Plasma glycated CD59 predicts postpartum glucose intolerance after gestational diabetes.


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
11 Oct 2021
Historique:
received: 15 06 2021
accepted: 15 09 2021
pubmed: 16 9 2021
medline: 16 10 2021
entrez: 15 9 2021
Statut: epublish

Résumé

To assess whether in women with gestational diabetes mellitus (GDM), postpartum plasma glycated CD59 (pGCD59) levels predict conversion to glucose intolerance diagnosed with an oral glucose tolerance test (OGTT). Blood levels of pGCD59 were measured in a case-control study of 105 women with GDM who underwent a 75 g OGTT 3 months postpartum. The 35 postpartum glucose intolerant cases were individually matched for age, BMI, ethnic origin, and parity with 70 women with GDM but normal postpartum OGTT (controls). The GDM cohort (105) was also matched with 105 normal glucose tolerant women during pregnancy. pGCD59 was measured by ELISA in standard peptide units (SPU). Mean pGCD59 postpartum was significantly higher in cases than in controls (1.5 ± 0.6 SPU vs 1.0 ± 0.6 SPU, P < 0.001). The area under the receiving operating characteristic curve (AUC) in cases vs controls was 0.72 (95% CI: 0.62-0.83) for postpartum pGCD59 and 0.50 (95% CI: 0.36-0.61) for postpartum HbA1c. A 0.5-unit increase in postpartum pGCD59 was associated with an odds ratio (OR) of 3.3 (95% CI: 1.82-6.16, P < 0.001) for glucose intolerance postpartum. A pGCD59 cut-off postpartum of 0.9 SPU had a sensitivity of 85.7% (95% CI: 69.7-95.2%), specificity of 47.8% (95% CI: 35.6-60.2%), positive predictive value of 45.4% (95% CI: 33.1-58.2%), and negative predictive value of 86.8% (95% CI: 71.9-95.6%). pGCD59 in pregnancy was a poor predictor for glucose intolerance postpartum (AUC of 0.61 (95% CI: 0.50-0.72)). pGCD59 might identify women at low risk for glucose intolerance postpartum and could help to avoid an OGTT.

Identifiants

pubmed: 34524975
doi: 10.1530/EJE-21-0635
pii: EJE-21-0635
pmc: PMC8511340
mid: NIHMS1744622
doi:
pii:

Substances chimiques

Blood Glucose 0
CD59 Antigens 0
Glycated Hemoglobin A 0
CD59 protein, human 101754-01-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

755-763

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK101442
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK118528
Pays : United States
Organisme : NIDDK NIH HHS
ID : R56 DK089206
Pays : United States

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Auteurs

Katrien Benhalima (K)

Department of Endocrinology, University Hospital Gasthuisberg, KU Leuven, Leuven, Belgium.

Diane D Ma (DD)

Divisions of Hematology, Bringham & Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Annouschka Laenen (A)

Center of Biostatics and Statistical bioinformatics, KU Leuven, Leuven, Belgium.

Chantal Mathieu (C)

Department of Endocrinology, University Hospital Gasthuisberg, KU Leuven, Leuven, Belgium.

Jose A Halperin (JA)

Divisions of Hematology, Bringham & Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

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Classifications MeSH