Cardiomyopathy, Dilated

"Cardiomyopathy, Dilated" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein.

Descriptor ID	D002311
MeSH Number(s)	C14.280.195.160 C14.280.238.070
Concept/Terms	Cardiomyopathy, Dilated Cardiomyopathy, Dilated Cardiomyopathies, Dilated Dilated Cardiomyopathies Dilated Cardiomyopathy Cardiomyopathy, Familial Idiopathic Cardiomyopathy, Familial Idiopathic Cardiomyopathies, Familial Idiopathic Familial Idiopathic Cardiomyopathies Familial Idiopathic Cardiomyopathy Idiopathic Cardiomyopathies, Familial Idiopathic Cardiomyopathy, Familial Cardiomyopathy, Congestive Cardiomyopathies, Congestive Congestive Cardiomyopathies Cardiomyopathy, Dilated, with Conduction Deffect1 Cardiomyopathy, Dilated, CMD1A Dilated cardiomyopathy 1A 1As, Dilated cardiomyopathy Dilated cardiomyopathy 1As cardiomyopathy 1A, Dilated cardiomyopathy 1As, Dilated Cardiomyopathy, Dilated, Autosomal Recessive Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, With Conduction Defect 1 Cardiomyopathy, Idiopathic Dilated Cardiomyopathies, Idiopathic Dilated Dilated Cardiomyopathies, Idiopathic Dilated Cardiomyopathy, Idiopathic Idiopathic Dilated Cardiomyopathies Idiopathic Dilated Cardiomyopathy Congestive Cardiomyopathy Cardiomyopathy, Dilated, LMNA

Below are MeSH descriptors whose meaning is more general than "Cardiomyopathy, Dilated".

Diseases [C]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Cardiomegaly [C14.280.195]
Cardiomyopathy, Dilated [C14.280.195.160]
Cardiomyopathies [C14.280.238]
Cardiomyopathy, Dilated [C14.280.238.070]

Below are MeSH descriptors whose meaning is related to "Cardiomyopathy, Dilated".

Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathy, Dilated".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Cardiomyopathy, Dilated" by people in this website by year, and whether "Cardiomyopathy, Dilated" was a major or minor topic of these publications.

Bar chart showing 127 publications over 27 distinct years, with a maximum of 9 publications in 2019

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	5	0	5
1996	2	1	3
1997	1	0	1
1998	2	0	2
1999	2	1	3
2000	3	2	5
2001	1	0	1
2002	5	0	5
2003	5	1	6
2004	2	2	4
2005	7	0	7
2006	1	4	5
2007	3	2	5
2008	3	1	4
2009	6	2	8
2010	6	2	8
2011	1	2	3
2012	5	1	6
2013	5	0	5
2014	5	0	5
2015	5	1	6
2016	6	1	7
2017	4	0	4
2018	3	0	3
2019	8	1	9
2020	4	1	5
2022	2	0	2

Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.

Lay E, Azamian MS, Denfield SW, Dreyer W, Spinner JA, Kearney D, Zhang L, Worley KC, Bi W, Lalani SR. LMOD2-related dilated cardiomyopathy presenting in late infancy. Am J Med Genet A. 2022 06; 188(6):1858-1862.

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Gorzynski JE, Goenka SD, Shafin K, Jensen TD, Fisk DG, Grove ME, Spiteri E, Pesout T, Monlong J, Bernstein JA, Ceresnak S, Chang PC, Christle JW, Chubb H, Dunn K, Garalde DR, Guillory J, Ruzhnikov MRZ, Wright C, Wusthoff CJ, Xiong K, Hollander SA, Berry GJ, Jain M, Sedlazeck FJ, Carroll A, Paten B, Ashley EA. Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock. Circ Genom Precis Med. 2022 Apr; 15(2):e003591.

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Tschöpe C, Ammirati E, Bozkurt B, Caforio ALP, Cooper LT, Felix SB, Hare JM, Heidecker B, Heymans S, Hübner N, Kelle S, Klingel K, Maatz H, Parwani AS, Spillmann F, Starling RC, Tsutsui H, Seferovic P, Van Linthout S. Myocarditis and inflammatory cardiomyopathy: current evidence and future directions. Nat Rev Cardiol. 2021 03; 18(3):169-193.

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Auguste G, Rouhi L, Matkovich SJ, Coarfa C, Robertson MJ, Czernuszewicz G, Gurha P, Marian AJ. BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific lamin A/C-deficient mice. J Clin Invest. 2020 09 01; 130(9):4740-4758.

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Solt SA, Hoffman TM, Sharma MS, Westreich KD, Kihlstrom M, Schwartz SP. Orthotopic Heart Transplantation in a Patient With Gitelman Syndrome and Dilated Cardiomyopathy. World J Pediatr Congenit Heart Surg. 2020 07; 11(4):520-521.

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Morales A, Kinnamon DD, Jordan E, Platt J, Vatta M, Dorschner MO, Starkey CA, Mead JO, Ai T, Burke W, Gastier-Foster J, Jarvik GP, Rehm HL, Nickerson DA, Hershberger RE. Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study. Circ Genom Precis Med. 2020 04; 13(2):e002480.

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Greenleaf CE, Binsalamah ZM, Adachi I. Replacement of Left Ventricular Assist Device Inflow Cannula Using a Right Angle Atrial Cannula. Ann Thorac Surg. 2020 05; 109(5):e389.

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Spigel ZA, Razzouk A, Nigro JJ, Karamlou TB, Kavarana MN, Roeser ME, Adachi I. Pulmonary Artery Banding for Children With Dilated Cardiomyopathy: US Experience. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2020; 23:69-76.

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Angelini A, Gorey MA, Dumont F, Mougenot N, Chatzifrangkeskou M, Muchir A, Li Z, Mericskay M, Decaux JF. Cardioprotective effects of a-cardiac actin on oxidative stress in a dilated cardiomyopathy mouse model. FASEB J. 2020 02; 34(2):2987-3005.

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Nakano SJ, Miyamoto SD, Price JF, Rossano JW, Cabrera AG. Pediatric Heart Failure: An Evolving Public Health Concern. J Pediatr. 2020 03; 218:217-221.

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