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Synchronous cardiac arrest in monozygotic twins with hypertrophic cardiomyopathy - Is sudden cardiac death genetically pre-programmed?
© Goh et al.; licensee BioMed Central. 2015
Received: 28 November 2014
Accepted: 18 February 2015
Published: 28 February 2015
Hypertrophic cardiomyopathy (HCM) is a myocardial disorder characterised by left ventricular hypertrophy (LVH) in the absence of another cardiac or systemic disease capable of producing the magnitude of LVH evident. HCM causes variable symptoms and is one of the leading causes of sudden cardiac death (SCD) in young adults. While various phenotypic features of HCM among monozygotic twin pairs are not uncommonly reported, occurrence of synchronous cardiac arrest among them is not known from literature.
We present a case of monozygotic twins with HCM who both had a cardiac arrest post physical exertion in 63rd year of their lives.
This case highlights potential genetics predisposition of cardiac arrest in patients with HCM despite having different phenotypic expression. SCD may be the only manifestation of patients with HCM. Decision of implantable cardioverter-defibrillator (ICD) placement for primary prevention of SCD should be based on the recommended guidelines, clinical judgment and patient’s preference.
HCM is a myocardial disorder characterised by left ventricular hypertrophy (LVH) in the absence of another cardiac or systemic disease capable of producing the magnitude of LVH evident. It is a genetic disorder, most commonly caused by autosomal dominant mutations in genes encoding protein components of sarcomere and myofilaments , characterised by variable disease expression and age-related penetrance . HCM causes variable symptoms and is one of the leading causes of SCD in young adults . We present a case of monozygotic twins with HCM who both had a cardiac arrest post physical exertion in 63rd year of their lives.
A 62-year-old man presented with first episode of unconscious collapse secondary to malignant ventricular tachyarrhythmia with underlying HCM. Fortunately he survived the episode as he had an implantable cardioverter-defibrillator (ICD) inserted two months ago, after his monozygotic twin brother suffered a fatal cardiac arrest.
Patient’s twin brother, in whom the basis of monozygosity was established by history taken from our patient, was diagnosed with HCM 30 years ago following a routine work-related medical check-up. He was a physically active person, with no known risk factors for ischaemic heart disease (IHD) and no regular medication. He had an excellent exercise tolerance including regular strenuous activities like surfing and skiing. He did not have any prior history of syncope or presyncope, or any family history of sudden death. His echocardiogram done 4 weeks prior to event showed normal left ventricular (LV) size and function, marked asymmetric septal hypertrophy of 1.9 cm and no evidence of left ventricular outflow tract (LVOT) obstruction. A 24-hour holter monitoring done 4 years ago showed no evidence of non-sustained ventricular tachycardia (NSVT). The only available stress echocardiogram done 9 years ago showed no inducible LVOT gradient with a normal blood pressure response. He suffered sudden cardiac death at the age of 62 when he collapsed immediately after completing few laps of swimming with pre-warning signs of dizziness.
Like his brother he was previously well with no significant cardiovascular risk factors for IHD and no regular medication. His physical examination was unremarkable with vital parameters within normal limits. His initial troponin was 0.06 (NR <0.04) with no serial increment. An urgent angiogram revealed no significant coronary artery disease. An echocardiogram two months before the incident showed normal LV size and systolic function, asymmetric septal hypertrophy of 2.8 cm, and no evidence of LVOT obstruction. His previous 24-hour holter monitoring done three years ago had shown no evidence of NSVT. He did not undergo any exercise test in the past 8 years.
He was admitted to intensive care unit (ICU) with cardiac monitoring and was commenced on sotalol. There was no further ventricular tachyarrhythmias noted on telemetry and he was discharged on day 4 with outpatient follow up.
As patient’s brother did not undergo a post-mortem examination, the exact cause of death could not be ascertained. Differential diagnosis to consider apart from sudden cardiac death secondary to HCM would include coronary artery disease or pulmonary embolism. For our patient, ventricular tachyarrhythmia arising from a proarrhythmic impulse from the recently implanted ICD could be an alternative explanation for his ventricular arrhythmia episode.
The exact mechanism of SCD in HCM is not known, but is thought to be secondary to malignant ventricular tachyarrhymias arising from abnormal myocardial fibres . While various phenotypic features of HCM among monozygotic twin pairs are not uncommonly reported , occurrence of synchronous cardiac arrest among them is not known from literature.
Indications for ICD implantation in HCM patients to prevent SCD
ICD Recommended (Class I)
ICD Reasonable (Class IIa)
ICD May be Useful (Class IIa)
● Prior cardiac arrest
● Family history of sudden death in first degree relative (age <50)
● Non-sustained VT or abnormal BP response in presence of other SCD risk modifiers.
● Sustained VT
● LV wall thickness ≥ 30 mm
Note: Role of ICD is uncertain in non-sustained VT or abnormal BP response in absence of other SCD risk modifiers (Class IIb)
● Recent unexplained syncope
Though currently available genetic testing is considered reasonable to identify first-degree relative at risk of developing HCM , it has not been proven useful in predicting clinical course and risk of SCD . Family members with similar genetic mutations may have entirely different phenotypic expression . While most phenotype of HCM in monozygotic twins are concordant, phenotype with discordant features has been reported . Our case report relates to twin brothers who had varying severity of asymmetrical LV hypertrophy, lived different life styles in two different geographical areas of Australia, and suffered cardiac arrest around the same time in their lives. This highlights the potential genetic predisposition of cardiac arrest in patients with HCM despite having different phenotypic expression. While it is likely to be a coincidence, the synchronous timing of cardiac arrest does raise a question whether an alternative explanation such as an underlying genetic cause could account for such synchronous timing. This however remains unlikely as lacks scientific evidence at this stage, and if such genetic factor did exist, more cases of synchronous cardiac arrests among siblings or relatives would have been reported in literature.
This case highlights potential genetic predisposition of cardiac arrest in patients with HCM despite having different phenotypic expression. SCD may be the only manifestation of patients with HCM. Decision of ICD placement for primary prevention of SCD should be based on the recommended guidelines, clinical judgment and patient’s preference.
Written informed consent was obtained from our patient and also from the deceased’s wife for publication of this case report and any accompanying images. Copies of the written consents are available for review by the Editor of this journal.
- Alcalai R, Seidman JG, Seidman CE. Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics. J Cardiovasc Electrophysiol. 2008;19(1):104–10.PubMedGoogle Scholar
- Maron BJ, Seidman CE, Ackerman MJ, Towbin JA, Maron MS, Ommen SR, et al. How should hypertrophic cardiomyopathy be classified?: What’s in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy. Circ Cardiovasc Genet. 2009;2(1):81–5. discussion 6.View ArticlePubMedGoogle Scholar
- Puranik R, Chow CK, Duflou JA, Kilborn MJ, McGuire MA. Sudden death in the young. Heart Rhythm. 2005;2(12):1277–82.View ArticlePubMedGoogle Scholar
- Adabag AS, Maron BJ. Implications of arrhythmias and prevention of sudden death in hypertrophic cardiomyopathy. Ann Noninvasive Electrocardiol. 2007;12(2):171–80.View ArticlePubMedGoogle Scholar
- Maron BJ, Casey SA, Almquist AK. Images in cardiovascular medicine. Hypertrophic cardiomyopathy in monozygotic twins. Circulation. 2002;105(18):2229.View ArticlePubMedGoogle Scholar
- Gersh BJ, Maron BJ, Bonow RO, Dearani JA, Fifer MA, Link MS, et al. 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation. 2011;124(24):2761–96.View ArticlePubMedGoogle Scholar
- Landstrom AP, Ackerman MJ. Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy. Circulation. 2010;122(23):2441–9. discussion 50.View ArticlePubMedGoogle Scholar
- Maron BJ, Maron MS, Semsarian C. Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives. J Am Coll Cardiol. 2012;60(8):705–15.View ArticlePubMedGoogle Scholar
- Palka P, Lange A, Burstow DJ. Different presentation of hypertrophic cardiomyopathy in monozygotic twins. Heart. 2003;89(7):751.View ArticlePubMedPubMed CentralGoogle Scholar
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