, 2017 - science.org
Despite current standard of care, the average 5-year mortality after an initial diagnosis of
heart failure (HF) is about 40%, reflecting an urgent need for new therapeutic approaches …

Hypertrophic cardiomyopathy: mutations to mechanisms to therapies

M Kawana, JA Spudich, KM Ruppel - Frontiers in Physiology, 2022 - frontiersin.org
Hypertrophic cardiomyopathy (HCM) affects more than 1 in 500 people in the general
population with an extensive burden of morbidity in the form of arrhythmia, heart failure, and …

Cardiomyocyte‐specific telomere shortening is a distinct signature of heart failure in humans

M Sharifi‐Sanjani, NM Oyster, ED Tichy… - Journal of the …, 2017 - Am Heart Assoc
Background Telomere defects are thought to play a role in cardiomyopathies, but the
specific cell type affected by the disease in human hearts is not yet identified. The aim of this …

Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review

D Fatkin, IG Huttner, JC Kovacic, JG Seidman… - Journal of the American …, 2019 - jacc.org
Precision medicine promises to dramatically improve patient outcomes and reduce health
care costs through a shift in focus from disease treatment to prevention and individualized …

Genetics of Dilated Cardiomyopathy

R Eldemire, L Mestroni… - Annual review of medicine, 2024 - annualreviews.org
Dilated cardiomyopathy (DCM) is defined as dilation and/or reduced function of one or both
ventricles and remains a common disease worldwide. An estimated 40% of cases of familial …

[HTML][HTML] Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

AE Minoche, C Horvat, R Johnson, V Gayevskiy… - Genetics in …, 2019 - Elsevier
Purpose We evaluated genome sequencing (GS) as an alternative to multigene panel
sequencing (PS) for genetic testing in dilated cardiomyopathy (DCM). Methods Forty-two …

Arrhythmic genotypes in familial dilated cardiomyopathy: implications for genetic testing and clinical management

S Peters, S Kumar, P Elliott, JM Kalman… - Heart, Lung and …, 2019 - Elsevier
Cardiac arrhythmias are frequently seen in patients with dilated cardiomyopathy (DCM) and
can precipitate heart failure and death. In patients with non-ischaemic DCM, evidence for the …