Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38331
Title: The association between dysregulated adipocytokines in early pregnancy and development of gestational diabetes.
Authors: De Courten B. ;Harrison C.L.;Hiam D.;Moreno-Asso A.;Stepto N.K.;Teede H.J. ;Abell S.K.;Shorakae S.
Institution: (Abell, Shorakae, Harrison, De Courten, Teede) Monash Centre for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Clayton, VIC, Australia (Abell, Shorakae, De Courten, Teede) Diabetes and Vascular Medicine Unit, Monash Health, Clayton, VIC, Australia (Hiam, Moreno-Asso, Stepto) Institute of Sport, Exercise and Active Living, Victoria University, Footscray, VIC, Australia
Issue Date: 10-Nov-2017
Copyright year: 2017
Publisher: John Wiley and Sons Ltd (Southern Gate, Chichester, West Sussex PO19 8SQ, United Kingdom. E-mail: vgorayska@wiley.com)
Place of publication: United Kingdom
Publication information: Diabetes/Metabolism Research and Reviews. 33 (8) (no pagination), 2017. Article Number: e2926. Date of Publication: November 2017.
Journal: Diabetes/Metabolism Research and Reviews
Abstract: Background: To investigate the association of adipocytokines and other inflammatory markers with development of GDM. Method(s): Serum adipocytokines and inflammatory markers were studied at 12 to 15 weeks gestation using biobanked control samples from a randomised trial. Study participants were identified as high risk for GDM using a validated clinical risk prediction tool. Markers were tested using commercial ELISA kits for high molecular weight (HMW) adiponectin, interleukin-6 (IL-6), plasminogen activator inhibitor-1, visfatin, omentin-1, sex-hormone binding globulin, monocyte chemoattractant protein, and asymmetrical dimethylarginine. The association between each biomarker and development of GDM at 24 to 28 weeks was evaluated using multivariable logistic regression analysis adjusted for maternal factors. Result(s): There were no differences in age, parity, country of birth, smoking, body mass index, or family history of diabetes in women with normal glucose tolerance (n = 78) and women who developed GDM (n = 25). Women with GDM were more likely to have a past history of GDM (P = 0.004). HMW adiponectin (odds ratio OR 0.37 [95% confidence interval 0.19-0.74]), omentin-1 (0.97 [0.94-0.99]), and IL-6 (1.87[1.03-3.37]) were associated with development of GDM, after adjustment for maternal age, body mass index, and past history of GDM. The other markers were not associated with GDM development. Conclusion(s): Decreased high molecular weight adiponectin and omentin-1 and increased IL-6 may enhance sensitivity of early risk prediction tools for women at high risk of GDM. This may allow early identification and opportunities for prevention of GDM and adverse outcomes. Further research is required in large validation studies to confirm these results.Copyright © 2017 John Wiley & Sons, Ltd.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1002/dmrr.2926
ORCID: Teede, Helena J.; ORCID: http://orcid.org/0000-0001-7609-577X
Link to associated publication: Click here for full text options
PubMed URL: 28806491 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28806491]
ISSN: 1520-7552
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38331
Type: Article
Subjects: *first trimester pregnancy
gestation period
high risk pregnancy
human
*immune dysregulation
inflammation
molecular weight
oral glucose tolerance test
*pregnancy diabetes mellitus
priority journal
*adipocytokine/ec [Endogenous Compound]
adiponectin/ec [Endogenous Compound]
biological marker/ec [Endogenous Compound]
glucose/ec [Endogenous Compound]
interleukin 6/ec [Endogenous Compound]
monocyte chemotactic protein/ec [Endogenous Compound]
n(g),n(g) dimethylarginine/ec [Endogenous Compound]
nicotinamide phosphoribosyltransferase/ec [Endogenous Compound]
plasminogen activator inhibitor 1/ec [Endogenous Compound]
sex hormone binding globulin/ec [Endogenous Compound]
unclassified drug
ELISA kit
omentin 1/ec [Endogenous Compound]
article
adult
clinical article
controlled study
female
adverse outcome
oral glucose tolerance test
molecular weight
inflammation
*immune dysregulation
human
high risk pregnancy
gestation period
*pregnancy diabetes mellitus
priority journal
controlled study
clinical article
Article
adverse outcome
adult
*first trimester pregnancy
female
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