Effect of metformin on adverse outcomes in T2DM patients: Systemic review and meta-analysis of observational studies
Zhicheng Xu
Haidong Zhang2*† 
Yuxiang Zheng- 1Department of Cardiology, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Nanchang, China
- 2Department of Nephrology, Peking University Third Hospital, Bejing, China
- 3School of Medicine, Sun Yat-sen University, Shenzhen, China
- 4Department of Anesthesiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
- 5Department of Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Background: The cardiovascular protection effect of metformin on patients with type 2 diabetes mellitus (T2DM) remains inconclusive. This systemic review and meta-analysis were to estimate the effect of metformin on mortality and cardiovascular events among patients with T2DM.
Methods: A search of the Pubmed and EMBASE databases up to December 2021 was performed. Adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) were pooled by a random-effects model with an inverse variance method.
Results: A total of 39 studies involving 2473009 T2DM patients were adopted. Compared to non-metformin therapy, the use of metformin was not significantly associated with a reduced risk of major adverse cardiovascular event (MACE) (HR = 1.06, 95%CI 0.91–1.22; I2 = 82%), hospitalization (HR = 0.85, 95%CI 0.64–1.13; I2 = 98%), heart failure (HR = 0.86, 95%CI 0.60–1.25; I2 = 99%), stroke (HR = 1.16, 95%CI 0.88–1.53; I2 = 84%), and risk of AMI (HR = 0.88, 95%CI 0.69–1.14; I2 = 88%) in T2DM patients. Metformin was also not associated with significantly lowered risk of MACE compared to dipeptidyl peptidase-4 inhibitor (DPP-4i) in T2DM patients (HR = 0.95, 95%CI 0.73–1.23; I2 = 84%).
Conclusions: The effect of metformin on some cardiovascular outcomes was not significantly better than the non-metformin therapy or DPP-4i in T2DM patients based on observational studies.
Introduction
Cardiovascular disease (CVD) is the predominant cause of death globally, resulting in a great economic burden and a tremendous threat to public health. Approximately 19.05 million deaths are estimated to CVD globally (1). Moreover, the incidence of CVD has been increasing or stagnating among younger individuals (aged 18–50 years) over the past few decades (2). Study shows that T2DM significantly increase the risk of CVD and aggressive glycemic control can reduce both macrovascular and microvascular events in T2DM patients (3).
Metformin, a biguanide derivative, has been used as a first-line hypoglycemic treatment for type 2 diabetes mellitus (T2DM) patients since 1957 when it was recommended by the European Association for the Study of Diabetes (EASD) and the American Diabetes Association (ADA) (4). Apart from its hypoglycemic effect, metformin has been found to confer protection against breast cancer (5), polycystic ovary syndrome (6), and neural recovery in patients with brain tumors (7). Metformin is also associated with a lower risk of major adverse cardiovascular events (MACEs) and all-cause mortality (8, 9). The UK Prospective Diabetes Study (UKPDS) shows that metformin has an effect of lowering the risk of cardiovascular morbidity and mortality over 20 years (10). Metformin can reduce the risk of heart failure, hospitalization, and stroke in patients with T2DM (10, 11). In T2DM patients with chronic kidney disease or heart failure, metformin may also show a cardiovascular protection effect (12, 13). Compared with other classic hypoglycemic agents (e.g., sulphonylurea), metformin reduces the risks of all-cause or cardiovascular mortality, stroke, and heart failure (14). When compared with new antidiabetic drugs such as sodium-glucose cotransporter-2 inhibitors, metformin is associated with a low rate of genital infection and ketoacidosis (15). However, recent conflicting reports have shown that metformin could not reduce all-cause and cardiovascular mortality (16, 17). Moreover, the combination of metformin and other hypoglycemic drugs may even impose higher death risks (17).
Han et al. (18) found Metformin could reduce cardiovascular mortality, all-cause mortality, and cardiovascular events in coronary artery disease (CAD) patients. However, Han's study only targeted CAD patients rather than the common population. Since more observational studies showed up and current observational evidence on the effect of metformin on CVD risk was still inconclusive, we carried out this meta-analysis on a synthesis of published data to estimate adverse cardiovascular outcomes following metformin treatment in patients with T2DM.
Methods
Overall, the corresponding authors designed the research criteria, and two reviewers independently performed the literature search, study selection, data abstraction, quality assessment, and data analysis. Disagreements were resolved by discussion between two reviewers, or consultation with the corresponding authors. Ethical approval was not necessary for this study because only the published studies were included.
Inclusion and exclusion criteria
We included observational retrospective or prospective cohort studies, in which the adverse outcomes were compared between patients with T2DM treated with metformin monotherapy and those treated with any other single drug or diet/lifestyle modification. The adverse outcomes of interest included all-cause mortality, MACE, hospitalization, heart failure, cardiovascular mortality, stroke, and AMI. The primary outcome was MACE, whereas others were secondary outcomes. The definitions of the studied outcomes were applied that were reported in the originally included studies.
We excluded studies focusing on patients with type 1 diabetes mellitus or patients without T2DM but with metformin treatment. Studies in which patients with T2DM were treated with two or more antidiabetic drugs or with one antidiabetic drug combined with insulin were also excluded. Certain publication types were excluded (e.g., reviews, comments, case reports, case series, letters, editorials, and meeting abstracts) due to insufficient data.
Literature search
A prior meta-analysis by Han et al. (18) has studied the effect of metformin on adverse outcomes in patients with T2DM, and the end date of the literature search in this study was October 2019. Therefore, we abstracted the included studies for the meta-analysis by Han et al., and then systemically searched the PubMed and Embase databases from January 2019 to December 2021 to identify studies about the effect of metformin monotherapy vs. other treatments on adverse outcomes in patients with T2DM. The search terms combined with “AND” were applied as follows: (1) “metformin,” (2) “diabetes mellitus” OR “diabetes.” No linguistic restrictions were applied in the literature search.
Study selection and data abstraction
We first screened the titles and abstracts of the retrieved studies from the PubMed and Embase databases, and subsequently, read the full texts of the potential studies. Those studies included in the prior meta-analysis by Han et al. (18) were also checked. Eligible studies would be chosen based on the pre-defined inclusion criteria. The following information of the included studies was collected: first author, publication year, country, study design, patient characteristics (study population, sample size, age, sex), follow-up time, type of treatment compared to metformin, sample size, and the number of events in the metformin and control groups, and adverse outcomes.
Study quality assessment
The Newcastle-Ottawa Scale (NOS) tool was used to assess the quality of cohort studies. The NOS tool had three domains with a total of nine points: the selection of population (0–4 points), the comparability between experimental groups and control groups in the study (0–2 points), and the assessment of the outcome (0–3 points). In this meta-analysis, the study with a NOS score of less than 6 points was defined as low quality (19). This assessment method was used previously (20).
Statistical analyzes
The statistical heterogeneity across the included studies was assessed using the P-value of the Cochrane Q test and the I2 statistic, where a P < 0.10 in the Cochrane Q test or an I2 > 50% suggested significant heterogeneity. The adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) were considered as the effect sizes, and we converted them to the natural logarithms and standard errors, which were pooled by a random-effects model with an inverse variance method. The data analyses were performed based on the type of treatment and complications of patients. In the sensitivity analysis, we re-performed the above-mentioned analyses by deleting studies in which the sample size was smaller than 1,000 in either the control group or the experimental group. The publication bias for the reported effect estimates was assessed by funnel plots, egger and begg tests, and trim and fill analyses.
All the statistical analyses of this meta-analysis were performed using the Review Manager version 5.4 software (the Cochrane Collaboration 2014, Nordic Cochrane Centre Copenhagen, Denmark; https://community.cochrane.org/). In this study, a P-value of less than 0.05 was considered statistically significant.
Results
Study selection
The flow chart of the literature retrieval is presented in Supplementary Figure 1. A total of 10,244 studies were retrieved from the PubMed and Embase databases for the title and abstract screenings, after which 32 potential studies from databases were pooled with the other 34 studies included in the prior meta-analysis by Han et al. (18) to receive full-text screenings. Then we excluded 27 studies for the following reasons: (1) 21 studies did not focus on the adverse outcomes we set in the inclusion criteria (21–39); (2) 3 studies included patients without type 2 diabetes mellitus (40–42); (3) 1 ongoing study without outcomes (43); (4) 1 research investigated methodology of estimating the effect of metformin (44); (5) 1 study used metformin as the baseline drug in combination therapy (45). Finally, 39 studies [8 prospective cohort studies (15, 46–52) and 31 retrospective cohort studies (11, 13, 19, 26, 53–79)] were included in this meta-analysis.
Baseline characteristics of the included studies
Table 1 shows the baseline characteristics of the included studies. Twenty-seven studies investigated the effect of metformin on all-cause mortality (13, 19, 46–53, 55–59, 61, 62, 64–66, 68, 72–74, 77–79), 16 studies investigated the effect of metformin on risk of MACE (26, 49, 52, 55, 60, 62, 64, 65, 69, 72, 74–79), 18 studies investigated the effect of metformin on risk of hospitalization (11, 13, 15, 47, 49, 50, 52, 56–60, 63, 67, 69, 71–73), 14 studies investigated the effect of metformin on risk of heart failure (11, 15, 49, 50, 52, 53, 56, 57, 59, 67–69, 71, 73), 14 studies investigated the effect of metformin on cardiovascular mortality (19, 26, 46, 47, 49, 50, 56, 59, 60, 62, 64, 71, 74, 75), 8 studies investigated the effect of metformin on risk of stroke (15, 26, 49, 57, 65, 68, 69, 74), and 6 studies investigated the effect of metformin on the risk of AMI (15, 26, 49, 54, 69, 74). Only 1 retrospective cohort study by Liu et al. (19) had a low quality with 4 points assessed by the NOS tool.
Table 1. Baseline characteristics of included studies.
Effect of metformin on MACE in T2DM patients
As shown in Figures 1A–C, the use of metformin was not associated with a decrease in the risk of MACE when compared to non-metformin (HR = 1.06, 95%CI 0.91–1.22; I2 = 82%). Specifically, metformin was associated with a decreased risk of MACE when compared to sulphonylurea (HR = 0.83, 95%CI 0.77–0.90; I2 = 48%). What's more, the use of metformin did not alter the risk of MACE significantly compared to dipeptidyl peptidase-4 inhibitor (DPP-4i) in T2DM patients (HR = 0.95, 95%CI 0.73–1.23; I2 = 84%).
Figure 1. (A) Forest plot of hazard ratio of MACE among patients with metformin therapy vs non-metformin therapy. (B) Forest plot of hazard ratio of MACE among patients with metformin therapy vs. sulphonylurea therapy. (C) Forest plot of hazard ratio of MACE among patients with metformin therapy vs. DPP-4i therapy. (D) Forest plot of hazard ratio of hospitalization among patients with metformin therapy vs non-metformin therapy. (E) Forest plot of hazard ratio of hospitalization among patients with metformin therapy vs. SGLT2i. (F) Forest plot of hazard ratio of hospitalization among heart failure patients with metformin therapy vs non-metformin therapy. CI, confidence interval; SE, standard error; IV, inverse of the variance.
Effect of metformin on all-cause mortality in T2DM patients
The results of the effect of metformin on all-cause mortality in T2DM patients were presented in Figures 2B–F, showing that the use of metformin was associated with a significantly lower all-cause mortality in T2DM patients compared to non-metformin therapy (HR = 0.82, 95%CI 0.77–0.88; I2 = 73%), sulphonylurea (HR = 0.58, 95%CI 0.49–0.68; I2 = 74%), and diet therapy (HR = 0.76, 95%CI 0.64–0.90; I2 = 0%). Also, there was a significant reduction in all-cause mortality in T2DM patients with heart failure (HR = 0.84, 95%CI 0.84–0.88; I2 = 40%) or CKD (HR = 0.79, 95%CI 0.75–0.82; I2 = 0%) using metformin vs. non-metformin therapy. In addition, two studies by Scheller et al. (78) and Chen et al. (57), respectively, compared the effect of metformin on all-cause mortality in T2DM patients with DPP-4i (HR = 0.8, 95%CI 0.58–1.09) and sodium-dependent glucose transporter-2 inhibitor (SGLT-2i) (HR = 2.04, 95%CI 1.82–2.27).
Figure 2. (A) Forest plot of hazard ratio of hospitalization among patients with metformin therapy vs. sulphonylurea therapy. (B) Forest plot of hazard ratio of all-cause mortality among patients with metformin therapy vs. non-metformin therapy. (C) Forest plot of hazard ratio of all-cause mortality among patients with metformin therapy vs. sulphonylurea therapy. (D) Forest plot of hazard ratio of all-cause mortality among patients with metformin vs. diet therapy. (E) Forest plot of hazard ratio of all-cause mortality among heart failure patients with metformin therapy vs. non-metformin therapy. (F) Forest plot of hazard ratio of all-cause mortality among patients with CKD treated with metformin therapy vs non-metformin therapy. CI, confidence interval; SE, standard error; IV, inverse of the variance.
Effect of metformin on the risk of hospitalization in T2DM patients
Figures 1D–F, 2A presented the effect of metformin on hospitalization in T2DM patients. Metformin was not associated with a significant lower risk of hospitalization in T2DM patients compared to non-metformin therapy (HR = 0.85, 95%CI 0.64–1.13; I2 = 98%) and SGLT2i (HR = 1.42, 95%CI 0.87–2.32; I2 = 49%), but it significantly lowered the risk of hospitalization compared to non-metformin therapy (HR = 0.86, 95%CI 0.78–0.95; I2 = 53%) in T2DM patients with heart failure and sulphonylurea (HR = 0.83, 95%CI 0.78–0.88; I2 = 40%) in T2DM patients. And as reported by Baksh (69) the use of metformin was not associated with a significantly lower risk of hospitalization compared with DPP-4i in T2DM patients (HR = 1.04, 95%CI 0.77–1.40).
Effect of metformin on the risk of heart failure in T2DM patients
As shown in Figure 3, the use of metformin was not associated with a significantly lower risk of heart failure in T2DM patients compared to non-metformin therapy (HR = 0.86, 95%CI 0.60–1.25; I2 = 99%). However, metformin significantly lowered the risk of heart failure compared to sulphonylurea (HR = 0.80, 95%CI 0.76–0.85; I2 = 0%) and the risk of recurrent incidents of heart failure compared to non-metformin therapy (HR = 0.82, 95%CI 0.76–0.87; I2 = 7%) in T2DM patients. And metformin was not significantly associated with reduced risk of heart failure compared to diet therapy (HR = 0.688, 95%CI 0.435–1.086) in T2DM patients in the study by Fung et al. (68) and compared to rosiglitazone (HR = 0.86, 95%CI 0.58–1.28) in T2DM patients in the study by Pantalone et al. (53).
Figure 3. (A) Forest plot of hazard ratio of heart failure among patients with metformin therapy vs non-metformin therapy. (B) Forest plot of hazard ratio of heart failure among patients with metformin therapy vs. sulphonylurea therapy. (C) Forest plot of hazard ratio of the recurrent incident of heart failure among heart failure patients with metformin therapy vs. non-metformin therapy. CI, confidence interval; SE, standard error; IV, inverse of the variance.
Effect of metformin on cardiovascular mortality in T2DM patients
Figures 4A–C showed the effect of metformin on cardiovascular mortality in T2DM patients. The use of metformin was not only significantly associated with lower cardiovascular mortality in T2DM patients (HR = 0.83, 95%CI 0.70–0.98; I2 = 85%) and in T2DM patients with heart failure (HR = 0.78, 95%CI 0.74–0.82; I2 = 0%) compared to non-metformin therapy, but also significantly lowering cardiovascular mortality compared to sulphonylurea in T2DM patients (HR = 0.70, 95%CI 0.58–0.84; I2 = 0%). Liu et al. (19) reported that metformin vs. diet therapy was not associated with significantly lower cardiovascular mortality (HR = 0.87, 95%CI 0.45–1.68).
Figure 4. (A) Forest plot of hazard ratio of cardiovascular mortality among patients with metformin therapy vs non-metformin therapy. (B) Forest plot of hazard ratio of cardiovascular mortality among heart failure patients with metformin therapy vs. non-metformin therapy. (C) Forest plot of hazard ratio of cardiovascular mortality among patients with metformin therapy vs. sulphonylurea. (D) Forest plot of hazard ratio of stroke among patients with metformin therapy vs. non-metformin therapy. (E) Forest plot of hazard ratio of stroke among patients with metformin therapy vs. SGLT2i. (F) Forest plot of hazard ratio of AMI among patients with metformin therapy vs. non-metformin therapy. CI, confidence interval; SE, standard error; IV, inverse of the variance.
Effect of metformin on the risk of stroke and AMI in T2DM patients
The effect of metformin on the risk of stroke and AMI in T2DM patients was shown in Figures 4D–F. The use of metformin was not associated with a significant decrease in the risk of stroke compared to non-metformin therapy (HR = 1.16, 95%CI 0.88–1.53; I2 = 84%) and SGLT2i (HR = 1.03, 95%CI 0.65–1.63; I2 = 87%) in T2DM patients. The use of metformin significantly lowered the risk of stroke compared to diet therapy in T2DM patients (HR = 0.698, 95%CI 0.511–0.954) in the study by Fung et al. (68) while the alteration of risk of stroke was not significant compared to DPP-4i (HR = 0.81, 95%CI 0.6–1.09) in T2DM patients in the study by Baksh et al. (69). And the risk of AMI did not decrease significantly in T2DM patients with metformin therapy vs. non-metformin therapy (HR = 0.88, 95%CI 0.69–1.14; I2 = 88%). What's more, the use of metformin was not associated with a significantly lower risk of AMI in T2DM patients compared to DPP-4i (HR = 0.95, 95%CI 0.72–1.27) and SGLT2i (HR = 1.10, 95%CI 0.66–1.85) in the study by Baksh et al. (69) and Fralick et al. (15), respectively.
Sensitivity analysis and publication bias
Supplementary Table 2 showed the results of sensitivity analysis for the outcomes. The majority of the re-analyses showed similar results as the analysis before deleting studies with a sample size smaller than 1,000 in either the control group or the experimental group. However, only 1 study by Roussel et al. (64) remained after deleting the data in the analyses studying the effect of metformin on all-cause mortality and cardiovascular mortality vs. non-metformin therapy in T2DM patients with heart failure. And 0 study was left in the analyses studying the effect of metformin on the risk of hospitalization and the risk of heart failure vs. non-metformin therapy in T2DM patients with heart failure. Besides, the effect of metformin on cardiovascular mortality vs. non-metformin therapy in T2DM patients altered significantly (HR = 0.85, 95%CI 0.69–1.06; I2 = 78%) in the re-analysis compared to the one before deleting the data (HR = 0.83, 95%CI 0.70–0.98; I2 = 85%). This might mainly result from the long follow-up period (9 years) in the study by Romero et al. (50), suggesting that a longer follow-up period might better demonstrate the efficacy of metformin.
Publication bias
The funnel plots and the results of egger and begg tests and trim and fill analyses in Supplementary Figures 2–22 indicated no potential publication biases for the adverse outcomes.
Discussion
We included 39 subjects in this study involving 2473009 T2DM patients. We found:
(1) Metformin couldn't remarkably reduce the risk of MACEs compared to non-metformin therapy but could remarkably reduce the risk when compared with sulphonylurea in T2DM patients. (2) Metformin could significantly reduce cardiovascular mortality compared to non-metformin therapy in T2DM patients with or without heart failure or when compared with sulphonylurea in T2DM patients. (3) Metformin could significantly reduce all-cause mortality compared to non-metformin therapy, sulphonylurea, and diet therapy, and it could also significantly reduce all-cause mortality compared to non-metformin therapy in T2DM patients with heart failure or CKD. (4) Compared with non-metformin therapy, metformin was not effective in reducing the risk of heart failure in patients with T2DM, but it did reduce the risk of heart failure recurrence. Metformin was effective in reducing the risk of heart failure when compared with sulphonylurea in T2DM patients. (5) Metformin couldn't significantly reduce the risk of hospitalization compared to non-metformin therapy but could remarkably reduce the risk when compared with sulphonylurea in T2DM patients. Particularly, in patients with T2DM and heart failure, metformin can significantly reduce the risk of hospitalization. (6) Metformin couldn't remarkably reduce the risk of stroke compared to non-metformin therapy and SGLT2i in T2DM patients. (7) Metformin couldn't remarkably reduce the risk of AMI compared to non-metformin therapy in T2DM patients.
Major adverse cardiovascular events (MACEs) have different definitions in different studies. In this meta-analysis, some of the events were counted together as follows: AMI, stroke, heart failure, cardiovascular death, cardiac arrest, hospitalization, coronary angioplasty, transient ischemic attack, and unstable angina. T2DM is always related to cardiovascular complications. Since 1988, the study showed that in patients with T2DM, lowering blood glucose could reduce microvascular complications (80). There are usually exit raised levels of inflammatory cytokines among patients with T2DM. hyperglycemia and these inflammatory cytokines would harm the vascular endothelial cells, which would result in atherosclerosis in T2DM patients (81). At the same time, this condition decreases pro-angiogenic factors especially vascular endothelial growth factors and other collateral vessel growth-related parameters, which would impede collateral vessel growth (82). All of these are associated with CVD in T2DM patients to a great extent. Metformin has been thought to be protective of the cardiovascular system in the human body and here are some possible mechanisms: (I) Metformin was found to decrease cardiovascular inflammation and/or oxidative stress through activation of (AMP sensitive protein kinase) AMPK phosphorylation (83). (II)Metformin would attenuate atherosclerosis by the Inhibition of Drp1-mediated mitochondrial fission (84). However, in this meta-analysis, we found that metformin could not significantly reduce the risk of MACEs in T2DM patients. It might indicate that SGLT2i and DPP-4i have relatively the same cardiovascular protection ability as metformin. Considering the cardiovascular protection mechanism we mentioned above, it seemed to be unreasonable. And these results are opposite to some previous studies. A meta-analysis of randomized controlled trials found that metformin is significantly associated with lower risks of MACEs compared to placebo or other anti-hyperglycemic drugs among T2DM patients (85). A retrospective cohort analysis in China showed that metformin monotherapy could reduce the risk of heart failure in T2DM patients when compared with no metformin medications (59). A recent retrospective cohort analysis in Korea showed that metformin would significantly decrease the risk of AMI in all patients (54). But there also exist some studies showing the same results. Chang-Qian Wang found that metformin wasn't associated with a reduced risk of MACEs (76). A meta-analysis of 13 randomized trials showed that metformin couldn't remarkably reduce AMI and stroke (86), so there remains uncertainty about whether metformin reduces the risk of MACEs, AMI, stroke, and heart failure in patients with T2DM or not, and our included studies were limited (3 AMI studies, 3 stroke studies, and 4 MACEs studies) in this meta-analysis. More studies need to be implemented to test them.
All-cause mortality and cardiovascular mortality, which are vital living indicators in CVD patients, were found to be reduced significantly in T2DM patients with the use of metformin in this study. These results are similar to lots of previous studies (9, 85). Research showed that heart disease, cancer, stroke, and diabetes are the major causes of death in the US population (87). Metformin, as one kind of classic first-line hypoglycemic agent, has cardiovascular protection, and it could also protect against many kinds of cancers (e.g., breast, colorectal, and prostate cancer) (88). These might lead to reduced risks of all-cause and cardiovascular mortality. However, Liu et al. (19) reported that metformin vs. diet therapy was not associated with significantly lower cardiovascular mortality in T2DM patients. Dietary therapy always refers to a low carbohydrate diet or/and a low-fat diet, which is also called a low-calorie diet (89). A low-calorie diet could reduce the risk of CVD by reducing the body weight, body mass index, fat mass, and low-density lipoprotein cholesterol levels (90, 91), which may contribute to lowing cardiovascular mortality. In T2DM patients, a low-calorie diet also could normalize insulin sensitivity and improve pancreatic beta-cell function by reducing pancreatic fat content (92, 93), which may show similar function as metformin.
The risk of hospitalization can be used to evaluate the quality of life among patients with T2DM. Studies show different opinions on whether metformin is associated with reducing the risk of hospitalization. A propensity-matched study in the community showed that metformin would remarkably reduce the hospitalization rate (50). While a 2021 retrospective cohort study found that metformin could not significantly reduce the risk of hospitalization (73). In this meta-analysis, we found metformin could not significantly reduce the risk of hospitalization in T2DM patients compared to the control group. We included 8 studies without differentiating the reasons for hospitalization, which may exist some biases. More research is needed to analyze the relationship between metformin management and the risk of hospitalization divided by different diseases.
Sulphonylurea, which has been existing for approximately 70 years, is recommended as a second-line treatment in the management of type 2 diabetes (94). Many studies have testified that compared with metformin, sulphonylurea was associated with higher risks of MACEs, heart failure, hospitalization rate, all-cause, and cardiovascular mortality (14, 71, 72). In our meta-analysis, these results were proved. Therefore, it is reasonable to recommend metformin considering its benefits above. SGLT2i and DPP-4i are relatively new hypoglycemic agents. In recent studies, these two kinds of drugs show cardiovascular benefits beyond glycemic control through anti-inflammatory pathways (95, 96). In this meta-analysis, we found there existed no significantly different effect of SGLT2i or DPP-4i vs. metformin on reducing the risk of MACEs, hospitalization, stroke, and AMI in different studies. It suggests that SGLT2i and DPP-4i may have cardiovascular protective capacity comparable to metformin. However, due to the data limitation, we couldn't make related assessments and we hope more studies could be included to find some results. In this meta-analysis, we also found metformin could reduce the risk of heart failure, and hospitalization compared with non-metformin therapy in T2DM patients with heart failure, while the difference was not significant in T2DM patients, which indicated that metformin might have higher cardiovascular protection among patients with heart failure. Related research needs to be implemented to find some mechanisms.
Our results support that metformin should be recommended as a first-line hypoglycemic drug to all T2DM patients, including those with heart failure or CKD. Because it can reduce all-cause mortality and cardiovascular mortality. Dietary management is supposed to popularize among all T2DM patients since its effect on reducing all-cause mortality has no significant difference with metformin. Metformin significantly reduced MACE, heart failure, in-hospital all-cause mortality, and cardiovascular mortality compared with sulfonylureas. Thus, we have more reasons to recommend metformin as an antidiabetic drug between these two drugs. Metformin could reduce cardiovascular mortality while it couldn't reduce the risk of MACEs, heart failure, and AMI. Perhaps metformin can reduce the severity of cardiovascular events and more studies need to testify to it. The studies on the effect of metformin monotherapy on the risk of AMI, stroke, heart failure, and hospitalization are insufficient, more multicenter studies should be implemented to guide us in the use of metformin on T2DM patients better.
Limitations
Our meta-analysis still had several limitations. First, although we included observational studies in this study, we didn't include RCTs in this study and therefore more data from large RCTs were still needed to bring clarity to the effect of metformin on adverse outcomes in T2DM patients. Second, the comparison between metformin and SGLT2i or DPP-4i needs to be further explored because of limited data in our study in which only 2 studies were pooled for analysis, and there was still limited data focusing on comparing the long-term effect of metformin and SGLT2i or DPP-4i in T2DM patients, remaining an empty field for meta-analysis in the future. Third, significant heterogeneity with I2 > 50% was found in a major part of our data analyses with a random-effects model, of which the results should be explained cautiously.
Conclusions
The effect of metformin on some of the adverse outcomes was not significantly better than the non-metformin therapy or DPP-4i in T2DM patients based on observational studies.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding authors.
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The handling editor declared a shared affiliation with the authors HZ, CW, and JJ at the time of review.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2022.944902/full#supplementary-material
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Keywords: metformin, type 2 diabetes mellitus, adverse outcomes, meta-analysis, cardiovascular
Citation: Xu Z, Zhang H, Wu C, Zheng Y and Jiang J (2022) Effect of metformin on adverse outcomes in T2DM patients: Systemic review and meta-analysis of observational studies. Front. Cardiovasc. Med. 9:944902. doi: 10.3389/fcvm.2022.944902
Received: 16 May 2022; Accepted: 08 July 2022;
Published: 23 September 2022.
Edited by:
Yuling Zhang, Sun Yat-sen Memorial Hospital, ChinaReviewed by:
Zhijian He, The First Affiliated Hospital of Guangdong Pharmaceutical University, ChinaFuwei Liu, Ganzhou People's Hospital, China
Copyright © 2022 Xu, Zhang, Wu, Zheng and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhicheng Xu, 532141796@qq.com; Haidong Zhang, 1013722016@qq.com; Jingzhou Jiang, 178009867@qq.com
†These authors have contributed equally to this work