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Improvement of both fasting and postprandial glycemic control by the two-step addition of miglitol and mitiglinide to basal insulin therapy: a pilot study
Diabetology & Metabolic Syndrome volume 6, Article number: 48 (2014)
Combination therapy consisting of basal insulin and oral hypoglycemic agents (OHAs) is effective for the treatment of type 2 diabetes (T2DM) that cannot be adequately controlled using OHAs alone. Though basal insulin with metformin or sulfonylurea is an effective therapy, it cannot reduce postprandial glycemia without the risk of hypoglycemia. We examined a two-step regimen consisting of the addition of postprandial hypoglycemic agents (an alpha-glucosidase inhibitor and a glinide) in patients whose T2DM was poorly controlled using basal insulin therapy.
Inpatients between the ages of 30–79 years who had T2DM and an HbA1c level of more than 7.0% were recruited. The patients were treated with once-daily insulin glargine with or without metformin, depending on the patient’s age and renal function. Insulin glargine was titrated to achieve a target fasting glucose level of 70–130 mg/dL as a first step (STEP0). If the 2-hour postprandial glucose (PBG) level was higher than the target of 180 mg/dL, miglitol treatment (150 mg/day) was initiated, with dose adjustments (75–225 mg) allowed depending on abdominal symptoms and the PBG (STEP1). If the PBG of the patients remained higher than the target after 3 days of treatment, mitiglinide (30 mg/day, titrated up to 60 mg) was added (STEP2). We then evaluated the proportion of patients who achieved the target PBG before and after the two-step regimen. Continuous Glucose Monitoring (CGM) was performed throughout the two-step protocol in most of the patients.
Of the 16 patients who were recruited (median age, 67.0 [58.0-71.0] years; body mass index, 25.0 [22.0-27.9] kg/m2; HbA1c level at admission, 9.1% [8.35-10.4%]), 1 patient (6.25%) achieved the target PBG at STEP 0 and 14 patients (87.5%) had achieved the target PBG at the end of the treatment protocol (P = 0.002). CGM showed a significant decrease in the glucose level at each step of the protocol. The standard deviations in the CGM glucose levels for 24 hours, MAGE, and M-value also improved.
The two-step addition of postprandial hypoglycemic agents to basal insulin therapy is potentially effective and safe for decreasing both the fasting and postprandial glucose levels.
Type 2 diabetes is characterized by both decreased insulin secretion and sensitivity . The impairment of insulin secretion derived from β cell dysfunction is a progressive process that occurs before diagnosis and throughout the course of type 2 diabetes [2, 3]. Therefore, many patients who are initially treated with oral hypoglycemic agents (OHAs) eventually require a treatment strategy that includes insulin to counteract persistent hyperglycemia.
One treatment strategy that includes insulin is the combination of basal insulin with oral hypoglycemic agents. Historically, a regimen combining basal insulin with sulfonylurea and metformin has been frequently used. Using this regimen, the insulin dose can be easily titrated to minimize the number of hypoglycemic episodes and weight gain, compared with multiple insulin injections or mixed insulin therapy [4, 5]. However, a drawback of this regimen is that it provides poor support against sustained post-breakfast hyperglycemia (a situation that is often observed in patients with poor glycemic control [6, 7]) and postprandial hyperglycemia, resulting in glucose fluctuations that can increase the risks of both cardiovascular disease [8–11] and microvascular disease [12, 13]. Attempts to lower the postprandial glucose level by increasing the dose of basal insulin can lead to an increased risk of severe hypoglycemia during the night and early morning, which might also be associated with an increased risk of cardiovascular disease [14, 15].
Accordingly, we have proposed a regimen consisting of a two-step administration of postprandial hypoglycemic agents, namely an alpha-glucosidase inhibitor and a glinide, to basal insulin therapy to target postprandial hyperglycemia. We then conducted a pilot study to examine the safety and efficacy of this regimen.
We enrolled patients with type 2 diabetes who were hospitalized at the National Center for Global Health and Medicine Center Hospital between November 2011 and August 2013. Candidate subjects were between the ages of 30–79 years and had insufficient glucose control (HbA1c ≧ 7.0%). Patients with severe renal dysfunction (estimated glomerular filtration rate <30 mL/min/1.73 m2 or continuous hemodialysis), severe liver dysfunction, type 1 diabetes, glutamic acid decarboxylase antibody positivity, malignancy, or other causes of hyperglycemia were excluded from the present study.
All the patients provided written informed consent a few days after hospitalization and prior to enrollment in the trial. The study protocol was approved by the ethics committee of the National Center of Global Health and Medicine Center Hospital and was implemented in accordance with the provisions of the Declaration of Helsinki.
First, patients were treated with diet therapy (25–30 kcal/ideal body weight/day: carbohydrates, 60%-67.5%; fat, 21%-24.2%; protein, 11.2%-18.4%) and insulin glargine with metformin. The metformin dosage was set as high as possible after considering the patient’s age, renal function, and other adverse effects. Metformin was not administered to subjects who were older than 75 years of age or who had a serum creatinine level higher than 1.3 mg/dL (for men) or 1.2 mg/dL (for women).
For the basal insulin therapy, insulin glargine was used. The dose was titrated at the physician’s discretion to achieve a target fasting blood glucose (FBG) level between 70–130 mg/dL. An evaluation of the daily glucose profiles indicated that at least 5 days after admission were required to regulate the FBG at the target level. If the postprandial 2-hour blood glucose (PBG) level corresponded to the target value (lower than 180 mg/dL), the study protocol ended (STEP 0 responder). Patients who did not achieve the target PBG value were additionally treated with postprandial hypoglycemic agents (refer to STEP 1 and STEP 2 below). The target PBG was defined according to the American Diabetes Association’s recommendation .
On day 1, miglitol (150 mg/day, 50 mg administered immediately before every meal) was administered and the PBG was evaluated. If the target PBG was not achieved on day 1, the dose of miglitol was increased to 225 mg/day (75 mg administered immediately before every meal) on day 2. If the patient experienced gastrointestinal symptoms, the dose of miglitol was decreased to a tolerable dose on day 3. The PBG was evaluated on day 2 or day 3. If the PBG was under 180 mg/dL, the study protocol was regarded as having been successful at STEP 1.
For patients who failed to achieve the target PBG with miglitol, mitiglinide (30 mg/day, 10 mg administered immediately before every meal) was added to the treatment regimen on day 4 (or day 5). If the target PBG was not reached, the dosage of mitiglinide was increased to 60 mg/day (20 mg administered immediately before every meal) on day 5 (or day 6) and the PBG was evaluated.
Biochemical and clinical measurements
We calculated the BMI using the body height and weight of each patient. The 24-h urine C peptide and serum C peptide levels were measured before and 6 minutes after the intravenous injection of 1 mg of glucagon (glucagon stimulation test).
The self-monitoring blood glucose (SMBG) levels were checked before and 2 hours after each meal and before sleep (7-point SMBG) using a Nipro StatStrip XP (Nova Biomedical K.K.). The M-value was calculated using the following equation:
The patients were observed using continuous glucose monitoring (CGMS® System Gold™; Medtronic Inc.); the CGMS device was calibrated four times a day. The results were then used to calculate the 24-h average, the standard deviation (SD) of the 24-h values, the 24-h area under the curve (AUC), every 4-h postprandial value, and from midnight to early morning (from 0:00 AM to 8:00 AM), and the mean amplitude of glycemic excursion (MAGE ) using the glucose values observed every 5 minutes. We failed to obtain CGM records in 2 of the 16 patients because of technical difficulties.
Primary and secondary outcomes
The primary endpoint was the change in the proportion of patients who reached the target PBG before and after the addition of the postprandial hypoglycemic agents (STEP 0 vs. end of protocol). We also calculated the M-value, MAGE, and the averages and SDs of the CGM data obtained on the days on which each of the steps were evaluated. We also compared the patient backgrounds of those in whom the treatment was or was not a success.
Exact McNemar test was used to compare the proportion of patients who achieved the target PBG at STEP 0 and at the end of the protocol. Continuous variables were compared using the Wilcoxon rank sum test. A two-sided P value <0.05 was regarded as significant. The results were described using the median and interquartile ranges. The statistical analysis was performed using Stata IC 11.
We enrolled 18 patients with type 2 diabetes who had been hospitalized in our institution. Two patients were excluded: one patient was diagnosed as having preclinical Cushing syndrome, and the other was excluded because of the presence of an insulin autoimmune antibody. One patient reached the target PBG at STEP 0 and did not proceed to the next step in the protocol (Figure 1) (Table 1). Of the 15 patients who were treated with miglitol, 8 patients reached the target PBG at the STEP 1 evaluation. Mitiglinide was then added to the treatments of the 7 patients who failed to reach the target PBG using the STEP 1 treatment; 5 of these patients achieved the target PBG at the STEP 2 evaluation. Finally, 1 of the 16 patients achieved the target PBG at STEP 0 and 14 patients achieved the target PBG at the end of the study protocol (6.25% vs. 87.5%, P = 0.0002). The 7-point SMBG and CGM were also improved (Figure 2). The characteristics of the patients who reached the target PBG at STEP 1 and the patients who proceeded to STEP 2 are presented in Additional file 1: Table S1.
At STEP 0, the 7-point glucose monitoring values exhibited sustained levels of post-breakfast hyperglycemia. With the administration of miglitol, the 7-point glucose monitoring values from after breakfast until after dinner were suppressed, but the values before sleep and before breakfast did not decrease significantly (Figure 3A). When the glycemic profiles were examined more precisely using CGM, the 24-h AUC and each of the 4-h postprandial AUC values were significantly decreased. The AUC from 0:00 AM to 8:00 AM (from evening until before breakfast) remained unchanged at the STEP1 evaluation after the addition of miglitol, compared with the values at STEP0 (Figure 3B).
Similarly, compared with STEP 1, the 7-point glucose monitoring values from after lunch through until after dinner were significantly decreased at the STEP 2 evaluation (Figure 3C), the same day of CGM profile was described (Figure 3D). The 24-h AUC, the 4-h after-lunch AUC, and the 4-h after dinner AUC recorded using CGM were significantly decreased at the STEP 2 evaluation. The details of the CGM data for each step are described in an Additional file 2: Table S2.
The markers of glucose fluctuations, namely the SDs of the glucose levels for 24-h and MAGE, improved and the M-values were also decreased at the end of protocol (Table 2).
Two patients were unable to achieve the target PBG. One patient was a 78-year-old man; although he exhibited a comparably sufficient endogenous insulin level, he was obese and could not use metformin because of his age. The other patient was a 61-year-old woman; she had a long duration of diabetes, and her endogenous insulin level was almost depleted. Both of these patients had highly fluctuating glucose levels, as shown by the M-value and the SDs of the 24-h data and MAGE obtained using CGM (Table 3).
No severe hypoglycemic events occurred. Regarding the CGM data, hypoglycemia of less than 70 mg/dL was rarely recorded from midnight until daytime (Table 2).
Postprandial hyperglycemia can have a harmful effect on the cardiovascular outcome. In this study, ten patients were treated with as high a dose of metformin as they could tolerate; metformin is recommended as a drug of first choice  in combination with insulin glargine at STEP 0. The remaining six patients were treated with insulin glargine alone at STEP 0 because of an advanced age or a reduced renal function. The administration of basal insulin with or without metformin decreases the fasting glucose level and the overall glycemic profile, but in our cases, it was insufficient to postprandial hyperglycemia in 15 of the 16 cases. Many studies have discussed the combination of basal insulin with metformin or sufonylurea or both drugs [5, 20–22]. However, their mechanisms of action can make them insufficient to prevent postprandial hyperglycemia. Consequently, we prescribed miglitol and mitiglinide as a two-step treatment. Using our treatment regimen, 14 of the 16 patients achieved the target PBG as defined by the American Diabetes Association’s recommendations . Though the duration of the hospital stay might have contributed to the gradual improvement in the glucose level and might have influenced the achievement of the target PBG, the fact that most of the subjects eventually attained an ideal glycemic control using this regimen is noteworthy. In addition, CGM highlighted the precise profiles of glucose excursion, showing the effectiveness of the miglitol and mitiglinide in lowering daytime blood glucose levels without causing hypoglycemia during the night as well as showing the improvement in glucose fluctuations as a result of treatment with the two drugs in more detail.
The two patients who were unable to attain the target PBG suggest that the present regimen has some limitations. One patient was an obese, elderly man who was unable to take metformin because of his age. In this patient, insulin resistance might have limited the effect of mitiglinide. The other patient was a woman with the lowest serum C-peptide at 6 minutes in the glucagon test. For this patient, the effect of mitiglinide might have been limited by the impaired secretion of insulin.
In this study, we used two postprandial hypoglycemic agents. Alpha-glucosidase inhibitors, which delay the absorption of carbohydrates in food, decrease the postprandial glucose level without inducing the secretion of insulin . As a result of this unique mechanism, alpha-glucosidase is effective for patients even if they have a comparatively long duration of diabetes and a severe deterioration of insulin secretion. In addition, miglitol provides incretin effects induced by GLP-1 secretion from L-cells . Glinide is a short-acting insulin secretagogue that functions through the KATP channel inhibition of β cells . Mitiglinide also suppresses postprandial free fat acid levels . These drugs decrease postprandial hyperglycemia effectively while causing fewer episodes of hypoglycemia and are relatively safe for patients with renal dysfunction and for elderly patients, in addition to being safe for long-term use.
Numerous studies have supported the effectiveness of basal insulin with sulfonylurea or metformin [5, 20–22] but as far as we know, few studies have examined the use of insulin glargine with postprandial hypoglycemic agents. Kim et al. reported the efficacy of adding either nateglinide or acarbose to insulin glargine, resulting in a 7-point reduction in the SMBG and with no difference in glucose variability between nateglinide and acarbose . Hirose et al. investigated the effect of mitiglinide with insulin glargine after switching from multiple daily injections and reported that 15 out of 30 patients maintained a fair glucose control after switching to mitiglinide [28, 29]. These reports suggested the effectiveness of using postprandial hypoglycemic agents with long-acting basal insulin and also indicated the limitations of the addition of single postprandial hypoglycemic agents.
To improve postprandial hypoglycemia, dipeptidyl peptidase-4 (DPP-4) inhibitors and GLP-1 analogs are other choices for use in combination with basal insulin [30, 31]. We are also attempting to construct new regimens composed of basal insulin and multiple hypoglycemic agents, including DPP-4 inhibitors or GLP-1 analogs .
Initiating basal insulin therapy in patients with poor glycemic control after the use of metformin is supported by the American Diabetes Association [33, 34] and the European Association for the Study of Diabetes . In addition, this treatment regimen may lead to better glycemic control, compared with only basal insulin with metformin, because both the fasting and postprandial blood glucose levels can be controlled. This regimen might also serve as a go-between for frequent insulin injections therapy.
This study had several limitations including the relatively small number of subjects, the absence of a control group, and the short-term results for inpatients. The patients’ satisfaction level after receiving this regimen and long-term diabetic complications, cardiovascular disease, and mortality also need to be evaluated. In addition, larger studies are needed to evaluate the reduction of hypoglycemia associated with this regimen. Confirming this hypothesis, further studies are required to confirm the efficacy of this regimen in outpatients; furthermore, the regimen should be simplified before being administered to outpatients.
Once such points have been clarified, our structured treatment regimen might be beneficial for many type 2 diabetes patients requiring insulin therapy.
In conclusion, in a pilot study of a two-step regimen consisting of the addition of postprandial hypoglycemic agents, more than 80% of the patients achieved a good glucose profile, indicating the potent efficacy of the two-step administration of postprandial hypoglycemic agents with basal insulin therapy.
Oral hypoglycemic agents
Continuous glucose monitoring
Self-monitoring blood glucose
Fasting blood glucose
Postprandial 2-hour blood glucose
Area under the curves
- DPP-4 inhibitor:
Dipeptidyl peptidase-4 inhibitor
Estimated glomerular filtration rate.
The Committee of the Japan Diabetes Society on the diagnostic criteria of diabetes mellitus: Report of the Committee on the classification and diagnostic criteria of diabetes mellitus. Diabetol Int. 2010, 1: 2-20. 10.1007/s13340-010-0006-7.
Kosaka K, Kuzuya T, Hagura R, Yoshinaga H: Insulin response to oral glucose load is consistently decreased in established non-insulin-dependent diabetes mellitus: the usefulness of decreased early insulin response as a predictor of non-insulin-dependent diabetes mellitus. Diabet Med. 1996, 13: S109-S119.
Yamamoto-Honda R, Osame K, Kitazato H, Shinkai-Goromaru M, Isogawa A, Yoshida Y, Kawzu S, Akanuma Y, Noda M: Insulin secretion and insulin sensitivity in Japanese patients with Type 2 diabetes: a cross-sectional study comparing the homeostasis model assessment-2 (HOMA2) indexes and indexes derived from the oral glucose tolerance test. Diabetology Int. 2011, 2: 72-78. 10.1007/s13340-011-0024-0.
Holman RR, Thorne KI, Farmer AJ, Davies MJ, Keenan JF, Paul S, Levy JC, 4-T Study Group: Addition of Biphasic, Prandial, or Basal Insulin to Oral Therapy in Type 2 Diabetes. N Engl J Med. 2007, 357: 1716-1730. 10.1056/NEJMoa075392.
Bretzel RG, Nuber U, Landgraf W, Owens DR, Brandley C, Linn T, Bretzel A, Nuber U, Landgraf W, Owens DR, Brandley C, Linn T: Once-daily basal insulin glargine versus thrice-daily prandial insulin lispro in people with type 2 diabetes on oral hypoglycaemic agents (APOLLO): an open randomized controlled trial. Lancet. 2008, 371: 1073-1084. 10.1016/S0140-6736(08)60485-7.
Monnier L, Colette C, Rabasa-Lhoret R, Lapinski H, Caubel C, Avignon A, Boniface H: Morning hyperglycemic excursions: a constant failure in the metabolic control of non-insulin-using patients with type 2 diabetes. Diabetes Care. 2002, 25 (4): 737-741. 10.2337/diacare.25.4.737.
Yamamoto-Honda R, Kitazato H, Hashimoto S, Takahashi Y, Yoshida Y, Hasegawa C, Akanuma Y, Noda M: Distribution of blood glucose and correlation between blood glucose and hemoglobin A1c levels in diabetic outpatients. Endocr J. 2008, 55 (5): 913-923. 10.1507/endocrj.K08E-071.
DECODE Study Group, on behalf of the European Diabetes Epidemiology Group: Glucose tolerance and cardiovascular mortality: comparison of fasting and 2-hour diagnostic criteria. Arch Intern Med. 2001, 161: 397-405.
Patel A, MacMahon S, Chalmers J, Neal B, Billot L, Woodward M, Marre M, Cooper M, Glasziou P, Grobbee D, Hamet P, Harrap S, Heller S, Liu L, Mancia G, Mogensen CE, Pan C, Poulter N, Rodgers A, Williams B, Bompoint S, de Galan BE, Joshi R, Travert F, The ADVANCE Collaborative Group: Intensive Blood Glucose Control and Vascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med. 2008, 358: 2560-2572.
Ceriello A, Hanefeld M, Leiter L, Monnier L, Moses A, Owens D, Tajima N, Tuomilehto J, for the International Prandial Glucose Regulation (PGR) Study Group: Postprandial glucose regulation and diabetic complications. Arch Intern Med. 2004, 164: 2090-2095. 10.1001/archinte.164.19.2090.
Cavalot F, Pagliarino A, Valle M, Di Martino L, Bonomo K, Massucco P, Anfossi G, Trovati M: Postprandial blood glucose predicts cardiovascular events and all-cause mortality in Type2 Diabetes in a 14-year follow-up: lessons from the San Luigi Gonzaga diabetes study. Diabetes Care. 2011, 34: 2237-2243. 10.2337/dc10-2414.
Shiraiwa T, Kaneto H, Miyatsuka T, Kato K, Yamamoto K, Kawashima A, Kanda T, Suzuki M, Imano E, Matsuhisa M, Hori M, Yamasaki Y: Postprandial hyperglycemia is a better predictor of the progression of diabetic retinopathy than HbA1c in Japanese type 2 diabetic patients. Diabetes Care. 2005, 28: 2806-2807. 10.2337/diacare.28.11.2806.
Chittari MV, MacTernan P, Bawazeer N, Constantinides K, Ciotola M, O’Hare JP, Kumar S, Ceriello A: Impact of acute hyperglycaemia on endothelial function and retinal vascular reactivity in patients with Type 2 diabetes. Diabet Med. 2011, 28: 450-454. 10.1111/j.1464-5491.2010.03223.x.
Goto A, Arah OA, Goto M, Terauchi Y, Noda M: Severe hypoglycaemia and cardiovascular disease: systematic review and meta-analysis with bias analysis. BMJ. 2013, 347: f4533-10.1136/bmj.f4533.
Tsujimoto T, Yamamoto-Honda R, Kajio H, Kishimoto M, Noto H, Hachiya R, Kimura A, Kakei M, Noda M: Vital Signs, QT Prolongation, and Newly Diagnosed Cardiovascular Disease during Severe Hypoglycemia in Type 1 and Type 2 Diabetic Patients. Diabetes Care. 2014, 37 (1): 217-25. 10.2337/dc13-0701.
American Diabetes Association: Standards of Medical Care in Diabetes-2013. Diabetes Care. 2013, 36 (Supplement): S11-S66.
Schichtkrull J, Munck O, Jersild M: The M-Value, an index of Blood-Sugar Control in Diabetics. Acta Med Scand. 1965, 177: 95-102.
Wójcicki JM: Mathematical descriptions of the glucose control in diabetes therapy. Analysis of the Schlichtkrull “M”-value. Horm Metab Res. 1995, 27: 1-5. 10.1055/s-2007-979895.
Service FJ, Molnar GD, Rosevear JW, Ackerman E, Gatewood LC, William FT: Mean amplitude of glycemic excursions, a measure of diabetic instability. Diabetes. 1970, 19 (9): 644-655.
Yuki-Järvinen H, Kauppinen-Mäkelin R, Tiikkainen M, Vähätalo M, Virtamo H, Nikkilä K, Tulokas T, Hulme S, Hardy K, McNulty S, Hänninen J, Levänen H, Lahdenperä S, Lehtonen R, Ryysy L: Insulin glargine or NPH combined with metformin in type 2 diabetes: the LANMET study. Diabetologia. 2006, 49: 442-451. 10.1007/s00125-005-0132-0.
Rosenstock J, Davies M, Home PD, Larsen J, Koenen C, Schernthaner G: A randomised, 52-week, treat-to-target trial comparing insulin detemir with insulin glargine when administrated as add-on to glucose-lowering drugs in insulin-naive people with type 2 diabetes. Diabetologia. 2008, 51: 408-416. 10.1007/s00125-007-0911-x.
Fonseca V, Gill J, Zhou R, Leahy J: An analysis of early insulin glargine added to metformin with or without sulfonylurea: impact on glycemic control and hypoglycemia. Diabetes, Obesity and Metabolism. 2011, 13: 814-822. 10.1111/j.1463-1326.2011.01412.x.
Kishimoto M, Noda M: A pilot study of the efficacy of miglitol and sitagliptin for type 2diabetes with a continuous glucose monitoring system and incretin-related markers. Cardiovasc Diabetol. 2011, 10: 115-10.1186/1475-2840-10-115.
Lee A, Patric P, Wishart J, Horowitz M, Morley JE: The effects of miglitol on glucagon-like peptide-1 secretion and appetite sensations in obese type 2 diabetics. Diabetes Obes Metab. 2002, 4 (5): 329-335. 10.1046/j.1463-1326.2002.00219.x.
Sunaga Y, Gonoi T, Shibasaki T, Ichikawa K, Kusama H, Yano H, Seino S: The effects of mitiglinide (KAD-1229), a new anti-diabetic drug, on ATP-sensitive K + channels and insulin secretion: comparison with the sulfonylureas and nateglinide. Eur J Pharmacol. 2001, 431 (1): 199-225.
Mori Y, Ojima K, Fuujimori Y, Aoyagi I, Kusama H, Yamazaki Y, Kojima M, Shibata N, Itoh Y, Tajima N: Effects of mitiglinide on glucose-induced insulin release into the portal vein and fat-induced triglyceride elevation in prediabetic and diabetic OLETF rats. Endocrine. 2006, 29 (2): 309-15. 10.1385/ENDO:29:2:309.
Kim MK, Suk JH, Kwon MJ, Chung HS, Yoon CS, Jun HJ, Ko JH, Kim TK, Lee SH, Oh MK, Rhee BD, Park JH: Nateglinide and acarbose for postprandial glucose control after optimizing fasting glucose with insulin glargine in patients with type 2 diabetes. Diabetes Res Clin Pract. 2011, 92 (3): 322-328. 10.1016/j.diabres.2011.01.022.
Yoshihara T, Kumashiro N, Kanazawa Y, Mita T, Sakurai Y, Kawai J, Abe M, Motojima K, Hara K, Yamazaki Y, Kanazawa A, Miwa S, Sato F, Kanno R, Shimizu T, Sakai K, Uchino H, Watada H, Tanaka Y, Kawamori R, Hirose T: Therapeutic efficacy of mitiglinide combined with once daily insulin glargine after switching from multiple daily insulin regimen of aspart insulin and glargine in patients with type 2 diabetes mellitus. Endocr J. 2006, 53 (1): 67-72. 10.1507/endocrj.53.67.
Kumashiro N, Yoshihara T, Kanazawa Y, Shimizu T, Watada H, Tanaka Y, Fujitani Y, Kawamori R, Hirose T: Long-term effect of combination therapy with mitiglinide and once daily insulin glargine in patients who were successfully switched from intensive insulin therapy in short-term study. Endocr J. 2007, 54 (1): 163-166. 10.1507/endocrj.K06-153.
Takahara M, Shiraiwa T, Kaneto H, Katakami N, Matsuoka TA, Shimomura I: Efficacy of sitagliptin on blood glucose fluctuation in Japanese type 2 diabetic patients with basal-supported oral therapy. Endocr J. 2013, 59 (12): 1131-1136.
Arnolds S, Dellweg S, Clair J, Dain MP, Nauck MA, Rave K, Kapitza C: Further improvement in postprandial glucose control with addition of exenatide or sitagliptin to combination therapy with insulin glargine and metformin: a proof-of-concept study. Diabetes Care. 2010, 33: 1509-1515. 10.2337/dc09-2191.
Kishimoto M, Noda M: Effect of the Addition of Sitagliptin and Miglitol on Insulin-Treated Type 2 Diabetes. Diabetes Ther. 2012, 3: 11-
American Diabetes Association: Standards of Medical Care in Diabetes-2014. Diabetes Care. 2014, 37: S14-80.
Inzucchi SE, Bergenstal RM, Buse JB, Diamant M, Ferrannini E, Nauck M, Peters AL, Tsapas A, Wender R, Matthews DR, American Diabetes Association (ADA); European Association for the Study of Diabetes (EASD): Management of hyperglycemia in type 2 diabetes: a patient-centered approach: position statement of the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care. 2012, 35 (6): 1364-79. 10.2337/dc12-0413.
This work was funded by a Health Sciences Research Grant (Comprehensive Research on Life-Style Related Diseases including Cardiovascular Diseases and Diabetes Mellitus H25-016) from the Ministry of Health, Labour and Welfare of Japan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare that they have no competing interests.
NI conceptualized the idea for the study, collected the data, performed the statistical analysis, and wrote the paper. TT participated in the design of the study, joined the discussion, and was involved in drafting the manuscript. R Y-H participated in the design of the study, joined the discussion, and was involved in drafting the manuscript. MKishimoto jointed the discussion and was involved in drafting the manuscript. HK and HN joined the discussion. MKakei joined the discussion and supervised the work. MN participated in the design of the study, supervised the work, and joined the discussion. All authors have read and approved the final manuscript.
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Ihana, N., Tsujimoto, T., Yamamoto-Honda, R. et al. Improvement of both fasting and postprandial glycemic control by the two-step addition of miglitol and mitiglinide to basal insulin therapy: a pilot study. Diabetol Metab Syndr 6, 48 (2014) doi:10.1186/1758-5996-6-48
- Insulin glargine
- Postprandial hyperglycemia
- Glucose fluctuation
- Continuous glucose monitoring (CGM)