Cardiac MRI and CT features of inheritable and congenital conditions associated with sudden cardiac death

European Radiology

Volumn 19, Issue 2, 2009, Pages 259-270

  Sparrow, Patrick ^a   Merchant, Naeem ^a   Provost, Yves ^a   Doyle, Deirdre ^a   Nguyen, Elsie ^a   Paul, Narinder ^a  

^a UNIVERSITY HEALTH NETWORK   (Canada)

Author keywords

Cardiac MRI; Cardiomyopathy; Multi detector computed tomography; Sudden cardiac death

Indexed keywords

ADENOSINE; GADOLINIUM; METOPROLOL; NONIONIC CONTRAST MEDIUM;

ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL HEART DISEASE; CONTRAST ENHANCEMENT; CORONARY ARTERY ANOMALY; CORONARY ARTERY DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; ELECTROCARDIOGRAPHY; FABRY DISEASE; HEART AMYLOIDOSIS; HEART LEFT VENTRICLE EJECTION FRACTION; HEART LEFT VENTRICLE OUTFLOW TRACT; HEART RIGHT VENTRICLE DYSPLASIA; HEART VENTRICLE ARRHYTHMIA; HERITABILITY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; IMAGE ENHANCEMENT; IMAGE PROCESSING; IMAGE QUALITY; MAGNETIC RESONANCE ANGIOGRAPHY; MORPHOLOGY; MULTIDETECTOR COMPUTED TOMOGRAPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RISK FACTOR; SENSITIVITY AND SPECIFICITY; SUDDEN DEATH;

ADULT; ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; CARDIOLOGY; CARDIOMEGALY; CARDIOMYOPATHIES; DEATH, SUDDEN, CARDIAC; DIAGNOSTIC TECHNIQUES, CARDIOVASCULAR; ELECTROCARDIOGRAPHY; FEMALE; HEART; HEART DEFECTS, CONGENITAL; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; TOMOGRAPHY, X-RAY COMPUTED;

EID: 59349100986     PISSN: 09387994     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00330-008-1169-5     Document Type: Article

References (55)

1. Priori SG, Aliot E, Blomstrom-Lundqvist C et al (2003) Update of the guidelines on sudden cardiac death of the European Society of Cardiology. Eur Heart J 24:13-15
2. Myerburg RJ, Castellanos A (2001) Cardiac arrest and sudden cardiac death. WB Saunders, Philadelphia
3. Kirchhof P, Breithardt G, Eckardt L (2006) Primary prevention of sudden cardiac death. Heart 92:1873-1878
4. Zheng ZJ, Croft JB, Giles WH et al (2001) Sudden cardiac death in the United States, 1989 to 1998. Circulation 104:2158-2163
5. Doolan A, Langlois N, Semsarian A (2004) Causes of sudden cardiac death in young Australians. Med J Aust 180:110-112
6. Wisten A, Forsberg H, Krantz P et al (2002) Sudden cardiac death in 15-35-year olds in Sweden during 1992-1999. J Intern Med 2552:529-536
7. Chugh SS, Senashova O, Watts A et al (2004) Post mortem molecular screening in unexplained sudden death. J Am Coll Cardiol 43:1625-1629
8. Olson TM, Michels VV, Thibodeau SN et al (1998) Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 280:750-752
9. Monserrat L, Hermida-Prieto M, Fernandez X et al (2007) Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Eur Heart J 28:1953-1961
10. Olson TM, Doan TP, Kishimoto NY et al (2000) Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J Mol Cell Cardiol 32:1687-1694
11. Maron BJ, Towbin JA, Thiene G et al (2006) Contemporary definitions and classification of the cardiomyopathies: An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 113:1807-1816
12. Marian AJ, Roberts R (2001) The molecular genetic basis for hypertrophic cardiomyopathy. J Mol Cell Cardiol 33:655-670
13. Niimura H, Bachinski LL, Sangwatanaroj S et al (1998) Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 338:1248-1257
14. Maron BJ, Olivotto I, Spirito P et al (2000) Epidemiology of hypertrophic cardiomyopathy related death: Revisited in a large non-referral-based patient population. Circulation 102:858-864
15. Hughes SE (2004) The pathology of hypertrophic cardiomyopathy. Histopathology 44:412-427
16. Choudry L, Mahrholdt H, Wagner A et al (2002) Myocardial scarring in asymptomatic or mildly symptomatic patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 40:2156-2164
17. Shirani J, Pick R, Roberts WC et al (2000) Morphology and significance of the left ventricular collagen network in young patients with hypertrophic cardiomyopathy and sudden cardiac death. J Am Coll Cardiol 35:36-44
18. Elliott PM, Gimeno Blanes JR, Mahon NG et al (2001) Relation between severity of left-ventricular hypertrophy and prognosis in patients with hypertrophic cardiomyopathy. Lancet 357:420-424
19. Tanaka M, Fujiwara H, Onodera T et al (1986) Quantitative analysis of myocardial fibrosis in normals, hypertensive hearts, and hypertrophic cardiomyopathy. Br Heart J 55:575-581
20. Kwon DH, Setser RM, Zoran B et al (2008) Association of myocardial fibrosis, electrocardiography and ventricular tachyarrhythmia in hypertrophic cardiomyopathy: A delayed contrast enhanced MRI study. Int J Cardiovasc Imaging 24(6):617-625, Epub 2008 Jan 19
21. Moon JC, McKenna WJ, McCrohon JA et al (2003) Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance. J Am Coll Cardiol 41:1561-1567
22. Teraoka K, Hirano M, Ookubo H et al (2004) Delayed contrast enhancement of MRI in hypertrophic cardiomyopathy. Magn Reson Imaging 22:155-161; erratum in Magn Reson Imaging (2004) 2022:2901
23. Adabag AS, Maron BJ, Appelbaum E et al (2008) Occurrence and frequency of arrhythmias in hypertrophic cardiomyopathy in relation to delayed enhancement on cardiovascular magnetic resonance. J Am Coll Cardiol 51:1369-1374
24. Pelliccia A, Culasso F, Di Paolo F et al (1999) Physiologic left ventricular cavity dilatation in elite athletes. Ann Intern med 130:23-31
25. Petersen SE, Selvanayagam JB, Francis JM et al (2005) Differentiation of athlete's heart from pathological forms of hypertrophy by means of geometric indices derived from cardiovascular magnetic resonance. J Cardiovasc Magn Reson 7:551-558
26. Maceira AM, Joshi J, Prasad SK et al (2005) Cardiovascular magnetic resonance in cardiac amyloidosis. Circulation 111:186-193
27. Sachdev B, Takenaka T, Teraguchi H et al (2002) Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy. Circulation 105:1407-1411
28. Shah JS, Hughes DA, Sachdev B et al (2005) Prevalence and clinical significance of cardiac arrhythmia in Anderson-Fabry disease. Am J Cardiol 96:842-846
29. Moon JC, Sachdev B, Elkington AG et al (2003) Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease: Evidence for a disease specific abnormality of the myocardial interstitium. Eur Heart J 24:2151-2155
30. Alcalai R, Metzger S, Rosenheck S et al (2003) A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair. J Am Coll Cardiol 42:319-327
31. McKoy G, Protonotarios N, Crosby A et al (2000) Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet 355:2119-2124
32. Rampazzo A, Nava A, Malacrida S et al (2002) Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet 71:1200-1206
33. Sen-Chowdry S, Lowe MD, Sporton SC et al (2004) Arrhythmogenic right ventricular cardiomyopathy: Clinical presentation, diagnosis and management. Am J Med 117:685-695
34. Sen-Chowdhry S, Syrris P, Ward D et al (2007) Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression. Circulation 115:1710-1720
35. McKenna WJ, Thiene G, Nava A et al (1994) Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. Br Heart J 71:215-218
36. Sen Chowdhry S, Prasad SK, Petros S et al (2006) Cardiovascular magnetic resonance in arrythmogenic right ventricular cardiomyopathy revisited. J Am Coll Cardiol 48:2132-2140
37. Hamid MS, Norman M, Queraishi A et al (2002) Prospective evaluation of relatives for familial Arrhythmogenic right ventricular cardiomyopathy/ dysplasia reveals a need to broaden diagnostic criteria. J Am Coll Cardiol 40:1445-1450
38. Jaoude SA, Leclercq JF, Coumel P (1996) Progressive ECG changes in arrhythmogenic right ventricular disease. Evidence for an evolving disease. Eur Heart J 17:1717-1722
39. Tandri H, Macedo R, Calkins H et al (2008) Role of magnetic resonance imaging in arrhythmogenic right ventricular dysplasia: Insights from the North American arrhythmogenic right ventricular dysplasia (ARVD/C) study. Am Heart J 155:147-153
40. Bluemke DA, Krupinski EA, Ovitt T et al (2003) MR Imaging of arrhythmogenic right ventricular cardiomyopathy: Morphologic findings and interobserver reliability. Cardiology 99:153-162
41. Burke AP, Farb A, Tashko G et al (1998) Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium: Are they different diseases? Circulation 97:1571-1580
42. Tandri H, Saranthan M, Rodriguez ER et al (2005) Noninvasive detection of myocardial fibrosis in arrhythmogenic right ventricular cardiomyopathy using delayed-enhancement magnetic resonance imaging. J Am Coll Cardiol 45:98-103
43. Kimura F, Sakai F, Sakomura Y et al (2002) Helical CT features of arrhythmogenic right ventricular cardiomyopathy. Radiographics 22:1111-1124
44. Bomma C, Tandri H, Nasir K et al (2003) Role of helical CT in qualitative and quantitative evaluation of arrhythmogenic right ventricular dysplasia. Pacing Clin Electrophysiol 26:965
45. Ritter M, Oechslin E, Sutsch G et al (1997) Isolated noncompaction of the myocardium in adults. Mayo Clin Proc 72:26-31
46. Ichida F, Tsubata S, Bowles KR et al (2001) Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Circulation 103:1256-1263
47. Sasse-Klaassen S, Gerull B, Oechslin E et al (2003) Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients. Am J Med Genet 119A:162-167
48. Oechslin EN, Attenhofer Jost CH, Rojas JR et al (2000) Long-term follow-up of 34 adults with isolated left ventricular noncompaction: A distinct cardiomyopathy with poor prognosis. J Am Coll Cardiol 36:493-500
49. Petersen SE, Selvanayagam JS, Wiesmann F et al (2005) Left ventricular non-compaction: Insights from cardiovascular magnetic resonance imaging. J Am Coll Cardiol 46:101-105
50. Murphy RT, Thaman R, Blanes JG et al (2004) Natural history and familial characteristics of isolated left ventricular non-compaction. Eur Heart J 26:187-192
51. Angelini P, Velasco JA, Flamm S (2002) Coronary anomalies: Incidence, pathophysiology, and clinical relevance. Circulation 105:2449-2454
52. Burke AP, Farb A, Virmani R et al (1991) Sports-related and non-sports-related sudden cardiac death in young adults. Am Heart J 121:568-575
53. Maron BJ, Thompson PD, Puffer JC et al (1996) Cardiovascular preparticipation screening of competitive athletes: A statement for health professionals from the Sudden Death Committee (Clinical Cardiology) and Congenital Cardiac Defects Committee (Cardiovascular Disease in the Young), American Heart Association. Circulation 94:850-856
54. Moustafa SE, Zehr K, Mookadam M et al (2007) Anomalous interarterial left coronary artery: An evidence based systematic overview. Int J Cardiol 126(1):13-20, Epub 2007 Aug 14
55. Angelini P, Villason S, Chan AV et al (1999) Normal and anomalous coronary arteries in humans. In: Angelini P (ed) Coronary artery anomalies: A comprehensive approach. Lippincott Williams & Wilkins, Philadelphia, pp 27-150