Electrocardiographic T Wave Abnormalities and the Risk of Sudden Cardiac Death: The Finnish Perspective (2024)

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  • Ann Noninvasive Electrocardiol
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Electrocardiographic TWave Abnormalities and the Risk of Sudden Cardiac Death: The Finnish Perspective (1)

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Ann Noninvasive Electrocardiol. 2015 Nov; 20(6): 526–533.

Published online 2015 Sep 22. doi:10.1111/anec.12310

PMCID: PMC6931827

PMID: 26391699

Jani T. Tikkanen, M.D., Ph.D.,Electrocardiographic TWave Abnormalities and the Risk of Sudden Cardiac Death: The Finnish Perspective (2)1,2 Tuomas Kenttä, Ph.D.,1 Kimmo Porthan, M.D., Ph.D.,3 Heikki V. Huikuri, M.D., Ph.D.,1 and M. Juhani Junttila, M.D., Ph.D.1

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Abstract

The identification of patients at risk for sudden cardiac death (SCD) is still a significant challenge to clinicians and scientists. Noninvasive identification of high‐risk patients has been of great interest, and several ventricular depolarization and repolarization abnormalities in the standard 12‐lead electrocardiogram (ECG) have been associated with increased vulnerability to lethal ventricular arrhythmias. Several benign and pathological conditions can induce changes in repolarization detected as alteration of the ST segment or Twave. Changes in the ST segment and Twaves can be early markers of an underlying cardiovascular disease, and even minor ST‐T abnormalities have predicted reduced survival and increased risk of SCD in the adult population. In this review, we will discuss the current knowledge of the SCD risk with standard 12‐lead ECG Twave abnormalities in the general population, and possible Twave changes in various cardiac conditions predisposing to SCD.

Keywords: electrophysiology‐cardiac arrest/sudden death, clinical; noninvasive techniques, electrocardiography, clinical

Sudden cardiac death (SCD) is the most common, and often the first manifestation, of coronary heart disease (CHD). It is estimated to cause approximately 50% of the annual cardiovascular deaths, and its occurrence in the general population is approximately 2 per thousand a year.1 The identification of patients at risk for SCD is still a significant challenge to clinicians and scientists. Noninvasive identification of high‐risk patients has been of great interest, and several ventricular depolarization and repolarization abnormalities in the standard 12‐lead electrocardiogram (ECG) have been associated with increased vulnerability to lethal ventricular arrhythmias. These ventricular repolarization abnormalities have among others included several Twave–associated ECG changes, which are found in apparently healthy subjects, but more frequently in hospital and clinical settings.

Several benign and pathological conditions can induce changes in repolarization detected as alteration of the ST segment or Twave. These primary repolarization abnormalities include myocardial ischemia, other structural heart diseases, electrolyte disturbances, drugs, changes in the sympathetic tone, and hyperventilation.2 Changes in the ST segment and Twaves can be early markers of an underlying cardiovascular disease, and even minor ST‐T abnormalities have predicted reduced survival and increased risk of SCD in the adult population 3, 4 In this review, we will discuss the current knowledge of the SCD risk with standard 12‐lead ECG Twave abnormalities in general population, and possible Twave changes in cardiac conditions predisposing to SCD.

TWAVE ABNORMALITIES AND THE RISK OF SCD IN GENERAL POPULATION

TWave Inversion

Generally, the Twave amplitude is usually upright in all leads, except the aVR and V1 leads, with maximal amplitudes in precordial leads V2 and V3. Especially in young adults and females, minor Twave inversion in V2 and in inferior leads can represent normal variation. Widespread Tinversion in general is rare in adults, although there is significant racial variation.2 An example ECG of Twave inversion in precordial leads is presented in Figure ​Figure11.

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In a large general population sample of asymptomatic Finnish middle‐aged subjects, Twave inversion was present in right precordial leads (leads V1 to V3) in 0.5% of individuals and in 0.7% of individuals in other leads.5 The prognosis associated with inverted Twaves in right precordial leads did not differ from the rest of the population, but inverted Twaves in leads other than V1–V3 and/or aVR were associated with a threefold risk for SCD. These changes were present in 0.5% and 0.7% of the population, respectively. The vast majority of these cases were women and had only mild‐to‐moderate Twave inversion and the findings persisted in repeated ECG recordings during several years. More recently, similar findings have been reported in another Finnish population of men aged 42 to 61 years,6 in which isolated negative Twaves were present in 2.4% of the population, and were similarly associated with a threefold risk of SCD after adjustments for age and clinical risk factors.

Abnormal QRS‐T Angle

The frontal QRS‐T angle is defined as the angle between the directions of ventricular depolarization and repolarization, which can be easily estimated from frontal plane QRS‐axis and Twave axis from standard ECG. A wide QRS‐T angle reflects either structural abnormalities affecting the depolarization or regional pathophysiological changes in ionic channels altering the sequence of repolarization. These underlying conditions may indicate subclinical diseases and an elevated risk of SCD.7, 8 An example of an abnormal frontal plane QRS‐T axis is presented in Figure ​Figure22.

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Figure 2

Abnormal frontal plane QRS‐T angle (>100°) due to abnormal Twave axis (in a middle‐aged individual). Abnormal QRS‐T angle is associated with twofold risk of SCD in general population.

In middle‐aged general population, QRS‐T angle ≥100° has been described to be present in 1.9% of the population and has been associated with over twofold risk of SCD.9 Although an abnormal Twave axis does not automatically mean abnormal QRS‐T angle, abnormal T axis seemed to confer most of the increased risk concomitant with wide QRS‐T angle, as it was associated with a similar twofold risk of SCD in that particular study.9 In another Finnish unselected male population, those with the highest quintile of QRS‐T angle (>67º) had similarly a twofold risk for SCD compared to others.6

TWave Peak‐to‐End Interval

The interval from the peak of the Twave to the end of the Twave (Tpeak‐to‐Tend interval; TPE) is a measure of transmural dispersion of repolarization. Its prolongation is known to represent a period of potential vulnerability to reentrant ventricular arrhythmias,10 and in a population‐based case‐control study.11 prolonged TPE measured from V5 was associated with SCD also in subjects with normal QTc values. In this study, most SCD cases had TPE values >100 ms, but although this value was high in specificity, it lacks in sensitivity, and lower values for arrhythmia risk have been reported elsewhere.

However, in a more recent and larger prospective study in general population sample, there was no association found between prolonged TPE and SCD.12 In this sample of >5600 individuals with nearly 8 years of follow‐up, maximum TPE interval had hazard ratios <1 before and after adjustments. Given these results, the significance of TPE interval in SCD prediction is questionable.

Computerized TWave Morphology Parameters

Several computerized and automatically calculated measures of the three‐dimensional Twave loop can also be obtained from the standard 12‐lead ECG. These Twave morphology parameters measure temporospatial changes throughout the ventricular repolarization phase and they have possessed some prognostic value for cardiovascular mortality in population‐based studies.13, 14, 15 These often include principal component analysis (PCA), Twave morphology dispersion (TMD), total cosine R‐to‐T (TCRT), and Twave residuum (TWR). The PCA ratio is a measure of the relative roundness or fatness of the three‐dimensional Twave loop.16 TMD is a measure of the variation in Twave morphology between different ECG leads,with similar Twave morphology in different ECG leads resulting in a small TMD value and repolarization abnormalities increasing the value. TCRT is an estimate of the spatial deviation between depolarization and repolarization phases, with a high TCRT value referring to a small angle between R and Twave loop vectors, resulting from normal depolarization and repolarization phases.17 TWR is a measure of nondipolar ECG signal content, with higher values indicating higher degrees of ventricular repolarization heterogeneity.18 In a recent prospective study referred to earlier,12 all of these Twave parameters stratified the SCD risk in general population. The strongest predictor of SCD in this sample was TMD with adjusted hazard ratio of 1.411, 7 for SCD. TCRT and TMD also remained significant predictors of SCD after multivariate adjustments including QT‐interval, indicating that Twave morphology parameters and QT‐interval characterize different aspects of the ventricular repolarization.

TWAVE ABNORMALITIES IN CARDIAC DISEASE

Twave abnormalities can be encountered in several cardiac conditions, including structural and ion channel disorders, and they can be an early sign of the underlying pathology. Thus, the recognition of these patterns is of importance for prediction and prevention of SCD also in asymptomatic individuals.

Arrhythmogenic Right Ventricular Dysplasia

Arrhythmogenic right ventricular dysplasia (ARVD) or cardiomyopathy is a rare genetic disease. The disease usually involves right ventricular outflow tract, where normal myocardium is replaced by fatty infiltration and fibrosis, and it is a common cause of SCD in young and athletes.19 The prevalence of ARVD is unknown due to challenging diagnosis, but it is estimated to be 0.02%.20, 21

Repolarization abnormalities in the ECG seem to be early and quite sensitive markers of disease expression in ARVD, and they are present in up to 90% of ARVD patients.22 Because a characteristic Epsilon wave is a rare finding in the general population,23 the most significant abnormalities in the ECG criteria of ARVD in addition to QRS changes in V1 to V3 are repolarization abnormalities manifested as Twave changes. Inverted Twaves in precordial leads V1–V3 are recognized as major criteria, because they have the optimal sensitivity and specificity for identifying ARVD patients.24 However, these changes are still mostly ignored in clinical situations. The presence of complete right bundle branch block and inverted Twaves beyond V3 are considered as minor criteria for ARVD.25 Please see Figure ​Figure33 for an example of ECG patient with ARVD.

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Figure 3

ECG of an individual with ARVD showing T‐inversion in V1 and V2.

Brugada Syndrome

The Brugada syndrome (BrS) is an inherited arrhythmic disorder, which is recognized as an important cause of SCD in young men, especially in Southeast Asia. There are three different subtypes of Brugada ECG patterns (see below), of which the type 1 is required for the diagnosis of BrS. Types 2 and 3 are considered as suggestive, but not diagnostic for BrS in the absence of documented arrhythmias, unexplained syncope or drug‐induced/spontaneous conversion to a typical type 1 pattern. The three types of Brugada ECG patterns are presented in Figure ​Figure4.4. The prevalence of Brugada type 1 ECG pattern among the general population in European region ranges from 0% to 0.2%.26, 27 The annual risk of malignant arrhythmias in BrS ranges from 0.5% to 8%, depending on prior symptoms.28, 29

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Figure 4

Example ECGs of the three phenotypes of Brugada ECG with various ST and Twave alterations. Type 1 is the typical coved ST‐elevation pattern with inverted Twaves. In type 2, the Twaves are upright, and type 3 has only mild ST changes. Reprinted from European Heart Journal with permission (2004;25:874–878).

The diagnosis of BrS can be made by recognizing its distinct ECG pattern from baseline or drug‐induced ECG changes. The electrocardiographic features include ST‐elevation in right precordial leads in combination with an atypical right bundle branch block pattern and Twave abnormalities. The type 1 pattern is described as a coved ST‐elevation over 2 mm followed by a negative Twave in at least two right precordial leads. In types 2 and 3, Twave inversion is not present.30

Early Repolarization

The term early repolarization has historically been used to describe benign ST‐elevations in precordial leads for decades, but recently Jwaves especially in the inferior and/or lateral leads of the ECG have been referred to as early repolarization after an apparent overpresentation of early repolarization in patients with unexplained VF. Several epidemiological studies have shown that this ECG pattern is associated with an increased risk of arrhythmic death and mortality either as a primary cause of sudden death in the general population or in conjunction with concurrent cardiac disease.31, 32, 33, 34 A recent meta‐analysis summarized the reported studies and showed that individuals with the early repolarization ECG pattern had a relative risk of 1.7 of experiencing an arrhythmia‐related death.35

High‐amplitude inferolateral J waves followed by horizontal or descending ST segments (and rarely Twave inversion), as shown in Figure ​Figure5,5, are believed to possess the highest risk of malignant arrhythmias in those with the early repolarization pattern.36 This ECG pattern with horizontal or descending ST segments has also been helpful in distinguishing idiopathic VF patients from matched controls, and thus it might be useful in clinical decision making separating the benign early repolarization patterns from potentially more malignant forms.37

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Figure 5

Early repolarization pattern, i.e., terminal QRS slurring and notching in two individuals, with horizontal/downsloping ST segments. This pattern of Jwave with horizontal/downsloping ST segment is associated with a twofold risk of SCD in general population. Reprinted from Circulation with permission (2011;123:2666–2673).

Left Ventricular Hypertrophy, Hypertrophic and Obstructive Cardiomyopathies

In patients with left ventricular hypertrophy (LVH), ST and Twave changes are observed in approximately 70% of the cases. These changes result from altered repolarization of the ventricular myocardium caused by LVH and are collectively referred to as strain patterns. Twave inversion has been reported to be present in 55% of patients with ECG‐diagnosed LVH.38, 39

Hypertrophic cardiomyopathy (HCM) involves myocardial hypertrophy in the absence of any obvious hemodynamic load that could cause extensive hypertrophy. It is a common cause of SCD in young adults, with prevalence estimation of 0.2%.40 In apical HCM, there is a possibility for the absence of increased voltages, but prominent Twave inversion in the anterolateral leads is usually present. Similar ECG changes can be observed among young male athletes, with so‐called athlete's hearts, but in those situations, repolarization changes are less prominent.41

Dilated cardiomyopathy (DCM) is a condition in which the left or both ventricles dilate leading to dysfunction of the heart and the symptoms of heart failure. The prevalence of DCM is estimated to be under 0.04%, but SCD is commonly the first manifestation of the disease. ST‐Twave abnormalities particularly in the lateral leads are common but nonspecific.

Long QT Syndrome

The long QT syndrome (LQTS) is an inherited syndrome characterized by prolongation of the heart rate‐corrected QT interval in a standard ECG with vulnerability for SCD. The prevalence of LQTS has been estimated to be 4/10,000.42 but the disorder remains underdiagnosed as some of the LQTS gene carriers have a normal QTc duration. In addition to QT interval prolongation, morphological Twave abnormalities, such as notched and/or biphasic Twaves, can be present. Several mutations have been associated with inherited LQTS, but three subtypes (LQT 1–3) account for the vast majority of cases.

Some typical ST‐T patterns exist in LQT1, LQT2, and LQT3 genotypes (Figure ​(Figure6),6), which can be used to identify those genotypes in LQTS patients and families.42 In LQT1, the Twaves are typically broad‐based, peaked and asymmetrical. Bifid Twaves are the hallmark of LQT2, and in LQT3, the Twaves are often distinct, peaked, late‐onset, and/or biphasic.

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Figure 6

Example ECGs of three different phenotypes in long QT syndrome. Reprinted from Circulation (1995;92:2929–2934).

SUMMARY

Standard 12‐lead ECG is not only an important tool in the diagnosis of various cardiac conditions, but it also provides valuable information in risk stratification. Among other electrocardiographic abnormalities, several Twave changes have recently been associated with increased risk of SCD in the general population. Those individuals with inverted Twaves and/or abnormal QRS‐T angle, as well as prolonged Twave peak‐to‐end interval seem to possess a two‐ to threefold risk of suffering SCD on a population level, even after adjusting for conventional risk factors. Although the positive predictive value of these variants remains low, those individuals with Twave abnormalities will often benefit from further clinical evaluation and closer follow‐up, as in some situations these changes may be an early sign of underlying cardiac pathology.

Notes

The authors declare that there are no conflicts of interest.

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Electrocardiographic T Wave Abnormalities and the Risk of Sudden Cardiac Death: The Finnish Perspective (2024)
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