Skip to content

Study · Randomized controlled trial · n = 146 · 2025

7 results

Improvement of β-Cell Function After Switching From DPP-4 Inhibitors to Oral Semaglutide: SWITCH-SEMA2 Post Hoc Analysis.

Nomoto H, Furusawa S, Yokoyama H, Suzuki Y, Izumihara R, Oe Y, Takahashi K, Miya A, Kameda H, Cho KY, Takeuchi J, Kurihara Y, Nakamura A, Atsumi T

The Journal of clinical endocrinology and metabolism1 Feb 2025Cited by 4 (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 study7

7 results from studies that gave the peptide. 7 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In adults with type 2 diabetes, switching from DPP-4 inhibitors to oral semaglutide raised HOMA2-beta more than continuing the DPP-4 inhibitor (+10.4 vs +0.6).

    In plain wordsIn adults with type 2 diabetes, switching to oral semaglutide improved beta-cell function scores more than staying on a DPP-4 inhibitor.

    Outcome
    IncreaseHOMA2-beta change
    Study

    n = 146

    Comparator
    DPP-4 inhibitor continuation
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Measurements

    HOMA2-beta change
    10.4 points
    semaglutide group
    HOMA2-beta change
    0.6 points
    DPP-4i group

    Source sentences

    Summary
    Regarding indices for β-cell function, changes in HOMA2-β as well as DI, reflecting the ability of β-cells to compensate for insulin resistance, were significantly higher in the semaglutide group compared with the DPP-4i group (mean change, +10.4 vs +0.6 in HOMA2-β [P = .001] and +0.09 vs 0.0 in DI [P < .001]).
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In adults with type 2 diabetes, switching from DPP-4 inhibitors to oral semaglutide raised the disposition index more than continuing the DPP-4 inhibitor (+0.09 vs 0.0).

    In plain wordsIn adults with type 2 diabetes, switching to oral semaglutide improved beta-cell compensation more than staying on a DPP-4 inhibitor.

    Outcome
    IncreaseDisposition index change
    Study

    n = 146

    Comparator
    DPP-4 inhibitor continuation
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Measurements

    Disposition index change
    0.09 units
    semaglutide group
    Disposition index change
    0 units
    DPP-4i group

    Source sentences

    Summary
    Regarding indices for β-cell function, changes in HOMA2-β as well as DI, reflecting the ability of β-cells to compensate for insulin resistance, were significantly higher in the semaglutide group compared with the DPP-4i group (mean change, +10.4 vs +0.6 in HOMA2-β [P = .001] and +0.09 vs 0.0 in DI [P < .001]).
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In adults with type 2 diabetes switched to oral semaglutide, glycemic control improved after 24 weeks.

    In plain wordsIn adults with type 2 diabetes switched to oral semaglutide, blood sugar control improved after 24 weeks.

    Outcome
    Not applicableGlycemic control after 24 weeks
    Study

    n = 69

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    In the semaglutide group, glycemic control, liver enzyme deviations, and lipid profiles improved after 24 weeks.
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In adults with type 2 diabetes switched to oral semaglutide, liver enzyme deviations improved after 24 weeks.

    In plain wordsIn adults with type 2 diabetes switched to oral semaglutide, abnormal liver enzyme results improved after 24 weeks.

    Outcome
    Not applicableLiver enzyme deviations after 24 weeks
    Study

    n = 69

    Outcome group
    Liver fat and liver function · Liver
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    In the semaglutide group, glycemic control, liver enzyme deviations, and lipid profiles improved after 24 weeks.
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  5. 05HumanRandomized controlled trialEfficacy outcome

    In adults with type 2 diabetes switched to oral semaglutide, lipid profiles improved after 24 weeks.

    In plain wordsIn adults with type 2 diabetes switched to oral semaglutide, blood fat levels improved after 24 weeks.

    Outcome
    Not applicableLipid profiles after 24 weeks
    Study

    n = 69

    Outcome group
    Lipids · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    In the semaglutide group, glycemic control, liver enzyme deviations, and lipid profiles improved after 24 weeks.
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  6. 06HumanRandomized controlled trialMechanism

    In the semaglutide group, improvement in disposition index correlated significantly with changes in BMI, HbA1c and fatty liver index.

    In plain wordsIn people on oral semaglutide, bigger gains in beta-cell compensation were linked to changes in weight, HbA1c and liver fat.

    Outcome
    Not applicableCorrelates of disposition index improvement
    Study

    n = 69

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    Improvement in DI in the semaglutide group was correlated significantly to changes in body mass index (BMI), HbA1c, and fatty liver index reflecting liver steatosis.
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.
  7. 07HumanRandomized controlled trialMechanism

    In multiple linear regression, semaglutide dose of 7 mg/day or more, reduction in fatty liver index and metformin nonuse were independently associated with disposition index improvement.

    In plain wordsHigher semaglutide dose, a bigger drop in the liver fat index and not taking metformin were each linked to a bigger gain in beta-cell compensation.

    Outcome
    Not applicableIndependent factors for disposition index improvement
    Study

    n: not reported in source

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated · oral · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    Multiple linear regression analysis revealed that dose of semaglutide (≥ 7 mg/day), reduction in fatty liver index, and metformin nonuse were independently associated with improvement of DI.
    2 context sentences
    Summary · context
    A total of 146 subjects (semaglutide group, 69; DPP-4i group, 77) were analyzed.
    Summary · context
    Post hoc analysis of SWITCH-SEMA 2, a multicenter prospective randomized controlled trial on the switch to oral semaglutide vs DPP-4i continuation without dose adjustment for 24 weeks in subjects with type 2 diabetes treated with DPP-4is, was conducted.

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

    11 Oct 2026, 00:04 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:06 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.