Skip to main content
Download PDF
Download ePub

Use of the energy waveform electrocardiogram to detect subclinical left ventricular dysfunction in patients with type 2 diabetes mellitus

Cardiovascular Diabetology volume 23, Article number: 91 (2024) Cite this article

Abstract

Background

Recent guidelines propose N-terminal pro-B-type natriuretic peptide (NT-proBNP) for recognition of asymptomatic left ventricular (LV) dysfunction (Stage B Heart Failure, SBHF) in type 2 diabetes mellitus (T2DM). Wavelet Transform based signal-processing transforms electrocardiogram (ECG) waveforms into an energy distribution waveform (ew)ECG, providing frequency and energy features that machine learning can use as additional inputs to improve the identification of SBHF. Accordingly, we sought whether machine learning model based on ewECG features was superior to NT-proBNP, as well as a conventional screening tool—the Atherosclerosis Risk in Communities (ARIC) HF risk score, in SBHF screening among patients with T2DM.

Methods

Participants in two clinical trials of SBHF (defined as diastolic dysfunction [DD], reduced global longitudinal strain [GLS ≤ 18%] or LV hypertrophy [LVH]) in T2DM underwent 12-lead ECG with additional ewECG feature and echocardiography. Supervised machine learning was adopted to identify the optimal combination of ewECG extracted features for SBHF screening in 178 participants in one trial and tested in 97 participants in the other trial. The accuracy of the ewECG model in SBHF screening was compared with NT-proBNP and ARIC HF.

Results

SBHF was identified in 128 (72%) participants in the training dataset (median 72 years, 41% female) and 64 (66%) in the validation dataset (median 70 years, 43% female). Fifteen ewECG features showed an area under the curve (AUC) of 0.81 (95% CI 0.787–0.794) in identifying SBHF, significantly better than both NT-proBNP (AUC 0.56, 95% CI 0.44–0.68, p < 0.001) and ARIC HF (AUC 0.67, 95%CI 0.56–0.79, p = 0.002). ewECG features were also led to robust models screening for DD (AUC 0.74, 95% CI 0.73–0.74), reduced GLS (AUC 0.76, 95% CI 0.73–0.74) and LVH (AUC 0.90, 95% CI 0.88–0.89).

Conclusions

Machine learning based modelling using additional ewECG extracted features are superior to NT-proBNP and ARIC HF in SBHF screening among patients with T2DM, providing an alternative HF screening strategy for asymptomatic patients and potentially act as a guidance tool to determine those who required echocardiogram to confirm diagnosis.

Trial registration LEAVE-DM, ACTRN 12619001393145 and Vic-ELF, ACTRN 12617000116325

Background

Heart failure (HF) may be the most common cardiovascular cause of death among patients with type 2 diabetes mellitus (T2DM) [1]. More than 25% of patients with T2DM are reported to have stage B HF (SBHF, also known as asymptomatic LVD) and this is even more prevalent among patients with long-standing diabetes or poor glycemic control [3,4,5]. HF is a progressive disorder [2], preceded by subclinical left ventricular dysfunction (LVD), detectable with global longitudinal strain (GLS), diastolic indices or LV mass [1]. The reliable detection of SBHF would allow earlier initiation of cardioprotective treatment and prevention or delay of symptomatic HF.

A 2022 consensus report from the American Diabetes Association recommended annual testing of N-terminal pro-B-type natriuretic peptide (NT-proBNP) among patients with T2DM to facilitate early detection of HF [6]. However, the standard cutoff value for NT-proBNP performs better in ruling out patients with no HF than identifying those with HF [7, 8]. This is mainly because comorbidities such as renal diseases, obesity and other cardiovascular diseases (CVD) may also result in the elevation of NT-proBNP value [9]. In our recent experience, neither clinical assessment nor NT-proBNP provided satisfactory discrimination for abnormal GLS (AUC 63%), diastolic indices (e′, AUC 54–61%) or LV mass (AUC 59–67%), and the high sensitivity needed for a screening test was attained only with an unacceptably low (< 50%) specificity [10]. An alternate approach in SBHF screening is the application of the Atherosclerosis Risk in Communities (ARIC) HF risk score, which consists of various risk factors such as age, sex, race, comorbidities and vital signs [11]. It has been previously reported as a strong predictor for HF and yet, the performance in screening for SBHF, an asymptomatic cardiovascular dysfunction, remained contentious.

The energy waveform electrocardiogram (ewECG) uses continuous wavelet transform (CWT) based signal processing to provide time-based Fourier Transform frequency domain information of the acquired ECG signal. This is a feasible screening tool as the 12-lead ECG is a standard test and no additional expertise is required and the ewECG waveform is simply post-acquisition signal processing that takes a few seconds. ewECG extracted features have been shown to be key machine learning model features that improve overall model performance above and beyond conventional ECG features for machine learning models built to be predictive for LV diastolic dysfunction [12, 13] and more recently SBHF in a community population at risk of HF [14]. However, although patients with T2DM have a heightened risk of HF, this is heterogeneous, with systolic as well as diastolic dysfunction being involved [15]. Accordingly, in order to determine an effective way to screen for SBHF and guide clinicians on those who required further echocardiogram, we used machine learning algorithms to develop a DM-specific screening model based on ewECG data to identify SBHF among asymptomatic patients and compare its performance with conventional clinical HF risk indicators in NT-proBNP and the ARIC HF risk score.

Methods

Study design and setting

The training dataset comprised asymptomatic participants with T2DM from the Determining the Effect of Dapagliflozin on Preventing Heart Failure in Patients with Type 2 Diabetes (LEAVE-DM, ACTRN 12619001393145) trial. These community-based participants were aged ≥ 65 years recruited from Melbourne but excluded those with: (i) moderate or severe valvular heart disease; (ii) history of HF or hypertrophic cardiomyopathy; (iii) currently undergoing therapy with SGLT2 inhibitors or GLP-1 receptor agonist; (iv) systolic blood pressure < 110 mmHg; (v) estimated glomerular filtration rate < 45 mL/min/1.73 m2; (vi) baseline New York Heart Association (NYHA) classification > 2 and (vii) oncologic life expectancy < 12 months.

The validation dataset comprised participants with T2DM In the Victorian Study of Echocardiographic Detection of Left Ventricular Dysfunction (Vic-ELF, ACTRN 12617000116325). This community-based study recruited participant aged ≥ 65 years with at least one of the following HF risk factors: (i) obesity (body mass index ≥ 30 kg/m2), (ii) diagnosed T2DM, or (iii) hypertension (systolic blood pressure ≥ 140 mmHg or on hypertensive medication). Exclusion criteria included LV ejection fraction ≤ 40%, symptomatic HF, known coronary artery disease (CAD), moderate or severe valvular heart disease, renal impairment and symptoms of HF.

Participant characteristics

Participants’ baseline characteristics such as age, sex, blood pressure, heart rate and body mass index (BMI) are summarised in Table 1. Risk factors for HF such as hypertension, peripheral vascular disease and family history of coronary artery disease (CAD) and HF were also included. In addition, the Charlson Comorbidity Index (CCI) and ARIC HF risk score were calculated to evaluate the severity of comorbidities and 4-year risk of incident symptomatic HF, respectively. Participants’ NT-proBNP levels were also measured.

Table 1 Baseline characteristics
Full size table

ewECG

Participants underwent ewECG evaluation using a commercially-available conventional 12-lead ECG device with additional signal processing to provide the ewECG waveform (MyoVista version 2.0, HeartSciences, Southlake, Texas). This ECG signal is deconstructed and presented in an energy scalogram which illustrates the distribution of energy over time and frequency, known as the “energy waveform”. Energy is expressed as coefficients that represent the agreement between wavelet and signal at different scales, rather than discrete energy measurements [13]. Fourier based signal processing is used extensively in medical devices to improve diagnostic performance. An example is the use of Fourier based Doppler signal processing to assess blood flow in echocardiography. A proprietary software generates a total of 643 CWT features at specific points throughout the cardiac cycle. The ewECG interface also provides a standard 12-lead ECG trace and an automated diagnostic interpretation based on the University of Glasgow 12-lead ECG interpretive analysis algorithm, offering both quantitative parameters and qualitative interpretations [16]. These CWT features are combined with conventional measurements to provide 1124 parameters (Additional file 1: Table S1).

Echocardiography

A transthoracic 2-dimensional and Doppler echocardiographic study was performed among using standard equipment (ACUSON SC2000, Siemens Healthcare USA, Mountain View, California and GE E95 ultrasound device, GE Healthcare, Chicago, Illinois, United States) and transducer (4V1c, 1.25 to 4.5 MHz; 4Z1c, 1.5 to 3.5 MHz) in accordance with the American Society of Echocardiography guidelines. Subclinical LV systolic function was assessed with GLS computed using speckle tracking (Syngo VVI; Siemens Healthcare USA) [17]. Diastolic function was assessed from transmitral flow (peak early [E] and late diastolic velocity E/A ratio), mitral annular early diastolic velocities (e′) and E/e′ ratio, left atrial volume index (LAVi) indexed to body surface area, and tricuspid regurgitation velocity [18].

SBHF was defined by the presence of one or more of: (i) diastolic dysfunction (DD) (E/e′ > 15 or E/e′ > 10 with left atrium enlargement (LAE) or impaired relaxation with LAE); (ii) reduced GLS (≤ 18%); or (iii) left ventricular hypertrophy (LVH, LV mass index > 95 g/m2 in women and > 115 g/m2 in men).

Machine learning classification model

A supervised machine learning approach was applied to develop a screening model for the primary outcome—SBHF and three secondary outcomes—(i) DD; (ii) reduced GLS and (iii) LVH. The proposed models for these outcomes included extremely randomised trees [19], random forest [20], explainable boosting machine (EBM) [21], and extreme gradient boosting (XGBoost) [22], all of which were applied using the Scikit-learn [23] and XGBoost and EBM libraries.

Given the high dimensionality of the data from the ewECG features, a bottom-up step-forward feature selection method was performed to identify high-predictive features for the selected outcomes. The feature selection started with zero features in the feature set and added one feature at a time across its iterative process. After including each feature, the feature set was evaluated using a k-fold cross-validation procedure over the training dataset on a machine learning model, where k was set to five based on the size of LEAVE-DM and Vic-ELF cohorts. In summary, k-fold cross-validation assessed the predictive performance of the model by splitting the data into k folds, training and learning it on k– 1 folds, and subsequently validating it on the remaining fold. The evaluation of each feature relied on both sensitivity and AUC of the model. After this step, the best performing feature was combined with the remaining feature set. This iterative process continued until all features were assessed or stopping criteria were achieved (e.g. deterioration or stabilisation of the predictive performance when including new features to the feature set).

The Shapley Additive Explanations (SHAP) method—which provides an overview of how the features are generally linked to the model’s prediction [24]—was then applied to explain the ewECG models. SHAP is a game theory-based method to derive explanations for individual prediction, in which combined results yield a global interpretation of the model’s behavior.

Statistical analysis

Descriptive statistics were used to present the participants’ baseline characteristics. Parametric variables were reported as means ± standard deviations while non-parametric variables were reported as medians [interquartile ranges (IQR)]. To compare participants’ baseline characteristics between the training and validation dataset, Kruskal–Wallis H test was performed on non-parametric variables and chi-square test on categorical variables.

The performance of each model in identifying the corresponding outcomes (SBHF, DD, reduced GLS and LVH) among the training and validation dataset were reported using the area under the receiver operating characteristics (ROC) curve (AUC). The optimal threshold for the machine learning model was set as 0.5 to identify the model’s sensitivity and specificity. The performance of NT-proBNP and ARIC HF risk score in identifying the outcomes among participants from the validation dataset was also evaluated and compared using the AUC. The optimal cut-off value for NT-proBNP and ARIC HF was identified using Youden’s Index and the accuracy in identifying participants with each outcome was demonstrated.

A p-value of < 0.05 was considered statistically significant for all analyses. Analyses were conducted using Stata 17.0 (StataCorp, College Station, Texas, USA) and Python (Python Software Foundation).

Results

Patient characteristics

The training (n = 178) and validation (n = 97) datasets comprised elderly patients with T2DM and risk factors, but participants from the training dataset were older, at higher risk of comorbidity and HF, and had a stronger family history of CAD and HF than in the validation dataset (Table 1). Participants from the training dataset had higher NT-proBNP, higher left ventricular mass index, and marginally worse cardiac function. Participants from the training dataset were also shown to have a higher risk of HF incidence given the significantly greater ARIC HF risk score than the validation dataset.

ewECG machine learning models

The ewECGs for T2DM patients with and without SBHF were demonstrated in Additional file 1. From the training dataset, models were developed for the four outcomes based on feature selection from the 643 ewECG features. Additional file 1 provides a detailed description for each of these ewECG features. The features selected in each model were also listed in Additional file 2: Figures. Overall, 15 features were selected with an explainable boosting machine model to identify participants with SBHF (Additional file 2: Fig. S2, n = 128, 71.9%); 11 features for DD (Additional file 2: Fig. S4, n = 66, 37.1%) with an XGBoost model; 18 features for reduced GLS (Additional file 2: Fig. S4, n = 99, 55.6%) with a random forest model and 22 features for LVH (Additional file 2: Fig. S5, n = 36, 20.2%) with an extremely randomised trees model. None of the 15 ewECG features from the SBHF screening model was also selected across all other three outcomes, although there was a preponderance of LV systolic markers, emphasized by differences in the energy signal in the parametric display (Fig. 1). In the training dataset, the SBHF model showed an AUC of 0.87 (95% CI 0.83–0.84), with 98% sensitivity and 58% specificity. Separate models were also developed for other outcomes with different constituents, which led to acceptable discrimination for DD (AUC 0.83 [95% CI 0.81–0.82]), impaired GLS (0.84 [95%CI 0.84–0.85]) and LVH (0.96 [95%CI 0.95–0.952]) in the training dataset.

Fig. 1
figure 1

Parametric display of ewECG for patients with and without Stage B Heart Failure. The detection of SBHF was predominantly based on LV systolic markers, emphasized by differences in the energy signal in the parametric display. The color display is referenced to The color displays peak energy relative to the peak of the R-wave (the highest energy component of the waveform)

Full size image

NT-pro-BNP and the ARIC HF risk score

The optimal cut-off value for NT-proBNP was identified in the validation dataset using Youden’s Index. Compared with the recommended cut-off value of 125 pg/mL, Youden's Index identified that 21 pg/mL in NT-proBNP showed the highest screening accuracy for SBHF, hence being deemed as the optimal cut-off value. Table 2 demonstrates the AUC for applying NT-proBNP as a screening tool for SBHF, DD, reduced GLS and LVH, as well as the sensitivity and specificity for both recommended (125 pg/mL) and optimal (21 pg/mL) cut-off values. Meanwhile, a score of 8% was deemed as the optimal cut-off value for the ARIC HF risk score for SBHF screening,

Table 2 The accuracy of NT-proBNP and ARIC HF in identifying Stage B Heart Failure, diastolic dysfunction, reduced global longitudinal strain and left ventricular hypertrophy in the validation dataset
Full size table

Interpretations of ewECG models

The SHAP plot in Additional file 2: Fig. S2 details and ranks the most important CWT features for the SBHF screening model. The amplitude of R-wave in lead II, early repolarization in lead V1 and duration of QRS interval in lead V3 are some of the key features identified in SBHF screening. Additional file 2: Fig. S2 demonstrates that higher R-wave amplitude in lead II and longer duration of QRS interval in lead V3 indicated a greater risk of SBHF. Conversely, a mixed pattern was identified for features such as R-wave amplitude in lead I and T-wave onset in lead II.

Correspondingly, the T-wave area in lead V2 and P-wave amplitude in lead III were key identifiers for DD (Additional file 2: Fig. S3). The amplitude of ST interval in lead II was the most impactful feature in the screening for reduced GLS (Additional file 2: Fig. S4). The frequency of peak depolarization origin measure in lead V3 and delta wave confidence in lead II were some of the key features in the ewECG screening model for LVH (Additional file 2: Fig. S5).

Comparison of the screening strategies for LV dysfunction

A total of 64 participants from the validation dataset (66%) had SBHF. The ewECG screening features were predictive for SBHF in the validation dataset (AUC = 0.81, 95%CI 0.787–0.794), outperforming both NT-proBNP and ARIC HF risk score significantly, with a sensitivity of 89% and specificity of 62% (Fig. 2). At a recommended cut-off value of 125 pg/mL, NT-proBNP was less discriminative for SBHF (AUC 0.55 [95%CI 0.43–0.66]), with a sensitivity of 15% and specificity of 94% (Table 2). On the other hand, applying the optimal cut-off value (21 pg/mL) for NT-proBNP resulted in a sensitivity of 85% and a specificity of 10%. Meanwhile, the ARIC HF yielded an AUC of 0.67 (95%CI 0.56–0.79) in SBHF screening.

Fig. 2
figure 2

Receiver operating characteristics curve for ewECG models developed to identify Stage B Heart Failure and its components. Similar levels of discrimination were obtained for Stage B Heart Failure, diastolic dysfunction and reduced global longitudinal strain. The curve for left ventricular hypertrophy should be interpreted with caution, because of sparse numbers with this manifestation. ewECG: Electrocardiographic with signal-processed via continuous wavelet transform

Full size image

Figure 3 illustrates the number of participants who would be advised to have echocardiography based on ewECG model versus NT-proBNP as a screening tool for SBHF. The ewECG model identified 67 out of the 97 participants from the validation dataset as participants who required echocardiography, of whom 85% were deemed to have SBHF. In comparison, the application of NT-proBNP, with cutoff values of 125 pg/mL and 21 pg/mL, as a screening tool resulted in unnecessary echocardiography in 85% and 35% of participants respectively.

Fig. 3
figure 3

Comparison of screening methods to identify Stage B Heart Failure and its components. This infographic compares the prediction and exclusion of SBHF with ewECG and NT-proBNP. CWT-ECG: Electrocardiographic with signal-processed via continuous wavelet transform; NT-proBNP: N-terminal pro-B-type natriuretic peptide; SBHF: Stage B Heart Failure; GLS: global longitudinal strain; LVH: left ventricular hypertrophy

Full size image

The prevalence of DD in participants from the validation dataset was 44% (n = 43). The ewECG model (AUC = 0.74, 95% CI 0.73–0.74) outperformed both NT-proBNP-21 pg/mL (AUC = 0.52, 95%CI 0.40–0.63) and ARIC HF (AUC = 0.61, 95%CI 0.50–0.73) in screening for DD. The sensitivities of the ewECG and NT-proBNP-21 pg/mL approaches were similar (81% and 88%, p = 0.347), but the specificity of ewECG exceeded that of NT-proBNP (71% vs 14%, p < 0.001). As for NT-proBNP with a cut-off value of 125 pg/mL, the sensitivity and specificity were 10% and 86% respectively.

Reduction in GLS (–18% or worse) was present in 51% of participants from the validation dataset (n = 49). Again, the ewECG model showed a higher AUC (0.76, 95%CI 0.73–0.74) in screening for reduced GLS than NT-proBNP-21 pg/mL (AUC = 0.52, 95%CI 0.41–0.64). The ewECG model for reduced GLS accurately screened 76% of the participants, compared to 48% using NT-proBNP. The ARIC HF risk score performed slightly better than NT-proBNP in screening for reduced GLS (AUC = 0.69, 95%CI 0.58–0.80).

Only 5 participants in the validation dataset (5.2%) had LVH. The AUC of the ewECG model was 0.90 (95%CI 0.88–0.89), with a sensitivity of 100% and specificity of 98%. The AUC for NT-proBNP and the ARIC HF risk score were 0.66 (95%CI 0.21–0.98) and 0.45 (95%CI 0.22–0.67) respectively.

Discussion

Our study demonstrates that machine learning models developed using ewECG features may provide a screening tool to provide clinical guidance for patients with T2DM who may benefit from echocardiography. The ewECG models for SBHF and other abnormalities (DD, reduced GLS and LVH) differed in the features selected, analogous to previous experience in people at risk of HF [14]. The ewECG model for SBHF had an accuracy of 83% in reflecting those who required further echocardiographic screening, compared to 60% with NT-proBNP and 69% with the ARIC HF risk score. These results suggest that ECG measures may be superior to current conventional tool for SBHF screening and that the ewECG could be routinely implemented and monitored among T2DM patients.

Importance of SBHF diagnoses in the prevention of HF progression

SBHF is relatively common in T2DM, especially in older individuals, those with long-standing diabetes and patients with poor glycemic control [3,4,5]. SBHF is an independent risk factor for incident HF—the cumulative probability of developing HF within 5 years is 37%—and increases with increasing SBHF severity [25]. Patients with T2DM typically develop HFpEF, and compared to people without T2DM, have a greater degree of LVH, higher circulating markers of oxidative stress, inflammation and fibrosis, and a greater risk of hospitalization [26]. Identification of SBHF among people with T2DM would provide an opportunity to initiate cardioprotective strategies, provide more intense follow-up, and facilitate treatment adherence. Despite being a precursor for subsequent HF incidence, SBHF is still underdiagnosed in T2DM [27]. Not all patients with T2DM are at equal risk, so a clinical score or biomarker would be helpful to identify the patients who need attention.

CVD screening using ECG assessment

A number of studies have reported the feasibility of applying advanced artificial intelligence (AI) methods to ECG assessment for predicting CVD [27]. AI algorithms such as convolutional neural networks require a training database of ECG interpretation to mimic human-like interpretation of the ECG [29]. ECG interpretation using this approach has been shown to predict low LV ejection fraction (≤ 35%) [30], atrial fibrillation [31], hypertrophic cardiomyopathy [32] and myocardial infarction [33]. Utilizing AI tools to guide clinicians in ECG interpretation can improve patient care by increasing the accuracy of identifying asymptomatic patients who may require further attention. In the context of left ventricular systolic dysfunction, previous study has shown that clinicians who adopted AI-ECG algorithm were twice as likely to diagnose patients with low ejection fraction as those who do not [34]. In addition, the implementation of AI-ECG in systolic dysfunction screening was reported to have an AUC of up to 0.93 [35], which would be highly cost-effective as a guideline for echocardiogram referral if such result is transferable in clinical setting. Nonetheless, AI-ECG approaches perform best in the type of population on which they have been trained, and potential issues with reproducibility may occur due to differences in population characteristics, including racial differences [28].

The potential number of ewECG features is huge, producing a highly-dimensional database for the ewECG assessment process. The sample size required to train the model is significantly smaller than the AI-approach. The predictive performance was generalizable when training and cross-validating these models on LEAVE-DM and independently validating them on the Vic-ELF cohorts. This is highlighted by only a small reduction in predictive performance, based on AUC, sensitivity and specificity, from cross-validation on the training dataset to the validation data.

The introduction of machine learning models based on ewECG as a screening tool provides a new alternative to the echocardiography selection process and yet requires no additional training to conduct the assessment as the acquisition is like a standard ECG. The implementation of a SBHF screening model based on ewECG features would improve selection for echocardiographic testing, while missing a few patients with SBHF.

Our study focuses on patients with T2DM because of a variety of reasons. First and foremost, hyperinsulinaemia-induced hypoglycemia can prolong the QTc interval and decrease T-wave area and amplitude, even among healthy individuals [36]. Furthermore, ECG alterations such as QT dispersion, changes in heart rate variability and ST-T changes may be observed even early in the course of DM [37]. Hence, given that the ECG interpretation would differ among diabetic patients, it raises the need to investigate if the accuracy is similar to what was previously reported of AI-ECG in screening for systolic dysfunction is [35].

Natriuretic peptides, the ARIC HF risk score, and ewECG in SBHF screening

The feasibility of NT-proBNP makes this an attractive option for annual testing [6]. However, while NT-proBNP is valuable for the recognition of unrecognized HF, it may be less sensitive in the recognition of LV dysfunction that is insufficiently advanced to increase myocardial wall stress [10]. A threshold of 125 pg/mL NT-proBNP is widely used in the diagnosis of acute HF [38], albeit as a “rule-out” test [39]. However, the use of this cut-off for the detection of subclinical HF yields a poor accuracy with high specificity but low sensitivity. In this study, we used the training set to identify a threshold for NT-proBNP (21 pg/mL) that provided a sensitive test. However, this change was at the cost of low specificity, and more patients with normal cardiac function were being falsely deemed as being at risk of SBHF. The result would inflate the numbers of unnecessary echocardiograms [40]. These results confirm our previous observations that question the use of NT-proBNP in the detection of LV dysfunction in T2DM.

In contrast, the ARIC HF risk score showed a slightly better discriminative performance than NT-proBNP. This is presumably due to its multifactorial nature as a screening tool which incorporated key risk factors including but not limited to age, sex, comorbidities and medication history [11]. However, it is important to note that the difficulty of identifying patients with SBHF lies on the condition being asymptomatic, which may result in clinicians overlooking the underlying risk factors presented by the patients. With the optimal cut-off value of 8% for SBHF screening, it may contribute further to clinicians' inability to identify those who have or are at risk of developing SBHF.

Among patients with T2DM, the accuracy of ewECG model in SBHF screening was shown to be significantly higher than both NT-proBNP and the ARIC HF risk score in this study. The ewECG model for SBHF screening was shown to reduce the number of echocardiography performed on patients with regular cardiac function by 64%, compared to NT-proBNP at the cut-off value of 21 pg/mL. In contrast, ewECG may be a sensitive first step to select those who require echocardiography and could ultimately improve the cost-effectiveness of echocardiographic screening for SBHF in T2DM. In addition, the ECG provides a widely-available biomarker that has the potential of identifying myocardial disease at an early stage. Regular ewECG assessment may be a feasible alternative to BNP among patients with T2DM who are already at higher risk of HF.

Study limitations

Our study has a few limitations. First, this is a cross-sectional study which does not capture the development of SBHF over time. The progressive nature of SBHF may impact the discriminative ability of ewECG, especially among patients in the early stage of SBHF. Second, the sample size for this study is relatively low for machine learning. Further studies with a larger and more diverse patient population are required to define broader implications in clinical settings. Lastly, the number of patients with LVH was very limited in the validation dataset, which is likely to have resulted in the overestimation of the ewECG performance in LVH screening.

Conclusions

Screening for SBHF, followed by the initiation of cardioprotective treatment, may prevent or delay HF occurrence among high-risk patients with T2DM. Nonetheless, clinical guidelines for referring patients to echocardiographic screening are lacking [2]. As ECG assessment is a routine clinical procedure, the application of ewECG is feasible and could act as a tool to identify asymptomatic T2DM patients who require echocardiography for SBHF diagnosis. Future studies should look into whether the findings from our study is consistent in a larger cohort of T2DM patients and investigate the cost-effectiveness of integrating ewECG in clinical settings for SBHF screening.

Availability of data and materials

The datasets used and analysed in this study are available from the corresponding author on reasonable request.

Abbreviations

ARIC:

Atherosclerosis risk in communities

CAD:

Coronary artery disease

CWT:

Continuous wave transform

ECG:

Electrocardiogram

ewECG:

Energy waveform electrocardiogram

GLS:

Global longitudinal strain

HF:

Heart failure

LV:

Left ventricle

LVH:

Left ventricle hypertrophy

NT-proBNP:

N-terminal pro-B-type natriuretic peptide

SBHF:

Stage B heart failure

T2DM:

Type 2 diabetes mellitus

References

  1. Fang ZY, Schull-Meade R, Downey M, Prins J, Marwick TH. Determinants of subclinical diabetic heart disease. Diabetologia. 2005;48(2):394–402.

    Article  CAS  PubMed  Google Scholar 

  2. Goldberg LR, Jessup M. Stage B heart failure. Circulation. 2006;113(24):2851–60.

    Article  PubMed  Google Scholar 

  3. Gori M, Gupta DK, Claggett B, Selvin E, Folsom AR, Matsushita K, et al. Natriuretic peptide and high-sensitivity troponin for cardiovascular risk prediction in diabetes: the atherosclerosis risk in communities (ARIC) study. Diabet Care. 2016;39(5):677–85.

    Article  CAS  Google Scholar 

  4. Selvin E, Lazo M, Chen Y, Shen L, Rubin J, McEvoy JW, et al. Diabetes mellitus, prediabetes, and incidence of subclinical myocardial damage. Circulation. 2014;130(16):1374–82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Rubin J, Matsushita K, Ballantyne Christie M, Hoogeveen R, Coresh J, Selvin E. Chronic hyperglycemia and subclinical myocardial injury. J Am Coll Cardiol. 2012;59(5):484–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Pop-Busui R, Januzzi JL, Bruemmer D, Butalia S, Green JB, Horton WB, et al. Heart failure: an underappreciated complication of diabetes. a consensus report of the American Diabetes Association. Diabet Care. 2022;45(7):1670–90.

    Article  Google Scholar 

  7. Heidenreich PA, Bozkurt B, Aguilar D, Allen LA, Byun JJ, Colvin MM, et al. 2022 AHA/ACC/HFSA guideline for the management of heart failure: a report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. 2022;145(18):e895–1032.

    PubMed  Google Scholar 

  8. Rørth R, Jhund PS, Yilmaz MB, Kristensen SL, Welsh P, Desai AS, et al. Comparison of BNP and NT-proBNP in patients with heart failure and reduced ejection fraction. Circ Heart Fail. 2020;13(2): e006541.

    Article  PubMed  Google Scholar 

  9. Ferrell PD, Oristian KM, Puranam I, Pizzo SV. Serum Pro-N-Cadherin is a marker of subclinical heart failure in the general population. J Am Heart Assoc. 2023;12(6): e028234.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Halabi A, Potter E, Yang H, Wright L, Sacre JW, Shaw JE, et al. Association of biomarkers and risk scores with subclinical left ventricular dysfunction in patients with type 2 diabetes mellitus. Cardiovasc Diabetol. 2022;21(1):278.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Agarwal SK, Chambless LE, Ballantyne CM, Astor B, Bertoni AG, Chang PP, et al. Prediction of incident heart failure in general practice. Circ Heart Fail. 2012;5(4):422–9.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Kagiyama N, Piccirilli M, Yanamala N, Shrestha S, Farjo PD, Casaclang-Verzosa G, et al. Machine learning assessment of left ventricular diastolic function based on electrocardiographic features. J Am Coll Cardiol. 2020;76(8):930–41.

    Article  PubMed  Google Scholar 

  13. Sengupta PP, Kulkarni H, Narula J. Prediction of abnormal myocardial relaxation from signal processed surface ECG. J Am Coll Cardiol. 2018;71(15):1650–60.

    Article  PubMed  Google Scholar 

  14. Potter EL, Rodrigues CHM, Ascher DB, Abhayaratna WP, Sengupta PP, Marwick TH. Machine learning of ECG waveforms to improve selection for testing for asymptomatic left ventricular dysfunction. JACC Cardiovasc Imaging. 2021;14(10):1904–15.

    Article  PubMed  Google Scholar 

  15. Ernande L, Audureau E, Jellis CL, Bergerot C, Henegar C, Sawaki D, et al. Clinical implications of echocardiographic phenotypes of patients with diabetes mellitus. J Am Coll Cardiol. 2017;70(14):1704–16.

    Article  PubMed  Google Scholar 

  16. Clark EN, Sejersten M, Clemmensen P, Macfarlane PW. Automated electrocardiogram interpretation programs versus cardiologists’ triage decision making based on teletransmitted data in patients with suspected acute coronary syndrome. Am J Cardiol. 2010;106(12):1696–702.

    Article  PubMed  Google Scholar 

  17. Reisner SA, Lysyansky P, Agmon Y, Mutlak D, Lessick J, Friedman Z. Global longitudinal strain: a novel index of left ventricular systolic function. J Am Soc Echocardiogr. 2004;17(6):630–3.

    Article  PubMed  Google Scholar 

  18. Nagueh SF, Smiseth OA, Appleton CP, Byrd BF, Dokainish H, Edvardsen T, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur J Echocardiogr. 2016;17(12):1321–60.

    Google Scholar 

  19. Geurts P, Ernst D, Wehenkel L. Extremely randomized trees. Mach Learn. 2006;63(1):3–42.

    Article  Google Scholar 

  20. Breiman L. Random forests. Mach Learn. 2001;45(1):5–32.

    Article  Google Scholar 

  21. Belle V, Papantonis I. Principles and practice of explainable machine learning. Front Big Data. 2021. https://doi.org/10.3389/fdata.2021.688969.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Chen T, Guestrin C. Xgboost: a scalable tree boosting system. In: Chen T, Guestrin C, editors. Proceedings of the 22nd acm sigkdd international conference on knowledge discovery and data mining. New York: Association for Computing Machinery; 2016.

    Google Scholar 

  23. Pedregosa F, Varoquaux G, Gramfort A, Michel V, Thirion B, Grisel O, et al. Scikit-learn: machine learning in python. J Mach Learn Res. 2011;12:2825–30.

    MathSciNet  Google Scholar 

  24. Lundberg SM, Lee S-I. A unified approach to interpreting model predictions. In: Guyon I, Von Luxburg U, Bengio S, Wallach H, Fergus R, Vishwanathan S, Garnett R, editors. Proceedings of the 31st international conference on neural information processing systems. California: Curran Associates Inc; 2017.

    Google Scholar 

  25. From AM, Scott CG, Chen HH. The development of heart failure in patients with diabetes mellitus and pre-clinical diastolic dysfunction: a population-based study. J Am Coll Cardiol. 2010;55(4):300–5.

    Article  PubMed  Google Scholar 

  26. Lindman BR, Dávila-Román VG, Mann DL, McNulty S, Semigran MJ, Lewis GD, et al. Cardiovascular phenotype in HFpEF patients with or without diabetes: a RELAX trial ancillary study. J Am Coll Cardiol. 2014;64(6):541–9.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Bell DS. Heart failure: the frequent, forgotten, and often fatal complication of diabetes. Diabet Care. 2003;26(8):2433–41.

    Article  ADS  Google Scholar 

  28. Siontis KC, Noseworthy PA, Attia ZI, Friedman PA. Artificial intelligence-enhanced electrocardiography in cardiovascular disease management. Nat Rev Cardiol. 2021;18(7):465–78.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ribeiro AH, Ribeiro MH, Paixão GM, Oliveira DM, Gomes PR, Canazart JA, et al. Automatic diagnosis of the 12-lead ECG using a deep neural network. Nat Commun. 2020;11(1):1760.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  30. Attia ZI, Kapa S, Lopez-Jimenez F, McKie PM, Ladewig DJ, Satam G, et al. Screening for cardiac contractile dysfunction using an artificial intelligence-enabled electrocardiogram. Nat Med. 2019;25(1):70–4.

    Article  CAS  PubMed  Google Scholar 

  31. Gladstone DJ, Spring M, Dorian P, Panzov V, Thorpe KE, Hall J, et al. Atrial fibrillation in patients with cryptogenic stroke. N Engl J Med. 2014;370(26):2467–77.

    Article  CAS  PubMed  Google Scholar 

  32. Ko W-Y, Siontis KC, Attia ZI, Carter RE, Kapa S, Ommen SR, et al. Detection of hypertrophic cardiomyopathy using a convolutional neural network-enabled electrocardiogram. J Am Coll Cardiol. 2020;75(7):722–33.

    Article  PubMed  Google Scholar 

  33. Liu W, Zhang M, Zhang Y, Liao Y, Huang Q, Chang S, et al. Real-time multilead convolutional neural network for myocardial infarction detection. IEEE J Biomed Health Inform. 2017;22(5):1434–44.

    Article  PubMed  Google Scholar 

  34. Rushlow DR, Croghan IT, Inselman JW, Thacher TD, Friedman PA, Yao X, Pellikka PA, Lopez-Jimenez F, Bernard ME, Barry BA, Attia IZ, Misra A, Foss RM, Molling PE, Rosas SL, Noseworthy PA. Clinician adoption of an artificial intelligence algorithm to detect left ventricular systolic dysfunction in primary care. Mayo Clin Proc. 2022;97(11):2076–85.

    Article  PubMed  Google Scholar 

  35. Attia ZI, Kapa S, Lopez-Jimenez F, et al. Screening for cardiac contractile dysfunction using an artificial intelligence-enabled electrocardiogram. Nat Med. 2019;25:70–4. https://doi.org/10.1038/s41591-018-0240-2.

    Article  CAS  PubMed  Google Scholar 

  36. Laitinen T, Lyyra-Laitinen T, Huopio H, Vauhkonen I, Halonen TP, Hartikainen J, Niskanen L, Laakso M. Electrocardiographic alterations during hyperinsulinemic hypoglycemia in healthy subjects. Ann Noninvasive Electrocardiol. 2008;13:97–105.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Gupta S, Gupta RK, Kulshrestha M, Chaudhary RR. Evaluation of ECG abnormalities in patients with asymptomatic type 2 diabetes mellitus. J Clin Diagn Res. 2017;11(4):39–41.

    Google Scholar 

  38. Roberts E, Ludman AJ, Dworzynski K, Al-Mohammad A, Cowie MR, McMurray JJV, et al. The diagnostic accuracy of the natriuretic peptides in heart failure: systematic review and diagnostic meta-analysis in the acute care setting. BMJ. 2015;350: h910.

    Article  PubMed  PubMed Central  Google Scholar 

  39. McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Böhm M, Dickstein K, et al. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the task force for the diagnosis and treatment of acute and chronic heart failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2012;33(14):1787–847.

    Article  PubMed  Google Scholar 

  40. Maisel A, Mueller C, Adams K Jr, Anker SD, Aspromonte N, Cleland JG, et al. State of the art: using natriuretic peptide levels in clinical practice. Eur J Heart Fail. 2008;10(9):824–39.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Accepted for moderated presentation at the 73rd Annual Scientific Session of the American College of Cardiology, April 6, 2024.

Funding

T.H.M. is supported by an Investigator grant from the National Health and Medical Research Council, Canberra, Australia (2008129).

Author information

Authors and Affiliations

  1. Imaging Research Laboratory, Baker Heart and Diabetes Institute, PO Box 6492, Melbourne, VIC, 3004, Australia

    Cheng Hwee Soh, Elizabeth Potter, Amera Halabi & Thomas H. Marwick

  2. Baker Department of Cardiometabolic Health, University of Melbourne, Melbourne, Australia

    Cheng Hwee Soh, Alex G. C. de Sá, David B. Ascher & Thomas H. Marwick

  3. Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, Melbourne, Australia

    Alex G. C. de Sá & David B. Ascher

  4. School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Australia

    Alex G. C. de Sá & David B. Ascher

  5. Systems and Computational Biology, Bio21 Institute, Parkville, Australia

    Alex G. C. de Sá & David B. Ascher

  6. Menzies Institute for Medical Research, Hobart, Australia

    Thomas H. Marwick

Authors
  1. Cheng Hwee Soh
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Alex G. C. de Sá
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Elizabeth Potter
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Amera Halabi
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. David B. Ascher
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Thomas H. Marwick
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

CHS researched data and wrote the first draft of the manuscript. ADS conducted the analysis. EP and AH researched data and contributed to the discussion. DBA provided supervision on the analysis conducted and contributed to the discussion. All authors reviewed and edited the manuscript, and subsequently approved the final version of the manuscript.

Corresponding author

Correspondence to Thomas H. Marwick.

Ethics declarations

Ethics approval and consent to participate

Both studies had obtained ethics approval (LEAVE-DM trial: Alfred Hospital Ethics Committee, ethics approval number HREC/324–19/Alfred-2019; Vic-ELF: Bellberry Limited, ethics approval number 2016–10-727) and followed the guidelines outlined in the Declaration of Helsinki and the National Statement on Ethical Conduct in Human Research. Written informed consent was provided by participants from the LEAVE-DM and Vic-ELF studies.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Soh, C.H., de Sá, A.G.C., Potter, E. et al. Use of the energy waveform electrocardiogram to detect subclinical left ventricular dysfunction in patients with type 2 diabetes mellitus. Cardiovasc Diabetol 23, 91 (2024). https://doi.org/10.1186/s12933-024-02141-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12933-024-02141-1

Keywords

Cardiovascular Diabetology

ISSN: 1475-2840