Effects of Metformin on Left Ventricular Size and Function in Hypertensive Patients with Type 2 Diabetes Mellitus: Results of a Randomized, Controlled, Multicenter, Phase IV Trial

Abstract

Background

Metformin is the most widely used oral antihyperglycemic agent for patients with type 2 diabetes mellitus (T2DM). Despite the possible benefits of metformin on diabetes mellitus (DM) and heart failure (HF), acute or unstable HF remains a precaution for its use.

Objective

The aim of the present prospective randomized controlled trial was to assess whether metformin treatment has beneficial effects on patients with T2DM with hypertension without overt HF.

Methods

A total of 164 patients (92 males, 72 females; median age 66 years) were included in this study. Patients with T2DM with a history of hypertension were randomized 1:1 to treatment for 1 year with either metformin (metformin-treated group) or other hypoglycemic agents (control group). The primary endpoints were changes in brain natriuretic peptide (BNP) levels, left ventricular (LV) mass index, and indicators of LV diastolic function. We also evaluated changes in both clinical findings and blood laboratory examination data.

Results

We observed no significant changes between baseline and 1-year post-treatment in LV mass index, BNP levels, or E/e′ (early diastolic transmitral flow velocity/early diastolic mitral annular velocity; an indicator of LV diastolic function) in either the metformin-treated (n = 83) or the control (n = 81) groups. The metformin-treated group had a significant reduction of body mass index (BMI) and low-density lipoprotein cholesterol (LDL-C), but the control group did not. We determined that renal function, including serum creatinine and estimated glomerular filtration rate, deteriorated significantly in the control group but not in the metformin-treated group.

Conclusion

LV mass and diastolic function were not affected after 1 year of metformin treatment in patients with T2DM. However, we observed benefits in terms of reductions in both BMI and LDL-C levels and preservation of renal function.

Trial Registration

UMIN000006504. Registered 7 October 2011.

Key Points

In addition to lowering blood glucose levels, metformin has been reported to exert cardio-protective effects.

One year of treatment with metformin did not affect the LV mass or diastolic function in patients with type 2 diabetes mellitus and hypertension.

Treatment with metformin was associated with a reduction of body mass index and serum LDL-C levels, and preservation of renal function.

Introduction

The prevalence of type 2 diabetes mellitus (T2DM) among patients with heart failure (HF) continues to increase, approaching 40% in recent clinical trials [1, 2]. Studies have reported that diabetes mellitus (DM) is the second most common pathology related to HF, after coronary artery disease, with a doubled risk of HF [3]. It has also been shown that HF is usually an initial manifestation of cardiovascular disease in patients with T2DM [4]. On the other hand, the severity of HF is associated with a slightly increased risk of developing DM [5].

Metformin is the most widely used oral antihyperglycemic agent in patients with T2DM. It has been shown to improve insulin sensitivity, mainly in the skeletal muscles and liver, and reduces blood glucose by decreasing gluconeogenesis in the liver. It also appears to have cardioprotective potential. Various experimental and clinical studies have demonstrated that metformin has a beneficial effect on lipid, atherosclerotic, and inflammatory profiles as well as on endothelial function [6, 7]. In dogs with pacing-induced HF, metformin also significantly reduced pulmonary capillary wedge pressure and left ventricular (LV) end-diastolic pressure versus control [8]. The mechanisms underlying these beneficial effects have been linked to the activation of 5′ adenosine monophosphate-activated protein kinase (AMPK) [9]. A recent study indicated that metformin also has AMPK-independent effects, including hepatic glucagon-signaling inhibition following decreased production of cyclic AMP [10]. Despite these possible benefits of metformin on DM and HF, Japan’s Ministry of Health, Labour and Welfare classifies HF as a contraindication to metformin therapy because of the risk of developing lactic acidosis [11]. The US FDA has removed HF as a contraindication to metformin use, but acute or unstable HF remains a precaution.

The aim of the present prospective randomized controlled trial was to assess whether metformin treatment has beneficial effects on patients with T2DM and hypertension without overt HF. To this end, we analyzed the effects of metformin on LV mass (LVM) and diastolic function in patients with T2DM with a history of hypertension.

Methods

Study Population

This multicenter, prospective, randomized controlled trial was conducted at 26 centers in Japan between September 2011 and December 2017. This trial (UMIN000006504) conformed to the Declaration of Helsinki and good clinical practice guidelines and was approved by independent ethics committees. All patients provided written informed consent before participating in trial-related activities. Key inclusion criteria were as follows: (1) patients aged 30–75 years with a history of hypertension; (2) blood pressure < 140/90 mmHg and stable for at least 1 month; (3) T2DM with glycated hemoglobin (HbA_1c) levels > 6.5% in the absence of metformin, thiazolidinediones, or insulin treatment; and (4) absence of renal dysfunction (serum creatinine < 1.3 mg/dL in males and < 1.2 mg/dL in females). Key exclusion criteria included a diagnosis of type 1 or secondary DM; severe liver dysfunction or cirrhosis; acute coronary syndrome, severe coronary heart disease (left main trunk disease or triple vessel disease); atrial fibrillation or implanted pacemaker; and shock, congestive HF, or pulmonary embolism with hypoxia. Additional exclusion criteria were as follows: a history of lactic acidosis; alcohol abuse or dehydration with gastrointestinal dysfunction; severe ketosis, diabetic coma, or pre-coma; severe infection or perioperative condition or severe trauma; malnutrition, weakness, dysfunction in pituitary or adrenal gland; history of allergic reaction to metformin; pregnancy or plans to become pregnant; and individuals recognized as inappropriate by the physician. Following initial screening, eligible patients were randomized 1:1 into one of the following groups: to be treated with metformin (metformin-treated group) or other hypoglycemic agents without metformin (control group). Both groups received therapy for 1 year. Since earlier studies have shown that thiazolidinediones affect cardiac hypertrophy [12], they were not used in this trial for either group.

Patients were allocated using a secure web response system, in accordance with the sequence from the randomization list. We adjusted the following factors as confounding for randomization: age, sex, blood pressure, and HbA_1c levels. All patients received diabetes education at enrollment and reinforcement of this throughout the study. Specifically, the latter consisted of routine clinical practice, including dietary and exercise suggestions according to Japanese guidelines. Metformin was initiated at 500 mg/day and titrated up to 2250 mg/day. If required, antihyperglycemic agents were added to the therapeutic protocol, with the exception of thiazolidinediones.

At baseline, eligible patients underwent the following procedures: physical examination, urine test (including urine albumin and creatinine concentration), and fasting blood sampling for biological measurements (including brain natriuretic peptide [BNP], liver enzyme, plasma lipids, and HbA_1c). Plasma BNP was measured with a chemiluminescent enzyme immunoassay. We also performed chest X-ray examination, electrocardiogram, and echocardiography. Similar examinations were also performed at 6 months and 1 year post-randomization.

Echocardiography

Echocardiography was performed at rest. During the test, patients were in the partial left decubitus position, and we used standard parasternal and apical views. M-mode echocardiograms of the LV chamber were recorded under two-dimensional control. We followed the recommendations of the American Society of Echocardiography in performing the measurements of the interventricular septal thickness at end-diastole (IVSd), LV end-diastolic dimension (LVEDD), and posterior wall thickness at end-diastole (PWd). LVM was measured according to the following formula:

$$\text{LVM}=0.8\left[1.04\left\{{(\text{IVSd}+\text{LVEDD}+\text{PWd})}^3\right\}\right]+0.6.$$

LVM index (LVMI) was calculated by dividing LVM with body surface area (BSA) using weight (W) and height (H), defined as follows:

$$\text{BSA}=W^{0.425}\times H^{0.725}\times 0.007184.$$

We measured the peak flow velocity of early diastole (E wave). Color tissue Doppler imaging loops were obtained in the apical four-chamber view. Peak early diastolic mitral annulus velocity (e′) was measured at the base of the septum, and the E/e′ ratio was calculated.

Definitions

The primary endpoints for the current analysis were as follows: changes in LVMI, plasma BNP levels, and echocardiographic parameters that indicate LV diastolic function, including the E/e′ ratio. Other evaluation items included clinical findings and blood laboratory examination data.

Statistical Analysis

Data are presented as numbers and percentages, mean value ± standard deviation, or median and interquartile range (IQR). We used Fisher’s exact test to compare categorical variables. Continuous two variables were compared using the Student’s t test or the Mann–Whitney U test, according to their distributions. We compared continuous three variables using repeated-measures analysis of variance (ANOVA), the Friedman test, the paired t test with Bonferroni correction, or the Wilcoxon signed-rank test with Bonferroni correction according to their distributions. We used JMP 10.0 (SAS Institute Inc, Cary, NC, USA) to perform all analyses. We considered all p values < 0.05 to be statistically significant.

Results

Baseline Characteristics

A total of 231 patients with T2DM with a history of hypertension without metformin treatment were included in the study (randomized 1:1 into metformin-treated and control groups). Serial echocardiography and BNP data were missing in 64 and 52 patients, respectively, and a further 67 patients were excluded, leaving 164 patients for analysis (see Fig. 1). As Table 1 shows, despite randomization, we observed significant differences in body mass index (BMI) within the baseline characteristics of the metformin-treated and control groups (p < 0.01).

Fig. 1.

Flow chart of study process. BNP brain natriuretic peptide, E/e′ early diastolic transmitral flow velocity/early diastolic mitral annular velocity, T2DM type 2 diabetes mellitus

Table 1.

Patients’ baseline characteristics

Characteristics	Control group	Metformin-treated group	p value
Sex, M/F	81; 46/35	83; 46/37	0.876a
Age, (years)	81; 66 (60–70)	83; 66 (61–70)	0.936b
BMI	80; 24.8 (22.8–28.4)	83; 26.8 (24.0–30.1)	0.008b
SBP	81; 129 (123–135)	83; 130 (122–138)	0.235b
DBP	81; 74.7 ± 10.5	83; 75.4 ± 9.0	0.634c
PR	81; 71.5 ± 11.6	83; 74.7 ± 11.8	0.075c
LVDd	81; 46.2 ± 4.5	83; 45.9 ± 4.6	0.693c
LVEF	81; 69.0 ± 7.9	83; 68.9 ± 6.7	0.937c
LAD	81; 38.2 ± 5.0	83; 38.7 ± 5.4	0.550c
E/e′ (septal)	81; 10.5 (9.0–13.1)	83; 10.8 (8.1–14.8)	0.781b
LVM	81; 155 (125–184)	83; 147 (127–188)	0.713b
LVMI	80; 93.4 (77.6–108.7)	83; 88.2 (75.6–108.3)	0.414b
BNP	81; 14.2 (6.9–27.2)	83; 15.8 (7.3–24.8)	0.652b
Cre	81; 0.7 (0.6–0.9)	83; 0.7 (0.6–0.8)	0.329b
eGFR	81; 73.0 (62.6–85.0)	83; 76.5 (66.2–89.2)	0.276b
TC	80; 190 (161–216)	82; 183 (165–208)	0.442b
TG	81; 124 (91–164)	83; 133 (99–197)	0.252b
HDL-C	81; 53 (46–61)	83; 51 (43–61)	0.295b
LDL-C	80; 113 (96–134)	82; 110 (96–128)	0.374b
Non-HDL-C	80; 132 (109–158)	82; 132 (113–152)	0.782b
HbA1c	81; 7.0 (6.7–7.6)	83; 7.2 (6.7–7.9)	0.167b

Data are presented as N; mean ± standard deviation and median (interquartile range) unless otherwise indicated

BMI body mass index, BNP brain natriuretic peptide, Cre creatinine, DBP diastolic blood pressure, E/e′ early diastolic transmitral flow velocity/early diastolic mitral annular velocity, eGFR estimated glomerular filtration rate, F female, HbA_1c glycated hemoglobin, HDL-C high-density lipoprotein cholesterol, LAD left atrial diameter, LDL-C low-density lipoprotein cholesterol, LVDd left ventricular diastolic diameter, LVEF left ventricular ejection fraction, LVM left ventricular mass, LVMI left ventricular mass index, M male, PR pulse rate, SBP systolic blood pressure, TC total cholesterol, TG triglyceride

^aFisher’s exact test

^bMann–Whitney U test

^cUnpaired t test

Primary Efficacy Endpoint

We observed no difference in serial changes in LVMI in both groups during the 1-year treatment period. BNP levels were significantly changed in the control group (p < 0.017) (Table 2) but were unchanged in the metformin-treated group (Table 3). Comparing BNP changes between two timepoints showed no statistical significance following Bonferroni correction in the control group (Table 3). When percentage change between baseline and 1 year in each parameter between control and metformin-treated groups was compared, no difference in changes in BNP levels was found (Table 4). E/e′, which indicates LV diastolic function, was unchanged during the treatment period in both groups.

Table 2.

Changes in primary and secondary endpoints (control group)

Endpoint	n	Baseline (time1; T1)	6 months (time2; T2)	1 year (time3; T3)	p value (time)	p value (Bonferroni correction)
						T1 vs. T2	T1 vs. T3	T2 vs. T3
BMI	80	24.8 (22.8–28.4)	24.7 (22.7–27.0)	25.2 (22.7–27.6)	0.699a	> 0.999	> 0.999	0.952b
SBP	79	129 (123–135)	130 (121–138)	131 (120–140)	0.696a	0.982	> 0.999	> 0.999b
DBP	79	75.0 ± 10.3	73.4 ± 10.1	74.1 ± 11.7	0.360c	0.429	> 0.999	> 0.999d
PR	79	71.5 ± 11.6	73.1 ± 11.6	73.4 ± 13.0	0.213c	0.496	0.349	> 0.999d
LVDd	80	46.3 ± 4.5	46.4 ± 4.9	46.3 ± 4.5	0.971c	> 0.999	> 0.999	> 0.999d
LVEF	80	68.9 ± 8.0	68.3 ± 7.1	68.3 ± 6.8	0.593c	> 0.999	> 0.999	> 0.999d
LAD	80	38.3 ± 5.0	38.2 ± 5.0	38.0 ± 4.6	0.831c	> 0.999	> 0.999	> 0.999d
E/e′ (septal)	77	10.7 (9.0–13.1)	11.4 (9.2–14.1)	11.5 (9.4–13.2)	0.200a	0.334	0.176	> 0.999b
LVM	80	156.8 (124.0–184.3)	158.8 (124.1–183.2)	158.2 (133.6–175.8)	0.857a	> 0.999	> 0.999	> 0.999b
LVMI	79	94.0 (76.9–109.3)	96.6 (82.1–108.4)	93.9 (84.6–108.6)	0.987a	> 0.999	> 0.999	> 0.999b
BNP	80	14.5 (6.8–28.1)	16.6 (9.7–28.4)	17.0 (8.7–29.2)	0.017a	0.138	0.114	> 0.999b
Cre	81	0.7 (0.6–0.9)	0.7 (0.7–0.9)	0.8 (0.7–0.9)	0.007a	0.013	0.019	> 0.999b
eGFR	81	73.0 (62.6–85.0)	69.6 (61.6–81.4)	70.4 (60.5–81.9)	0.007a	0.002	0.016	> 0.999b
TC	79	190 (161–217)	180 (163–208)	186 (159–210)	0.540a	0.359	> 0.999	0.879b
TG	81	124 (91–164)	112 (87–180)	119 (87–153)	0.634a	> 0.999	0.421	0.941b
HDL-C	81	53 (46–61)	52 (45–63)	55 (44–66)	0.331a	> 0.999	> 0.999	0.084b
LDL-C	80	113 (96–134)	108 (91.3–125.5)	113 (92–137)	0.419a	0.188	> 0.999	0.515b
Non-HDL-C	79	133 (108–158)	130 (105–148)	133 (110–153)	0.451a	0.584	> 0.999	> 0.999b
HbA1c	81	7.0 (6.7–7.6)	6.4 (6.1–7.1)	6.4 (6.0–6.9)	0.000a	0.000	0.000	> 0.999b

Data are presented as N, mean ± standard deviation and median (interquartile range) unless otherwise indicated

ANOVA analysis of variance, BMI body mass index, BNP brain natriuretic peptide, Cre creatinine, DBP diastolic blood pressure, E/e′ early diastolic transmitral flow velocity/early diastolic mitral annular velocity, eGFR estimated glomerular filtration rate, HbA_1c glycated hemoglobin, HDL-C high-density lipoprotein cholesterol, LAD left atrial diameter, LDL-C low-density lipoprotein cholesterol, LVDd left ventricular diastolic diameter, LVEF left ventricular ejection fraction, LVM left ventricular mass, LVMI left ventricular mass index, PR pulse rate, SBP systolic blood pressure, TC total cholesterol, TG triglyceride

^aThe Friedman test

^bThe Wilcoxon signed-rank test (Bonferroni correction)

^cRepeated-measures ANOVA

^dPaired t test (Bonferroni correction)

Table 3.

Changes in primary and secondary endpoints (metformin-treated group)

Endpoint	n	Baseline (time1; T1)	6 months (time2; T2)	1 year (time3; T3)	p value (time)	p value (Bonferroni correction)
						T1 vs. T2	T1 vs. T3	T2 vs. T3
BMI	78	27.2 (24.5–30.5)	26.5 (24.1–30.6)	26.1 (23.7–30.1)	0.001a	0.014	0.003	0.562b
SBP	82	131 (122–138)	131 (121–141)	134 (124–143)	0.821a	> 0.999	0.354	0.294b
DBP	82	75.5 ± 9.1	74.3 ± 9.9	75.2 ± 9.9	0.575c	0.905	> 0.999	> 0.999d
PR	80	74.8 ± 12.0	76.0 ± 11.0	75.1 ± 12.0	0.453c	0.616	> 0.999	> 0.999d
LVDd	83	45.9 ± 4.6	45.4 ± 5.5	45.6 ± 4.8	0.470c	0.759	> 0.999	> 0.999d
LVEF	83	68.9 ± 6.7	69.3 ± 7.0	68.9 ± 6.4	0.763c	> 0.999	> 0.999	> 0.999d
LAD	83	38.7 ± 5.4	38.8 ± 5.1	38.5 ± 5.3	0.655c	> 0.999	> 0.999	> 0.999d
E/e′ (septal)	81	10.8 (8.1–14.7)	11.5 (9.2–15.0)	10.9 (9.4–14.0)	0.013a	0.119	0.962	0.482b
LVM	83	146.8 (127.1–188.4)	147.8 (128.0–188.0)	149.9 (127.8–188.0)	0.701a	> 0.999	> 0.999	> 0.999b
LVMI	78	88.4 (76.9–108.6)	88.8 (76.8–107.7)	88.7 (76.4–104.4)	0.905a	> 0.999	> 0.999	> 0.999b
BNP	82	15.7 (7.2–23.9)	15.4 (7.7–29.0)	15.8 (8.8–28.9)	0.520a	0.100	0.064	> 0.999b
Cre	83	0.7 (0.6–0.8)	0.7 (0.6–0.9)	0.7 (0.6–0.8)	0.627a	0.727	> 0.999	0.407b
eGFR	83	76.5 (66.2–89.2)	76.9 (62.8–87.4)	76.3 (63.6–89.3)	0.627a	0.478	> 0.999	0.486b
TC	82	183 (165–208)	174 (156–196)	180 (161–200)	0.059a	0.039	0.417	0.650b
TG	83	133 (99–197)	132 (88–191)	130 (104–188)	0.918a	> 0.999	> 0.999	> 0.999b
HDL-C	83	51 (43–61)	50 (43–60)	51 (44–63)	0.167a	> 0.999	0.445	0.609b
LDL-C	81	110 (96–129)	96 (82–115)	103 (86–122)	0.000a	0.000	0.027	0.063b
Non-HDL-C	82	132 (113–152)	120 (101–144)	125 (107–146)	0.012a	0.035	0.153	> 0.999b
HbA1c	82	7.2 (6.7–7.9)	6.4 (6.0–6.9)	6.4 (6.2–7.1)	0.000a	0.000	0.000	> 0.999b

Data are presented as N, mean ± standard deviation and median (interquartile range) unless otherwise indicated

ANOVA analysis of variance, BMI body mass index, BNP brain natriuretic peptide, Cre creatinine, DBP diastolic blood pressure, E/e′ early diastolic transmitral flow velocity/early diastolic mitral annular velocity, eGFR estimate glomerular filtration rate, HbA_1c glycated hemoglobin, HDL-C high-density lipoprotein cholesterol, LAD left atrial diameter, LDL-C low-density lipoprotein cholesterol, LVDd left ventricular diastolic diameter, LVEF left ventricular ejection fraction, LVM left ventricular mass, LVMI left ventricular mass index, PR pulse rate, SBP systolic blood pressure, TC total cholesterol, TG triglyceride

^aThe Friedman test

^bThe Wilcoxon signed-rank test (Bonferroni correction)

^cRepeated-measures ANOVA

^dPaired t test (Bonferroni correction)

Table 4.

Percent changes of primary and secondary endpoints 1 year post-treatment with or without metformin

Endpoint (%)	Control group	Metformin-treated group	p value
BMI	80; 0.6 (− 2.2 to 2.8)	79; − 1.9 (− 4.6 to 1.5)	0.006a
SBP	80; 0.7 (− 7.8 to 10.6)	82; 1.1 (− 6.3 to 12.5)	0.685a
DBP	80; − 0.4 ± 13.7	82; 0.7 ± 15.6	0.654b
PR	80; 3.5 ± 13.8	82; 1.7 ± 12.8	0.407b
LVDd	81; 0.42 ± 7.47	83; − 0.46 ± 8.80	0.492b
LVEF	81; − 0.2 ± 10.3	83; 0.5 ± 10.3	0.642b
LAD	81; 0.1 ± 10.4	83; 0.0 ± 9.9	0.945b
E/e′ (septal)	81; 2.7 (− 7.5 to 25.5)	83; 5.1 (− 15.8 to 19.3)	0.611a
LVM	81; 0.0 (− 9.7 to 14.8)	83; 0.0 (− 13.4 to 12.2)	0.343a
LVMI	80; 0.6 (− 9.4 to 13.3)	79; 0.4 (− 12.0 to 13.0)	0.608a
BNP	81; 13.3 (− 23.0 to 65.5)	83; 0.0 (− 19.6 to 76.7)	0.951a
Cre	81; 2.9 (− 3.0 to 10.3)	83; 0.0 (− 5.6 to 8.9)	0.142a
eGFR	81; − 3.0 (− 10.2 to 3.4)	83; 0.0 (− 8.9 to 6.5)	0.142a
TC	79; − 1.1 (− 8.4 to 7.5)	82; − 2.5 (− 14.0 to 9.0)	0.420a
TG	81; − 3.9 (− 30.8 to 26.3)	83; 0.0 (− 22.1 to 26.3)	0.387a
HDL-C	81; 1.7 (− 6.4 to 9.0)	83; 3.8 (− 8.3 to 14.5)	0.497a
LDL-C	80; − 3.1 (− 10.7 to 10.3)	81; − 5.4 (− 23.1 to 4.4)	0.139a
Non-HDL-C	79; − 0.8 (− 7.7 to 7.1)	82; − 4.2 (− 17.5 to 7.3)	0.238a
HbA1c	81; − 8.2 (− 13.0 to − 1.5)	82; − 9.1 (− 17.1 to − 4.5)	0.083a

Data are presented as N; mean ± standard deviation and median (interquartile range) unless otherwise indicated

BMI body mass index, BNP brain natriuretic peptide, Cre creatinine, DBP diastolic blood pressure, E/e′ early diastolic transmitral flow velocity/early diastolic mitral annular velocity, eGFR estimate glomerular filtration rate, HbA_1c glycated hemoglobin, HDL-C high-density lipoprotein cholesterol, LAD left atrial diameter, LDL-C low-density lipoprotein cholesterol, LVDd left ventricular diastolic diameter, LVEF left ventricular ejection fraction, LVM left ventricular mass, LVMI left ventricular mass index, PR pulse rate, SBP systolic blood pressure, TC total cholesterol, TG triglyceride

^aUnpaired t test

^bMann–Whitney U test

Other Evaluation Data

Over the study period, the median HbA_1c significantly reduced in both groups (p < 0.001). Of note, the median BMI was significantly reduced only in the metformin-treated group (p = 0.001). A post-hoc analysis of the Friedman test indicated that BMI changes were statistically significant between the baseline versus 6 months and baseline versus 1 year, even after Bonferroni correction. When comparing percentage change between baseline and 1 year in each parameter, only BMI was significantly reduced in the metformin-treated versus the control group (p < 0.01). We observed that serum creatinine and estimated glomerular filtration rate (eGFR) levels were significantly changed in the control group (p < 0.0074 for creatinine; p < 0.0074, for eGFR) (Table 2) but not in the metformin-treated group (Table 3). A comparison of changes in creatinine and eGFR between two time points showed a statistically significant difference between baseline versus 6 months and baseline versus 1 year in the control group. Conversely, low-density lipoprotein cholesterol (LDL-C) and non-high-density lipoprotein cholesterol (HDL-C) levels were significantly changed in the metformin-treated group (p < 0.00016 for LDL-C; p < 0.0012 for non-HDL-C) (Table 3). However, no changes were found in the control group. Comparing changes in LDL-C between the two time points identified a significant reduction between baseline and 6 months and between baseline and 1 year. The reduction in non-HDL-C was significant only between baseline and 6 months. Comparing percentage change between baseline and 1 year in each parameter between control and metformin-treated groups showed no changes in creatinine, eGFR, LDL-C, or non-HDL-C (Table 4). Mean metformin doses at 6 months and 1 year were 857 and 909 mg/day, respectively. Table 5 summarizes the changes of metformin doses. Oral hypoglycemic agents used at baseline included sulfonylureas, dipeptidyl peptidase-4 (DPP-4) inhibitors, and α-glucosidase inhibitors (Table 5). Tables 6, 7 and 8 summarize the serial changes of other medications. No differences were observed in the use of lipid-lowering agents between the two groups in the course of the treatment period.

Table 5.

Changes in metformin doses

Metformin dose (mg)	6 months (time2)	1 year (time3)	p valuea
250	2 (2.44)	2 (2.44)	0.040636
500	33 (40.2)	27 (32.9)
750	16 (19.5)	20 (24.4)
1000	11 (13.4)	10 (12.2)
1250	1 (1.22)	1 (1.22)
1500	18 (22.0)	20 (24.4)
2000	1 (1.22)	1 (1.22)
2250	0 (0)	1 (1.22)

Data are presented as n (%) unless otherwise indicated

^aThe Wilcoxon signed-rank test

Table 6.

Other medications at baseline

Medications	Control group	Metformin-treated group	p valuea
Oral hypoglycemic agents
Sulfonylureas	32 (39.5)	22 (26.5)	0.0967
DPP-4 inhibitor	47 (58.0)	29 (34.9)	0.0047
GLP-1 receptor agonist	0 (0.0)	0 (0.0)	–
α-Glucosidase inhibitor	23 (28.4)	14 (16.9)	0.0936
Lipid-lowering agents
Statins	46 (56.8)	54 (65.1)	0.3371
Ezetimibe	1 (1.2)	4 (4.8)	0.3675
Antihypertensive agents
Angiotensin II receptor antagonists	38 (46.9)	43 (51.8)	0.5371
Angiotensin-converting enzyme inhibitors	7 ((8.6)	7 (8.4)	> 0.999
Aldosterone antagonists	3 (3.7)	1 (1.2)	0.3643
Calcium channel inhibitors	50 (61.7)	52 (62.7)	> 0.999
β-Blockers	18 (22.2)	14 (16.9)	0.4341
Others	9 (11.1)	12 (14.5)	0.6417

Data are presented as n (%) unless otherwise indicated

DPP-4 dipeptidyl peptidase-4, GLP-1 glucagon-like peptide-1

^aFisher’s exact test

Table 7.

Other medications at 6 months

Medications	Control group	Metformin-treated group	p valuea
Oral hypoglycemic agents
Sulfonylureas	32 (39.5)	21 (25.3)	0.0662
DPP-4 inhibitor	58 (71.6)	30 (36.1)	0.0000
GLP-1 receptor agonist	0 (0.0)	0 (0.0)	–
α-Glucosidase inhibitor	27 (33.3)	15 (18.1)	0.0317
Lipid-lowering agents
Statins	46 (56.8)	54 (65.1)	0.3371
Ezetimibe	1 (1.2)	4 (4.8)	0.3675
Antihypertensive agents
Angiotensin II receptor antagonists	38 (46.9)	42 (50.6)	0.6433
Angiotensin-converting enzyme inhibitors	7 (8.6)	9 (10.8)	0.7936
Aldosterone antagonists	4 (4.9)	1 (1.2)	0.2073
Calcium channel inhibitors	54 (66.7)	53 (63.9)	0.7447
β-Blockers	18 (22.2)	13 (15.7)	0.3223
Others	9 (11.1)	12 (14.5)	0.6417

Data are presented as n (%) unless otherwise indicated

DPP-4 dipeptidyl peptidase-4, GLP-1 glucagon-like peptide-1

^aFisher’s exact test

Table 8.

Other medications at 1 year

Medication	Control group	Metformin-treated group	p valuea
Oral hypoglycemic agents
Sulfonylureas	32 (39.5)	21 (25.3)	0.0662
DPP-4 inhibitor	57 (70.4)	30 (36.1)	0.0000
GLP-1 receptor agonist	0 (0.0)	0 (0.0)	–
α-Glucosidase inhibitor	27 (33.3)	16 (19.3)	0.0509
Lipid-lowering agents
Statins	48 (59.3)	56 (67.5)	0.3311
Ezetimibe	2 (2.5)	4 (4.8)	0.6818
Antihypertensive agents
Angiotensin II receptor antagonists	38 (46.9)	42 (50.6)	0.6433
Angiotensin-converting enzyme inhibitors	7 (8.6)	9 (10.8)	0.7936
Aldosterone antagonists	4 (4.9)	1 (1.2)	0.2073
Calcium channel inhibitors	55 (67.9)	55 (66.3)	0.8689
β-Blockers	18 (22.2)	13 (15.7)	0.3223
Others	10 (12.3)	10 (12.0)	> 0.999

Data are presented as n (%) unless otherwise indicated

DPP-4 dipeptidyl peptidase-4, GLP-1 glucagon-like peptide-1

^aFisher’s exact test

Discussion

The main finding of this study was that 1 year of metformin treatment in patients with T2DM did not affect LVM or LV diastolic function versus treatments with other hypoglycemic agents. However, it significantly reduced BMI and LDL-C levels and preserved renal function.

Metformin is an oral hypoglycemic drug of the biguanide class that lowers blood glucose levels by decreasing hepatic glucose production and improving the insulin sensitivity of the peripheral tissues by increasing glucose uptake. It is currently used as a first-line treatment for T2DM. The drug is recommended during all stages of therapy as monotherapy and in combination with other oral antihyperglycemic drugs as well as insulin. Such guidelines are due to its low cost, safety, and association with a reduction in the risk of cardiovascular events [13–15].

T2DM is an independent risk factor for cardiovascular disease and is associated with a higher incidence of HF, as first reported in the Framingham study [16]. The risk of HF in patients with T2DM is almost two times higher for men and five times higher for women than in the general population, and patients with T2DM account for one-third of all HF cases [17]. However, concerns regarding the development of lactic acidosis with the use of phenformin led the US FDA to apply a black box warning to metformin cautioning against using it in the setting of chronic kidney disease because of possible impaired drug excretion. It also recommended caution in patients with conditions that may promote lactate accumulation. Examples of the latter include congestive HF and chronic liver disease. The FDA has removed congestive HF as a contraindication to metformin use. However, acute or unstable congestive HF remains a precaution. In Japan, to date, HF is classified as a contraindication to metformin therapy because of the risk of lactic acidosis [11]. Therefore, we aimed to verify the effects of metformin on cardiac morphology and function in patients with hypertension who were at risk for HF development.

Our study showed no clear changes in the indicators of LV diastolic function and LVM. There are various reasons for not having proved our working hypothesis. First, the previously observed effects of metformin on the reduction of cardiovascular events differ from the prevention of cardiac hypertrophy and/or diastolic dysfunction observed in the early phase of hypertension. Several events are associated with HF development, and additional factors may be associated with metformin treatment. Second, the use of DPP-4 inhibitors increased in the control group over the treatment period. Several reports have shown beneficial effects from DPP-4 inhibitors on cardiac hypertrophy in animal experiments. They act by suppressing sodium-proton pump exchanger type 1 or insulin-like growth factor-I [18, 19]. However, several clinical studies have reported that the use of DDP-4 inhibitors was associated with worsening of HF [20]. A meta-analysis [21] of randomized controlled trials investigating the effects of hypoglycemic agents on LVM recently showed that gliclazide was the only medication to significantly reduce LVM in patients with T2DM. Additionally, metformin exhibited negative effects on the prevention of cardiac hypertrophy. Our results are in line with this report. Sodium–glucose co-transporter 2 (SGLT2) inhibitors have proven effective in reducing HF hospitalization in patients with DM, and glucagon-like peptide-1 (GLP-1) receptor agonists are beneficial for patients with ischemic heart disease [22, 23]. However, GLP-1 receptor agonists were not used in either of our groups in this study. The use of SGLT2 inhibitors had not been approved by the Japan Ministry of Health, Labor, and Welfare when this study was conducted.

We observed several beneficial effects of metformin in our study population. Like previous reports, we observed a significant decrease in BMI following metformin treatment, and its effect was more evident in the first 6 months of treatment [24–26]. A possible explanation for this effect is the higher usage of sulfonylureas in the control group than in the metformin-treated group. However, other explanations for the mechanisms of metformin-induced weight loss may be considered. An earlier study suggested that metformin reduces weight by affecting appetite signals in the brain, fat oxidation, and fat storage in the liver [27]. An additional report suggested that metformin-induced weight loss, secretion of GLP-1 and peptide YY, and increases in conjugated bile acid are associated with alterations of the gut microbiota [28, 29].

Renal function in the control group deteriorated during the 1-year study but was unchanged in the metformin-treated group. Uncertainty remains about the underlying mechanisms. Recently published data support the use of metformin in patients with renal diseases [30]. An analysis by the REACH (Reduction of Atherothrombosis for Continued Health) registry suggested that the proposed cardiovascular benefits of metformin may include patients with established atherosclerosis and moderate chronic kidney disease [31]. However, the abovementioned reports do not support the hypothesis of a renoprotective effect. Metformin has previously been shown to attenuate renal fibrosis in both AMPKα2-dependent and -independent manners [32]. In our study group, kidney function may have been preserved by such antifibrotic effects. Hypertension causes renal damage, which in turn further increases blood pressure. Consequently, patients with DM and hypertension may be good candidates for metformin treatment.

In the metformin-treated group, LDL-C significantly decreased in the study period. This was more evident during the first half of the study than the last. It has been recently shown in patients with T2DM that metformin treatment reduces the levels of three acyl-alkyl-phosphatidylcholine metabolites [33]. The reduction of LDL-C levels may be due to such changes in metabolic profiles. The latter is most likely induced by metformin-induced activation of AMPK and consequent suppression of sterol regulatory element-binding protein 1c (SREBP1c) and fatty acid desaturation [33]. These findings suggest that metformin may have a beneficial effect on lipid metabolism for the prevention of atherosclerosis in patients with hypertension.

The present study has several limitations. First, our protocol set the target sample size at 440 patients (UMIN000006504). We assumed the annual LV weight reduction with metformin treatment would be 6 g [34]. To determine the superiority of these values with 80% power and a two-sided overall significance level of 5% required 185 patients per arm. To allow for a loss-to-follow-up rate of 15%, we determined that we would need to enroll 220 patients in each study arm. However, slow recruitment meant we only recruited 231 patients, which reduced the power of this trial. Second, our findings are subject to confounding factors because the two study groups had different BMI values at baseline. Finally, the metformin dose was relatively small compared with that used in other countries, which may have limited the effects of metformin.

Conclusion

Treatment of patients with T2DM with metformin did not affect LVM or LV diastolic function versus treatments with other hypoglycemic agents over the course of 1 year. However, metformin reduced BMI, lowered LDL-C, and preserved renal function.

Author Contributions

Conception and design: KO and KH; Analysis and interpretation of the data: KO, HW, NA, HI, KU, JF, AO, TH, MF, AS, and KH; Drafting of the article: KO and KH. Statistical expertise: KH; Collection and assembly of data: KO, HW, NA, HI, KU, JF, AO, TH, MF, AS, and KH. All authors read and approved the final manuscript.

Compliance with Ethical Standards

Ethics Approval and Consent to Participate

This study was approved by the institutional review board of each institute.

Consent for Publication

Not applicable.

Availability of Data and Material

The datasets used or analyzed during the current study are available from the corresponding author on reasonable request.

Conflict of interest

Koh Ono, Hiromichi Wada, Noriko Satoh-Asahara, Hitoki Inoue, Keita Uehara, Junichi Funada, Atsushi Ogo, Takahiro Horie, Masatoshi Fujita, Akira Shimatsu, and Koji Hasegawa have no conflicts of interest that are directly relevant to the content of this article.

Funding

This work was supported by Grants to KO and KH for a large-scale clinical study for the promotion of evidence-based medical practices by the National Hospital Organization.