Comparison of the Effects of Various Antidiabetic Medication on Bone Mineral Density in Patients with Type 2 Diabetes Mellitus.

BACKGROUND: Prospective comparative studies on the effects of various antidiabetic agents on bone metabolism are limited. This study aimed to assess changes in bone mass and biochemical bone markers in postmenopausal patients with type 2 diabetes mellitus (T2DM).
METHODS: This prospective, multicenter, open-label, comparative trial included 264 patients with T2DM. Patients who had received a metformin, or sulfonylurea/metformin combination (Group 1); a thiazolidinedione combination (Group 2); a dipeptidyl peptidase-4 inhibitor (gemigliptin) combination (Group 3); or an sodium-glucose cotransporter 2 inhibitor (empagliflozin) combination (Group 4) were prospectively treated for 12 months; bone mineral density (BMD) and bone turnover marker (BTM) changes were evaluated.
RESULTS: The femoral neck BMD percentage changes were -0.79%±2.86% (Group 1), -2.50%±3.08% (Group 2), -1.05%±2.74% (Group 3), and -1.24%±2.91% (Group 4) (P<0.05). The total hip BMD percentage changes were -0.57%±1.79% (Group 1), -1.74%±1.48% (Group 2), -0.75%±1.87% (Group 3), and -1.27%±1.72% (Group 4) (P<0.05). Mean serum BTM (C-terminal type 1 collagen telopeptide and procollagen type 1 amino-terminal propeptide) levels measured during the study period did not change over time or differ between groups.
CONCLUSION: Significant bone loss in the femoral neck and total hip was associated with thiazolidinedione combination regimens. However, bone loss was not significantly associated with combination regimens including gemigliptin or empagliflozin. Caution should be exercised during treatment with antidiabetic medications that adversely affect the bone in patients with diabetes at a high risk of bone loss.

INTRODUCTION

Osteoporosis is defined as low bone mass and microarchitectural bone deterioration leading to increased bone fragility and fracture susceptibility [1]. Osteoporosis is a systemic skeletal disease that progresses gradually, and as the elderly population increases, the worldwide prevalence and associated socioeconomic burden are rising [2-4].

Bone is an important target organ subject to diabetic complications, and there is increasing evidence of a link between diabetes and osteoporosis. Type 1 diabetes is an important secondary cause of osteoporosis and is characterized by lower bone mass and higher fracture than those observed in the healthy population [5]. In patients with type 2 diabetes mellitus (T2DM), the bone mineral density (BMD) of the lumbar spine and hip was found to be normal or even higher than that of healthy subjects, and the results were consistent even after adjusting for age, sex, ethnicity, and body mass index [6,7]. However, the risk of fragility fractures is higher in patients with T2DM. An increased risk of fracture in patients with T2DM is associated with the duration of diabetes, the presence of diabetes complications, the type of antidiabetic medication, or frequent falls [5,7,8]. In the Women’s Health Initiative Observational Study, women with T2DM were at increased risk for fractures despite BMD being increased; this result remained consistent even after adjustment for multiple risk factors for fracture [8].

Some antidiabetic medications are known to increase fractures in patients with diabetes. According to the Diabetes Outcome Progression Trial (ADOPT), fractures were more common in patients treated with a peroxisome proliferator-activated receptor γ agonist than in the patients treated with metformin or glyburide [9]. Recent data from a randomized phase 3 study suggest that canagliflozin, a sodium-glucose cotransporter 2 inhibitor (SGLT2i), lowers BMD and increases fracture risk compared with the respective outcomes in the placebo group [10]. However, other SGLT2i, dapagliflozin or empagliflozin, did not report a decrease in bone density or an increase in fractures [11]. Alternatively, metformin and sulfonylurea have a neutral effect on bone, while incretin-based treatments may have a positive effect [5]. Most studies to date have performed comparisons with placebo or between single drugs; however, in practice, it is more common to combine multiple antidiabetic agents with different mechanisms to lower blood glucose than to administer a single agent. Moreover, data on the effects of gemigliptin and empagliflozin on bone metabolism in real practice are limited. Therefore, in this prospective study, patients who had previously been treated with various regimens of oral combination therapy were divided into groups, changes in bone mass and bone markers were prospectively observed for 12 months, and differences between groups were compared.

METHODS

Patients and sample collection

We conducted a prospective, multicenter, open-label, comparative study to determine the effects of antidiabetic medications on bone metabolism in patients with T2DM. The study flow for study subject evaluation is depicted in Fig. 1. Subjects with T2DM who had previously been treated with metformin monotherapy or combination metformin/sulfonylurea were divided into four groups (n=227): Group 1, continued metformin monotherapy or combination metformin/sulfonylurea (n=52); Group 2, addition of thiazolidinedione (TZD) (n=60); Group 3, addition of dipeptidyl peptidase-4 inhibitor (DPP4i) (n=61); and Group 4, addition of SGLT2i (n=54). BMD and bone turnover markers (BTMs) were prospectively observed for 12 months (Fig. 1). After exclusion, a total of 193 subjects (45 subjects in Group 1, 47 subjects in Group 2, 53 subjects in Group 3, and 48 subjects in Group 4) were eligible for the analysis (Fig. 1). The type and dosage of medications were determined according to the physician’s clinical discretion. Subjects with other underlying diseases that would affect bone metabolism were excluded from the enrollment. Subjects were excluded if they were treated with any of the following drugs: corticosteroid, anticonvulsants, thyroid hormones, aromatase inhibitors, bisphosphonates, estrogen or selective estrogen receptor modulator, parathyroid hormone (PTH), teriparatide, or denosumab. For sulfonylureas, glimepiride was employed, with daily doses between 0.5 and 2 mg. Daily metformin titration ranged from 500 to 1,500 mg, depending on the physician’s discretion. Among TZDs, pioglitazone accounted for 76.6% and lobeglitazone accounted for 23.4%. Gemigliptin 50 mg was administered as a DPP4i, and empagliflozin 10 or 25 mg was administered as an SGLT2i. All study subjects received calcium and vitamin D supplements, with the aim of maintaining serum 25-hydroxyvitamin D levels ≥20 ng/mL. Performing moderate-intensity exercise for 150 minutes per week was recommended to all study participants. For the analysis, patients in each group were prospectively observed for 12 months, and changes in BMD and biochemical markers, including BTMs, were evaluated. BMD was measured at baseline and 12 months. Subjects’ body weight and height were simultaneously measured while measuring BMD. Blood was sampled between 7:00 AM and 9:00 AM after 8 hours of overnight fasting to evaluate serum glucose, calcium, phosphorus, creatinine, albumin, PTH, 25-hydroxyvitamin D, total procollagen type 1 amino-terminal propeptide (P1NP), and C-terminal type 1 collagen telopeptide (CTx). Biochemical testing, except BTM measurement, was performed five times during the study period: at baseline, 3, 6, 9, and 12 months. BTM was measured three times: at baseline, between 3 and 6 months of the study, and between 9 and 12 months of the study. Serum calcium was corrected for changes in serum albumin concentration according to the following formula: corrected calcium (mg/dL)=actual calcium+(4–serum albumin)×0.8. As a part of standard care monitoring, glycated hemoglobin (HbA1c) and fasting serum glucose were measured at every follow-up to provide a standard of care for patients with diabetes. This study protocol was reviewed and approved by the Institutional Review Board of Yeouido St. Mary’s Hospital (Seoul, Korea), and all patients signed an informed consent form before entering the study (XC16OIMI0031S).

Fig. 1

Enrollment, randomization, and follow-up of participants. T2DM, type 2 diabetes mellitus; DPP4i, dipeptidyl peptidase-4 inhibitor; SGLT2i, sodium-glucose cotransporter 2 inhibitor.

Assays

Serum calcium, phosphorus, albumin, and creatinine levels were determined using an autoanalyzer (747 automatic analyzer, Hitachi, Tokyo, Japan). HbA1c levels were measured using high-performance liquid chromatography (HLC-723G7, Tosoh, Tokyo, Japan). Serum P1NP (Elecsys total P1NP, Roche Diagnostics, Rotkreuz, Switzerland), CTx (Elecsys B-CrossLaps, Roche Diagnostics), and PTH (intact PTH, Elecsys PTH, Roche Diagnostics) concentrations were determined in duplicate using an ECLIA (Cobas e 801, Roche Diagnostics). 25-Hydroxyvitamin D (Access 25(OH) Vitamin D Total DXI reagent, Beckman Coulter Inc., Brea, CA, USA) was measured using a UniCel DxI 800 Immunoassay Analyzer (Beckman Coulter Inc.). The maximum inter- and intra-assay coefficients of variation (CVs) for the range of concentrations evaluated were 4.1% and 2.6% for P1NP and 6.5% and 3.6% for CTx. The manufacturer suggested a reference range for CTx in postmenopausal women <1.008 ng/mL and a reference range for P1NP in postmenopausal women without postmenopausal hormone replacement therapy of 20.25 to 76.31 ng/mL.

BMD measurement

The BMD of the lumbar spine (lumbar vertebrae L1–L4), femoral neck, and total hip were measured by dual-energy X-ray absorptiometry using a Hologic Delphi W (Hologic Inc., Bedford, MA, USA) at baseline and after 12 months. The CV was determined to be 1.2% at the lumbar spine and 1.9% at the femoral neck. The BMD measurement was performed by one technician with >10 years of experience. To properly control the quality of bone density measurement, our institution performed quality control for the bone density equipment and the bone density tester according to the protocol.

Statistical analysis

All data were analyzed using SPSS version 20.0 for Windows (IBM Co., Armonk, NY, USA). The data are presented as the mean±standard deviation, unless otherwise stated. Graphics were produced using GraphPad Prism version 5.0 (GraphPad Software Inc., San Diego, CA, USA). In the evaluation of clinical features, we used the chi-square test for analysis of categorical variables and Student’s t test for the analysis of continuous variables. The mean percentage changes for BMD and other biochemical markers from baseline were analyzed using repeated measures analysis of variation (ANOVA) and Dunnett’s method, if appropriate. P values <0.05 were considered to represent statistically significant results for all comparisons.

RESULTS

Baseline characteristics

Clinical characteristics at baseline are summarized in Table 1. The subjects were postmenopausal women with a mean age of 66.5±7.1 years and experienced menopause an average of 16.1± 8.0 years prior. There was no difference between the four groups in regard to age, years after menopause, or body mass index. The mean duration of diabetes was 10.4±7.9 years, with Group 1 having the shortest duration at 8.0±6.5 years, but there was no significant difference among the groups. The mean baseline HbA1c level was 6.5%±0.6%, without significant differences among groups. The baseline BMD was 0.942±0.132 for the lumbar spine, 0.790±0.104 for the femoral neck, and 0.887±0.120 for the total hip, and T-score at baseline was −1.6±1.1. There was no significant difference in the T-score or BMD at baseline for all measurement sites among the groups. In addition, detailed information on the prescription patterns of each group is provided in Table 2. In each group, a dual combination with metformin was the most commonly prescribed combination.

Table 1

Baseline Characteristics of the Study Population by Group

Characteristic	Total (n=193)	Group 1 (n=45)	Group 2 (n=47)	Group 3 (n=53)	Group 4 (n=48)	P value
Age, yr	66.5±7.1	65.4±7.0	65.9±7.0	67.9±7.2	66.5±7.0	0.309
Years since menopause	16.1±8.0	17.1±9.4	15.5±7.2	17.4±8.6	14.1±6.4	0.277
Height, cm	153.2±12.0	153.4±4.9	153.7±4.8	151.6±3.6	154.5±4.4	0.640
Weight, kg	60.0±7.8	59.8±7.2	60.5±8.2	59.4±8.2	60.5±7.4	0.473
Body mass index, kg/m2	25.3±3.0	25.7±3.0	25.6±3.1	24.9±3.1	25.4±2.8	0.321
Diabetes duration, yr	10.4±7.9	8.0±6.5	11.5±7.7	11.5±7.7	10.5±9.2	0.820
Glycated hemoglobin, %	6.5±0.6	6.5±0.5	6.5±0.6	6.4±0.5	6.6±0.6	0.184
Previous clinical fracture	16 (8.3)	4 (8.9)	3 (6.4)	5 (9.4)	4 (8.3)	0.439
T-score
Lumbar spine	−1.6±1.1	−1.8±1.1	−1.7±1.2	−1.7±1.0	−1.3±1.1	0.199
Femoral neck	−1.3±0.9	−1.3±1.0	−1.3±0.8	−1.3±0.9	−1.2±0.8	0.959
Total hip	−0.7±1.0	−0.8±1.1	−0.8±1.0	−0.8±1.0	−0.6±0.9	0.719
BMD, g/cm2
Lumbar spine	0.942±0.132	0.928±0.129	0.932±0.142	0.932±0.127	0.977±0.131	0.226
Femoral neck	0.790±0.104	0.790±0.121	0.790±0.095	0.784±0.103	0.795±0.100	0.953
Total hip	0.887±0.120	0.881±0.126	0.883±0.120	0.883±0.120	0.905±0.112	0.681
Serum CTx, ng/mL	0.44±0.20	0.44±0.22	0.42±0.17	0.43±0.20	0.49±0.22	0.385
Serum P1NP, ng/mL	47.2±16.6	49.1±16.7	45.3±11.8	45.2±15.3	49.5±21.9	0.509
Serum 25-hydroxyvitamin D, ng/mL	25.9±7.5	25.8±6.6	25.4±9.3	26.0±7.2	26.4±6.8	0.928
Serum calcium, mg/dL	9.2±0.4	9.2±0.4	9.1±0.3	9.2±0.4	9.2±0.4	0.510
Serum creatinine, mg/dL	0.67±0.16	0.63±0.14	0.74±0.23	0.67±0.13	0.65±0.14	0.097

Values are expressed as mean±standard deviation or number (%). Group 1, metformin or metformin/sulfonylurea combination; Group 2, thiazolidinedione with metformin and/or sulfonylurea combination; Group 3, dipeptidyl peptidase-4 inhibitor (gemigliptin) with metformin and/or sulfonylurea combination; Group 4, sodium-glucose cotransporter 2 inhibitor (empagliflozin) with metformin and/or sulfonylurea combination.

BMD, bone mineral density; CTx, C-terminal telopeptides of type I collagen; P1NP, total procollagen type 1 amino-terminal propeptide.

Table 2

Prescription Patterns of Antidiabetic Medications in Each Group

	Patterns	No. (%)
Group 1 (n=45)	Metformin+Sulfonylurea	41 (91.1)
	Metformin monotherapy	4 (8.9)
Group 2 (n=47)	Metformin+Thiazolidinedione	38 (80.9)
	Metformin+Thiazolidinedione+Sulfonylurea	9 (19.1)
Group 3 (n=53)	Metformin+DPP4i	43 (81.1)
	Metformin+DPP4i+Sulfonylurea	10 (18.9)
Group 4 (n=48)	Metformin+SGLT2i	38 (79.2)
	Metformin+SGLT2i+Sulfonylurea	10 (20.8)

Group 1, metformin or metformin/sulfonylurea combination; Group 2, thiazolidinedione with metformin and/or sulfonylurea combination, pioglitazone accounted for 76.6% and lobeglitazone accounted for 23.4%; Group 3, DPP4i (gemigliptin) with metformin and/or sulfonylurea combination; Group 4, SGLT2i (empagliflozin) with metformin and/or sulfonylurea combination.

DPP4i, dipeptidyl peptidase-4 inhibitor; SGLT2i, sodium-glucose cotransporter 2 inhibitor.

Changes in BMD

The percentage changes in BMD from baseline to 12 months were analyzed according to groups (Table 3, Fig. 2). The lumbar spine BMD reduction was found to be the highest in the SGLT2i group (Group 4) (−1.28%±2.65%), despite not exhibiting a significant decrease compared to baseline (P=0.314) or a statistically significant difference among groups (P=0.265). The decrease in femoral neck BMD in the TZD group (Group 2) at 12 months was found to be significant compared to the baseline value (−2.50%±3.08%, P=0.015), and the reduction was also significant in comparison with the other three groups (P=0.012). For the total hip, BMD decreased significantly from baseline at 12 months in the TZD group (Group 2) (−1.74%±1.48%, P= 0.046) and was also significantly different from sulfonylurea group (Group 1) (P=0.007) and the DPP4i group (Group 3) (P=0.024) but not from the SGLT2i group (Group 4) (P=0.638).

Table 3

Difference in Percentage Changes of Bone Mineral Density from Baseline to 12 Months between Groups

	Lumbar spine, %	Femoral neck, %	Total hip, %
Group 1	−0.24±2.32	−0.79±2.86	−0.57±1.79
Group 2	−1.00±2.94	−2.50±3.08a	−1.74±1.48b
Group 3	−0.62±2.50	−1.05±2.74	−0.75±1.87
Group 4	−1.28±2.65	−1.24±2.91	−1.27±1.72

Values are expressed as mean±standard deviation. Group 1, metformin or metformin/sulfonylurea combination; Group 2, thiazolidinedione with metformin and/or sulfonylurea combination; Group 3, dipeptidyl peptidase-4 inhibitor (gemigliptin) with metformin and/or sulfonylurea combination; Group 4, sodium-glucose cotransporter 2 inhibitor (empagliflozin) with metformin and/or sulfonylurea combination. P for trend compared with the baseline; P value by one-way analysis of variation (ANOVA) and post hoc analysis. Dunnett’s method was applied for post hoc analysis.

P<0.05 compared to baseline and other groups;

P<0.05 compared to baseline and Group 1 and 3.

Fig. 2

Percentage change of bone mineral density (BMD) from baseline to 12 months. (A) Lumbar spine, (B) femoral neck, (C) total hip. Group 1, metformin or metformin/sulfonylurea combination; Group 2, thiazolidinedione with metformin and/or sulfonylurea combination; Group 3, dipeptidyl peptidase 4 inhibitor with metformin and/or sulfonylurea combination; Group 4, sodium-glucose cotransporter 2 inhibitors with metformin and/or sulfonylurea combination. aP<0.05 compared with Group 1, 3, and 4; bP<0.05 compared with baseline; cP<0.05 compared with Group 1 and 3.

Levels of bone turnover markers

Serum levels of CTx and P1NP during the study period are summarized in Table 4. No significant changes in CTx or P1NP were observed during the study period in any group. During the 9- to 12-month period of the study, the lowest CTx was measured in the TZD group (Group 2) (0.43±0.16 ng/mL), but it was not significantly different from the other groups. In all groups, CTx was maintained below 1.008 ng/mL, the reference range for postmenopausal women, and P1NP was also maintained between 20.25 and 76.31 ng/mL, the reference range for postmenopausal women without postmenopausal hormone replacement therapy.

Table 4

Bone Turnover Markers during the Study Period

	Baseline	Point 1	Point 2	P for trend
CTx, ng/mL
Group 1	0.44±0.22	0.50±0.25	0.45±0.22	0.368
Group 2	0.42±0.17	0.43±0.16	0.43±0.16	0.713
Group 3	0.43±0.20	0.45±0.17	0.44±0.17	0.215
Group 4	0.49±0.22	0.48±0.17	0.47±0.20	0.709
P1NP, ng/mL
Group 1	49.1±16.7	52.1±13.8	51.5±18.6	0.448
Group 2	45.3±11.8	47.2±13.9	47.1±12.4	0.543
Group 3	45.2±15.3	47.9±15.5	45.7±15.4	0.198
Group 4	49.5±21.9	51.6±18.2	50.4±18.7	0.253

Values are expressed as mean±standard deviation. Point 1, between 3–6 months of the study; Point 2, between 9–12 months of the study. Group 1, metformin or metformin/sulfonylurea combination; Group 2, thiazolidinedione with metformin and/or sulfonylurea combination; Group 3, dipeptidyl peptidase-4 inhibitor (gemigliptin) with metformin and/or sulfonylurea combination; Group 4, sodium-glucose cotransporter 2 inhibitor (empagliflozin) with metformin and/or sulfonylurea combination. P for trend compared with the baseline; P value by one-way analysis of variation (ANOVA) and post hoc analysis. Dunnett’s method was applied for post hoc analysis.

CTx, C-terminal type 1 collagen telopeptide; P1NP, total procollagen type 1 amino-terminal propeptide.

Metabolic parameters

During the study period, weight gain in the TZD group and weight loss in the SGLT2i group were seen; however, the change was not significant, and the final weight was not statistically different between the four groups. No significant changes in HbA1c levels were observed during the study period. At 12 months, HbA1c was 6.4%±0.5% for Group 1, 6.4%±0.8% for Group 2, 6.4%±0.6% for Group 3, and 6.7%±0.8% for Group 4. Neither differences between groups nor differences within groups were significant.

Adverse events and safety

In the TZD group (Group 2), three (6.4%) patients reported peripheral edema, but none stopped taking medication for this reason. In the SGLT2i group (Group 4), urinary tract infection was reported in two patients (4.2%), and genital infection was reported in one patient (2.1%). No symptomatic hypoglycemia was reported in any of the four groups during the study period. No serious adverse events resulting in discontinuation of the medication were reported in any group during the study period.

DISCUSSION

In this prospective study, significant reductions in femoral neck and total hip BMD were confirmed in postmenopausal T2DM patients treated with combination therapy with TZD. The femoral neck was the site with the largest decrease (−2.50%±3.08%) compared to the baseline level, which was also significantly higher than the levels in the other groups. Administration of combination regimens containing empagliflozin, an SGLT2i, did not cause significant bone loss.

TZDs are an antidiabetic medication that improves insulin sensitivity, but their use is associated with reduced bone mass [12,13] and increased risk for fracture [14]. However, lobeglitazone showed no detrimental effect on osteoblast differentiation in vitro [15]. An important mechanistic explanation for the effect of TZDs on bone is that TZDs induce adipogenesis and inhibits regulators of bone differentiation [16]. A meta-analysis of 22 randomized controlled trials concluded that pioglitazone treatment is associated with an increased risk of fractures in women (odds ratio of 1.73) [17]. Schwartz et al. [13] reported that TZD treatment, namely, pioglitazone, may cause bone loss in the whole body of older women with T2DM. Similar results were found in a study of nondiabetic subjects. In a large randomized controlled trial, pioglitazone was associated with a significant reduction in the risk of stroke and myocardial infarction in nondiabetic patients with cerebrovascular disease but was associated with an increased fracture risk [9]. Most previous studies have compared pioglitazone with placebo or with a single comparative agent. However, in an actual clinical environment, not only pioglitazone monotherapy but also combination therapy containing pioglitazone are prescribed for T2DM treatment. In this study, the harmful effect of TZD monotherapy on bone metabolism was also reproduced in the group treated with combination therapy containing TZD. Despite the great advantages of TZD for the treatment of T2DM, the benefits and harm of pioglitazone treatment must be carefully considered in T2DM patients at a high risk of fracture.

SGLT2i block glucose reabsorption in the proximal kidney tubule by blocking sodium-glucose cotransporters, resulting in a lower serum glucose concentration [18]. Dapagliflozin, empaglifozin, and canagliflozin are agents belonging to this class and have common characteristics of lowering blood glucose and preventing cardiovascular disease but seem to have different effects on bone metabolism. In a recent randomized controlled trial, canagliflozin was shown to be associated with a decrease in total hip BMD (−1.2% of placebo-subtracted changes in canagliflozin 300 mg) and an increase in CTx and osteocalcin over 104 weeks [19]. Blau et al. [20] suggested that canagliflozin has adverse effects on bone because it induces an immediate increase in serum phosphorous, causing downstream changes in fibroblast growth factor-23, 1,25-dihydroxyvitamin D, and PTH. However, studies on dapagliflozin and empagliflozin (mostly dapagliflozin) have reported neutral effects on BMD, BTM, and risk of fracture [5,21,22]. Although these agents belong to the same SGLT2i class, the physiological mechanism leading to different bone safety profiles has not yet been elucidated. We found that total hip BMD decreased by 1.27%±1.72% during the 12-month study period in Group 4 treated with empagliflozin, but this was not a significant decrease compared to the baseline value. There have been few studies on the effects of empagliflozin on bone metabolism, and our studies have shown that empagliflozin does not cause significant bone loss, as observed in the TZD group. Moreover, since the combination of empagliflozin and metformin accounted for most of the prescriptions in Group 4, it realistically reflects the current T2DM treatment in which metformin is administered as a first-line agent. Currently, canagliflozin is not available in Korea. A prospective comparative study of SGLT2i, including canagliflozin, will help to elucidate the effect of SGLT2i on bone metabolism more clearly.

In T2DM patients, BTM levels are altered. Based on the pooled data in a meta-analysis including 22 studies, CTx and osteocalcin were significantly lower in patients with diabetes than in the nondiabetic population [23]. Farr et al. [24] reported significantly lower serum CTx and serum P1NP levels in 30 postmenopausal patients with T2DM durations >10 years. Consistent with previous reports [24-27], our analysis revealed that BTM levels were lowered in T2DM patients. However, in our study, there was no nondiabetic control, but BTM levels were maintained at lower than the reference value in postmenopausal women. The mechanisms for reduced BTM, in particular, reduced bone formation in T2DM patients, are not well understood. T2DM may deteriorate bone homeostasis by suppressing osteoblast differentiation and accelerating osteoblast apoptosis, which is expressed as a reduced formation marker [28]. Advanced glycation end-products (AGEs) and oxidative stress are identified as possible causes of BTM changes. In T2DM patients with prolonged exposure to high glucose concentrations, more AGE accumulates in bone tissue, which negatively affects bone quality, resulting in fragile bones [28-30]. BTM changes after administration of a single agent have been differently reported. With TZD treatment, bone resorption markers increase but formation markers decrease, while both resorption and formation markers increase with SGLT2i [31]. Furthermore, DPP4i and sulfonylurea have a neutral effect on changes in bone resorption markers [31], whereas metformin decreased serum CTx/P1NP levels in the ADOPT trial [32]. The effect of a combination therapy on BTM is expected to show varied patterns, but clear evidence is lacking. In our study, we intended to determine the change in BTM levels under various combination regimens, and we found that BTM levels were not altered during the 12-month study period in any of the four groups. However, it is difficult to provide a clear basis for these results.

Our study has several limitations. First, the duration of diabetes was shorter in Group 1 than in the other groups. Guidelines recommend metformin as the first-line therapy in the treatment of T2DM patients unless it is contraindicated [33,34], and Group 1 includes patients undergoing metformin monotherapy, resulting in a relatively short duration of disease. However, no significant difference was observed between groups in regard to the duration of diabetes. Second, there was no quantitative analysis of dietary calcium intake. However, elemental calcium (250 mg of calcium carbonate) and cholecalciferol (1,000 IU) were administered to all subjects, and serum 25-hydroxyvitamin D levels were maintained at ≥20 ng/mL during the study period, with no difference among the four groups. Another drawback is that the prescription of diabetic medication was heterogeneous. Our study included participants with various prescriptions from monotherapy to dual and triple combination, and it may be difficult to conclude that the result represents the specific effect of a distinct medication. With metformin as the baseline treatment, the dual combinations of sulfonylurea (Group 1), TZD (mainly pioglitazone) (Group 2), gemigliptin (Group 3), and empagliflozin (Group 4) were the most prescribed patterns in each group. Therefore, the results primarily represent the effect of the dual combination with metformin. Lastly, it was difficult to identify new fractures during the study period due to the short study period and the limited number of study subjects.

This is the first study to compare the effects of combination therapy on BMD and BTM based on previous findings on the bone-related effects of antidiabetic agents. To regulate the various pathophysiological mechanisms of diabetes, it is recommended to administer a combination of antidiabetic agents from the early stages of the disease [35]. As prevalence of combination therapy rather than a single drug prescription continues to increase, careful attention is needed on how combination therapy affects BMD and BTM. In conclusion, patients on combination therapy with TZD exhibited noticeable cortical bone loss. On the other hand, in patients treated with empagliflozin (SGLT2i) combination, gemigliptin (DPP4i) combination, or sulfonylurea combination, bone loss was not significant at any measurement site during the 12-month follow-up period. Thus, caution should be exercised during treatment with antidiabetic medications or combinations that adversely affect bone in patients with a high risk of bone loss.