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Fasting C-peptide in Gestational Diabetes Mellitus

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IntroductionInsulin secretion and sensitivity are thought to vary in gestational diabetes mellitus (GDM) as well as in different trimesters within the same individual.ObjectivesTo see the fasting serum C-peptide in subjects with GDM as an indicator of basal insulin secretion and to compare it to the normal glucose tolerance (NGT) control.MethodThis case-control study investigated and compared fasting serum C-peptide in 35 GDM subjects with 37, age, BMI, and trimester-matched control. GDM was diagnosed by WHO 2013 criteria. Plasma glucose was measured by the glucose oxidase method and C-peptide by a chemiluminescent immunometric assay.ResultFasting serum C-peptides were significantly higher in the GDM group than that of the NGT (NGT vs. GDM: 1.45±0.76 vs. 1.99±1.28, mean±SD, p=0.032), but no difference was observed between GDM and NGT with a BMI <25kg/m2(NGT vs. GDM: 1.25±0.44 vs. 1.37±0.77, mean±SD, p=0.597). Within the NGT group, fasting C-peptide was similar with a BMI cut-off 25kg/m2(<25 vs. ≥ 25: 1.25±0.44 vs. 1.61±0.94, p=0.159); however, within the GDM group, the fasting C-peptide was significantly higher with a BMI ≥25 kg/m2(<25 vs. ≥ 25: 1.37±0.77 vs. 2.45±1.41, mean ±SD, p=0.011). We did not observe any trimester-specific difference in fasting C-peptide between the NGT and the GDM (NGT vs. GDM: 1.55±0.45 vs. 1.67±0.57, p=0.736; 1.43±0.95 vs. 2.13±1.10, p=0.085; 1.43±0.71 vs. 1.97±1.60, p= 0.204; ng/dl, mean ± SD, for 1st, 2nd, and 3rdtrimester, respectively). Pearson correlation revealed BMI (r=0.389, p=0.001), Systolic BP (r=0.531, p<0.001), Diastolic BP (r=0.355, p=0.002), FPG (r=0.32, p=0.006) and 1hr PG on OGTT (r=0.423, p<0.001) had significant positive correlation with fasting C-peptide.ConclusionFasting C-peptide increased significantly in GDM with BMI ≥25kg/m2, but not with <25kg/m2
Title: Fasting C-peptide in Gestational Diabetes Mellitus
Description:
IntroductionInsulin secretion and sensitivity are thought to vary in gestational diabetes mellitus (GDM) as well as in different trimesters within the same individual.
ObjectivesTo see the fasting serum C-peptide in subjects with GDM as an indicator of basal insulin secretion and to compare it to the normal glucose tolerance (NGT) control.
MethodThis case-control study investigated and compared fasting serum C-peptide in 35 GDM subjects with 37, age, BMI, and trimester-matched control.
GDM was diagnosed by WHO 2013 criteria.
Plasma glucose was measured by the glucose oxidase method and C-peptide by a chemiluminescent immunometric assay.
ResultFasting serum C-peptides were significantly higher in the GDM group than that of the NGT (NGT vs.
GDM: 1.
45±0.
76 vs.
1.
99±1.
28, mean±SD, p=0.
032), but no difference was observed between GDM and NGT with a BMI <25kg/m2(NGT vs.
GDM: 1.
25±0.
44 vs.
1.
37±0.
77, mean±SD, p=0.
597).
Within the NGT group, fasting C-peptide was similar with a BMI cut-off 25kg/m2(<25 vs.
≥ 25: 1.
25±0.
44 vs.
1.
61±0.
94, p=0.
159); however, within the GDM group, the fasting C-peptide was significantly higher with a BMI ≥25 kg/m2(<25 vs.
≥ 25: 1.
37±0.
77 vs.
2.
45±1.
41, mean ±SD, p=0.
011).
We did not observe any trimester-specific difference in fasting C-peptide between the NGT and the GDM (NGT vs.
GDM: 1.
55±0.
45 vs.
1.
67±0.
57, p=0.
736; 1.
43±0.
95 vs.
2.
13±1.
10, p=0.
085; 1.
43±0.
71 vs.
1.
97±1.
60, p= 0.
204; ng/dl, mean ± SD, for 1st, 2nd, and 3rdtrimester, respectively).
Pearson correlation revealed BMI (r=0.
389, p=0.
001), Systolic BP (r=0.
531, p<0.
001), Diastolic BP (r=0.
355, p=0.
002), FPG (r=0.
32, p=0.
006) and 1hr PG on OGTT (r=0.
423, p<0.
001) had significant positive correlation with fasting C-peptide.
ConclusionFasting C-peptide increased significantly in GDM with BMI ≥25kg/m2, but not with <25kg/m2.

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