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Study · Observational study · n = 116 · 2014

4 results

The association between postprandial urinary C-peptide creatinine ratio and the treatment response to liraglutide: a multi-centre observational study.

Thong KY, McDonald TJ, Hattersley AT, Blann AD, Ramtoola S, Duncan C, Carr S, Adamson K, Nayak AU, Khurana R, Hunter SJ, Ali A, Au S, Ryder RE

Diabetic medicine : a journal of the British Diabetic Association6 Dec 2013Cited by 22 (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 study4

4 results from studies that gave the peptide. 4 results from people.

  1. 01HumanObservational studyOther

    In adults with type 2 diabetes starting or on liraglutide, neither pretreatment nor on-treatment urinary C-peptide creatinine ratio correlated with HbA1c change in univariate analyses.

    In plain wordsIn adults with type 2 diabetes on liraglutide, urinary C-peptide ratio was not linked to HbA1c change in simple analyses.

    Outcome
    No significant changeCorrelation of urinary C-peptide creatinine ratio with HbA1c change (univariate)
    Study

    n = 116

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.6 → 1.2 mg daily · 32 weeksAs given in this study (human).

    Measurements

    Spearman r
    −0.17
    pretreatment ratio
    Spearman r
    −0.2
    on-treatment ratio

    Source sentences

    Summary
    In univariate analyses, neither pretreatment nor on-treatment urinary C-peptide creatinine ratio correlated with HbA1c change (Spearman rank correlation coefficient, r = -0.17, P = 0.17 and r = -0.20, P = 0.19, respectively).
    2 context sentences
    Summary · context
    One hundred and sixteen subjects (70 pretreatment, 46 on treatment) with Type 2 diabetes from 10 diabetes centres were studied.
    Summary · context
    A single, outpatient urine sample for urinary C-peptide creatinine ratio was collected 2 h after the largest meal of the day among two separate groups: (1) subjects initiating liraglutide (0.6 → 1.2 mg daily) or (2) subjects already treated with liraglutide for 20-32 weeks.
  2. 02HumanObservational studyOther

    In adults with type 2 diabetes on liraglutide, after adjusting for baseline HbA1c, pretreatment and on-treatment log urinary C-peptide creatinine ratio were significantly associated with HbA1c change.

    In plain wordsIn adults with type 2 diabetes on liraglutide, after adjusting for baseline HbA1c, urinary C-peptide ratio was linked to how much HbA1c changed.

    Outcome
    Not applicableAssociation of urinary C-peptide creatinine ratio with HbA1c change (multivariate)
    Study

    n = 116

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.6 → 1.2 mg daily · 32 weeksAs given in this study (human).

    Measurements

    P value
    0.048
    pretreatment
    P value
    0.04
    on-treatment

    Source sentences

    Summary
    In multi-linear regression analyses, entering baseline HbA1c and log urinary C-peptide creatinine ratio, pretreatment and on-treatment log urinary C-peptide creatinine ratio became significantly associated with HbA1c change (P = 0.048 and P = 0.040, respectively).
    2 context sentences
    Summary · context
    One hundred and sixteen subjects (70 pretreatment, 46 on treatment) with Type 2 diabetes from 10 diabetes centres were studied.
    Summary · context
    A single, outpatient urine sample for urinary C-peptide creatinine ratio was collected 2 h after the largest meal of the day among two separate groups: (1) subjects initiating liraglutide (0.6 → 1.2 mg daily) or (2) subjects already treated with liraglutide for 20-32 weeks.
  3. 03HumanObservational studyOther

    In adults with type 2 diabetes starting liraglutide, HbA1c did not change significantly in the lowest quartile of pretreatment urinary C-peptide creatinine ratio.

    In plain wordsIn adults with type 2 diabetes starting liraglutide, those with the lowest urinary C-peptide ratio had no clear HbA1c change.

    Outcome
    No significant changeHbA1c change in lowest quartile of pretreatment urinary C-peptide creatinine ratio
    Study

    n: not reported in source

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.6 → 1.2 mg daily · 32 weeksAs given in this study (human).

    Measurements

    HbA1c change
    −3 mmol/mol
    quartile 1

    Source sentences

    Summary
    -3 ± 17 mmol/mol (-0.3 ± 1.6%) (P = 0.52)
    1 context sentence
    Summary · context
    A single, outpatient urine sample for urinary C-peptide creatinine ratio was collected 2 h after the largest meal of the day among two separate groups: (1) subjects initiating liraglutide (0.6 → 1.2 mg daily) or (2) subjects already treated with liraglutide for 20-32 weeks.
  4. 04HumanObservational studyOther

    In adults with type 2 diabetes starting liraglutide, HbA1c fell by 11-12 mmol/mol in quartiles 2 to 4 of pretreatment urinary C-peptide creatinine ratio.

    In plain wordsIn adults with type 2 diabetes starting liraglutide, HbA1c fell in those with higher urinary C-peptide ratios.

    Outcome
    DecreaseHbA1c change in quartiles 2 to 4 of pretreatment urinary C-peptide creatinine ratio
    Study

    n: not reported in source

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.6 → 1.2 mg daily · 32 weeksAs given in this study (human).

    Measurements

    HbA1c change
    −12 mmol/mol
    quartile 2
    HbA1c change
    −11 mmol/mol
    quartile 3
    HbA1c change
    −12 mmol/mol
    quartile 4

    Source sentences

    Summary
    -12 ± 15 mmol/mol (-1.1 ± 1.4%) (P = 0.003), -11 ± 13 mmol/mol (-1.0 ± 1.2%) (P = 0.002) and -12±17 mmol/mol (-1.1±1.6%) (P=0.016), respectively.
    1 context sentence
    Summary · context
    A single, outpatient urine sample for urinary C-peptide creatinine ratio was collected 2 h after the largest meal of the day among two separate groups: (1) subjects initiating liraglutide (0.6 → 1.2 mg daily) or (2) subjects already treated with liraglutide for 20-32 weeks.

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

    12 Oct 2026, 12:10 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:05 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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