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Left ventricular noncompaction 8(LVNC8)

MedGen UID:
815618
Concept ID:
C3809288
Disease or Syndrome
Synonym: LVNC8
 
Gene (location): PRDM16 (1p36.32)
 
Monarch Initiative: MONDO:0014152
OMIM®: 615373

Definition

Some individuals with left ventricular noncompaction experience no symptoms at all; others have heart problems that can include sudden cardiac death. Additional signs and symptoms include abnormal blood clots, irregular heart rhythm (arrhythmia), a sensation of fluttering or pounding in the chest (palpitations), extreme fatigue during exercise (exercise intolerance), shortness of breath (dyspnea), fainting (syncope), swelling of the legs (lymphedema), and trouble laying down flat. Some affected individuals have features of other heart defects. Left ventricular noncompaction can be diagnosed at any age, from birth to late adulthood. Approximately two-thirds of individuals with left ventricular noncompaction develop heart failure.

Left ventricular noncompaction is a heart (cardiac) muscle disorder that occurs when the lower left chamber of the heart (left ventricle), which helps the heart pump blood, does not develop correctly. Instead of the muscle being smooth and firm, the cardiac muscle in the left ventricle is thick and appears spongy. The abnormal cardiac muscle is weak and has an impaired ability to pump blood because it either cannot completely contract or it cannot completely relax. For the heart to pump blood normally, cardiac muscle must contract and relax fully. [from MedlinePlus Genetics]

Clinical features

From HPO
Cardiac arrhythmia
MedGen UID:
2039
Concept ID:
C0003811
Finding
Any cardiac rhythm other than the normal sinus rhythm. Such a rhythm may be either of sinus or ectopic origin and either regular or irregular. An arrhythmia may be due to a disturbance in impulse formation or conduction or both.
Primary dilated cardiomyopathy
MedGen UID:
2880
Concept ID:
C0007193
Disease or Syndrome
Familial dilated cardiomyopathy is a genetic form of heart disease. It occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.\n\nIt usually takes many years for symptoms of familial dilated cardiomyopathy to cause health problems. They typically begin in mid-adulthood, but can occur at any time from infancy to late adulthood. Signs and symptoms of familial dilated cardiomyopathy can include an irregular heartbeat (arrhythmia), shortness of breath (dyspnea), extreme tiredness (fatigue), fainting episodes (syncope), and swelling of the legs and feet. In some cases, the first sign of the disorder is sudden cardiac death. The severity of the condition varies among affected individuals, even in members of the same family.
Congestive heart failure
MedGen UID:
9169
Concept ID:
C0018802
Disease or Syndrome
The presence of an abnormality of cardiac function that is responsible for the failure of the heart to pump blood at a rate that is commensurate with the needs of the tissues or a state in which abnormally elevated filling pressures are required for the heart to do so. Heart failure is frequently related to a defect in myocardial contraction.
Mitral regurgitation
MedGen UID:
7670
Concept ID:
C0026266
Disease or Syndrome
An abnormality of the mitral valve characterized by insufficiency or incompetence of the mitral valve resulting in retrograde leaking of blood through the mitral valve upon ventricular contraction.
Left ventricular diastolic dysfunction
MedGen UID:
696562
Concept ID:
C1273070
Disease or Syndrome
Abnormal function of the left ventricule during left ventricular relaxation and filling.
Left ventricular systolic dysfunction
MedGen UID:
226908
Concept ID:
C1277187
Disease or Syndrome
Abnormality of left ventricular contraction, often defined operationally as an ejection fraction of less than 40 percent.
Left ventricular noncompaction
MedGen UID:
450531
Concept ID:
C1960469
Disease or Syndrome
Left ventricular noncompaction is a heart (cardiac) muscle disorder that occurs when the lower left chamber of the heart (left ventricle), which helps the heart pump blood, does not develop correctly. Instead of the muscle being smooth and firm, the cardiac muscle in the left ventricle is thick and appears spongy. The abnormal cardiac muscle is weak and has an impaired ability to pump blood because it either cannot completely contract or it cannot completely relax. For the heart to pump blood normally, cardiac muscle must contract and relax fully.\n\nSome individuals with left ventricular noncompaction experience no symptoms at all; others have heart problems that can include sudden cardiac death. Additional signs and symptoms include abnormal blood clots, irregular heart rhythm (arrhythmia), a sensation of fluttering or pounding in the chest (palpitations), extreme fatigue during exercise (exercise intolerance), shortness of breath (dyspnea), fainting (syncope), swelling of the legs (lymphedema), and trouble laying down flat. Some affected individuals have features of other heart defects. Left ventricular noncompaction can be diagnosed at any age, from birth to late adulthood. Approximately two-thirds of individuals with left ventricular noncompaction develop heart failure.

Professional guidelines

PubMed

Wanert C, El Louali F, Al Dybiat S, Nguyen K, Zaffran S, Ovaert C
Arch Cardiovasc Dis 2023 Jun-Jul;116(6-7):309-315. Epub 2023 May 16 doi: 10.1016/j.acvd.2023.04.008. PMID: 37246080
Grassi S, Campuzano O, Coll M, Cazzato F, Sarquella-Brugada G, Rossi R, Arena V, Brugada J, Brugada R, Oliva A
Int J Mol Sci 2021 Apr 16;22(8) doi: 10.3390/ijms22084124. PMID: 33923560Free PMC Article
Fuchs TA, Erhart L, Ghadri JR, Herzog BA, Giannopoulos A, Buechel RR, Stämpfli SF, Gruner C, Pazhenkottil AP, Niemann M, Kaufmann PA, Tanner FC
PLoS One 2020;15(7):e0235751. Epub 2020 Jul 10 doi: 10.1371/journal.pone.0235751. PMID: 32649698Free PMC Article

Recent clinical studies

Etiology

Schiebel K, Finsterer J, Lazarevic P, Stöllberger C
J Stroke Cerebrovasc Dis 2022 Sep;31(9):106623. Epub 2022 Jul 6 doi: 10.1016/j.jstrokecerebrovasdis.2022.106623. PMID: 35803121
Gregor Z, Kiss AR, Grebur K, Szabó LE, Merkely B, Vágó H, Szűcs A
Int J Cardiol 2022 Jul 15;359:69-75. Epub 2022 Apr 15 doi: 10.1016/j.ijcard.2022.04.026. PMID: 35436556
Stöllberger C, Finsterer J
Rev Cardiovasc Med 2021 Dec 22;22(4):1413-1420. doi: 10.31083/j.rcm2204146. PMID: 34957781
Ichida F
J Cardiol 2020 Jan;75(1):1-9. Epub 2019 Oct 17 doi: 10.1016/j.jjcc.2019.09.011. PMID: 31629663
van Waning JI, Caliskan K, Hoedemaekers YM, van Spaendonck-Zwarts KY, Baas AF, Boekholdt SM, van Melle JP, Teske AJ, Asselbergs FW, Backx APCM, du Marchie Sarvaas GJ, Dalinghaus M, Breur JMPJ, Linschoten MPM, Verlooij LA, Kardys I, Dooijes D, Lekanne Deprez RH, IJpma AS, van den Berg MP, Hofstra RMW, van Slegtenhorst MA, Jongbloed JDH, Majoor-Krakauer D
J Am Coll Cardiol 2018 Feb 20;71(7):711-722. doi: 10.1016/j.jacc.2017.12.019. PMID: 29447731

Diagnosis

de Frutos F, Ochoa JP, Navarro-Peñalver M, Baas A, Bjerre JV, Zorio E, Méndez I, Lorca R, Verdonschot JAJ, García-Granja PE, Bilinska Z, Fatkin D, Fuentes-Cañamero ME, García-Pinilla JM, García-Álvarez MI, Girolami F, Barriales-Villa R, Díez-López C, Lopes LR, Wahbi K, García-Álvarez A, Rodríguez-Sánchez I, Rekondo-Olaetxea J, Rodríguez-Palomares JF, Gallego-Delgado M, Meder B, Kubanek M, Hansen FG, Restrepo-Córdoba MA, Palomino-Doza J, Ruiz-Guerrero L, Sarquella-Brugada G, Perez-Perez AJ, Bermúdez-Jiménez FJ, Ripoll-Vera T, Rasmussen TB, Jansen M, Sabater-Molina M, Elliot PM, Garcia-Pavia P; European Genetic Cardiomyopathies Initiative Investigators
J Am Coll Cardiol 2022 Oct 11;80(15):1447-1461. Epub 2022 Aug 22 doi: 10.1016/j.jacc.2022.07.023. PMID: 36007715
Stöllberger C, Finsterer J
Rev Cardiovasc Med 2021 Dec 22;22(4):1413-1420. doi: 10.31083/j.rcm2204146. PMID: 34957781
Ichida F
J Cardiol 2020 Jan;75(1):1-9. Epub 2019 Oct 17 doi: 10.1016/j.jjcc.2019.09.011. PMID: 31629663
van Waning JI, Caliskan K, Hoedemaekers YM, van Spaendonck-Zwarts KY, Baas AF, Boekholdt SM, van Melle JP, Teske AJ, Asselbergs FW, Backx APCM, du Marchie Sarvaas GJ, Dalinghaus M, Breur JMPJ, Linschoten MPM, Verlooij LA, Kardys I, Dooijes D, Lekanne Deprez RH, IJpma AS, van den Berg MP, Hofstra RMW, van Slegtenhorst MA, Jongbloed JDH, Majoor-Krakauer D
J Am Coll Cardiol 2018 Feb 20;71(7):711-722. doi: 10.1016/j.jacc.2017.12.019. PMID: 29447731
Clarke SL, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG
Orphanet J Rare Dis 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23. PMID: 23398819Free PMC Article

Therapy

Kazmirczak F, Martin CM, Shenoy C
Circulation 2020 Feb 25;141(8):696-701. Epub 2020 Feb 24 doi: 10.1161/CIRCULATIONAHA.119.043716. PMID: 32091931Free PMC Article
Muser D, Liang JJ, Witschey WR, Pathak RK, Castro S, Magnani S, Zado ES, Garcia FC, Desjardins B, Callans DJ, Frankel DS, Marchlinski FE, Santangeli P
Heart Rhythm 2017 Feb;14(2):166-175. Epub 2016 Nov 24 doi: 10.1016/j.hrthm.2016.11.014. PMID: 27890738
Peters F, Khandheria BK, Botha F, Libhaber E, Matioda H, Dos Santos C, Govender S, Meel R, Essop MR
J Card Fail 2014 Oct;20(10):709-715. Epub 2014 Jul 29 doi: 10.1016/j.cardfail.2014.07.007. PMID: 25079299
Bhatia NL, Tajik AJ, Wilansky S, Steidley DE, Mookadam F
J Card Fail 2011 Sep;17(9):771-8. doi: 10.1016/j.cardfail.2011.05.002. PMID: 21872148
Stöllberger C, Blazek G, Dobias C, Hanafin A, Wegner C, Finsterer J
Am J Cardiol 2011 Oct 1;108(7):1021-3. Epub 2011 Jul 23 doi: 10.1016/j.amjcard.2011.05.039. PMID: 21784395

Prognosis

de Frutos F, Ochoa JP, Navarro-Peñalver M, Baas A, Bjerre JV, Zorio E, Méndez I, Lorca R, Verdonschot JAJ, García-Granja PE, Bilinska Z, Fatkin D, Fuentes-Cañamero ME, García-Pinilla JM, García-Álvarez MI, Girolami F, Barriales-Villa R, Díez-López C, Lopes LR, Wahbi K, García-Álvarez A, Rodríguez-Sánchez I, Rekondo-Olaetxea J, Rodríguez-Palomares JF, Gallego-Delgado M, Meder B, Kubanek M, Hansen FG, Restrepo-Córdoba MA, Palomino-Doza J, Ruiz-Guerrero L, Sarquella-Brugada G, Perez-Perez AJ, Bermúdez-Jiménez FJ, Ripoll-Vera T, Rasmussen TB, Jansen M, Sabater-Molina M, Elliot PM, Garcia-Pavia P; European Genetic Cardiomyopathies Initiative Investigators
J Am Coll Cardiol 2022 Oct 11;80(15):1447-1461. Epub 2022 Aug 22 doi: 10.1016/j.jacc.2022.07.023. PMID: 36007715
Schiebel K, Finsterer J, Lazarevic P, Stöllberger C
J Stroke Cerebrovasc Dis 2022 Sep;31(9):106623. Epub 2022 Jul 6 doi: 10.1016/j.jstrokecerebrovasdis.2022.106623. PMID: 35803121
Stöllberger C, Finsterer J
Rev Cardiovasc Med 2021 Dec 22;22(4):1413-1420. doi: 10.31083/j.rcm2204146. PMID: 34957781
Ichida F
J Cardiol 2020 Jan;75(1):1-9. Epub 2019 Oct 17 doi: 10.1016/j.jjcc.2019.09.011. PMID: 31629663
van Waning JI, Caliskan K, Hoedemaekers YM, van Spaendonck-Zwarts KY, Baas AF, Boekholdt SM, van Melle JP, Teske AJ, Asselbergs FW, Backx APCM, du Marchie Sarvaas GJ, Dalinghaus M, Breur JMPJ, Linschoten MPM, Verlooij LA, Kardys I, Dooijes D, Lekanne Deprez RH, IJpma AS, van den Berg MP, Hofstra RMW, van Slegtenhorst MA, Jongbloed JDH, Majoor-Krakauer D
J Am Coll Cardiol 2018 Feb 20;71(7):711-722. doi: 10.1016/j.jacc.2017.12.019. PMID: 29447731

Clinical prediction guides

Stöllberger C, Finsterer J
Rev Cardiovasc Med 2021 Dec 22;22(4):1413-1420. doi: 10.31083/j.rcm2204146. PMID: 34957781
de la Chica JA, Gómez-Talavera S, García-Ruiz JM, García-Lunar I, Oliva B, Fernández-Alvira JM, López-Melgar B, Sánchez-González J, de la Pompa JL, Mendiguren JM, Martínez de Vega V, Fernández-Ortiz A, Sanz J, Fernández-Friera L, Ibáñez B, Fuster V
J Am Coll Cardiol 2020 Oct 13;76(15):1723-1733. doi: 10.1016/j.jacc.2020.08.030. PMID: 33032733
Ichida F
J Cardiol 2020 Jan;75(1):1-9. Epub 2019 Oct 17 doi: 10.1016/j.jjcc.2019.09.011. PMID: 31629663
Stöllberger C, Wegner C, Finsterer J
Herz 2019 Nov;44(7):659-665. Epub 2018 Apr 6 doi: 10.1007/s00059-018-4695-1. PMID: 29626229
van Waning JI, Caliskan K, Hoedemaekers YM, van Spaendonck-Zwarts KY, Baas AF, Boekholdt SM, van Melle JP, Teske AJ, Asselbergs FW, Backx APCM, du Marchie Sarvaas GJ, Dalinghaus M, Breur JMPJ, Linschoten MPM, Verlooij LA, Kardys I, Dooijes D, Lekanne Deprez RH, IJpma AS, van den Berg MP, Hofstra RMW, van Slegtenhorst MA, Jongbloed JDH, Majoor-Krakauer D
J Am Coll Cardiol 2018 Feb 20;71(7):711-722. doi: 10.1016/j.jacc.2017.12.019. PMID: 29447731

Recent systematic reviews

Fan P, Yang KQ, Han B, Kong D, Yin WH, Li JH, Yang ZX, Niu LL, Fu CS, Rong CZ, Lin YH, Wang H, Zhou XL, Gao LG, Qin XC, Tian T
Pediatr Res 2023 Aug;94(2):683-690. Epub 2023 Feb 9 doi: 10.1038/s41390-023-02515-3. PMID: 36759750
Bardhi E, Faralli I, Deroma M, Galoppi P, Ventriglia F, Giancotti A, Perrone G, Brunelli R
J Matern Fetal Neonatal Med 2021 Sep;34(17):2910-2917. Epub 2019 Oct 1 doi: 10.1080/14767058.2019.1671337. PMID: 31570025
van Waning JI, Moesker J, Heijsman D, Boersma E, Majoor-Krakauer D
J Am Heart Assoc 2019 Dec 3;8(23):e012993. Epub 2019 Nov 27 doi: 10.1161/JAHA.119.012993. PMID: 31771441Free PMC Article
Grigoratos C, Barison A, Ivanov A, Andreini D, Amzulescu MS, Mazurkiewicz L, De Luca A, Grzybowski J, Masci PG, Marczak M, Heitner JF, Schwitter J, Gerber BL, Emdin M, Aquaro GD
JACC Cardiovasc Imaging 2019 Nov;12(11 Pt 1):2141-2151. Epub 2019 Mar 13 doi: 10.1016/j.jcmg.2018.12.029. PMID: 30878415
Bertini M, Balla C, Pavasini R, Boriani G
J Cardiovasc Med (Hagerstown) 2018 Jul;19(7):324-328. doi: 10.2459/JCM.0000000000000657. PMID: 29877973

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