AI Article Synopsis

  • The study aimed to analyze the metabolic and phenotypic differences in pregnant women with one abnormal glucose value (OAV) during an oral glucose tolerance test (OGTT) compared to normal and gestational diabetes mellitus (GDM) groups.
  • It involved 7,618 pregnant women, dividing the OAV group based on when hyperglycemia occurred during the OGTT: fasting, 1 hour, or 2-3 hours post-glucose intake.
  • Results showed the OAV group had intermediate insulin sensitivity and secretion levels, with specific characteristics: fasting OAV exhibited higher insulin resistance and lower insulin secretion, while the 1-hour OAV indicated lower insulin responsiveness.

Article Abstract

Objective: To examine the phenotypic and metabolic characteristics of pregnant women with one abnormal glucose value (OAV) in the OGTT compared to normals (N) and to gestational diabetes mellitus (GDM) subjects and also to test if the timing of the observed hyperglycemia is related to any difference in their phenotype.

Materials And Methods: 7618 pregnant women underwent a 100g OGTT (N = 3813, OAV = 1290, GDM = 2515). The OAV Group was further subdivided according to the time of hyperglycemia: fasting OAV, 1h OAV and 2-3h OAV. Demographic data were recorded and indices of insulin sensitivity and secretion were calculated.

Results: The OAV Group presented intermediate values in all demographic parameters and in indices of insulin sensitivity and secretion compared to N and GDM Groups (p < 0.01). Regarding the three OAV subgroups: OAV-Fasting was heavier, had increased HOMA-IR and lower HOMA-B index, than the other two. In contrast, the OAV-1h subgroup had the lower Stumvoll first and second phase indices compared to the others, and also the lowest ISSI (p < 0.01).

Conclusion: Isolated hyperglycemia appeared to be heterogeneous. Fasting hyperglycemia was mainly characterized by increased hepatic insulin resistance and impaired basal insulin secretion, while OAV at 1h presented increased muscle insulin resistance and diminished stimulated insulin secretion.

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Source
http://dx.doi.org/10.1016/j.diabres.2010.08.024DOI Listing

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