Evidence mapPaperPMID 35044568Full record

ArticleDiabetes therapy : research, treatment and education of diabetes and related disorders2022

Postprandial Glucose Excursions in Asian Versus Non-Asian Patients with Type 2 Diabetes: A Post Hoc Analysis of Baseline Data from Phase 3 Randomised Controlled Trials of IDegAsp.

Wenying Yang, Shahid Akhtar, Edward Franek, Martin Haluzík, Takahisa Hirose, Balamurali Kalyanam, Soumitra Kar, Ted Wu, Dilek Gogas Yavuz, Ambika Gopalakrishnan Unnikrishnan

13 registry-linked trialsAbstract read
In one paragraph

Article in Diabetes therapy : research, treatment and education of diabetes and related disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 13 registered trials, which are not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01009580 phase3completednot on this map

A 26-week, Randomised, Open-labelled, Two-arm, Parallel-group, Treat-to-target Trial Comparing Efficacy and Safety of Soluble Insulin Analogue Combination (SIAC) Twice Daily (BID) With Biphasic Insulin Aspart (BIAsp) 30 BID, With or Without Metformin, With or Without DPP-4 Inhibitor, With or Without Pioglitazone in Subjects With Type 2 Diabetes in Inadequate Glycaemic Control on Once or Twice Daily Premixed or Self-mixed Insulin Regimen With or Without OADs (BOOST™: Intensify Premix 1)

TypeinterventionalSponsorNovo Nordisk A/SRan2009 to 2010Enrolled447ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, biphasic insulin aspart 30
NCT01045447 phase3completednot on this map

A Trial Comparing Efficacy and Safety of NN5401 With Insulin Glargine, Both in Combination With Oral Antidiabetic Drugs in Subjects With Type 2 Diabetes (BOOST™ : INTENSIFY BASAL)

TypeinterventionalSponsorNovo Nordisk A/SRan2010 to 2010Enrolled465ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, insulin glargine
NCT01045707 phase3completednot on this map

NN5401-3590: A Trial Comparing Efficacy and Safety of NN5401 With Insulin Glargine in Insulin Naive Subjects With Type 2 Diabetes (BOOST™ : START 1) / NN5401-3726: An Extension Trial Comparing Safety and Efficacy of NN5401 With Insulin Glargine in Subjects With Type 2 Diabetes (BOOST™: START 1)

TypeinterventionalSponsorNovo Nordisk A/SRan2010 to 2010Enrolled530ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, insulin glargine
NCT01059812 phase3completednot on this map

A Pan Asian Trial Comparing Efficacy and Safety of NN5401 and Biphasic Insulin Aspart 30 in Type 2 Diabetes (BOOST™: INTENSIFY ALL)

TypeinterventionalSponsorNovo Nordisk A/SRan2010 to 2010Enrolled424ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, biphasic insulin aspart 30
NCT01272193 phase3completednot on this map

A Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart With Insulin Glargine in Insulin Naive Subjects With Type 2 Diabetes (BOOST™: JAPAN)

TypeinterventionalSponsorNovo Nordisk A/SRan2011 to 2011Enrolled296ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, insulin glargine
NCT01365507 phase3completednot on this map

A Trial Comparing the Efficacy and Safety of Insulin Degludec/Insulin Aspart Once Daily in Insulin-naïve Subjects With Type 2 Diabetes Mellitus When Using Two Different Titration Algorithms (BOOST™: SIMPLE USE)

TypeinterventionalSponsorNovo Nordisk A/SRan2011 to 2012Enrolled276ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart
NCT01513590 phase3completednot on this map

A 26-week, Randomised, Open-label, Multinational, Treat-to-target Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart (IDegAsp) Twice Daily (BID) and BIAsp 30 BID Both With Metformin in Insulin naïve Subjects With Type 2 Diabetes Mellitus Inadequately Controlled on Metformin Monotherapy or Metformin in Combination With One Additional Oral Antidiabetic Drug (OAD)

TypeinterventionalSponsorNovo Nordisk A/SRan2012 to 2012Enrolled394ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart
NCT01680341 phase3completednot on this map

A Trial Comparing the Efficacy and Safety of Two Different Titration Algorithms for Insulin Degludec/Insulin Aspart in Subjects With Type 2 Diabetes Mellitus Previously Treated With Insulin Glargine (BOOST®: SIMPLE vs. STEPWISE)

TypeinterventionalSponsorNovo Nordisk A/SRan2012 to 2013Enrolled272ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart
NCT01713530 phase3completednot on this map

A 26-week Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart BID and Insulin Degludec OD Plus Insulin Aspart in Subjects With Type 2 Diabetes Mellitus Treated With Basal Insulin in Need of Treatment Intensification With Mealtime Insulin

TypeinterventionalSponsorNovo Nordisk A/SRan2013 to 2014Enrolled274ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, insulin degludec, insulin aspart
NCT01814137 phase3completednot on this map

A Randomised Trial Comparing Efficacy and Safety After Intensification With Either Insulin Aspart Once Daily as add-on or Changing to Basal Bolus Treatment With Insulin Degludec and Insulin Aspart in Subjects With Type 2 Diabetes Previously Treated With Insulin Degludec/Insulin Aspart Twice Daily (BOOST®: INTENSIFY BID)

TypeinterventionalSponsorNovo Nordisk A/SRan2013 to 2014Enrolled40ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, insulin degludec, insulin aspart
NCT02648217 phase3completednot on this map

A Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart Twice Daily and Biphasic Insulin Aspart Twice Daily in Subjects With Type 2 Diabetes Mellitus Before, During and After Ramadan

TypeinterventionalSponsorNovo Nordisk A/SRan2016 to 2016Enrolled263ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, biphasic insulin aspart
NCT02762578 phase3completednot on this map

A Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart and BIAsp 30 in Subjects With Type 2 Diabetes BOOST: INTENSIFY PREMIX/ALL 2

TypeinterventionalSponsorNovo Nordisk A/SRan2016 to 2017Enrolled543ConditionsDiabetes, Diabetes Mellitus, Type 2Armsinsulin degludec/insulin aspart, biphasic insulin aspart
NCT02906917 phase3completednot on this map

This Trial is Conducted Globally. The Aim of This Trial is to Compare the Effect and Safety of Insulin Degludec/Insulin Aspart vs. Insulin Glargine Plus Insulin Aspart in Subjects With Type 2 Diabetes Treated With Basal Insulin With or Without Oral Antidiabetic Treatment in Need of Treatment Intensification.

TypeinterventionalSponsorNovo Nordisk A/SRan2016 to 2017Enrolled532ConditionsDiabetes, Diabetes Mellitus, Type 2ArmsInsulin degludec/insulin aspart, Insulin glargine, Insulin aspart
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Treatment Patterns and Glycaemic Control Between 2015 and 2019 in Tianjin, China: A Real-World Study of Adults with Type 2 Diabetes.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2025
    Article
  7. Barriers to the Use of Insulin Therapy and Potential Solutions: A Narrative Review of Perspectives from the Asia-Pacific Region.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Wenying YangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, 100029, China. ywying_1010@163.com.ORCID http://orcid.org/0000-0002-7997-9404
Shahid AkhtarClinical, Medical and Regulatory Department, Novo Nordisk Pharma Gulf FZ-LLC, Dubai, United Arab Emirates.
Edward FranekMossakowski Medical Research Centre, Warsaw, Poland.
Martin HaluzíkInstitute for Clinical and Experimental Medicine and Charles University, Prague, Czech Republic.
Takahisa HiroseToho University Graduate School of Medicine, Tokyo, Japan.
Balamurali KalyanamNovo Nordisk Service Centre India Private Ltd., Bangalore, India.
Soumitra KarNovo Nordisk Service Centre India Private Ltd., Bangalore, India.
Ted WuDiabetes Centre, Royal Prince Alfred Hospital, Sydney, Australia.
Dilek Gogas YavuzMarmara University School of Medicine, Istanbul, Turkey.
Ambika Gopalakrishnan UnnikrishnanChellaram Diabetes Institute, Pune, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIncreased postprandial glucose (PPG) is associated with high glycated haemoglobin levels and is an independent risk factor for cardiovascular diseases. The aim of this study was to compare PPG increments in Asian versus non-Asian adults with type 2 diabetes (T2D), who were insulin-naïve or insulin-experienced, from the phase 3 insulin degludec/insulin aspart (IDegAsp) clinical trials.

methodsThis was a post hoc analysis of data from 13 phase 3, randomised, parallel-group, open-label IDegAsp trials in patients with T2D. The pooled baseline clinical data were analysed for insulin-naïve and insulin-experienced groups; and each group was split into subgroups of Asian and non-Asian patients, respectively, and analysed accordingly. Baseline self-monitored blood glucose (SMBG) values at breakfast, lunch and the evening meal (before and 90 min after each meal) were used to assess PPG increments. The estimated differences in baseline SMBG increment between the Asian and non-Asian subgroups were analysed.

resultsClinical data from 4750 participants (insulin-naïve, n = 1495; insulin-experienced, n = 3255) were evaluated. In the insulin-naïve group, the postprandial SMBG increment was significantly greater in the Asian versus the non-Asian subgroup at breakfast (estimated difference 28.67 mg/dL, 95% confidence interval [CI] 18.35, 38.99; p < 0.0001), lunch (17.34 mg/dL, 95% CI 6.47, 28.21; p = 0.0018) and the evening meal (16.19 mg/dL, 95% CI 5.04, 27.34; p = 0.0045). In the insulin-experienced group, the postprandial SMBG increment was significantly greater in the Asian versus non-Asian subgroup at breakfast (estimated difference 13.81 mg/dL, 95% CI 9.19, 18.44; p < 0.0001) and lunch (29.18 mg/dL, 95% CI 24.22, 34.14; p < 0.0001), but not significantly different at the evening meal.

conclusionIn this post hoc analysis, baseline PPG increments were significantly greater in Asian participants with T2D than in their non-Asian counterparts at all mealtimes, with the exception of the evening meal in insulin-experienced participants. Asian adults with T2D may benefit from the use of regimens that control PPG excursions. CLINICAL TRIAL NUMBERS: NCT02762578, NCT01814137, NCT01513590, NCT01009580, NCT01713530, NCT02648217, NCT01045447, NCT01365507, NCT01045707, NCT01272193, NCT01059812, NCT01680341, NCT02906917.

Indexed as

AsianDiabetes managementIDegAspPostprandial glucose excursionType 2 diabetes

Identifiers

PMID35044568
PMCPMC8873325

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

and 7 more above

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.