 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.
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
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| MeSH Number(s) |
C14.280.195.160 C14.280.238.070
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| 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, Dilated, Autosomal Recessive
- Cardiomyopathy, Dilated, CMD1A
- Cardiomyopathy, Dilated, LMNA
- Congestive Cardiomyopathy
- Cardiomyopathy, Dilated, with Conduction Deffect1
- Cardiomyopathy, Idiopathic Dilated
- Cardiomyopathies, Idiopathic Dilated
- Dilated Cardiomyopathies, Idiopathic
- Dilated Cardiomyopathy, Idiopathic
- Idiopathic Dilated Cardiomyopathies
- Idiopathic Dilated Cardiomyopathy
- Dilated cardiomyopathy 1A
- 1A, Dilated cardiomyopathy
- 1As, Dilated cardiomyopathy
- Dilated cardiomyopathy 1As
- cardiomyopathy 1A, Dilated
- cardiomyopathy 1As, Dilated
- Cardiomyopathy, Congestive
- Cardiomyopathies, Congestive
- Congestive Cardiomyopathies
- Cardiomyopathy, Dilated, 1a
- Cardiomyopathy, Dilated, With Conduction Defect 1
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Below are MeSH descriptors whose meaning is more general than "Cardiomyopathy, Dilated".
Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathy, Dilated".
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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1989 | 1 | 0 | 1 | | 1999 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2009 | 2 | 0 | 2 | | 2011 | 1 | 0 | 1 | | 2012 | 0 | 1 | 1 | | 2016 | 3 | 0 | 3 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.
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Arif M, Alam P, Ahmed RP, Pandey R, Faridi HM, Sadayappan S. Upregulated Angiogenesis Is Incompetent to Rescue Dilated Cardiomyopathy Phenotype in Mice. Cells. 2021 03 31; 10(4).
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Boldizsar F, Tarjanyi O, Olasz K, Hegyi A, Mikecz K, Glant TT, Rauch TA. FTY720 (Gilenya) treatment prevents spontaneous autoimmune myocarditis and dilated cardiomyopathy in transgenic HLA-DQ8-BALB/c mice. Cardiovasc Pathol. 2016 Sep-Oct; 25(5):353-61.
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Patel AN, Henry TD, Quyyumi AA, Schaer GL, Anderson RD, Toma C, East C, Remmers AE, Goodrich J, Desai AS, Recker D, DeMaria A. Ixmyelocel-T for patients with ischaemic heart failure: a prospective randomised double-blind trial. Lancet. 2016 Jun 11; 387(10036):2412-21.
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Henry TD, Schaer GL, DeMaria A, Recker D, Remmers AE, Goodrich J, Patel AN. The ixCELL-DCM Trial: Rationale and Design. Cell Transplant. 2016; 25(9):1689-1699.
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Respress JL, van Oort RJ, Li N, Rolim N, Dixit SS, deAlmeida A, Voigt N, Lawrence WS, Skapura DG, Sk?rdal K, Wisl?ff U, Wieland T, Ai X, Pogwizd SM, Dobrev D, Wehrens XH. Role of RyR2 phosphorylation at S2814 during heart failure progression. Circ Res. 2012 May 25; 110(11):1474-83.
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Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Z?chner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Am J Hum Genet. 2011 Mar 11; 88(3):273-82.
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Shannon TR. Ryanodine receptor Ca2+ sensitivity and excitation-contraction coupling in muscular dystrophy and heart failure: similar and yet different. Am J Physiol Heart Circ Physiol. 2009 Dec; 297(6):H1965-6.
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Catalucci D, Zhang DH, DeSantiago J, Aimond F, Barbara G, Chemin J, Bonci D, Picht E, Rusconi F, Dalton ND, Peterson KL, Richard S, Bers DM, Brown JH, Condorelli G. Akt regulates L-type Ca2+ channel activity by modulating Cavalpha1 protein stability. J Cell Biol. 2009 Mar 23; 184(6):923-33.
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Ai X, Pogwizd SM. Connexin 43 downregulation and dephosphorylation in nonischemic heart failure is associated with enhanced colocalized protein phosphatase type 2A. Circ Res. 2005 Jan 07; 96(1):54-63.
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Shah PJ, Hare DL, Raman JS, Gordon I, Chan RK, Horowitz JD, Rosalion A, Buxton BF. Survival after myocardial revascularization for ischemic cardiomyopathy: a prospective ten-year follow-up study. J Thorac Cardiovasc Surg. 2003 Nov; 126(5):1320-7.
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