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Study · Randomized controlled trial · n = 36 · 2016

8 results

Exenatide improves β-cell function up to 3 years of treatment in patients with type 2 diabetes: a randomised controlled trial.

van Raalte DH, Bunck MC, Smits MM, Hoekstra T, Cornér A, Diamant M, Eliasson B, Marja-RiittaTaskinen, Heine RJ, Smith U, HanneleYki-Järvinen, Mari A

European journal of endocrinology27 Jul 2016Cited by 26 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study8

5 results from studies that gave the peptide. 5 results from people.

  1. 01HumanRandomized controlled trialMechanism

    In type 2 diabetes patients, only exenatide sustained improved beta-cell glucose sensitivity for 3 years, unlike insulin glargine.

    In plain wordsIn patients with diabetes, exenatide sustained improved glucose sensitivity for 3 years, unlike insulin glargine.

    Outcome
    IncreaseSustained beta-cell glucose sensitivity
    Study

    n = 36

    Comparator
    Insulin glargine
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · 3 yearsAs given in this study (human).

    Source sentences

    Summary
    However, only EXE treatment sustained this improvement for 3 years.
    2 context sentences
    Summary · context
    Both treatments improved β-cell glucose sensitivity after 1-year treatment.
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).
  2. 02HumanRandomized controlled trialEfficacy outcome

    In metformin-treated type 2 diabetes patients, HbA1c was comparable with exenatide and insulin glargine after 3 years.

    In plain wordsIn patients with diabetes, HbA1c was similar with exenatide and insulin glargine after 3 years.

    Outcome
    No significant changeHbA1c at three years
    Study

    n: not reported in source

    Comparator
    Insulin glargine
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · 3 yearsAs given in this study (human).

    Measurements

    HbA1c
    6.6%
    exenatide
    HbA1c
    6.9%
    glargine

    Source sentences

    Summary
    After 3 years, groups had comparable glycaemic control (HbA1c: EXE 6.6 ± 0.2% and GLAR 6.9 ± 0.2%; P = 0.216).
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).
  3. 03HumanRandomized controlled trialEfficacy outcome

    In type 2 diabetes patients, exenatide reduced post-breakfast glucose more than insulin glargine at 1 and 3 years.

    In plain wordsIn patients with diabetes, exenatide lowered blood sugar after breakfast more than insulin glargine at 1 and 3 years.

    Outcome
    DecreasePost-breakfast glucose
    Study

    n: not reported in source

    Comparator
    Insulin glargine
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · 3 yearsAs given in this study (human).

    Source sentences

    Summary
    Compared with GLAR, at 1 and 3 years, EXE induced a stronger reduction in post-breakfast glucose concentrations (P < 0.001), with lower C-peptide levels (P < 0.001).
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).
  4. 04HumanRandomized controlled trialMechanism

    In type 2 diabetes patients, exenatide produced lower post-breakfast C-peptide than insulin glargine at 1 and 3 years.

    In plain wordsIn patients with diabetes, C-peptide after breakfast was lower with exenatide than insulin glargine at 1 and 3 years.

    Outcome
    DecreasePost-breakfast C-peptide
    Study

    n: not reported in source

    Comparator
    Insulin glargine
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · 3 yearsAs given in this study (human).

    Source sentences

    Summary
    Compared with GLAR, at 1 and 3 years, EXE induced a stronger reduction in post-breakfast glucose concentrations (P < 0.001), with lower C-peptide levels (P < 0.001).
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).
  5. 05HumanRandomized controlled trialMechanism

    In type 2 diabetes patients, exenatide increased insulin secretion at 8 mmol/L glucose compared with insulin glargine throughout treatment.

    In plain wordsIn patients with diabetes, exenatide increased insulin release at matched blood sugar compared with insulin glargine.

    Outcome
    IncreaseInsulin secretion at fixed glucose
    Study

    n: not reported in source

    Comparator
    Insulin glargine
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · 3 yearsAs given in this study (human).

    Source sentences

    Summary
    Compared with GLAR, EXE increased insulin secretion at 8 mmol/L glucose throughout the study period (P < 0.01).
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).

Studies that did not test the peptide alone3

In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Exenatide (exendin-4).

  1. 06HumanNot a test of Exenatide (exendin-4) aloneRandomized controlled trialMechanism

    In type 2 diabetes patients, beta-cell glucose sensitivity improved after one year with both exenatide and insulin glargine.

    In plain wordsIn patients with diabetes, insulin-producing cells became more sensitive to glucose with both exenatide and insulin glargine compared with baseline.

    Outcome
    IncreaseBeta-cell glucose sensitivity at one year
    Study

    n = 59

    Comparator
    Baseline
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    Both treatments improved β-cell glucose sensitivity after 1-year treatment.
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).

    In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Exenatide (exendin-4).

  2. 07HumanNot a test of Exenatide (exendin-4) aloneRandomized controlled trialMechanism

    In type 2 diabetes patients receiving exenatide or insulin glargine, rate sensitivity showed no consistent change.

    In plain wordsIn patients with diabetes receiving exenatide or insulin glargine, rate sensitivity showed no consistent change from baseline.

    Outcome
    Direction not reportedRate sensitivity
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    No consistent changes in other β-cell parameters including rate sensitivity and potentiation were observed.
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).

    In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Exenatide (exendin-4).

  3. 08HumanNot a test of Exenatide (exendin-4) aloneRandomized controlled trialMechanism

    In type 2 diabetes patients receiving exenatide or insulin glargine, potentiation showed no consistent change.

    In plain wordsIn patients with diabetes receiving exenatide or insulin glargine, potentiation showed no consistent change from baseline.

    Outcome
    Direction not reportedPotentiation
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    No consistent changes in other β-cell parameters including rate sensitivity and potentiation were observed.
    1 context sentence
    Summary · context
    Sixty-nine metformin-treated type 2 diabetes patients were randomised to the GLP1 receptor agonist, exenatide (EXE) twice daily (BID) or to insulin glargine (GLAR).

    In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Exenatide (exendin-4).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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