 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, 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
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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 |
|---|
| 1996 | 4 | 0 | 4 | | 1997 | 3 | 0 | 3 | | 1998 | 1 | 0 | 1 | | 1999 | 7 | 2 | 9 | | 2000 | 1 | 0 | 1 | | 2001 | 3 | 0 | 3 | | 2002 | 4 | 0 | 4 | | 2003 | 2 | 1 | 3 | | 2004 | 4 | 1 | 5 | | 2005 | 2 | 1 | 3 | | 2006 | 1 | 2 | 3 | | 2007 | 4 | 1 | 5 | | 2008 | 3 | 1 | 4 | | 2009 | 5 | 0 | 5 | | 2010 | 1 | 0 | 1 | | 2011 | 2 | 1 | 3 | | 2012 | 5 | 2 | 7 | | 2013 | 5 | 0 | 5 | | 2014 | 4 | 2 | 6 | | 2015 | 7 | 3 | 10 | | 2016 | 6 | 0 | 6 | | 2017 | 7 | 1 | 8 | | 2018 | 9 | 2 | 11 | | 2019 | 7 | 1 | 8 | | 2020 | 6 | 1 | 7 | | 2021 | 7 | 1 | 8 | | 2022 | 11 | 0 | 11 | | 2023 | 5 | 0 | 5 | | 2024 | 5 | 1 | 6 | | 2025 | 9 | 2 | 11 | | 2026 | 3 | 0 | 3 |
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Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.
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Stroeks SLVM, Bart NK, Rossano J, Claggett B, Beelen NJ, Buchan RJ, Day S, Fornaro A, Halliday BP, Wheeler MT, Hammersley DJ, Helms A, Heymans ABM, Ho CY, Khan SS, Lin K, Lota A, Merlo M, Mestroni L, Olivotto I, Owens A, Seidman CE, Shore S, Sinnette C, Sinagra G, Stevenson LW, Stewart GC, Theotakis P, Venner MFGHM, Ware JS, Taylor MRG, Verdonschot JAJ, Wilsbacher L, Prasad S, Heymans SR, Parikh VN, Tayal U, Lakdawala NK. Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe Registry. J Am Coll Cardiol. 2026 Jun 30; 87(25):3573-3588.
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Floyd BJ, Njoroge JN, Krysov VA, Gomes B, Murtha R, Aribeana C, Cannie D, Smith E, Paldino A, Brown EE, Barth A, Ilhan E, Johnson R, Wojciak J, Alkhayat M, Graw S, Medo K, Haas J, Chahal CAA, Fenzl K, Steinmetz L, Gollob M, Ashley E, Day S, Judge D, Roberts JD, Vedantham V, Mao CY, Fatkin D, Lakdawala NK, Taylor MRG, Mestroni L, Saguner AM, Tayal U, Cadrin-Tourigny J, Krahn AD, James C, Dal Ferro M, Sinagra G, Merlo M, Owens A, Reza N, Saberi S, Helms A, Elliott P, Meder B, Lancaster M, Parikh VN. RBM20 Truncating Variants and Human Cardiomyopathy. JAMA Cardiol. 2026 May 01; 11(5):439-445.
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Wang M, Ghazal R, Srinivas AN, Nguyen TTL, Murthy V, McNamara DM, Skime MK, Batzler A, Jenkins GD, Barlera S, Pileggi S, Mestroni L, Merlo M, Pinet F, Krejcí J, Chaloupka A, de Groote P, Weinshilboum RM, Tschumperlin DJ, Liu D, Pereira NL. Novel association of NAV3 with dilated cardiomyopathy and its role in cardiac fibrosis. Am J Physiol Heart Circ Physiol. 2026 Mar 01; 330(3):H686-H696.
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Johnson R, Fletcher RA, Peters S, Ohanian M, Soka M, Smolnikov A, Abihider KE, Ackerman MJ, Ader F, Akhtar MM, Amin AS, Ashley EA, Atherton JJ, Austin R, Baas AF, Bagnall RD, Ross SB, Blouin JL, Brown EE, Bundgaard H, Cannie D, Chmielewski P, Correnti G, Crespo-Leiro MG, Dal Ferro M, Dellefave-Castillo LM, Dominguez F, Dooijes D, Dybro AM, Ed Demri Y, El Hachmi M, Escobar-Lopez L, Foye SJ, Franaszczyk M, Gigli M, Lopez EG, Goudal A, Graw S, Guipponi M, Haan E, Haas J, Hammersley DJ, Hansen FG, Hayward CS, Hey TM, Heymans S, Ho CY, Houweling AC, Ingles J, Ingrey A, Jabbour A, James PA, Jansweijer JA, Jongbloed JDH, Keogh AM, Larrañaga-Moreira JM, Lekanne Deprez RH, Macciocca I, Macdonald PS, Mansencal N, Mansour J, Martinez-Veira C, McDonough B, McGaughran J, Medo K, Merlo M, Michalak E, Monserrat L, Mountain H, Muller SA, Murphy AM, Murray B, Oates EC, Ormondroyd E, Pachter N, Paldino A, Palmyre A, Pereira NL, Picard KC, Poplawski N, Prasad S, Proukhnitzky J, Pruny JF, Reant P, Richard P, Ronan A, Sedaghat-Hamedani F, Semsarian C, Storm G, Stroeks S, Syrris P, Taylor MRG, Thomson K, Thompson T, van Tintelen JP, Vissing CR, Waddell-Smith KE, Wallis M, Zentner D, Arnott C, Marian AJ, Oh J, Fokstuen S, James CA, Barriales-Villa R, Meder B, Wahbi K, Giudicessi JR, Parikh VN, Ware JS, Piriou N, Rooryck C, Lakdawala NK, Mestroni L, Sinagra G, Elliott PM, Watkins H, McNally EM, Charron P, van Spaendonck-Zwarts KY, Garcia-Pavia P, Peña-Peña ML, Mogensen J, Christensen AH, Bilinska ZT, Rasmussen TB, Seidman JG, Seidman CE, Te Riele ASJM, Verdonschot JAJ, Pinto YM, Christiaans I, Fatkin D. Titin-related familial dilated cardiomyopathy: factors associated with disease onset. Eur Heart J. 2025 Dec 22; 46(48):5240-5257.
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Stroeks SLVM, Merlo M, Mora-Ayestaran N, Jason M, Tayal U, Wang P, Cannatà A, Sikking MA, Dal Ferro M, Peiro B, Willemars M, Hellebrekers DMEI, van Leeuwen REW, Setti M, Gonzalez-Lopez E, Krapels IPC, Pio Loco Detto Gava C, van den Wijngaard A, Henkens MTHM, Iseppi M, Raafs AG, Hoes MF, van Empel VPM, Jones EAV, Nabben M, Taylor M, Brunner HG, Ochoa JP, Dominguez F, Lakdawala NK, Sinagra G, Garcia-Pavia P, Mestroni L, Heymans SRB, Verdonschot JAJ. Sex Differences in Prognosis of Patients With Genetic Dilated Cardiomyopathy. Circ Heart Fail. 2025 Nov; 18(11):e012592.
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Gigli M, Verdonschot JAJ, Garcia-Pavia P, Stolfo D, Monserrat L, Prasad S, Mazzanti A, Asselbergs FW, Bauce B, Charron P, Dawson D, Halliday BP, Mestroni L, Seferovic P, Tayal U, Esteban MTT, Van Tintelen P, Heymans S, Pantazis A, Metra M, Sinagra G. Future development of arrhythmogenic risk scores in patients with heart failure and inherited dilated cardiomyopathy. A scientific statement of the Heart Failure Association of the ESC. Eur J Heart Fail. 2025 Nov; 27(11):2229-2243.
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Stroeks SLVM, Wang P, Merlo M, Muller S, Paldino A, Mora-Ayestaran N, Jason M, Ferro MD, Pio Loco Detto Gava C, Dominguez F, Gonzalez-Lopez E, van den Wijngaard A, Venner MFGHM, Sikking M, Minten M, Nihant B, Beelen N, Graw S, Medo K, de Koning B, Taylor M, van Tintelen JP, Mestroni L, Sinagra G, Te Riele ASJM, Garcia-Pavia P, Heymans S, Verdonschot JAJ. Impact of genotype-phenotype associations on prognosis in dilated cardiomyopathy. Eur J Heart Fail. 2025 Dec; 27(12):3205-3218.
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Pitsava G, Hawley M, Auriga L, de Dios I, Ko A, Marmolejos S, Almalvez M, Chen I, Scozzaro K, Zhao J, Barrick R, Ah Mew N, Fusaro VA, LoTempio J, Taylor M, Mestroni L, Graw S, Milewicz D, Guo D, Murdock DR, Bujakowska KM, Xiao C, Délot EC, Berger SI, Vilain E. Genome sequencing reveals the impact of pseudoexons in rare genetic disease. Genet Med. 2025 Nov; 27(11):101574.
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Perotto M, Paldino A, Mazzarotto F, Barbati G, Stroeks SLVM, Verdonschot JAJ, Akhtar M, Elliott P, Ochoa JP, Garcia-Pavia P, de Frutos F, Sepp R, Hategan L, Prasad S, Yazdani M, Morris-Rosendahl D, Palinkas ED, Girolami F, Olivotto I, Parikh VN, Fatkin D, Lakdawala N, McKenna WJ, Stolfo D, Gigli M, Brun F, Collesi C, Giacca M, Zacchigna S, Severini GM, Lenarduzzi S, Spedicati B, Santin A, Girotto G, Gasparini P, Taylor MRG, Mestroni L, Merlo M, Sinagra G, Dal Ferro M. Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study. JACC Heart Fail. 2025 Sep; 13(9):102529.
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Jeffrey DA, Dockstader K, Revoredo Vicentino A, Slavov DB, Miyamoto SD, Stauffer BL, Sucharov CC. Muscle-specific isoforms of FXR1 are necessary for miR-1-mediated repression of connexin 43 and are downregulated in pediatric dilated cardiomyopathy. Am J Physiol Heart Circ Physiol. 2025 06 01; 328(6):H1380-H1390.
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