Application of machine learning tools: Potential and useful approach for the prediction of type 2 diabetes mellitus based on the gut microbiome profile
- Authors:
- Published online on: February 23, 2022 https://doi.org/10.3892/etm.2022.11234
- Article Number: 305
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Copyright: © Ge et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Type 2 diabetes mellitus (T2DM) is one of the most common metabolic disorders worldwide and is primarily caused by defective insulin secretion (1). Over the past 30 years, the number of individuals with T2DM and prediabetes has increased two-fold globally, indicating T2DM as a rapidly growing public health challenge. However, T2DM is a multifactorial disease that slowly progresses over several years (2). Environmental factors including obesity, aging, an unhealthy diet, a lack of physical activity, smoking, as well as genetic factors and epigenetic modifications all contribute to the accelerating diabetes epidemic in China (3). However, genetic variation accounts for only a small ratio of risk of T2DM development and environmental factors play a pivotal role in driving the progression of T2DM. In addition, several studies have reported increased hypertension rates among T2DM subjects (4-6). It is estimated that the incidence of hypertension is increased ~two-fold in patients with T2DM compared with those without T2DM (7). A previous study indicated that moderate consumption of alcohol has been associated with a reduced risk of T2DM (8). However, moderate drinking needs to be monitored cautiously under a culturally appropriate context, particularly considering the stable increase in alcohol consumption in several Asian countries (9) and the excess increase in alcohol consumption in European countries (10).
Recent studies reported the occurrence of gut microbiota (GM) dysbiosis in obese patients with T2DM and indicated that the gut microflora may be a major environmental factor involved in the onset and progression of diabetes. Additionally, intestinal microbiome changes were also associated with the onset of type 1 DM and gestational DM (11,12). Therefore, it is necessary to develop a reliable early method for detecting T2DM that could lead to earlier interventions and treatments for T2DM.
The human gut microbiome has been demonstrated to possess 500-1,000 bacterial species, which are estimated to encompass ~2,000,000 genes. Surprisingly, the bacterial genes possess 100 times more genes than the human genes (13). The GM is a very diversified ecosystem and its function is dependent on several factors, such as host genetics, species, sex, age, body mass index (BMI), diet, smoking and drugs (14,15). GM may be key to the management of T2DM development. The aim of the present study was to develop a rapid machine learning-based method to predict the risk of T2DM.
Materials and methods
Sample and clinical data collection
A total of 118 newly diagnosed patients with T2DM and 89 controls (non-T2DM) were randomly recruited between January 2019 and October 2020 from the affiliated Hospital of Chengde Medical University (Chengde, China). The inclusion criteria for T2DM were as follows: i) Patients with T2DM were enrolled in accordance with the 1999 WHO diagnostic criteria as previously described (16); and ii) were aged >18 years. The exclusion criteria were as follows: i) Acute infection, trauma or surgery within the past month; ii) use of antibiotics, glucocorticoids or other immune regulators within the past month; iii) severe coronary heart disease, stroke or malignant disease; iv) pregnancy or lactation; v) autoimmune diseases, such as hyperthyroidism; and vi) other types of diabetes (17). The exclusion criteria for the controls were the same as those aforementioned.
All procedures were performed and approved (approval no. CYFYLL2021171) in accordance with the ethical standards of the Clinical Research Ethics Committee of the affiliated Hospital of Chengde Medical University (Chengde, China), and written informed consent was obtained from all participants included in the study.
Fecal sample collection and DNA extraction
A total of 207 fresh fecal samples were collected in sterile collection tubes (Thermo Fisher Scientific, Inc.). All samples were stored at -20˚C for temporary preservation and then transferred to -80˚C for longer term storage. Specifically, 200 mg fecal sample was added to 1 ml PBS in a 1.5 ml tube, vortexed at maximum speed for 3 min and centrifuged at 167.7 x g for 5 min at 4˚C and then the supernatant was collected and transferred to a 2-ml tube. A total of ~800 µl supernatant was centrifuged at 1,677 x g for 5 min at 4˚C and then the supernatant was removed. Subsequently, the microbial DNA was extracted from the fecal samples using a nucleic acid extraction kit (cat. no. T221S) according to the manufacturer's protocol (Xi'an Tianlong Science & Technology Co., Ltd,). Finally, ~60 µl DNA was obtained for downstream experiments.
Primers and PCR amplification
A total of 10 microbial oligonucleotide primers were synthesized and purified by General Biol (generalbiol.com/) (Table SI). Quantitative PCR (qPCR) was performed using an ABI-7500 real-time PCR system (Thermo Fisher Scientific, Inc.). The thermocycling conditions were: Pre-denaturation at 95˚C for 10 min; followed by 45 cycles of denaturation at 95˚C for 15 sec and annealing at 60˚C for 45 sec. Following amplification, melting temperature analysis of PCR products was performed to determine the specificity of the PCR amplification. The melting curves were obtained by heating from 60 to 95˚C at a rate of 0.3˚C/sec, with continuous fluorescence measurement. Differences in threshold cycles between the positive control (universal 16S rDNA) and each bacteria were quantified using the 2-ΔCq method as previously described (18), where ΔCq was the differences in Cq values for each bacteria and universal 16S rDNA and the relative abundance of each bacteria was calculated.
Construction of the prediction models
In the present study, three machine learning tools were established to predict T2DM development, including an artificial neural network of the multilayer perceptron (MLP) model, an XGboost model and a support vector machine (SVM) model and combined 6 clinical features and 10 bacterial species. The SVM model has been reported to predict chronic kidney disease in clinical applications (19), the XGBoost model exhibits improved performance in predicting patients with postoperative sepsis (20), and the MLP model performed well when applied to computed tomography for coronary artery disease and myocardial perfusion (21). K-fold is a common cross validation approach, particularly when the datasets are limited (22). Therefore, k-fold (k=5) was used to train, construct and compare the three predictive models. Additionally, the parameters of the three predictive models were tuned for the optimization of the equations in Python (Table SII).
A total of 207 participants (118 patients with T2DM and 89 controls) were randomly allocated into a training set (80%) and a test set (20%). In the training set, k=5 was used and various parameter combinations were exhausted using grid search. For each model, the confusion matrix, area under the receiver operating characteristic (ROC) curve (AUC), accuracy, sensitivity (recall), specificity, positive predictive value [ppv (precision)] and negative predictive value (npv) and were used to evaluate and compare the comprehensive performance of feature selection as previously described (23).
Statistical analysis
The three models were used to predict the risk of T2DM and evaluated using Python (version 3.6.12; Python Software Foundation) and incorporated including 6 clinical features and 10 bacterial species. The diagnostic values of the three models were assessed using ROC analysis. After preprocessing the data with pandas and sklearn, XGboost was used to analyze the importance of features and evaluated by Python as previously described (24). Categorical variables were presented by numbers or proportions, and differences in distribution between the two groups were analyzed using a χ2 test in SPSS (version 19.0; IBM Corp.) Continuous variables are presented as the median and range. Continuous variables between the two groups were compared using a nonparametric Mann-Whitney U test (for two groups) or nonparametric Kruskal-Wallis test followed by Dunn's post hoc test (for more than two groups). Statistical calculations were performed in GraphPad Prism (version 8.0; GraphPad Software, Inc.). P≤0.05 was considered to indicate a statistically significant difference.
Results
Clinical characteristics of the participants
The clinical characteristics of the patients with T2DM and controls are shown in Table SIII. There were no significant differences in age (P=0.502), sex (P=0.683), BMI (P=0.230), smoking (P=0.146), alcohol consumption (P=0.220) and hypertension status (P=0.055) between patients with T2DM and controls.
Comparison of the 10 bacteria between patients with T2DM and controls
A total of 10 bacteria, including Veillonellaceae, Clostridium leptum, Roseburia inulinivorans, Bacteroides, Prevotella, Bifidobacterium, Lactobacillus, Faecalibacterium prausnitzii, Enterococcus and Eubacterium rectale were detected by qPCR. The abundance of Bacteroides (P=0.0055), Eubacterium rectale (P=0.0432) and Roseburia inulinivorans (P=0.0019) was significantly lower in the T2DM group than in the control group (Fig. 1A-C). In addition, the abundance of Enterococcus (P=0.0002) was significantly higher in the T2DM group than in the control group (Fig. 1D). However, there were no significant differences in Prevotella (P=0.164), Bifidobacterium (P=0.103), Veillonellaceae (P=0.642), Faecalibacterium prausnitzii (P=0.157), Lactobacillus (P=0.078) and Clostridium leptum (P=0.493) between the two groups (Fig. S1).
In addition, Faecalibacterium prausnitzii was significantly higher in the control female subgroup than in the T2DM female subgroup (P=0.032; Fig. 2A). Furthermore, the abundance of Enterococcus was higher in the T2DM male subgroup than in both control female (P=0.025) and male (P=0.0121) subgroups (Fig. 2B). Roseburia inulinivorans was significantly higher in both control female and male subgroups than in the T2DM female subgroup (P=0.0008 and P=0.0026, respectively) (Fig. 2C). However, there were no significant differences in the abundance of the Bacteroides (P=0.0477), Prevotella (P=0.468), Bifidobacterium (P=0.35), Lactobacillus (P=0.326), Eubacterium rectale (P=0.118), Veillonellaceae (P=0.124) and Clostridium leptum (P=0.178) between each subgroup (Fig. S2).
The abundance of Bacteroides in the control older age (>60 years old) subgroup was higher than that in the T2DM older age subgroup (P=0.0208; Fig. 3A). The abundance of Bifidobacterium in the T2DM older age subgroup (>60 years old) was higher than that in the T2DM younger age (≤60 years old) subgroup (P=0.0343) and the control older age subgroup (P=0.0041; Fig. 3B). The abundance of Enterococcus was significantly higher in both the T2DM older age and younger age subgroups (P=0.0012 and P=0.0012, respectively; Fig. 3C), compared with control participants less than 60 years old. Furthermore, Roseburia inulinivorans was significantly higher in the control younger age subgroup than in the T2DM older age subgroup (P=0.0007; Fig. 3D). However, there were no significant differences in the abundance of Prevotella (P=0.0975), Lactobacillus (P=0.0697), Eubacterium rectale (P=0.102), Faecalibacterium prausnitzii (P=0.455), Veillonellaceae (P=0.507) and Clostridium leptum (P=0.904) between each subgroup (Fig. S3).
Comparison of the 3 machine learning models
SVM, XGboost and MLP models were used to predict the risk of T2DM by incorporating 6 clinical features and 10 bacterial species. A total of 207 samples were randomly divided into a training set (80%) and test set (20%). The ROC curve is widely used to validate the performance of prediction models, and the average AUC and 95% CI are shown in Fig. 4A. In the training set, the results indicated that the AUC values of SVM, XGboost and MLP models were 0.72, 0.70 and 0.69, respectively. Furthermore, the accuracy, ppv (precision) and sensitivity (recall) were >0.61 in all models (Table SIV). However, specificity and npv were poor in the three models. In the test set, the results showed that the SVM obtained the highest AUC value (0.77); the XGboost and MLP model AUC values were 0.69 and 0.67, respectively (Fig. 4B). The accuracy was >0.67 in the three models and the specificity and precision were >0.72 (Table SV). However, recall and npv did not perform well in all the models. Furthermore, the XGboost model was used to analyze the importance of the 16 features, and then the feature score rankings were measured (Fig. 5). The results showed that Bifidobacterium, age and Roseburia inulinivorans were the top three features in the model.
Discussion
The prevalence of T2DM has become a major public concern, with its continuingly increasing incidence worldwide. Gut dysbiosis in patients with T2DM is caused by not only environmental factors but also the host genetics. Studies have suggested that the composition of the intestinal microbiota can trigger T2DM (25-27). Therefore, further research is required to elucidate the connection between GM and T2DM.
T2DM is a systemic disease which is characterized by hyperglycemia, hyperlipidemia and organismic insulin resistance (28). In the present study, six clinical data including age, sex, BMI, smoking, alcohol consumption and hypertension status which were associated with T2DM development were collected. Additionally, numerous studies have shown that non-alcoholic fatty liver disease (NAFLD) is commonly observed in patients with T2DM (29,30). However, whether NAFLD is a cause or consequence of the diabetic pathology remains a source of debate (28). Thus, this relationship is bidirectional, since T2DM substantially predicts the development of these metabolic disorders (3). Therefore, the NAFLD status, hyperlipidemia and disorders of glucose and lipid metabolism status were not collected to predict the risk of T2DM in the present study. According to previous studies, 10 bacteria including Veillonellaceae, Clostridium leptum, Roseburia inulinivorans, Bacteroides, Prevotella, Bifidobacterium, Lactobacillus, Faecalibacterium prausnitzii, Enterococcus and Eubacterium rectale were associated with T2DM (31,32). The abundance of Bacteroides was significantly lower in the T2DM group, which is consistent with a previous study in animals, which revealed that after administration of metformin, the relative abundance of Bacteroides was increased in mice and rats treated with metformin (33). Roseburia inulinivorans was more abundant in the control group in the present study, which is similar to a study which showed that the abundance of Roseburia inulinivorans was increased in patients after diabetic remission, achieved by both laparoscopic Roux-en-Y gastric bypass or sleeve gastrectomy surgery (34). Interestingly, Roseburia inulinivorans was significantly higher in both control female and male subgroups than in the T2DM female subgroup. Moreover, Roseburia inulinivorans was significantly higher in the control younger age subgroup than in the T2DM older age subgroup. In the present study, the abundance of Eubacterium rectale was significantly higher in the control group than in the T2DM group, which is consistent with a metagenome-wide association study which revealed that the relative abundance of Eubacterium rectale was higher in the control group than in the patients with T2DM (31). A previous study found that Enterococcus was positively correlated with obesity (35). Enterococcus was significantly higher in the patients with T2DM in the present study, which is in accordance with a study that showed that Enterococcus was more enriched in the DM group than in the control group (36). Interestingly, the abundance of Enterococcus was higher in both T2DM younger and older age subgroups than in the control younger age subgroup. Additionally, Enterococcus was higher in the T2DM male subgroup than in both control female and male subgroups.
Additionally, several studies have shown that Bifidobacterium was negatively associated with T2DM (37,38). Conversely, Sasaki et al (39) reported that Bifidobacterium was significantly increased in the patients with T2DM when compared with the healthy controls. However, in the present study, the abundance of Bifidobacterium did not significantly differ between the control group and the T2DM group. Interestingly, Bifidobacterium exhibited the higher abundance in the T2DM older age subgroup than in the T2DM younger age subgroup and the control older age subgroup. Faecalibacterium prausnitzii was found to be negatively associated with T2DM (32,40). Interestingly, Faecalibacterium prausnitzii was significantly higher in the control female subgroup than in the T2DM female subgroup; although there was no significant difference in Faecalibacterium prausnitzii abundance between the control group and T2DM group. Penckofer et al (41) reported that Lactobacillus was more abundant in women with T2DM than in the controls. Conversely, previous studies have demonstrated the beneficial effects of Lactobacillus for human health, including improving T2DM, exhibiting anti-inflammatory effects and reducing body weight (42-44). Human gut Lactobacillus can reduce blood glucose responses in vivo (45). The aforementioned studies indicated that Lactobacillus shows the most discrepant results among studies. Furthermore, Prevotella was significantly correlated with lipid metabolites, such as lysophosphatidylglycerol and phosphatidylinositol-3, resembling obese and diabetic phenotypes (46). The abundance of Clostridium leptum in the probiotic group was significantly higher than in the control group who did not take probiotics than in Japanese patients with T2DM (47). In a previous study, it was demonstrated that Veillonellaceae was significantly higher in the acarbose group than in the placebo group (48). However, in the present study, the abundance of Lactobacillus, Prevotella, Clostridium leptum and Veillonellaceae did not significantly differ between the control and T2DM groups.
In order to improve earlier warnings in patients with T2DM, the SVM, XGboost and MLP models were used, incorporating 6 clinical features and 10 bacterial species to predict the risk of T2DM. A total of 207 samples were randomly divided into a training set (80%) and test set (20%). Among the three models, SVM and XGboost models obtained AUC values of 0.72 and 0.70, respectively, in the training set, and the accuracy, precision and recall were >0.61. While in the test set, only the SVM model obtained an AUC value of 0.77, the precision and specificity were >0.77, and the accuracy, recall, and npv were >0.60. Previous studies reported that if the model AUC is >0.70, the model has high accuracy (49,50). Although the SVM model had the highest overall predictive power, the sample size in the training and test set were small. Thus, large samples are required to verify this result.
In addition, the XGboost model was used to analyze the importance of the 16 features, including 6 clinical features and 10 bacterial species. The results revealed that Bifidobacterium, age and Roseburia inulinivorans played major roles in the model, while alcohol consumption, smoking status and sex were less important. Bifidobacterium represents beneficial genera, most frequently reported in studies of T2DM, and appears to be the most consistent genus supported by the literature, exhibiting potentially protective effects against T2DM (51). Roseburia inulinivorans is also the most consistently reported to exhibit a negative association with T2DM (51). Therefore, the results indicated that the gut microbiome can be a potential marker for predicting the risk of T2DM. Yang et al (52) reported that the meta-analysis of the prevalence T2DM rate at the age of 55-74 years was six- to seven-fold higher than that of individuals aged 20-34 years, in China. Thus, age may be a major factor in the risk of T2DM. In the present study, age was ranked as the second most important factor in the model. Additionally, Bifidobacterium, Roseburia inulinivorans and Enterococcus were associated with an older age. Bifidobacterium, Roseburia inulinivorans and Enterococcus were ranked as the top 5 important features in the model. In addition, a previous study showed that a high BMI was the single strongest risk factor for T2DM (53), and was associated with several metabolic abnormalities that result in insulin resistance (54). According to a series of nationwide surveys reported in China (55), the prevalence of being overweight (23 kg/m2 ≤ BMI <27.5 kg/m2) in Chinese adults aged 20-59 years old increased from 37.4% in 2000 to 39.2% in 2005, 40.7% in 2010, and 41.2% in 2014. The prevalence of obesity (BMI ≥27.5 kg/m2) increased from 8.6% in 2000 to 10.3% in 2005, 12.2% in 2010 and 12.9% in 2014. Notably, T2DM develops at a considerably lower BMI in the Chinese population than in European populations. The relatively high risk of diabetes at a lower BMI could be partially attributed to the tendency towards visceral adiposity in East Asian populations, including the Chinese population (56). Therefore, BMI may not play an important role in developing T2DM in the Chinese population. In the present study, BMI ranked as the fifth most important feature in the model. In addition, smoking has shown to induce insulin resistance and compensatory insulin-secretion responses (57), which may explain the increased risk of T2DM in individuals who smoke. On the one hand, moderate consumption of alcohol has been associated with a reduced risk of T2DM (8). On the other hand, it may be due to the public education campaigns to reduce the prevalence of smoking in China in recent years. A meta-analysis indicated that the prevalence of T2DM was 9.9% for men and 11.6% for women in China (2000-2014) (52). It appears that the effect of sex on the prevalence of T2DM amongst the Chinese is equal. Thus, alcohol consumption, smoking and sex are less important in the model ranking. Meanwhile, the abundance of Faecalibacterium prausnitzii, Veillonellaceae, Clostridium leptum and Lactobacillus did not differ between the control and T2DM groups, which may explain why they were ranked lower.
There are several limitations in the present study. First, the sample size used was relatively small and the total cohort of patients with T2DM and cohort of controls was unbalanced. Second, only 6 clinical features and 10 bacterial species were used to establish the models between the two groups. The 16S rRNA gene is a promising method for detecting GM, but in the present study, the abundance of the 10 bacterial species between the two groups was assessed by qPCR instead. Third, although the SVM model obtained an AUC value of 0.77 in the test set, larger cohorts are required to validate in the model before the model can be assessed in the clinic for detection of early stage T2DM.
In conclusion, three machine learning models were constructed and compared to predict the risk of T2DM, revealing that the SVM model exhibited the highest overall predictive power. In addition, Bifidobacterium, age and Roseburia inulinivorans had important impacts in predicting early stage T2DM. Therefore, SVM machine learning may have potential to aid in the early prediction and treatment of patients with T2DM in the near feature.
Supplementary Material
Comparison of the abundance of the 6 bacterial species between the patients with T2DM and controls. No significant difference was observed in the abundance of (A) Prevotella, (B) Bifidobacterium, (C) Veillonellaceae, (D) Faecalibacter iumprausnitzii, (E) Lactobacillus and (F) Clostridium leptum between the two groups. Results represent the median and range. T2DM, type 2 diabetes mellitus.
Comparison of the abundance of the 7 bacterial species between the control female and male subgroups, and the T2DM female and male subgroups. No significant difference was observed in the abundance of (A) Bacteroides, (B) Prevotella, (C) Bifidobacterium, (D) Lactobacillus, (E) Eubacterium rectale, (F) Veillonellaceae and (G) Clostridium leptum between the four subgroups. Results represent the median and range. T2DM, type 2 diabetes mellitus.
Comparison of the abundance of the 6 bacterial species between the control older age and younger age subgroups, and the T2DM older age and younger age subgroups. No significant difference was observed in the abundance of (A) Prevotella, (B) Lactobacillus, (C) Eubacterium rectale, (D) Faecalibacter iumprausnitzii, (E) Veillonellaceae and (F) Clostridium leptum between the four subgroups. Results represent the median and range. T2DM, type 2 diabetes mellitus.
Sequences of the primers used in the present study.
Selection of parameters in the predictive models.
Clinical characteristics of patients with T2DM and control subjects.
Summary of the efficacy of the SVM, MLP and XGboost models in the training set.
Summary of the efficacy of the SVM, MLP and XGboost models in the test set.
Acknowledgements
Not applicable.
Funding
Funding: No funding was received.
Availability of data and materials
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
XG, HT, JZ and YG designed the experiments. AZ, LL, QS, JH and YW collected the samples and performed the experiments. XG, RT, YX, JZ and YP analyzed the data. XG, HT, JZ and YG confirm the authenticity of all the raw data. XG, HT, YX and YG wrote the manuscript. JZ, YX, HT and YG revised the manuscript. All authors have read and approved the final manuscript.
Ethics approval and informed consent
The present study was approved (approval no. CYFYLL2021171) by the Ethics Committee of the affiliated Hospital of Chengde Medical University (Chengde, China). Written informed consent was obtained from all participants involved in the present study.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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