Journal of Endocrinological Investigation

, Volume 41, Issue 5, pp 567–573 | Cite as

Abnormal 1-hour post-load glycemia during pregnancy impairs post-partum metabolic status: a single-center experience

  • A. Tumminia
  • A. Milluzzo
  • F. Cinti
  • M. Parisi
  • F. Tata
  • F. Frasca
  • L. Frittitta
  • R. Vigneri
  • L. Sciacca
Original Article



Recent evidence indicates that people with normal glucose tolerance (NGT) but 1-h post-load plasma glucose (1-h OGTT) ≥ 155 mg/dl have an increased risk for developing Type 2 diabetes mellitus (T2DM), determining a new risk category with deeper metabolic impairment. The aim of this study was to identify, among women with gestational diabetes (GDM), which alterations at OGTT during pregnancy are more frequently associated with 1-h OGTT ≥ 155 mg/dl at post-partum examination.


Among 297 women affected by GDM, we retrospectively evaluated 244 resulted NGT after delivery. Based on post-partum glucose levels at 1-h OGTT, these people were divided into 188 cases (77.0%) with 1-h OGTT < 155 mg/dl (L-NGT) and 56 (23.0%) with 1-h OGTT ≥ 155 mg/dl (H-NGT).


Abnormal glucose levels at 1-h OGTT during pregnancy (≥ 180 mg/dl) were more frequent in H-NGT than in L-NGT (39.3 vs. 24.6%, odds ratio 3.7 [95% CI 1.4–9.6]; p = 0.016). Moreover, H-NGT showed more frequently the simultaneous alteration of all three OGTT plasma glucose values during pregnancy (10.7 vs. 2.1%, odds ratio 4.5 [95% CI 1.5–20.3]; p = 0.038) and less frequently the alteration of fasting plasma glucose alone (14.3 vs. 30.8%, odds ratio 0.4 [95% CI 0.1–0.7]; p = 0.028).


Abnormal 1-h OGTT during pregnancy predicts an increased risk for post-partum 1-h OGTT ≥ 155 mg/dl in women with previous GDM. Even if NGT after delivery, these women may require a closer long-term post-partum follow-up, being at higher risk to develop future glucose intolerance.


Gestational diabetes Pregnancy Oral glucose tolerance test Type 2 diabetes mellitus 



The authors thank Prof. Giuliana Arcidiacono, Ph.D. in English and Anglo-American Studies, University of Catania, for the language revision of the manuscript.

Compliance with ethical standards

Conflict of interest

RV. participated in the Novo Nordisk Advisory Board in 2015 and 2016. L.S. participated in the Lilly Advisory Board in 2017. The other authors have nothing to disclose.

Ethical approval

The ethical committee approval is not required in our institution for retrospective studies. The study was conducted in accordance with the ethical principles of the Declaration of Helsinki and its later amendments.

Informed consent

For this type of study formal consent is not required.

Supplementary material

40618_2017_774_MOESM1_ESM.docx (59 kb)
Supplementary material 1 (DOCX 59 kb)


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Copyright information

© Italian Society of Endocrinology (SIE) 2017

Authors and Affiliations

  • A. Tumminia
    • 1
  • A. Milluzzo
    • 1
  • F. Cinti
    • 1
  • M. Parisi
    • 1
  • F. Tata
    • 1
  • F. Frasca
    • 1
  • L. Frittitta
    • 1
  • R. Vigneri
    • 1
    • 2
  • L. Sciacca
    • 1
  1. 1.Endocrinology Section, Department of Clinical and Experimental Medicine, Garibaldi-Nesima HospitalUniversity of CataniaCataniaItaly
  2. 2.Institute of Bioimages and Biostructures, CNRCataniaItaly

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