Brugada Syndrome

Typical ECG abnormalities in Brugada syndrome: ST elevation in V1-V3, without ischemia.

Typical ECG abnormalities in Brugada syndrome

Dr. Pedro Brugada. Pedro and Josep Brugada described in 1992 a landmark publication with a case-series of 8 patients with sudden cardiac death. [1] Currently, three brothers of the Brugada family (Pedro, Josep and Ramon Brugada) conduct research in the syndrome that has been named after them.

The SCN5a gen is located on the short arm (p) of chromosome 3

Brugada syndrome refers to a hereditary disease that is associated with a risk of sudden cardiac death. It is characterized by typical ECG abnormalities: ST segment elevation in the precordial leads (V1 - V3).

The Brugada brothers were the first to describe the characteristic ECG findings and link them to sudden death. Before that, the characteristic ECG findings, were often mistaken for a right ventricle myocardial infarction and already in 1953, a publication mentions that the ECG findings were not associated with ischemia as people often expected.

General features

• The diagnosis is based on ECG findings.
• It is an inheritable cardiac arrhythmia syndrome with an autosomal dominant inheritance.
• Males are often more symptomatic than females, probably by the influence of sex hormones on cardiac arrhythmias and/or ion channels.
• The arrhythmias typically occur in patients between 30-40 years of age and often during rest or while sleeping.
• The right ventricle is most affected in Brugada syndrome, and particularly (but not specifically) the right ventricular outflow tract.
• The prevalence varies between 5-50:10.000, largely depending on the geographic location (especially in some Southeast Asian countries the disease is more prevalent).

Clinical diagnosis

The clinical diagnosis of Brugada syndrome is confirmed in an individual with the following:

Table 2: Here is a list of the Genes linked to the Brugada syndrome.
Type	OMIM	Gene	Protein	Functional role in cardiomyocytes	Effect of mutation
Autosomal dominant inheritance
BrS1	#601144	SCN5A	Nav1.5	α subunit of INa channel	Loss of function of INa
BrS2	#611777	GPD1-L	G3PD1L	Not fully established	Loss of function of INa
BrS3	#611875	CACNA1C	Cav1.2	α1C subunit of ICa,L channel	Loss of function of ICa,L
BrS4	#611876	CACNB2b	Cavβ2b	β2b subunit of ICa,L channel	Loss of function of ICa,L
BrS5	#612838	SCN1B	Navβ1	β subunit of INa channel	Loss of function of INa
BrS6	#613119	KCNE3	KCNE3 (MiRP2)	β subunit of voltage-dependent K+ channels	Gain of function of Ito
BrS7	#613120	SCN3B	Navβ 3	β subunit of INa channel	Loss of function of INa
NC	#613123	HCN4	HCN4	α subunit of If	Gain of function of If
NC		CACNA2D1	Cavα2δ-1	α2δ subunit of ICa,L channel	Loss of function of ICa,L
NC		MOG1	MOG1	Regulates trafficking of Nav1.5 to the membrance	Loss of function of INa
NC		KCND3	Kv4.3	α subunit of Ito channel	Gain of function of Ito
NC		KCNE1L (KCNE5)	KCNE1L	β subunit of voltage-dependent K+ channels	Gain of function of Ito
NC		KCNJ8	Kir6.1	α subunit of IK,ATP	Gain of function of IK,ATP
NC		SCN1Bb	Navβ1B	β subunit of INa	Loss of function of INa and Gain of function of Ito
OMIM: Online Mendelian Inheritance in Man compendium of human genes and genetic phenotypes; BrS1–BrS7: Brugada syndrome types 1–7; NC: no consensus; ICa,L: L-type calcium current; If: hyperpolarization-activated current; IK,ATP: ATP-sensitive potassium current; INa: fast sodium current; Ito: transient outward potassium current.

Diagnosis and treatment

• Patients who are symptomatic (unexplained syncopes, ventricular tachycardias or aborted sudden cardiac death) may have a symptom recurrence risk of 2 to 10% per year. In these patients an ICD implant is advisable. Further, life-style advice is given (see below).
• Some groups advise an electrophysiological investigation (inducibility of ventricular fibrillation) for risk assessment in Brugada patients,[2][3] but others could not reproduce the predictive value of these tests,[4][5] so the value of inducibility is controversial.
• In large studies familial sudden death did not appear to be a risk factor for sudden death in siblings.
• In asymptomatic patients in whom the Brugada ECG characteristics are present (either spontaneously or provoked by fever or sodium channel blockers like ajmaline, procainimde or flecainide) life style advice is given. This advice includes:
  • A number of medications should not be taken (including sodium channel blockers and certain anti-depressants and anti-arrhythmics, see www.BrugadaDrugs.org)
  • Rigorous treatment of fever with paracetamol/Tylenol, as fever may elicit a Brugada ECG and arrhythmias in some patients.
• Spontaneous Type I ECGs do appear to be more prevalent in patients who experienced symptoms.

For a full list of the diagnostic criteria, see [6]

Electrocardiographic criteria

Changed lead positions of leads V3 and V5 to increase the sensitiviy to 'catch' a Brugada pattern on the ECG

Three ECG repolarization patterns in the right precordial leads are recognized in the diagnosis of Brugada syndrome.

Type I is the only ECG criterion that is diagnostic of Brugada syndrome. The type I ECG is characterized by a J elevation >=2 mm (0.2 mV) a coved type ST segment followed by a negative T wave (see figure). Brugada syndrome is definitively diagnosed when a type 1 ST-segment is observed in >1 right precordial lead (V1 to V3) in the presence or absence of a sodium channel–blocking agent, and in conjunction with one of the following:

• documented ventricular fibrillation (VF)
• polymorphic ventricular tachycardia (VT)
• a family history of sudden cardiac death at <45 years old
• coved-type ECGs in family members
• inducibility of VT with programmed electrical stimulation
• syncope
• nocturnal agonal respiration.

The sensitivity of the ECG for Brugada syndrome can be increased with placement of ECG leads in the intercostal space above V1 and V2 (V1ic3 and V2ic3)

Electrocardiograms of Brugada patients can change over time from type I to type II and/or normal ECGs and back. A type III ECG is rather common and is considered a normal variant, but also the Type II is a normal variant (albeit suggestive of Brugada syndrome).

A recent study suggests that fractionation of the QRS complex is a marker of a worse prognosis in Brugada syndrome.[7]

ST segment abnormalities in the different types of Brugada syndrome[8]

	Type I	Type II	Type III
J wave amplitude	>= 2mm	>= 2mm	>= 2mm
T wave	Negative	Positive or biphasis	Positive
ST-T configuration	Coved type	Saddleback	Saddleback
ST segment (terminal portion)	Gradually descending	Elevated >= 1mm	Elevated < 1mm

• Examples of Brugada syndrome type I
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  Brugada ECG during ajmaline testing

• Examples of Brugada syndrome type II
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External links

• Cardiogenetics website of the AMC cardiogentica.nl
• Brugada.org
• Genereview Brugada
• Brugada drugs contains lists of medications that should be avoided in patients with Brugada syndrome and medication that can be used to diagnose the syndrome

References

1. Brugada P and Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol. 1992 Nov 15;20(6):1391-6. DOI:10.1016/0735-1097(92)90253-j |
2. Brugada J, Brugada R, Antzelevitch C, Towbin J, Nademanee K, and Brugada P. Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3. Circulation. 2002 Jan 1;105(1):73-8. DOI:10.1161/hc0102.101354 |
3. Brugada P, Brugada R, Mont L, Rivero M, Geelen P, and Brugada J. Natural history of Brugada syndrome: the prognostic value of programmed electrical stimulation of the heart. J Cardiovasc Electrophysiol. 2003 May;14(5):455-7. DOI:10.1046/j.1540-8167.2003.02517.x |
4. Priori SG, Napolitano C, Gasparini M, Pappone C, Della Bella P, Giordano U, Bloise R, Giustetto C, De Nardis R, Grillo M, Ronchetti E, Faggiano G, and Nastoli J. Natural history of Brugada syndrome: insights for risk stratification and management. Circulation. 2002 Mar 19;105(11):1342-7. DOI:10.1161/hc1102.105288 |
5. Eckardt L, Probst V, Smits JP, Bahr ES, Wolpert C, Schimpf R, Wichter T, Boisseau P, Heinecke A, Breithardt G, Borggrefe M, LeMarec H, Böcker D, and Wilde AA. Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome. Circulation. 2005 Jan 25;111(3):257-63. DOI:10.1161/01.CIR.0000153267.21278.8D |
6. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, Gussak I, LeMarec H, Nademanee K, Perez Riera AR, Shimizu W, Schulze-Bahr E, Tan H, and Wilde A. Brugada syndrome: report of the second consensus conference. Heart Rhythm. 2005 Apr;2(4):429-40. DOI:10.1016/j.hrthm.2005.01.005 |
7. Morita H, Kusano KF, Miura D, Nagase S, Nakamura K, Morita ST, Ohe T, Zipes DP, and Wu J. Fragmented QRS as a marker of conduction abnormality and a predictor of prognosis of Brugada syndrome. Circulation. 2008 Oct 21;118(17):1697-704. DOI:10.1161/CIRCULATIONAHA.108.770917 |
8. Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA, and Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Proposed diagnostic criteria for the Brugada syndrome: consensus report. Circulation. 2002 Nov 5;106(19):2514-9. DOI:10.1161/01.cir.0000034169.45752.4a |
9. OSHER HL and WOLFF L. Electrocardiographic pattern simulating acute myocardial injury. Am J Med Sci. 1953 Nov;226(5):541-5.