학술논문

Clinical and biomarker modifiers of vitamin D treatment response: the Multi-Ethnic Study of Atherosclerosis
Document Type
article
Source
American Journal of Clinical Nutrition. 115(3)
Subject
Biomedical and Clinical Sciences
Nutrition and Dietetics
Clinical Research
Prevention
Clinical Trials and Supportive Activities
Atherosclerosis
Complementary and Integrative Health
Aging
Nutrition
Aged
Biomarkers
Calcifediol
Cholecalciferol
Dietary Supplements
Ethnicity
Female
Humans
Male
Minority Groups
Parathyroid Hormone
Vitamin D
Vitamin D Deficiency
Vitamins
vitamin D
cholecalciferol
vitamin D deficiency
vitamin D insufficiency
randomized clinical trial
standardization
HbA1c harmonization program
vitamin D standardization program
Engineering
Medical and Health Sciences
Nutrition & Dietetics
Clinical sciences
Nutrition and dietetics
Language
Abstract
BackgroundDifferent 25-hydroxyvitamin D [25(OH)D] thresholds for treatment with vitamin D supplementation have been suggested and are derived almost exclusively from observational studies. Whether other characteristics, including race/ethnicity, BMI, and estimated glomerular filtration rate (eGFR), should also influence the threshold for treatment is unknown.ObjectivesThe aim was to identify clinical and biomarker characteristics that modify the response to vitamin D supplementation.MethodsA total of 666 older adults in the Multi-Ethnic Study of Atherosclerosis (MESA) were randomly assigned to 16 wk of oral vitamin D3 (2000 IU/d; n = 499) or placebo (n = 167). Primary outcomes were changes in serum parathyroid hormone (PTH) and 1,25-dihydroxyvitamin D [1,25(OH)2D] concentrations from baseline to 16 wk.ResultsAmong 666 participants randomly assigned (mean age: 72 y; 53% female; 66% racial/ethnic minority), 611 (92%) completed the study. The mean (SD) change in PTH was -3 (16) pg/mL with vitamin D3 compared with 2 (18) pg/mL with placebo (estimated mean difference: -5; 95% CI: -8, -2 pg/mL). Within the vitamin D3 group, lower baseline 25-hydroxyvitamin D [25(OH)D] was associated with a larger decline in PTH in a nonlinear fashion. With baseline 25(OH)D ≥30 ng/mL as the reference, 25(OH)D