- Original investigation
- Open Access
Machine-learning to stratify diabetic patients using novel cardiac biomarkers and integrative genomics
Cardiovascular Diabetology volume 18, Article number: 78 (2019)
Diabetes mellitus is a chronic disease that impacts an increasing percentage of people each year. Among its comorbidities, diabetics are two to four times more likely to develop cardiovascular diseases. While HbA1c remains the primary diagnostic for diabetics, its ability to predict long-term, health outcomes across diverse demographics, ethnic groups, and at a personalized level are limited. The purpose of this study was to provide a model for precision medicine through the implementation of machine-learning algorithms using multiple cardiac biomarkers as a means for predicting diabetes mellitus development.
Right atrial appendages from 50 patients, 30 non-diabetic and 20 type 2 diabetic, were procured from the WVU Ruby Memorial Hospital. Machine-learning was applied to physiological, biochemical, and sequencing data for each patient. Supervised learning implementing SHapley Additive exPlanations (SHAP) allowed binary (no diabetes or type 2 diabetes) and multiple classification (no diabetes, prediabetes, and type 2 diabetes) of the patient cohort with and without the inclusion of HbA1c levels. Findings were validated through Logistic Regression (LR), Linear Discriminant Analysis (LDA), Gaussian Naïve Bayes (NB), Support Vector Machine (SVM), and Classification and Regression Tree (CART) models with tenfold cross validation.
Total nuclear methylation and hydroxymethylation were highly correlated to diabetic status, with nuclear methylation and mitochondrial electron transport chain (ETC) activities achieving superior testing accuracies in the predictive model (~ 84% testing, binary). Mitochondrial DNA SNPs found in the D-Loop region (SNP-73G, -16126C, and -16362C) were highly associated with diabetes mellitus. The CpG island of transcription factor A, mitochondrial (TFAM) revealed CpG24 (chr10:58385262, P = 0.003) and CpG29 (chr10:58385324, P = 0.001) as markers correlating with diabetic progression. When combining the most predictive factors from each set, total nuclear methylation and CpG24 methylation were the best diagnostic measures in both binary and multiple classification sets.
Using machine-learning, we were able to identify novel as well as the most relevant biomarkers associated with type 2 diabetes mellitus by integrating physiological, biochemical, and sequencing datasets. Ultimately, this approach may be used as a guideline for future investigations into disease pathogenesis and novel biomarker discovery.
A disconnect continues to persist in the diagnosis and pathogenesis of diabetes-induced cardiovascular dysfunction. While diabetics are at a two to fourfold greater risk of developing cardiovascular diseases [1, 2], understanding how the numerous biochemical markers involved in the pathology integrate and influence disease progression has not been fully explicated. In a clinical setting, the ability to better calculate prognostics of a patient’s health through the integration of biomarkers facilitates the potential for developing personalized and generalized medicine, as well as treatment strategies . While glycated hemoglobin (HbA1c) remains a hallmark for disease diagnosis , other biomarkers may exist that more unequivocally define the severity of the pathology, characterize the mechanisms involved, and/or provide a better predictive tool of future cardiovascular events.
Diabetes mellitus is a multifaceted disease, consisting of systemic comorbidities which necessitate a variety of treatment modalities and stratify those affected with the disease . Before the implementation of machine-learning algorithms in medicine, linear statistical models have highlighted measures, such as HbA1c, as diagnostic staples for the evaluation of diabetes mellitus onset and progression . By exploring these previously published metadata sets, machine-learning has been applied in refining the accuracy of biomarkers used to characterize the pathology as well as to highlight vulnerable populations in need of clinical intervention . Machine-learning has also revealed that coupling HbA1c with additional biomarkers, such as 8-hydroxy-2-deoxyguanosine (8-OhdG) and other metabolites, can increase the accuracy of the predictive model and better characterize the severity of the disease .
In cardiology, machine-learning approaches have been applied primarily to imaging-based diagnostics, including echocardiography and computed tomography angiography to evaluate cardiovascular health and outcomes [9, 10]. It is estimated that machine-learning applications in the field of cardiovascular research will continue to grow at an exponential rate . While image-derived deep learning models are increasing in popularity, little is known about the predicative power of machine-learning models on basic genomic, epigenomic, proteomic, and metabolomic profiles of the heart. While the beginning of the “big data” age was characterized by the accumulation and compartmentalization of datasets, the recent advent of combining metadata, deep sequencing, and “omics”-based approaches warrants the union between hierarchical predictive algorithms and biological processes. As more patients have access to their personal “omics” profiles, machine-learning will be instrumental in providing feedback for the individual patient and the general population of patients impacted by the disease, enhancing health practice by the caregiver.
While demographic information and physical examination data are more easily procured from patients, the genomic and transcriptomic characterization of a tissue or cell type provides a much finer granularity and uniqueness when predicting phenotypic outcomes in patients . HbA1c, fasting blood glucose, and BMI are examples of easily accessible, valuable measurements when evaluating diabetes progression and onset [6, 13], but genetic components, including epigenetic, epitranscriptomic, single nucleotide polymorphisms (SNPs), and others, provide a wealth of undiscovered information for disease classification. This genetic component may be specifically important when understanding the pathogenesis of diabetes in ethnic groups, when BMI [14, 15] and HbA1c  show distinct differences between ethnicities. Though applying patient-matched, genomic information is currently unrealistic for disease diagnosis, it may hold the key for revealing commonalities across ethnic and demographic groups when classifying diabetic onset, progression, and severity.
In the current study, machine-learning was used as a predictive tool to integrate cardiac physiological, biochemical, genomic, and epigenomic biomarker data in a patient-matched fashion and enable determination of type 2 diabetic status. In 50 patients, machine-learning algorithms revealed the interconnectedness between diabetic classification, mitochondrial function, and methylation status. Our study highlights how novel biomarkers can be used to augment existing diagnostic standards as well as provide new, and more precise, methods for identifying the development and severity of type 2 diabetes mellitus in potentially at-risk populations, such as those with prediabetes. While we examine physiological, biochemical, and molecular datasets using machine-learning algorithms, our goal was to understand which features possessed the best predictive accuracies and if these specific features could be used alone, or in conjunction, with HbA1c. The purpose for the inclusion of models that do not rise above 50% predictive accuracy was to contrast them against those models that do rise above 50% in the absence of HbA1c, to determine which biomarkers are the best overall predictors.
Research design and methods
All tissue and patient information was acquired in a double de-identified fashion, and was approved by the West Virginia University Institutional Review Board and Institutional Biosafety Committee . Patients were all consented by the Heart and Vascular Institute, J.W. Ruby Memorial Hospital at the West Virginia University School of Medicine. Right atrial appendages were removed during open-heart and/or valvular surgeries. Both groups of patients (non-diabetic and type 2 diabetic) who were receiving open-heart surgery could elect for their tissues to be used for research purposes, with no direct or indirect incentivisation. A total of 50 patients were selected for the study (between August 2016 and May 2018), 30 of which were non-diabetic (ND) and 20 that were type 2 diabetic (T2DM) and existed along a spectrum of measured HbA1c levels. Patient inclusion into the study was determined by (a) election for open heart surgery and release of tissue for research purposes (b) was not undergoing surgery due to heart failure, and (c) demographic data was provided. Patient characteristics are provided in Table 1, listing patients classified as non-diabetic and those who have been clinically diagnosed as type 2 diabetic. Patient information is also provided for separation of the groups into those with no diabetes, prediabetes, and type 2 diabetes (Additional file 1: Table S1). Additional file 1: Table S1 contains the matching 50 patient cohort analyzed in Table 1 but with the creation of a new non-diabetic cohort (n = 16), comprised of those individuals with an HbA1c < 5.7, and prediabetic cohort (n = 14), comprised of clinically non-diabetic patients whose HbA1c is between 5.7 and 6.4.
Mitochondria were isolated from a portion of the right atrial appendage as previously described , with modifications by our laboratory [19,20,21]. Mitochondrial subpopulations of subsarcolemmal and interfibrillar mitochondria were extracted and combined to achieve a total mitochondrial population.
Electron transport chain (ETC) complex activities
A portion of the tissue from all 50 patients was homogenized using a Polytron PowerGen 500 S1 tissue homogenizer (Fisher Scientific, Hampton, NH) in NP-40 buffer (150 mM NaCl, 50 mM, pH 8.0 Tris-Cl, and 1.0% NP-40). Protein homogenates were used to measure electron transport chain complexes I, III, IV, and V (ATP synthase) spectrophotometrically, as previously described  and implemented by our laboratory [19, 23,24,25,26]. Protein concentrations were normalized using the Bradford method, with standardization to bovine serum albumin .
Citrate synthase activity
Isolated mitochondria from all 50 patients, was used to measure citrate synthase activity using a colorimetric Citrate Synthase Assay Kit (Sciencell, San Diego, CA), as previously described . Citrate synthase activity, normalized to protein content, was used to determine mitochondrial content.
Using a colorimetric Methyltransferase Assay Kit (Caymen, Ann Arbor, Michigan), S-adenosylmethionine (SAM)-dependent methyltransferase activity was assessed, per manufacturer’s instructions. Briefly, nuclear homogenates were used to assess total SAM-dependent methyltransferase activity in all 50 patients.
DNA 5mC and 5hmC quantification
Using a DNeasy Blood & Tissue Kit (Qiagen, Hilden, Germany), DNA was isolated from both 10 mg of atrial appendage tissue and mitochondria, per manufacturer’s instructions. Levels of 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) were measured through a 5mC and 5hmC ELISA Kit (Zymo Research, Irvine, CA), per manufacturer’s instructions. DNA was quantified using a NanoDrop™ 1000 Spectrophotometer (Thermo Fisher, Waltham, MA). 100 ng of nuclear (tissue extract) and mitochondrial DNA were used to assess total 5mC and 5hmC content spectrophotometrically for all 50 patients.
Using 4–12% gradient gels, immunoblotting was performed through MES SDS-PAGE, as previously described [21, 26, 29,30,31]. Protein was normalized using the Bradford method. Primary antibodies used in the study included: anti-TFAM, transcription factor A, mitochondrial, 1:500 (SCBT, Dallas, TX), anti-GAPDH 1:1000 (Abcam, Cambridge, MA). The secondary antibody used in the study was a goat anti-mouse IgG (H&L) horseradish peroxidase (HRP) conjugate 1:10,000 (Thermo Fisher). GAPDH expression was used to normalize protein content. Chemiluminescence was measured through Radiance Chemiluminescent Substrate (Azure Biosystems, Dublin, CA), per manufacturer’s instructions and imaged using the G:Box Bioimaging system (Syngene, Frederick, MD). Images were captured through GeneSnap/GeneTools software (Syngene). Densitometry was analyzed using ImageJ and Fiji Software (NIH, Bethesda, MD). Data is represented as optical density with arbitrary units.
Chromatin immunoprecipitation (ChIP)-qPCR
The SimpleChIP® Plus Sonication Chromatin IP Kit (Cell Signaling Technology, Danvers, MA) was used, per manufacturer’s instructions. Briefly, 100 mg of atrial tissue was minced into ~ 2 mm3 pieces and treated with freshly prepared 37% formaldehyde for 30 min. Sonicated DNA was assessed for sheering and further immunoprecipitated with anti-TFAM (SCBT) bound Protein G magnetic beads overnight at 4 °C. The beads were washed, DNA reverse cross-linked, and DNA eluted as previously described [24, 32]. DNA bound to TFAM was further examined through qPCR. 2% chromatin inputs for each sample were used for normalization of expression. An Applied Biosystems 7900HT Fast Real-Time PCR system (Applied Biosystems, Foster City, CA) was used to assess expression through SYBR Green. Quantification was achieved using the 2−ΔΔCT method . All primer pairs to assess the mitochondrial D-Loop are provided (Additional file 1: Table S2).
DNA was extracted from patient tissue as described above. DNA was bisulfite-treated using the EZ DNA Methylation-Lightning Kit (Zymo Research), per manufacturer’s instructions. Primers were designed for the CpG island of TFAM; primer set 1 amplified the 3′ end and primer set 2 amplified the 5′ end of the CpG island (Additional file 1: Table S2). Bisulfite DNA was prepared for sequencing using a 2-Step PCR amplification process . Step-1 PCR adapters included a base pairing region (~ 23 bp) and an overhang Illumina adapter arm (~ 33 bp). Bisulfite DNA was PCR amplified using Step-1 primers utilizing Platinum™ Taq DNA Polymerase (Thermo Fisher), run on 2% agarose gels, extracted through a QIAquick Gel Extraction Kit (Qiagen), and DNA purified. DNA was then further amplified using Step-2 Illumina barcoded adapters and prepared using a 300-cycle MiSeq Reagent Micro Kit v2 (Illumina, San Diego, CA). PCR amplicons were sequenced on the MiSeq with paired-end (PE) 250 base pair reads. Files were aligned to the bisulfite converted reference genome GRCh38 release 94 implementing Bismark [35, 36]. Alignment was obtained through Bismark using the Bowtie2  engine using “non-directional” and “paired-end.” Complete sequencing code is provided (https://github.com/qahathaway/WVU_Machine-Learning-50/tree/master).
Mitochondrial SNP sequencing
Mitochondrial DNA was isolated as described above and further amplified using the REPLI-g Mitochondrial DNA Kit (Qiagen), per manufacturer’s instructions. Libraries for amplified DNA were prepared using the MiSeq Reagent Kit v3 (Illumina). Mitochondrial DNA was sequenced on the MiSeq with paired-end (PE) 300 base pair reads. Files were aligned to the reference genome GRCh38 release 94 through Bowtie2 using “sensitive-local.” BAM files were sorted, run through variant calling, and single-nucleotide polymorphisms (SNPs) were identified in the mitochondria through SAMtools [38,39,40]. Complete sequencing code is provided (https://github.com/qahathaway/WVU_Machine-Learning-50/tree/master).
Decision tree classifier algorithms were created in python (v3.6.5) using scikit-learn  and pandas  libraries (Fig. 1a). In binary classification, patient labels were determined through previous clinical diagnoses, where diabetic status was retained even if current HbA1c levels were below 6.5%. In multiple classification, patients with an HbA1c value in the range of 5.7% to 6.4% were designated as having prediabetes. Due to this, the HbA1c feature was excluded from all tested trials, and the derived accuracies are in comparison to that of the “perfect” accuracy obtained from HbA1c classification. A decision tree classifier model was created using the functions of scikit-learn tree. The data file was split into 80% training and 20% testing partitions using a defined seed value. Different seeds were chosen for each set to maintain the training and testing set distributions. Selected seed values maintained a binary classification testing set of five diabetics and five non-diabetics. In the multiple classification testing set, seed values maintained a distribution of three diabetics, three non-diabetics, and four pre-diabetics. Seeds were only chosen such that the resulting training and testing accuracies were similar; ensuring that the created classification tree did not over fit to the small sample size and remained generalizable to future testing samples.
Within the model, tenfold cross validation was implemented. CART analysis was then performed on each of the datasets using the scikit-learn model, and the features of importance extracted using the feature importance parameter. The physiological/biochemical, genomic, and epigenomic datasets were combined into a single file to serve as the “all features” dataset used to extract the best and most influential biomarkers. For each trial, selected combinations of biomarkers from each dataset were utilized, and within each trial CART analysis was performed five times. After each of the five iterations, average feature importance, average training, and average testing accuracies were obtained. Standard deviations were taken over each of the five iterations per trial. For each dataset, the first iteration of CART analysis included all biomarkers of each set. If the average feature importance was less than 1%, the feature was no longer included in subsequent trials. After all iterations, if the average feature importance was less than or equal to 8% it was assigned to a category titled “other.” These same trials were repeated with other default scikit-learn machine-learning frameworks (Logistic Regression, Linear Discriminant Analysis, K-Nearest Neighbors Classifier, Gaussian Naïve Bayes, and Support Vector Machine). Tenfold cross validation and the same seed parameters were used in analysis of these five models and the resulting training and testing accuracies are provided (Additional file 1: Tables S3–S10). The six models tested include few modifications and utilize no additional regularization techniques aside from those default to the scikit-learn library models. Only the Support Vector Machine model received modifications, with the probability parameter set to “true” to provide probability estimates for each data point and a linear kernel used over the default Radial Basis Function ‘rbf’ kernel. Code for analyses is also provided (https://github.com/qahathaway/WVU_Machine-Learning-50/tree/master).
Machine-learning feature extraction and accuracy
To determine which model(s) would provide the most accurate predictions on the current data, we assessed the 345 total features across all six models in binary (Table 2) and multiple (Table 3) classification of diabetic status. Through assessment of individual datasets (i.e. physiological/biochemical, genetic, and epigenetic), a set of 18 features was further used to classify diabetic status in binary (Additional file 1: Table S11) and multiple (Additional file 1: Table S12) classification. Model analysis was enacted for each dataset, and the established tenfold cross validation and seed parameters for binary and multiple classification were utilized. Each dataset was tested five times per model. Averages were obtained for training accuracy, training standard deviation, testing accuracy, testing standard deviation, model average F1 score, and area under the curve (AUC). AUC values were provided for each of the six tested algorithms for the testing data under binary classification using the roc_auc_score function of scikit-learn, but not for multiple classification. AUC was determined as 1.0 for LR and SVM models when evaluating the 345 total features due to the large sample size of biomarkers. From the available 345 features, two predictors were chosen that perfectly distinguished diabetic and nondiabetic status for this particular dataset. As such, these AUC values were removed from Table 2 for LR and SVM, as this was not an accurate indicator of the model’s predictive ability. As the feature set was restricted to the 18 “best” features from each dataset, AUC values of 1.0 were no longer observed (Additional file 1: Tables S11 and S12).
Extracted important features and corresponding feature bias within each model, with the exception of KNN, were determined and are provided for binary and multiple classification. CART feature importance was extracted from the trained model using the feature importance parameter. For the NB model, feature influence was determined using the predict_log_proba function to return the most important biomarker per class in both binary (0,1) and multiple (0,1,2) classification schemes. Feature importance was not determined for the KNN model due to the restrictions of the default model. LDA, LR, and SVM feature influence was determined by taking the magnitude of the model coefficients, coef_ parameter, times the standard deviation of that biomarker in the testing data. The resulting values are ranked based off magnitude and are reported with sign under the “Important Feature Bias” (Tables 2 and 3, Additional file 1: Tables S11 and S12). A positive influence value indicates a biomarker favoring classification towards one label while a negative value favors the opposite classification label. The larger the magnitude, the more strongly that feature shifts classification.
SHapley Additive exPlanations (SHAP)
SHAP framework, from slundberg (https://github.com/slundberg/shap), was used to visually explain the classification trees developed for the 50 patient samples using an XGBoost model (Fig. 1b) [43,44,45]. Figure 1b illustrates how SHAP plots are presented in three dimensions, with the “X” and “Y” dimensions plotted spatially while the “Z” dimension is indicated only through color; allowing for the examination of how variables, “X” and “Z”, can influence the nature of the model and classification of patients, “Y”, into non-diabetic and diabetic cohorts. Through Jupyter Notebook (v0.34.9)  with a Python 3 kernel and importing pandas, shap, and xgboost libraries, SHAP plots were derived. Delineation of binary and multiple classification systems are defined above. The entire 50 patient population was utilized during training of the XGBoost model and both the patient biomarker values and patient labels were provided during training. The XGBoost and SHAP tree explainer utilized were left unaltered. The number of influential features shown in the summary plot were selected using the max display parameter. Plot generation utilized force plot, dependency plot, and summary plot SHAP functions. Force plots depict the effect of biomarker values on the model’s output. Dependency plots relate specific biomarker values to model prediction and show how the chosen biomarker depends on other tested biomarkers. Summary plots depict the top influential biomarkers and how they influence the model prediction. Code for analyses is also provided (https://github.com/qahathaway/WVU_Machine-Learning-50/tree/master).
Significance was determined using a two-tailed Student’s t-test or one-way analysis of variance (ANOVA), where appropriate. Tukey’s multiple comparisons test was implemented following the ANOVA to derive significance between multiple groups. Differences between groups were considered statistically different if P ≤ 0.05, denoted by * if statistically different from non-diabetic or # if statistically different from pre-diabetic. All data are presented as the mean ± standard error of the mean (SEM).
Mitochondrial DNA-Seq: Sequence Read Archive PRJNA520920 https://dataview.ncbi.nlm.nih.gov/?search=SUB5124294.
TFAM Promoter Methylation Amplicon-Seq: Sequence Read Archive PRJNA520920 https://dataview.ncbi.nlm.nih.gov/?search=SUB5125264.
Bioinformatics and Machine-learning Scripts: Github https://github.com/qahathaway/WVU_Machine-Learning-50/tree/master.
Alterations to the interaction networks that exist between the nucleus and mitochondrion play a significant role in the development of diabetic cardiomyopathy [47,48,49,50]. As a result, we wanted to determine how observed changes in these parameters could predict diabetic status using machine-learning algorithms. All of the machine-learning algorithms in this study implemented to draw conclusions were constructed around tree ensembles, such as Classification and Regression Trees (CART). CART algorithms proved to have the overall highest testing and training accuracies when compared to other models (Additional file 1: Tables S3–S10), while also performing superiorly in multiple classification of prediabetes (Tables 2, 3). When examining the testing, training, and area under the curve (AUC) values that depict model performance, CART performed consistently at, or near, the top of the six models in both the binary (Table 2) and multiple (Table 3) classification sets when assessing all 345 features. SHapley Additive exPlanations (SHAP) which implement CART functions were used to provide binary (non-diabetic or type 2 diabetic) as well as multiple (non-diabetic, prediabetic, and type 2 diabetic) classification analyses. SHAP analysis maps a particular biomarker’s numeric values to a computationally defined SHAP value that represents the degree to which specific biomarker values classify the patient to a particular label (non-diabetic or type 2 diabetic). We wanted to demonstrate how machine-learning algorithms, applied across a variety of health outcome datasets, could be implemented to identify novel biomarkers, with and without HbA1c, to provide better assessment of type 2 diabetes mellitus. By presenting each dataset distinctly, we were able to assess which biomarkers provided the best overall predictive power.
Physiological and biochemical analyses
Those with type 2 diabetes mellitus had significantly lower electron transport chain (ETC) complex I and III activities, along with a decreased methyltransferase activity (Additional file 1: Table S13). Using CART analysis and machine-learning, total nuclear methylation, total mitochondrial hydroxymethylation, and total nuclear hydroxymethylation were shown to be the most important factors influencing the model (Fig. 2a). Total nuclear methylation was also shown to be significantly increased in type 2 diabetics (Fig. 2b) with a corresponding decrease in total nuclear hydroxymethylation (Fig. 2c). Nuclear methylation increased as HbA1c levels increased (Fig. 2d) while the rate of hydroxymethylation, generally inversely correlated with methylation levels, decreased as HbA1c increased (Fig. 2e). Methyltransferase activity, total mitochondrial hydroxymethylation, total nuclear methylation, and total nuclear hydroxymethylation were shown to be important features in predicting type 2 diabetes mellitus in the absence of HbA1c (Fig. 2f). High s-adenosyl methionine (SAM) methyltransferase activity was also shown to be strongly associated with lower total nuclear methylation levels in the absence of HbA1c (Fig. 2g).
A decrease in mitochondrial ETC complex III activity was associated with a higher BMI (Fig. 2h). While those who were considered to be prediabetic (HbA1c 5.7–6.4) did not show significant differences between any of the biochemical measures except total TFAM CpG methylation (Additional file 1: Table S14), total nuclear methylation was still shown to provide partial classification of patients into non-diabetic, prediabetic, and type 2 diabetic designations (Fig. 2i, j). CART tenfold cross validation confirmed findings for binary [testing (0.838), training (0.7448)] and multiple [testing (0.598), training (0.545)] classification (Additional file 1: Figure S1A–D).
The complete mitochondrial genomes of all patients were sequenced, and a list of all single nucleotide polymorphisms (SNPs) was compiled. The binary nature of SNPs, i.e. either being converted or not, allowed the dynamic HbA1c levels to influence the machine-learning model much more efficiently (Fig. 3a). When HbA1c was removed, classification of diabetic or non-diabetic through SNPs was much more apparent, revealing that the 16,362 base pair was most significantly impacted (Fig. 3b). When examining the distribution of SNPs across the mitochondrial genome, the most significant area for base pair alterations to occur was shown to be the D-Loop, or control region (Fig. 3c).
The D-Loop (mtDNA 16,025–576 bp), as compared to all other regions in the mitochondrial genome, contained the highest frequency of SNPs used to predict type 2 diabetes mellitus (Fig. 3a, b, Additional file 1: Figure S2A, B). We further investigated how transcription factor binding could be altered at the D-Loop through chromatin immunoprecipitation (ChIP) of mitochondrial transcription factor A, mitochondrial (TFAM). Though protein levels of TFAM were unchanged (Additional file 1: Figure S3A), ChIP-qPCR revealed decreased binding of TFAM to the proximal and distal end of the control region in type 2 diabetics (Additional file 1: Figure S3B). SNPs near the replication of the H strand (Fig. 3d) or at the end of the D-Loop region (Fig. 3e) could impact TFAM binding and mitochondrial genome transcription. CART tenfold cross validation confirmed findings for binary [testing (0.79), training (0.92)] and multiple [testing (0.576), training (0.808)] classification (Additional file 1: Figure S2A–D).
The cytosine nucleotide followed by a guanine nucleotide (CpG) island of TFAM was examined (Fig. 4a), using overhang bisulfite PCR to amplify regions of the island for sequencing (Fig. 4b). Though total methylation of the gene was low (~ 3%) and showed no significant differences between non-diabetic and type 2 diabetic patients (Additional file 1: Table S13), site-specific CpG island methylation changes revealed significant differences between groups (Fig. 4a). Specifically, the 24th (CpG24) and 29th (CpG29) CpGs in the amplified region revealed significant hypomethylation in type 2 diabetic patients (Fig. 4c, d).
Without using the HbA1c parameter, methylation levels at CpG24, 1, 29, and 35 were shown to be significant contributors to the prediction of diabetic status (Fig. 4e). When comparing the interactions of CpG24 and CpG29, methylation levels at CpG24 were shown to allow distinct separation of the non-diabetic and type 2 diabetic population (Fig. 4f). CpG24 methylation remained a primary predictor, even in the presence of HbA1c for multiple classification (Fig. 4g). Examining total methylation of the TFAM CpG island, prediabetics exhibited an overall increase in methylation, while non-diabetics and type 2 diabetics with similar HbA1c levels showed much lower expression (Fig. 4h). CART tenfold cross validation confirmed findings for binary [testing (0.79), training (0.925)] and multiple [testing (0.668), training (0.767)] classification (Additional file 1: Figure S4A–D).
Those physiological, biochemical, genomic, and/or epigenomic markers that provided the best association within their class for predicting type 2 diabetes mellitus status were used in the final analyses. With the combined list of features, CART algorithms continued to perform consistently at, or near, the top for testing and training accuracies in binary (Additional file 1: Table S11) and multiple (Additional file 1: Table S12) classification. Total nuclear hydroxymethylation and total nuclear methylation levels provided the most powerful predictors in delineating between binary (non-diabetic and type 2 diabetic) (Fig. 5a) and multiple (non-diabetic, prediabetic, type 2 diabetic) (Fig. 5b) classifications, distinguishing them as potentially suitable biomarkers to accompany diagnostic practices using HbA1c. When using machine-learning to predict diabetic status without HbA1c, CpG24 methylation status and total nuclear methylation proved to be the most powerful predictors in both the binary (Fig. 5c) and multiple (Fig. 5d) classification datasets. Ultimately, both in the prediction of type 2 diabetes mellitus (Fig. 5e) and in assessing the onset (Fig. 5f), CpG24 hypomethylation was strongly correlated with total nuclear hypermethylation. CART tenfold cross validation confirmed findings for binary [testing (0.78), training (0.832)] and multiple [testing (0.67), training (0.542)] classification (Additional file 1: Figure S5A–D). Within our datasets, CpG24 methylation status and total nuclear methylation provided the best predictive measures for assessing type 2 diabetes mellitus. The incorporation of physiological, biochemical, genetic, and epigenetic features with machine-learning algorithms exemplifies the potential for more informative diagnostics in the future, as well as personalized approaches to generalized treatment modalities (Fig. 6).
Machine-learning can be applied as a systems biology approach, integrating multiple classes of biometric data to assess the importance of specific factors, while also predicting future outcomes. Whereas conventional assessments of disease identification exist, more detailed genomic and epigenomic testing is likely to reveal a comprehensive, systemic valuation of an etiology. To-date, studies have applied machine-learning algorithms in examining the physiological, biochemical, and/or genetic components of disease onset or progression . The advantage of our current study is through the assimilation of patient-matched data across a variety of critically impacted systems, providing an archetype for developing novel, descriptive, diagnostic measures through machine-learning algorithms that are specific for each disease type. By individually representing our datasets in Figs. 2, 3 and 4, we were able to reach more conclusive data in Fig. 5 by choosing the most predictive features for our final model. For the first time, a multi-omics, machine-learning approach was used to assess the progression and development of type 2 diabetes mellitus in a patient population, identifying potential biomarkers for cardiovascular risk and revealing the fundamental role of genetics in the pathology.
Molecular pathogenesis and machine-learning
While clinical practice has recently experienced a surge in deep learning applications used for non-invasive imaging , implementing machine-learning algorithms to the fundamental biochemistry and cellular and molecular processes of the body is now only blossoming. Onset and progression of type 2 diabetes has been traditionally measured through blood glucose levels, but, the multifaceted aspects of the disease could create variability in prognosis between vastly different demographic and ethnic groups. Owusu Adjah et al.  recently identified BMI as a risk factor for determining ethnic group disposition to type 2 diabetes mellitus. Specifically, the relationship between BMI and increased incidence of diabetes mellitus is non-linear; some groups, such as South Asian populations, were more disposed to developing the disease even at lower BMIs. While the current manuscript examines cardiovascular tissue, other less invasive approaches have been used to apply machine-learning algorithms. By retrieving blood from the basilica vein, circulating biomarkers were examined for their role in predicting early recurrence of atrial fibrillation following cryoballoon ablation . Support vector machines confirmed that decreased levels of creatine-kinase (CK-MB) and Troponin T (TnT) were associated with increased early recurrence of atrial fibrillation following cryoballoon ablation. Additionally, a unique, non-invasive approach for potentially diagnosing type 2 diabetes in patients was performed through the examination of toenails. Carter et al. , through a variety of machine learning algorithms, focused on 22 elements, including aluminum, cesium, nickel, vanadium, and zinc, and was able to get an AUC of 0.90 when predicting diabetic status using a random forest model.
Similar to parts of the aims of this study, other groups have attempted to use machine learning to separate diabetic and non-diabetic patients without the inclusion of blood glucose or HbA1c . In a testing set of 13,700 patients from the Luzhou, China region, random forest machine-learning algorithms provided a 0.7225 accuracy when predicting diabetic status from physical examination data in the absence of blood glucose . Also using a random forest model, Tang et al.  revealed how CpG island methylation data, combined with microRNA expression profiles, can be instrumental in cancer pathogenesis; implementing this two-feature selection process, they were able to identify the best tissue specific features, ultimately allowing for the identification of the originating tissue where tumor progression began. In a similar fashion, the machine-learning algorithm HeteSim , which examines heterogeneous datasets and calculates their relatedness, was employed in ascribing how gene profiles can be related to phenotypic outcomes, specifically in the validation and prediction of genes classified within major diseases .
While understanding how to better form prognoses and treat cardiac dysfunction in patients with type 2 diabetes mellitus remains a critical mission, more than 80 million American adults, most of which are undiagnosed, are prediabetic . In the current work, we have implemented predictive algorithms to assess biomarkers likely involved in the onset, as well as prediabetic progression, of type 2 diabetes mellitus. Although multiple classification categories further reduce the predictive power of the model, separation into distinct groupings revealed a unique phenotype for prediabetics (Fig. 4h). The effects of diabetes mellitus on the body is a high glucose stressed condition, altering substrate metabolism and causing systemic inflammation . Due to this environmental change, researchers have shown how epigenetic changes occur across most, if not all, tissues that are impacted by diabetes mellitus [49, 61].
In the cardiovascular system, the heart, circulatory system, and regulating immune system are all transcriptionally regulated through epigenetic alterations [48, 62], resulting in cellular adaptations to the environmental stress. Examining atrial appendages, the results obtained in this study are a direct reflection of changes within the heart. While blood is more easily acquired in type 2 diabetic patients, cardiac tissue, which is mitochondrially rich, provides a direct connection between physiological dysfunction observed in the heart and the impact of altered genomic profiles in the mitochondrion and nucleus. Machine-learning, which at current has been applied to very few genetic applications, may play a significant role in defining the epigenome of those with diabetes mellitus, likely unveiling genes and molecular pathways first impacted by the pathology.
The challenges of machine learning in the clinical setting
Machine-learning algorithms produce generalizations as they are inherently predictive, which means a smaller sample size can occasionally result in increased emphasis on outliers within the patient dataset and determination of the outliers’ biomarker features to be most influential in disease diagnosis. With a limited 50 patient dataset, there are concerns of overfitting the model, where the derived classification tree would have branches for each patient sample encountered during training. If this was to occur, the produced tree would fail future test cases while maintaining near perfect training accuracy, which was not observed. Tenfold cross validation ensured that no single developed tree was composed solely of outliers or a group of patient data of one label type, allowing patients of different labels to train the algorithm. Additionally, choosing seed values provided an even patient distribution during model training and testing. Both tenfold cross validation and setting a seed allowed the derived models to not over fit the training data. With this being said, it should be noted that the small sample size limits the conclusions and predictions made by the machine-learning algorithms within the manuscript, and future investigations will need to validate specific features, including CpG24 of TFAM and global nuclear DNA methylation.
For developed frameworks and the implemented SHAP visualization, the results are inherently regulated by HbA1c since patient HbA1c values were used to assign the labels from which the machine-learning algorithm then proceeded to train. HbA1c is used as a guide in this study to help clarify how clinically assessed progression of diabetes (commonly through HbA1c levels) is related to the biochemical and genetic signatures found in the heart. Although no specific biomarker or biomarker combinations can replace HbA1c due to the apparent diagnostic bias in this study (essentially ~ 100% accuracy when included), they can provide predictive accuracies near that of HbA1c. While previous clinical diagnoses determined a patients’ diabetic status in this study, some patients diagnosed as type 2 diabetics had HbA1c levels within normal ranges; begging the question of whether sustained, or attenuated, health effects can be accurately assessed through HbA1c levels alone when intervention (lifestyle or medicinally) occurs? Ultimately, this study provides a machine-learning algorithm utilizing the respective advantages of HbA1c in combination with other biomarkers to help circumvent the limitations of modern HbA1c diagnosis, as well as introduces completely novel cardiac risk stratification paradigms for patients with type 2 diabetes mellitus.
The quantity and diversity of omics-based approaches continues to expand. Convenience and increasingly inexpensive options for biometric-based valuations incite a growing demand for the incorporation and meaningful explanation of large and diverse patient datasets. The methodology outlined in this manuscript can serve as an archetype for the development and implementation of machine-learning to other disciplines seeking to evaluate disease progression. By using various health outcomes datasets, we were able to identify, and combine, the most prominent biomarkers into an accurate predictive algorithm engineered around 50 patients. While we have identified specific genetic features that are highly predictive in 50 patients, as a much larger patient population is applied to this model, the prioritization of other features is likely to occur, enhancing the diagnostic potential for the individual diabetic or prediabetic patient. Indeed, this is the advantage of using machine-learning models, in that they continue to learn and develop more accurate predictions as the number of features and sampled population grows.
Our work highlights the importance of identifying biomarkers in systems known to be disturbed during the disease (i.e. the mitochondrion and nucleus), and further applying these biological systems to personalized prognostics. By implementing classification tree, machine-learning algorithms to cardiac tissue from type 2 diabetic patients, we determined that hypermethylation of the nuclear genome was predictive of diabetic status and that it may provide added benefit to diagnostic applications in the future. Additionally, through our machine-learning model, as little as a ~ 5% change in methylation status of a gene promoter could provide valuable predictive data when determining diabetic status. Defining new diagnostic parameters, better predicting future health outcomes, and specializing modalities of care begins with the integration of “big data” into machine-learning systems; this study reveals how integration of data assists in the determination of diabetic status in the heart.
Availability of data and materials
area under the curve
Classification and Regression Trees
cytosine nucleotide followed by a guanine nucleotide
electron transport chain
Linear Discriminant Analysis
SHapley Additive exPlanations
Support Vector Machine
type 2 diabetes mellitus
transcription factor A, mitochondrial
Bertoluci MC, Rocha VZ. Cardiovascular risk assessment in patients with diabetes. Diabetol Metab Syndr. 2017;9:25.
Gregg EW, Cheng YJ, Srinivasan M, Lin J, Geiss LS, Albright AL, Imperatore G. Trends in cause-specific mortality among adults with and without diagnosed diabetes in the USA: an epidemiological analysis of linked national survey and vital statistics data. Lancet. 2018;391(10138):2430–40.
Scirica BM. Use of biomarkers in predicting the onset, monitoring the progression, and risk stratification for patients with type 2 diabetes mellitus. Clin Chem. 2017;63(1):186–95.
Bonora E, Tuomilehto J. The pros and cons of diagnosing diabetes with A1C. Diabetes Care. 2011;34(Suppl 2):S184–90.
Capobianco E. Systems and precision medicine approaches to diabetes heterogeneity: a Big Data perspective. Clin Transl Med. 2017;6(1):23.
Massi-Benedetti M. Changing targets in the treatment of type 2 diabetes. Curr Med Res Opin. 2006;22(Suppl 2):S5–13.
Kavakiotis I, Tsave O, Salifoglou A, Maglaveras N, Vlahavas I, Chouvarda I. Machine learning and data mining methods in diabetes research. Comput Struct Biotechnol J. 2017;15:104–16.
Jelinek HF, Stranieri A, Yatsko A, Venkatraman S. Data analytics identify glycated haemoglobin co-markers for type 2 diabetes mellitus diagnosis. Comput Biol Med. 2016;75:90–7.
Al’Aref SJ, Anchouche K, Singh G, Slomka PJ, Kolli KK, Kumar A, Pandey M, Maliakal G, van Rosendael AR, Beecy AN, et al. Clinical applications of machine learning in cardiovascular disease and its relevance to cardiac imaging. Eur Heart J. 2018. https://doi.org/10.1093/eurheartj/ehy404.
Tsay D, Patterson C. From machine learning to artificial intelligence applications in cardiac care. Circulation. 2018;138(22):2569–75.
Shameer K, Johnson KW, Glicksberg BS, Dudley JT, Sengupta PP. Machine learning in cardiovascular medicine: are we there yet? Heart. 2018;104(14):1156–64.
Libbrecht MW, Noble WS. Machine learning applications in genetics and genomics. Nat Rev Genet. 2015;16(6):321–32.
Norberg M, Eriksson JW, Lindahl B, Andersson C, Rolandsson O, Stenlund H, Weinehall L. A combination of HbA1c, fasting glucose and BMI is effective in screening for individuals at risk of future type 2 diabetes: OGTT is not needed. J Intern Med. 2006;260(3):263–71.
Owusu Adjah ES, Bellary S, Hanif W, Patel K, Khunti K, Paul SK. Prevalence and incidence of complications at diagnosis of T2DM and during follow-up by BMI and ethnicity: a matched case–control analysis. Cardiovasc Diabetol. 2018;17(1):70.
Almajwal AM, Al-Baghli NA, Batterham MJ, Williams PG, Al-Turki KA, Al-Ghamdi AJ. Performance of body mass index in predicting diabetes and hypertension in the Eastern Province of Saudi Arabia. Ann Saudi Med. 2009;29(6):437–45.
Cavagnolli G, Pimentel AL, Freitas PA, Gross JL, Camargo JL. Effect of ethnicity on HbA1c levels in individuals without diabetes: systematic review and meta-analysis. PLoS ONE. 2017;12(2):e0171315.
Croston TL, Thapa D, Holden AA, Tveter KJ, Lewis SE, Shepherd DL, Nichols CE, Long DM, Olfert IM, Jagannathan R, et al. Functional deficiencies of subsarcolemmal mitochondria in the type 2 diabetic human heart. Am J Physiol Heart Circ Physiol. 2014;307(1):H54–65.
Palmer JW, Tandler B, Hoppel CL. Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle. J Biol Chem. 1977;252(23):8731–9.
Baseler WA, Dabkowski ER, Jagannathan R, Thapa D, Nichols CE, Shepherd DL, Croston TL, Powell M, Razunguzwa TT, Lewis SE, et al. Reversal of mitochondrial proteomic loss in Type 1 diabetic heart with overexpression of phospholipid hydroperoxide glutathione peroxidase. Am J Physiol Regul Integr Comp Physiol. 2013;304(7):R553–65.
Baseler WA, Dabkowski ER, Williamson CL, Croston TL, Thapa D, Powell MJ, Razunguzwa TT, Hollander JM. Proteomic alterations of distinct mitochondrial subpopulations in the type 1 diabetic heart: contribution of protein import dysfunction. Am J Physiol Regul Integr Comp Physiol. 2011;300(2):R186–200.
Dabkowski ER, Baseler WA, Williamson CL, Powell M, Razunguzwa TT, Frisbee JC, Hollander JM. Mitochondrial dysfunction in the type 2 diabetic heart is associated with alterations in spatially distinct mitochondrial proteomes. Am J Physiol Heart Circ Physiol. 2010;299(2):H529–40.
Barrientos A, Fontanesi F, Diaz F. Evaluation of the mitochondrial respiratory chain and oxidative phosphorylation system using polarography and spectrophotometric enzyme assays. Curr Protoc Hum Genet. 2009; Chapter 19:Unit19 13.
Hathaway QA, Nichols CE, Shepherd DL, Stapleton PA, McLaughlin SL, Stricker JC, Rellick SL, Pinti MV, Abukabda AB, McBride CR, et al. Maternal-engineered nanomaterial exposure disrupts progeny cardiac function and bioenergetics. Am J Physiol Heart Circ Physiol. 2017;312(3):H446–58.
Shepherd DL, Hathaway QA, Nichols CE, Durr AJ, Pinti MV, Hughes KM, Kunovac A, Stine SM, Hollander JM. Mitochondrial proteome disruption in the diabetic heart through targeted epigenetic regulation at the mitochondrial heat shock protein 70 (mtHsp70) nuclear locus. J Mol Cell Cardiol. 2018;119:104–15.
Shepherd DL, Hathaway QA, Pinti MV, Nichols CE, Durr AJ, Sreekumar S, Hughes KM, Stine SM, Martinez I, Hollander JM. Exploring the mitochondrial microRNA import pathway through Polynucleotide Phosphorylase (PNPase). J Mol Cell Cardiol. 2017;110:15–25.
Hathaway QA, Durr AJ, Shepherd DL, Pinti MV, Brandebura AN, Nichols CE, Kunovac A, Goldsmith WT, Friend SA, Abukabda AB, et al. miRNA-378a as a key regulator of cardiovascular health following engineered nanomaterial inhalation exposure. Nanotoxicology. 2019. https://doi.org/10.1080/17435390.2019.1570372.
Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248–54.
Jagannathan R, Thapa D, Nichols CE, Shepherd DL, Stricker JC, Croston TL, Baseler WA, Lewis SE, Martinez I, Hollander JM. Translational regulation of the mitochondrial genome following redistribution of mitochondrial MicroRNA in the diabetic heart. Circ Cardiovasc Genet. 2015;8(6):785–802.
Croston TL, Shepherd DL, Thapa D, Nichols CE, Lewis SE, Dabkowski ER, Jagannathan R, Baseler WA, Hollander JM. Evaluation of the cardiolipin biosynthetic pathway and its interactions in the diabetic heart. Life Sci. 2013;93(8):313–22.
Thapa D, Nichols CE, Lewis SE, Shepherd DL, Jagannathan R, Croston TL, Tveter KJ, Holden AA, Baseler WA, Hollander JM. Transgenic overexpression of mitofilin attenuates diabetes mellitus-associated cardiac and mitochondria dysfunction. J Mol Cell Cardiol. 2015;79:212–23.
Nichols CE, Shepherd DL, Knuckles TL, Thapa D, Stricker JC, Stapleton PA, Minarchick VC, Erdely A, Zeidler-Erdely PC, Alway SE, et al. Cardiac and mitochondrial dysfunction following acute pulmonary exposure to mountaintop removal mining particulate matter. Am J Physiol Heart Circ Physiol. 2015;309(12):H2017–30.
Stapleton PA, Hathaway QA, Nichols CE, Abukabda AB, Pinti MV, Shepherd DL, McBride CR, Yi J, Castranova VC, Hollander JM, et al. Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome. Part Fibre Toxicol. 2018;15(1):3.
Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008;3(6):1101–8.
Bernstein DL, Kameswaran V, Le Lay JE, Sheaffer KL, Kaestner KH. The BisPCR(2) method for targeted bisulfite sequencing. Epigenetics Chromatin. 2015;8:27.
Krueger F, Kreck B, Franke A, Andrews SR. DNA methylome analysis using short bisulfite sequencing data. Nat Methods. 2012;9(2):145–51.
Krueger F, Andrews SR. Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications. Bioinformatics. 2011;27(11):1571–2.
Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012;9(4):357–9.
Li H. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data. Bioinformatics. 2011;27(21):2987–93.
Danecek P, Auton A, Abecasis G, Albers CA, Banks E, DePristo MA, Handsaker RE, Lunter G, Marth GT, Sherry ST, et al. The variant call format and VCFtools. Bioinformatics. 2011;27(15):2156–8.
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R, Genome Project Data Processing S. The sequence alignment/map format and SAMtools. Bioinformatics. 2009;25(16):2078–9.
Pedregosa F, Varoquaux G, Gramfort A, Michel V, Thirion B, Grisel O, Blondel M, Prettenhofer P, Weiss R, Dubourg V, et al. Scikit-learn: machine learning in Python. J Mach Learn Res. 2011;12:2825–30.
McKinney W. Data Structures for Statistical Computing in Python. In: Proc of the 9th Python in Science Conf: 2010; SCIPY 2010; 2010.
Lundberg SM, Erion GG, Lee S-I. Consistent individualized feature attribution for tree ensembles. CoRR 2018. abs/1802.03888.
Lundberg SM, Lee SI. A unified approach to interpreting model predictions. In: Advances in Neural Information Processing system. Vol. 30. 2017.
Chen T, Guestrin C. XGBoost: a scalable tree boosting system. In: Proceedings of the 22nd ACM SIGKDD international conference on knowledge discovery and data mining. San Francisco, California, USA: ACM; 2016. p. 785–94.
Kluyver T, Ragan-Kelley B, Pérez F, Granger B, Bussonnier M, Frederic J, Kelley K, Hamrick J, Grout J, Corlay S et al. Jupyter notebooks—a publishing format for reproducible computational workflows. In: Loizides F, Scmidt B, editors. 20th International conference on electronic publishing. Göttingen, Germany; 2016. p. 87–90.
Bugger H, Abel ED. Mitochondria in the diabetic heart. Cardiovasc Res. 2010;88(2):229–40.
Costantino S, Libby P, Kishore R, Tardif JC, El-Osta A, Paneni F. Epigenetics and precision medicine in cardiovascular patients: from basic concepts to the clinical arena. Eur Heart J. 2018;39(47):4150–8.
Villeneuve LM, Natarajan R. The role of epigenetics in the pathology of diabetic complications. Am J Physiol Renal Physiol. 2010;299(1):F14–25.
Pinti MV, Fink GK, Hathaway QA, Durr AJ, Kunovac A, Hollander JM. Mitochondrial dysfunction in type 2 diabetes mellitus: an organ-based analysis. Am J Physiol Endocrinol Metab. 2019;316:268–85.
Chaudhary K, Poirion OB, Lu L, Garmire LX. Deep learning-based multi-omics integration robustly predicts survival in liver cancer. Clin Cancer Res. 2018;24(6):1248–59.
Klang E. Deep learning and medical imaging. J Thorac Dis. 2018;10(3):1325–8.
Budzianowski J, Hiczkiewicz J, Burchardt P, Pieszko K, Rzezniczak J, Budzianowski P, Korybalska K. Predictors of atrial fibrillation early recurrence following cryoballoon ablation of pulmonary veins using statistical assessment and machine learning algorithms. Heart Vessels. 2019;34(2):352–9.
Carter JA, Long CS, Smith BR, Smith TL, Donati GL. Combining elemental analysis of toenails and machine learning techniques as a non-invasive diagnostic tool for the robust classification of type-2 diabetes. Expert Syst Appl. 2019;115:245–55.
Zou Q, Qu K, Luo Y, Yin D, Ju Y, Tang H. Predicting diabetes mellitus with machine learning techniques. Front Genet. 2018;9:515.
Tang W, Wan S, Yang Z, Teschendorff AE, Zou Q. Tumor origin detection with tissue-specific miRNA and DNA methylation markers. Bioinformatics. 2018;34(3):398–406.
Shi C, Kong XN, Huang Y, Yu PS, Wu B. HeteSim: a general framework for relevance measure in heterogeneous networks. IEEE Trans Knowl Data Eng. 2014;26(10):2479–92.
Zeng XX, Liao YL, Liu YS, Zou Q. Prediction and validation of disease genes using HeteSim scores. IEEE ACM Trans Comput Biol. 2017;14(3):687–95.
Centers for Disease Control and Prevention. Prediabetes: your chance to prevent type 2 diabetes. In: National Center for Chronic Disease Prevention and Health Promotion, Division of Diabetes Translation, editor. Diabetes. 2018. Updated 25 June 2018. https://www.cdc.gov/diabetes/basics/prediabetes.html.
Shoelson SE, Lee J, Goldfine AB. Inflammation and insulin resistance. J Clin Invest. 2006;116(7):1793–801.
Ling C, Groop L. Epigenetics: a molecular link between environmental factors and type 2 diabetes. Diabetes. 2009;58(12):2718–25.
Keating ST, Plutzky J, El-Osta A. Epigenetic changes in diabetes and cardiovascular risk. Circ Res. 2016;118(11):1706–22.
The authors have declared that no conflict of interest exists. We would like to acknowledge the WVU Genomics Core Facility, Morgantown WV for support provided to help make this publication possible. We would like to thank the West Virginia University Ruby Memorial Hospital Heart and Vascular Institute as well as surgeons Vinay Badwar, Harold Roberts, Muhammad Salman, and Lawrence Wei for promoting this collaborative work.
This work was supported by: R01 HL-128485 (JMH), American Heart Association AHA-17PRE33660333 (QAH), West Virginia IDeA Network of Biomedical Research WV-INBRE support by NIH Grant P20GM103434, and the Community Foundation for the Ohio Valley Whipkey Trust. Portions of this work have been accepted in abstract form to Experimental Biology, Orlando, FL 2019.
Ethics approval and consent to participate
All tissue and patient information was acquired in a double de-identified fashion, and was approved by the West Virginia University Institutional Review Board and Institutional Biosafety Committee. Patients were all consented by the Heart and Vascular Institute, J.W. Ruby Memorial Hospital at West Virginia University School of Medicine. Right atrial appendages were removed during open-heart and/or valvular surgeries (Refer to “Methods”, section “Study approval”).
Consent for publication
The authors declare that they have no competing interests.
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