The Weak Relationship between Vitamin D Compounds and Glucose Homeostasis Measures in Pregnant Women with Obesity: An Exploratory Sub-Analysis of the DALI Study.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
09 Aug 2022
Historique:
received: 22 06 2022
revised: 02 08 2022
accepted: 05 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

Studies on the relationship between vitamin D (VitD) and glucose homeostasis usually consider either total VitD or 25OHD3 but not 25OHD2 and epimers. We aimed to evaluate the cross-sectional association of VitD compounds with glucose homeostasis measurements in pregnant women with overweight/obesity participating in the Vitamin D And Lifestyle Intervention for Gestational Diabetes Mellitus Prevention study. Methods: The analysis included 912 women. Inclusion criteria: <20 weeks gestation, body mass index ≥29 kg/m2 and information on exposure and outcome variables at baseline. Measurements: A 75 g OGTT at <20, 24−28 and 35−37 weeks gestation (except if previous diabetes diagnosis). Exposure variables: 25OHD2, 25OHD3 and C3-epimer. Outcome variables: fasting and post-challenge insulin sensitivity and secretion indices, corresponding disposition indices (DI), plasma glucose at fasting and 1 and 2 h, hyperglycemia in pregnancy (HiP). Statistics: Multivariate regression analyses with adjustment. Results: Baseline VitD sufficiency was 66.3%. Overall, VitD compounds did not show strong associations with any glucose homeostasis measures. 25OHD3 showed direct significant associations with: FPG at <20 and 24−28 weeks (standardized β coefficient (β) 0.124, p = 0.030 and 0.111, p = 0.026 respectively), 2 h plasma glucose at 24−28 weeks (β 0.120, p = 0.018), and insulin sensitivity (1/HOMA-IR, β 0.127, p = 0.027) at 35−37 weeks; it showed an inverse association with fasting DI (QUCKI*HOMA-β) at <20 and 24−28 weeks (β −0.124, p = 0.045 and β −0.148, p = 0.004 respectively). 25OHD2 showed direct associations with post-challenge insulin sensitivity (Matsuda, β 0.149, p = 0.048) at 24−28 weeks) and post-challenge DI (Matsuda*Stumvoll phase 1) at 24−28 and 35−37 weeks (β 0.168, p = 0.030, β 0.239, p = 0.006). No significant association with C3-epimer was observed at any time period. Conclusions: In these women with average baseline VitD in sufficiency range, VitD compounds did not show clear beneficial associations with glucose homeostasis measures.

Identifiants

pubmed: 36014761
pii: nu14163256
doi: 10.3390/nu14163256
pmc: PMC9415540
pii:
doi:

Substances chimiques

Blood Glucose 0
Insulin 0
Vitamins 0
Vitamin D 1406-16-2
Calcifediol P6YZ13C99Q

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Spanish Diabetes Society (SED)
ID : XI Grant for clinical research projects in diabetes lead by young investigators to LM in 2020

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Auteurs

Lilian Cristina Mendoza (LC)

Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain.
CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), 28029 Madrid, Spain.

Jürgen Harreiter (J)

Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Gender Medicine Unit, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.

Gernot Desoye (G)

Department of Obstetrics and Gynecology, Medical University of Graz, 8036 Graz, Austria.

David Simmons (D)

Macarthur Clinical School, School of Medicine, Western Sydney University, Campbelltown, NSE 2560, Australia.

Juan M Adelantado (JM)

Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain.

Alexandra Kautzky-Willer (A)

Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Gender Medicine Unit, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.

Agnieszka Zawiejska (A)

Department of Reproduction, Poznan University of Medical Sciences, 60-525 Poznan, Poland.

Ewa Wender-Ozegowska (E)

Department of Reproduction, Poznan University of Medical Sciences, 60-525 Poznan, Poland.

Annunziata Lapolla (A)

Department of Medicine, University of Padova, 35128 Padova, Italy.

Maria G Dalfra (MG)

Department of Medicine, University of Padova, 35128 Padova, Italy.

Alessandra Bertolotto (A)

Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.

Roland Devlieger (R)

Obstetrics and Gynecology, University Hospitals KU Leuven, 3000 Leuven, Belgium.

Fidelma Dunne (F)

College of Medicine, Nursing and Health Sciences, School of Medicine, National University of Ireland, H91 TK33 Galway, Ireland.

Elisabeth R Mathiesen (ER)

Center for Pregnant Women with Diabetes, Departments of Endocrinology and Obstetrics, Rigshospitalet, University of Copenhagen, DK-1165 Copenhagen, Denmark.

Peter Damm (P)

Center for Pregnant Women with Diabetes, Departments of Endocrinology and Obstetrics, Rigshospitalet, University of Copenhagen, DK-1165 Copenhagen, Denmark.

Lisse Lotte Andersen (LL)

Department of Gynecology and Obstetrics, Odense University Hospital, 5000 Odense, Denmark.

Dorte Moller Jensen (DM)

Department of Gynecology and Obstetrics, Odense University Hospital, 5000 Odense, Denmark.

David Hill (D)

Lawson Health Research Institute, St. Joseph Health Care, London, ON N6A 4V2, Canada.

Mireille Nicoline Maria van Poppel (MNM)

Institute of Sport Science, University of Graz, 8010 Graz, Austria.

Rosa Corcoy (R)

Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain.
CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), 28029 Madrid, Spain.
Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain.

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