Efficacy and Safety of Insulin Degludec versus Insulin Glargine: A Systematic Review and Meta-Analysis of Fifteen Clinical Trials

Liu, Wei; Yang, Xiaojie; Huang, Jing

doi:https://doi.org/10.1155/2018/8726046

International Journal of Endocrinology

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Abstract Introduction Methods Results Discussion Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Review Article | Open Access

Volume 2018 | Article ID 8726046 | https://doi.org/10.1155/2018/8726046

Efficacy and Safety of Insulin Degludec versus Insulin Glargine: A Systematic Review and Meta-Analysis of Fifteen Clinical Trials

Wei Liu,¹Xiaojie Yang,²and Jing Huang¹

Academic Editor: Michael Horowitz

Received02 Oct 2017

Revised17 Dec 2017

Accepted01 Jan 2018

Published12 Mar 2018

Abstract

Aims. Insulin degludec (IDeg) and insulin glargine (IGlar) are both proved to be effective in diabetes. This study aimed to assess the effects and safety of IDeg versus IGlar. Methods. A systematic literature search was conducted using the PubMed, EMBASE, and Cochrane Library electronic databases to identify all randomized controlled trials (RCTs). Results. Fifteen RCTs were identified. The combined data showed that the decrease in the glycosylated hemoglobin (HbA1c) level was slightly different, and the proportion of patients who achieved HbA1c < 7% was similar between the IDeg and IGlar groups. Further, a statistically significant decrease in the fasting plasma glucose level was observed in the IDeg group as compared to the IGlar group. In patients with T2DM, IDeg was associated with lower rates of overall hypoglycemia. Nocturnal hypoglycemia was significantly lower in the case of IDeg than in the case of IGlar in both T1DM and T2DM patients. No statistically significant differences were observed between the groups. Conclusions. Compared with IGlar, IDeg is associated with equivalent glycemic control and a statistically significantly lower rate of nocturnal hypoglycemia in patients with T1DM and T2DM. In T2DM patients, IDeg also provides better results in terms of overall hypoglycemia.

1. Introduction

Diabetes mellitus (DM) is a major risk factor for cardiovascular diseases and stroke. Improved glycemic control delays and prevents the development of these complications [1]. Unfortunately, a large number of people with DM are unable to achieve the guideline-recommended glycosylated hemoglobin (HbA1c) level [2, 3]. Tighter glycemic control is typically associated with an increased risk of hypoglycemia [4]. The burden and fear of hypoglycemia have become major barriers to patients reaching the recommended HbA1c level [5].

Insulin glargine (IGlar) has been proven to pose a lower risk of hypoglycemia than older human insulin formulations [6]. Nonetheless, the occurrence of hypoglycemia with IGlar treatment is still noticeable [7]. Insulin degludec (IDeg) is a new basal insulin drug with an ultralong duration of action. Experimental studies show that IDeg has a long half-life with a flatter and more stable glucose-lowering effect, resulting in a four times lower within-patient variability than IGlar [8, 9]. Therefore, many randomized controlled trials (RCTs) have been carried out to evaluate the effect of glycemic control and the prevalence of hypoglycemia in the case of IDeg as compared to IGlar [10–14]. A previously published meta-analysis of seven clinical trials showed that IDeg is associated with equivalent HbA1c control and a significantly lower nocturnal hypoglycemia rate than IGlar [15]. However, since then, several new clinical trials with different results have been reported, particularly with respect to nocturnal hypoglycemia; for instance, trials conducted by Pan et al. and Warren et al. showed neutral results [16, 17], while trials from Wysham et al. showed better result for IDeg [18]. Therefore, a systematic review and meta-analysis with updated data are necessary to further assess the efficacy and safety of IDeg compared to that of IGlar.

2. Methods

2.1. Search Strategy

The PubMed, EMBASE, and Cochrane Library electronic databases were searched for studies published up to July 15, 2017, to identify all publications that compare the effects of the administration of IDeg and that of IGlar in patients with DM. The following terms were used in combination with appropriate logical connectors: “insulin,” “degludec,” “IDeg,” “glargine,” “IGlar,” “randomized,” “randomly,” “diabetes,” and “diabetes mellitus.” Further, a manual search was performed by scanning the references of the identified articles to find studies that were potentially missed by the electronic searches.

2.2. Study Selection and Data Collection

The inclusion criteria of the present systematic review and meta-analysis were as follows: (1) an RCT with a no less than 12-week follow-up, (2) patients diagnosed with type 1 DM (T1DM) or type 2 DM (T2DM), and (3) studies that compared the effects of the administration of IDeg once a day with those of IGlar treatment. The exclusion criteria were as follows: (1) IDeg coformulated with other hypoglycemic agents, (2) IDeg injected three times a week, (3) trials with a duration of less than 12 weeks, and (4) short reports, letters to editors, abstracts, or proceedings of scientific meetings.

The study selection was strictly in compliance with the inclusion and exclusion criteria. Two authors (Wei Liu and Xiaojie Yang) independently assessed all the potentially relevant studies. The selection process was carried out by crude screening to exclude a majority of the irrelevant studies at the level of title and abstract, and the remaining studies were double-examined by perusing through the full text to reach the final decision. A consensus was reached on all eligible studies between the two screening authors. Any discrepancies were resolved by discussion.

Two authors (Wei Liu and Jing Huang) independently extracted all the relevant information from the eligible studies. A prespecified table that contained the relevant items was used to help with the data collection.

2.3. Endpoints

The treatment efficacy was evaluated on the basis of the change in the HbA1c and fasting plasma glucose (FPG) levels from the baseline to the end of the study and the proportion of patients who achieved HbA1c levels of <7%. The safety assessments considered adverse events, hypoglycemia, and body weight. The same hypoglycemia criteria were used for all the included studies in our manuscript. Hypoglycemia was defined as a symptomatic or an asymptomatic event with plasma glucose of <3.1 mmol/L (56 mg/dL) [13].

2.4. Evaluation of Study Quality and Publication Bias

The quality of the included studies was evaluated by using the Jadad scale. The Jadad scale consists of three items pertaining to the descriptions of randomization (0–2 points), double blinding (0–2 points), and dropouts and withdrawals (0-1 point), totaling to five points, with a higher score indicating better quality. Trials that scored 3 points or more were considered to be high-quality trials.

Publication bias was evaluated by using a funnel plot and visually inspecting its symmetry.

2.5. Data Synthesis and Statistical Analysis

The I² statistic was used to test statistical heterogeneity, with values of >50% representing important heterogeneity, then a random-effects model was used to perform the meta-analysis. The mean difference (MD) with the 95% confidence interval (CI) between the IDeg and the IGlar cases was calculated to represent the difference in the changes in the HbA1c and FPG levels. For the efficacy analysis, the odds ratio (OR) or the risk ratio (RR) was calculated as the effect size. A subgroup analysis was performed between patients with T1DM and those with T2DM.

The present systematic review and meta-analysis were performed in compliance with the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [19]. All meta-analyses of the present study were pooled according to Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0. The statistical significance was set at . All analyses were conducted using the software Review Manager 5.3.

3. Results

Finally, 15 studies were found to be eligible for this research [10–14, 16–18, 20–26]. All the included studies were multicenter studies, except the study by Iga et al., which was a single-center study [25]. The duration of intervention ranged from 12 weeks to 2 years. Four of these studies used a crossover design [17, 18, 25, 26]. All 15 studies had a so-called treat-to-target design.

In all, 16,328 patients were included in the present study. Five studies recruited patients with T1DM [11, 14, 22, 25, 26], and the other ten studies enrolled patients with T2DM [10, 12, 13, 16–18, 20, 21, 23, 24]. In all the considered studies, the authors used an intention-to-treat analysis. Withdrawals and dropouts were described adequately in all these studies, and the rates of completed treatment varied from 76.7% to 100%. The clinical characteristics of each trial are summarized in Table 1.

3.1. Glycemic Control

The HbA1c and the changes from the baseline to the endpoint levels were reported in all the 15 included studies. The overall meta-analysis revealed statistically significant difference with a MD of 0.04% in the HbA1c level between the IDeg and the IGlar treatment groups, with nonsignificant heterogeneity (MD = 0.04%, 95% CI = 0.01% to 0.07%, , I² = 0%, Figure 1 and Table 2). The subgroup analyses showed nonsignificant difference in T1DM (MD = 0.05%, 95% CI = −0.01% to 0.10%, , I² = 0%) and slight difference in T2DM (MD = 0.04%, 95% CI = 0.00 to 0.07%, , I² = 0%). In the case of FPG level, the IDeg treatment was associated with a statistically significant reduction as compared to the IGlar treatment (MD = −0.41, 95% CI = −0.54 to −0.28, , I² = 27%, Figure 2 and Table 2); this association was observed in the cases of both T1DM (MD = −0.84, 95% CI = −1.18 to −0.51, , I² = 0%) and T2DM (MD = −0.34, 95% CI = −0.45 to −0.23, , I² = 0%).

Eight studies reported the following proportions of patients who achieved HbA1c levels of <7%: 1704 (46.1%) of 3693 patients achieved HbA1c < 7% in the IDeg group, and 793 (46.9%) of 1690 patients achieved HbA1c < 7% in the IGlar group. The meta-analysis showed that the proportions of patients who achieved HbA1c levels of <7% were similar in the two groups (, Table 2).

3.2. Safety Endpoints

All 15 included studies evaluated the changes in body weight. The pooled result showed a similar change in body weight between the examined groups (MD = 0.03, 95% CI = −0.11 to 0.18, , I² = 36%, Table 2), of both patients with T1DM (MD = −0.04, 95% CI = −0.35 to 0.26, , I² = 0%) and those with T2DM (MD = 0.05, 95% CI = −0.11 to 0.22, , I² = 51%).

With respect to overall hypoglycemia, events per patient-year of exposure were integrated. We identified 13 studies that reported the events per patient-year of overall hypoglycemia. The meta-analyses showed that the incidence of overall hypoglycemia was lower in the IDeg treatment group (RR = 0.88, 95% CI = 0.81 to 0.96, , I² = 67%, random-effects model, Figure 3 and Table 2). Subgroup analyses revealed that IDeg reduced overall hypoglycemia only in patients with T2DM (RR = 0.82, 95% CI = 0.73 to 0.92, , I² = 56%) and not in patients with T1DM.

With respect to nocturnal hypoglycemia, events per patient-year of the episodes were lower in the IDeg group in the cases of both T1DM and T2DM (overall analysis: RR = 0.74, 95% CI = 0.69 to 0.79, , I² = 0%; T1DM: RR = 0.74, 95% CI = 0.68 to 0.81, , I² = 0%; T2DM: RR = 0.74, 95% CI = 0.66 to 0.82, , I² = 0%, Figure 4 and Table 2).

3.3. Adverse Events

Twelve studies reported the adverse events in detail. The proportion of patients reporting adverse events did not differ between the groups (4785 [53.7%] of the 8911 patients in the IDeg group versus 3336 [49.7%] of the 6715 patients in the IGlar group, pooled OR = 0.94, 95% CI = 0.88 to 1.01, , I² = 0%, Table 2), both for patients with T1DM and for those with T2DM. Of the three studies that did not report the adverse events in detail, one study did not report any adverse events [25], and the remaining two studies reported that the rates of adverse events were comparable between the groups [11, 17].

No statistically significant differences were observed between the groups for the serious adverse events and the adverse events possibly related to the trial product (Table 2).

3.4. Quality and Publication Bias of the Included Studies

The quality of the included studies was quantitatively assessed by using the Jadad scale. 14 of the 15 included studies were multicenter designs. Further, all the studies had Jadad scores of 3 points or more. Therefore, all the included studies were of high quality (Table 3). Publication bias was determined on the basis of the asymmetrical funnel plots.

4. Discussion

The present systematic review and meta-analysis included 15 high-quality RCTs to evaluate the efficacy and safety of two long-acting insulin analogs. The pooled results demonstrated the following: (1) although the IDeg treatment achieved a significantly better result than the IGlar treatment in terms of the FPG level, the reduction of HbA1c was comparable between the IDeg and the IGlar treatments. The results were robust across the T1DM and T2DM subgroups. (2) The risk of hypoglycemia was statistically significantly decreased in the IDeg treatment group as compared to that in the IGlar treatment group of patients with T2DM, as was nocturnal hypoglycemia. While in patients with T1DM, the IDeg treatment was associated with a lower risk of nocturnal hypoglycemia, but not associated with a lower risk of overall hypoglycemia. (3) The adverse events and the serious adverse events were similar between the IDeg and the IGlar treatment groups and across the T1DM and T2DM subgroups.

Glycemic control is vital for patients with DM. The microvascular and macrovascular complications of DM declined dramatically over the past two decades [27] but have reappeared with a higher rate of hospital admissions for hypoglycemic events [7]. Therefore, the development of an effective antidiabetic treatment with a lower rate of hypoglycemic events than that with the current treatment is important.

The present study showed that the IDeg treatment exhibited a slight increase of HbA1c to that observed in the case of IGlar treatment with no clinical significant effect, followed with a greater decrease in the FPG level. Therefore, we inferred that IDeg is noninferior to IGlar with respect to glycemic control. Similar efficacy is expected because all the included studies were treat-to-target trials, and noninferiority was observed in each trial. This finding is of great importance to confirm that the lower rates of hypoglycemia observed in the case of the IDeg treatment are not achieved at the cost of poor glycemic control.

Hypoglycemia is a common complication of insulin treatment in patients with DM [7]. Hypoglycemia has been considered to be one of the main barriers to good glycemic control, resulting in patients becoming unwilling to optimize treatment with insulin and in clinicians conservatively recommending more aggressive treatment targets [28]. In the present study, we found that the IDeg treatment was associated with a significant reduction in the risk of hypoglycemia, particularly nocturnal hypoglycemia. Besides, several studies showed that IDeg treatment not only decreased the risk of hypoglycemia but also led to improvements in both mental and physical health status [12, 13].

In patients with T2DM, the rate of nocturnal hypoglycemia decreased significantly along with a reduction in overall hypoglycemia. Although a previous meta-analysis reported that IDeg did not decrease the rate of overall hypoglycemia [15], the present meta-analysis including more recent studies showed a statistically significant decline in hypoglycemia. With respect to nocturnal hypoglycemia, a more statistically significant effect was observed than that for overall hypoglycemia in the case of the IDeg treatment.

In patients with T1DM, the IDeg treatment was associated with a reduction in nocturnal hypoglycemia, but not in overall hypoglycemia. Concerns about the increase in the rate of daytime hypoglycemia were raised. However, nocturnal hypoglycemia poses a considerably greater risk to patients with DM than daytime hypoglycemia [29]. Therefore, IDeg is still a safer basal insulin option than IGlar. Nonetheless, only four studies evaluated the hypoglycemia rate in the T1DM subgroup; therefore, the explanation of the results should be cautious.

It is striking that despite the lower rates of hypoglycemia, glycemic control was not evidently compensated. The present meta-analysis showed that IDeg exhibited significantly better results than IGlar in terms of the FPG level and the hypoglycemia rate, with similar reductions in the HbA1c level. Lower FPG values are typically expected to be followed by higher rates of nocturnal hypoglycemia, but in the case of IDeg, the results were the opposite. This difference in results could be attributed to the fact that IDeg has a stable and consistent glucose-lowering effect, with its ultralong duration of action and lower within-patient day-to-day variability than IGlar [8, 9].

Although our study included 15 high-quality RCTs, it has some important limitations. Firstly, most of the included studies had self-reporting of hypoglycemic episodes; this posed a potential risk of failure in the reporting of the episodes. Secondly, hypoglycemia has different definitions across the European Medicines Agency and American Diabetes Association [30]. However, in the present systematic review and meta-analysis, only a symptomatic or an asymptomatic event with plasma glucose of <3.1 mmol/L (56 mg/dL) was defined as hypoglycemia. Therefore, the effects of hypoglycemia were not covered by other definitions, and the extrapolation of the results should be cautious to other definitions of hyperglycemia. Nonetheless, a previous meta-analysis reported similar results for hypoglycemia defined differently [30]. Thirdly, the inherent limitations of a meta-analysis cannot be ignored, such as publication bias.

In conclusion, this systematic review and meta-analysis of 15 RCTs demonstrate that IDeg exhibits a similar reduction of HbA1c to that of IGlar but a lower FPG value. The rates of nocturnal hypoglycemia were significantly decreased in the IDeg group for both T1DM and T2DM patients, while the overall hypoglycemia was only reduced in patients with T2DM. These findings indicate that IDeg might be a safer option to patients with diabetes mellitus who need basal insulin therapy.

Conflicts of Interest

No competing financial interests exist.

Authors’ Contributions

Wei Liu and Xiaojie Yang contributed equally to this manuscript.

Acknowledgments

This work was supported by grants from the National Clinical Key Specialty Construction Project of China (no. (2013)544) and Clinical Research Center Project of the Department of Science and Technology of Guizhou Province (no. (2017)5405).

References

D. M. Nathan, P. A. Cleary, J. Y. Backlund et al., “Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes,” The New England Journal of Medicine, vol. 353, no. 25, pp. 2643–2653, 2005.
View at: Publisher Site | Google Scholar
Writing Team for the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group, “Effect of intensive therapy on the microvascular complications of type 1 diabetes mellitus,” JAMA, vol. 287, no. 19, pp. 2563–2569, 2002.
View at: Publisher Site | Google Scholar
P. Gaede, P. Vedel, N. Larsen, G. V. Jensen, H. H. Parving, and O. Pedersen, “Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes,” The New England Journal of Medicine, vol. 348, no. 5, pp. 383–393, 2003.
View at: Publisher Site | Google Scholar
T. K. Mattila and A. de Boer, “Influence of intensive versus conventional glucose control on microvascular and macrovascular complications in type 1 and 2 diabetes mellitus,” Drugs, vol. 70, no. 17, pp. 2229–2245, 2010.
View at: Publisher Site | Google Scholar
P. E. Cryer, “Hypoglycaemia: the limiting factor in the glycaemic management of type I and type II diabetes,” Diabetologia, vol. 45, no. 7, pp. 937–948, 2002.
View at: Publisher Site | Google Scholar
K. Horvath, K. Jeitler, A. Berghold et al., “Long-acting insulin analogues versus NPH insulin (human isophane insulin) for type 2 diabetes mellitus,” Cochrane Database of Systematic Reviews, vol. 2, article D5613, 2007.
View at: Publisher Site | Google Scholar
K. J. Lipska, J. S. Ross, Y. Wang et al., “National trends in US hospital admissions for hyperglycemia and hypoglycemia among Medicare beneficiaries, 1999 to 2011,” JAMA Internal Medicine, vol. 174, no. 7, pp. 1116–1124, 2014.
View at: Publisher Site | Google Scholar
T. Heise, L. Hermanski, L. Nosek, A. Feldman, S. Rasmussen, and H. Haahr, “Insulin degludec: four times lower pharmacodynamic variability than insulin glargine under steady-state conditions in type 1 diabetes,” Diabetes, Obesity and Metabolism, vol. 14, no. 9, pp. 859–864, 2012.
View at: Publisher Site | Google Scholar
T. Heise, L. Nosek, S. G. Bottcher, H. Hastrup, and H. Haahr, “Ultra-long-acting insulin degludec has a flat and stable glucose-lowering effect in type 2 diabetes,” Diabetes, Obesity and Metabolism, vol. 14, no. 10, pp. 944–950, 2012.
View at: Publisher Site | Google Scholar
B. Zinman, G. Fulcher, P. V. Rao et al., “Insulin degludec, an ultra-long-acting basal insulin, once a day or three times a week versus insulin glargine once a day in patients with type 2 diabetes: a 16-week, randomised, open-label, phase 2 trial,” The Lancet, vol. 377, no. 9769, pp. 924–931, 2011.
View at: Publisher Site | Google Scholar
K. I. Birkeland, P. D. Home, U. Wendisch et al., “Insulin degludec in type 1 diabetes: a randomized controlled trial of a new-generation ultra-long-acting insulin compared with insulin glargine,” Diabetes Care, vol. 34, no. 3, pp. 661–665, 2011.
View at: Publisher Site | Google Scholar
B. Zinman, A. Philis-Tsimikas, B. Cariou et al., “Insulin degludec versus insulin glargine in insulin-naive patients with type 2 diabetes: a 1-year, randomized, treat-to-target trial (BEGIN Once Long),” Diabetes Care, vol. 35, no. 12, pp. 2464–2471, 2012.
View at: Publisher Site | Google Scholar
A. J. Garber, A. B. King, S. Del Prato et al., “Insulin degludec, an ultra-longacting basal insulin, versus insulin glargine in basal-bolus treatment with mealtime insulin aspart in type 2 diabetes (BEGIN Basal-Bolus Type 2): a phase 3, randomised, open-label, treat-to-target non-inferiority trial,” Lancet, vol. 379, no. 9825, pp. 1498–1507, 2012.
View at: Publisher Site | Google Scholar
S. Heller, J. Buse, M. Fisher et al., “Insulin degludec, an ultra-longacting basal insulin, versus insulin glargine in basal-bolus treatment with mealtime insulin aspart in type 1 diabetes (BEGIN Basal-Bolus Type 1): a phase 3, randomised, open-label, treat-to-target non-inferiority trial,” The Lancet, vol. 379, no. 9825, pp. 1489–1497, 2012.
View at: Publisher Site | Google Scholar
J. Vora, T. Christensen, A. Rana, and S. C. Bain, “Insulin degludec versus insulin glargine in type 1 and type 2 diabetes mellitus: a meta-analysis of endpoints in phase 3a trials,” Diabetes Therapy, vol. 5, no. 2, pp. 435–446, 2014.
View at: Publisher Site | Google Scholar
C. Pan, J. L. Gross, W. Yang et al., “A multinational, randomized, open-label, treat-to-target trial comparing insulin degludec and insulin glargine in insulin-naive patients with type 2 diabetes mellitus,” Drugs in R&D, vol. 16, no. 2, pp. 239–249, 2016.
View at: Publisher Site | Google Scholar
M. L. Warren, L. B. Chaykin, S. Jabbour et al., “Insulin degludec 200 units/mL is associated with lower injection frequency and improved patient-reported outcomes compared with insulin glargine 100 units/mL in patients with type 2 diabetes requiring high-dose insulin,” Clinical Diabetes, vol. 35, no. 2, pp. 90–95, 2017.
View at: Publisher Site | Google Scholar
C. Wysham, A. Bhargava, L. Chaykin et al., “Effect of insulin degludec vs insulin glargine U100 on hypoglycemia in patients with type 2 diabetes: the SWITCH 2 randomized clinical trial,” JAMA, vol. 318, no. 1, pp. 45–56, 2017.
View at: Publisher Site | Google Scholar
D. Moher, A. Liberati, J. Tetzlaff, and D. G. Altman, “Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement,” Annals of Internal Medicine, vol. 151, no. 4, pp. 264–269, 2009.
View at: Publisher Site | Google Scholar
Y. Onishi, Y. Iwamoto, S. J. Yoo, P. Clauson, S. C. Tamer, and S. Park, “Insulin degludec compared with insulin glargine in insulin-naïve patients with type 2 diabetes: a 26-week, randomized, controlled, Pan-Asian, treat-to-target trial,” Journal of Diabetes Investigation, vol. 4, no. 6, pp. 605–612, 2013.
View at: Publisher Site | Google Scholar
S. C. Gough, A. Bhargava, R. Jain, H. Mersebach, S. Rasmussen, and R. M. Bergenstal, “Low-volume insulin degludec 200 units/ml once daily improves glycemic control similarly to insulin glargine with a low risk of hypoglycemia in insulin-naïve patients with type 2 diabetes: a 26-week, randomized, controlled, multinational, treat-to-target trial: the BEGIN LOW VOLUME trial,” Diabetes Care, vol. 36, no. 9, pp. 2536–2542, 2013.
View at: Publisher Site | Google Scholar
C. Mathieu, P. Hollander, B. Miranda-Palma et al., “Efficacy and safety of insulin degludec in a flexible dosing regimen vs insulin glargine in patients with type 1 diabetes (BEGIN: Flex T1): a 26-week randomized, treat-to-target trial with a 26-week extension,” The Journal of Clinical Endocrinology and Metabolism, vol. 98, no. 3, pp. 1154–1162, 2013.
View at: Publisher Site | Google Scholar
L. Meneghini, S. L. Atkin, S. C. Gough et al., “The efficacy and safety of insulin degludec given in variable once-daily dosing intervals compared with insulin glargine and insulin degludec dosed at the same time daily: a 26-week, randomized, open-label, parallel-group, treat-to-target trial in individuals with type 2 diabetes,” Diabetes Care, vol. 36, no. 4, pp. 858–864, 2013.
View at: Publisher Site | Google Scholar
S. P. Marso, M. G. DK, B. Zinman et al., “Efficacy and safety of degludec versus glargine in type 2 diabetes,” The New England Journal of Medicine, vol. 377, no. 8, pp. 723–732, 2017.
View at: Publisher Site | Google Scholar
R. Iga, H. Uchino, K. Kanazawa et al., “Glycemic variability in type 1 diabetes compared with degludec and glargine on the morning injection: an open-label randomized controlled trial,” Diabetes Therapy, vol. 8, no. 4, pp. 783–792, 2017.
View at: Publisher Site | Google Scholar
W. Lane, T. S. Bailey, G. Gerety et al., “Effect of insulin degludec vs insulin glargine U100 on hypoglycemia in patients with type 1 diabetes: the SWITCH 1 randomized clinical trial,” JAMA, vol. 318, no. 1, pp. 33–44, 2017.
View at: Publisher Site | Google Scholar
E. W. Gregg, Y. Li, J. Wang et al., “Changes in diabetes-related complications in the United States, 1990–2010,” The New England Journal of Medicine, vol. 370, no. 16, pp. 1514–1523, 2014.
View at: Publisher Site | Google Scholar
T. Kunt and F. J. Snoek, “Barriers to insulin initiation and intensification and how to overcome them,” International Journal of Clinical Practice. Supplement, vol. 63, no. s164, pp. 6–10, 2009.
View at: Publisher Site | Google Scholar
E. Chow, A. Bernjak, S. Williams et al., “Risk of cardiac arrhythmias during hypoglycemia in patients with type 2 diabetes and cardiovascular risk,” Diabetes, vol. 63, no. 5, pp. 1738–1747, 2014.
View at: Publisher Site | Google Scholar
S. Heller, C. Mathieu, R. Kapur, M. L. Wolden, and B. Zinman, “A meta-analysis of rate ratios for nocturnal confirmed hypoglycaemia with insulin degludec vs. insulin glargine using different definitions for hypoglycaemia,” Diabetic Medicine, vol. 33, no. 4, pp. 478–487, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2018 Wei Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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