The effect of vitamin D supplementation on cardiovascular risk in patients with prediabetes: A secondary analysis of the D2d study.


Journal

Journal of diabetes and its complications
ISSN: 1873-460X
Titre abrégé: J Diabetes Complications
Pays: United States
ID NLM: 9204583

Informations de publication

Date de publication:
08 2022
Historique:
received: 08 04 2022
revised: 20 05 2022
accepted: 09 06 2022
pubmed: 27 6 2022
medline: 10 8 2022
entrez: 26 6 2022
Statut: ppublish

Résumé

Low blood 25(OH)D level is associated with increased cardiovascular disease (CVD) risk. Additionally, individuals with prediabetes are at higher risk for CVD than individuals with normoglycemia. We investigated the effects of vitamin D supplementation on CVD outcomes in the vitamin D and type 2 diabetes (D2d) study, a large trial among adults with prediabetes. 2423 participants were randomized to 4000 IU/day of vitamin D Mean age was 60 years, 45 % were women, 13 % had history of CVD. Twenty-one participants assigned to vitamin D and 12 participants assigned to placebo met the MACE outcome (HR 1.81, 95%CI 0.89 to 3.69). There were 27 expanded MACE outcomes in each group (HR 1.02, 95%CI, 0.59 to 1.76). There were no significant differences between vitamin D and placebo in individual CVD risk factors, but change in ASCVD risk score favored the vitamin D group (-0.45 %, 95%CI -0.75 to -0.15). In people with prediabetes not selected for vitamin D insufficiency and with intermediate CVD risk, vitamin D supplementation did not decrease MACE but had a small favorable effect on ASCVD risk score. D2d ClinicalTrials.gov number, NCT01942694, prospectively registered September 16, 2013.

Identifiants

pubmed: 35753926
pii: S1056-8727(22)00136-2
doi: 10.1016/j.jdiacomp.2022.108230
pii:
doi:

Substances chimiques

Vitamins 0
Vitamin D 1406-16-2

Banques de données

ClinicalTrials.gov
['NCT01942694']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't Research Support, N.I.H., Intramural Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

108230

Subventions

Organisme : NIDDK NIH HHS
ID : U34 DK091958
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK098245
Pays : United States

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Cyrus Desouza (C)

Omaha VA Medical Center, University of Nebraska Medical Center, Omaha, NE, United States of America. Electronic address: cdesouza@unmc.edu.

Ranee Chatterjee (R)

Department of Medicine, Duke University, Durham, NC, United States of America.

Ellen M Vickery (EM)

Division of Endocrinology, Diabetes and Metabolism, Tufts Medical Center, Boston, MA, United States of America.

Jason Nelson (J)

Tufts CTSI, BERD Center, Tufts Medical Center, Boston, MA, United States of America.

Karen C Johnson (KC)

Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, United States of America.

Sangeeta R Kashyap (SR)

Department of Endocrinology, Diabetes, and Metabolism, Cleveland Clinic, Cleveland, OH, United States of America.

Michael R Lewis (MR)

Department of Pathology, Banner MD Anderson Cancer Center, Gilbert, AZ, United State of America.

Karen Margolis (K)

Health Partners Institute, Minneapolis, MN, United States of America.

Richard Pratley (R)

AdventHealth Translational Research Institute, Orlando, FL, United States of America.

Neda Rasouli (N)

University of Colorado, School of Medicine and VA Eastern Colorado Health Care System, Aurora, CO, United States of America.

Patricia R Sheehan (PR)

Division of Endocrinology, Diabetes and Metabolism, Tufts Medical Center, Boston, MA, United States of America.

Anastassios G Pittas (AG)

Division of Endocrinology, Diabetes and Metabolism, Tufts Medical Center, Boston, MA, United States of America.

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Classifications MeSH