共 13 条
Scientific opinion on the tolerable upper intake level for vitamin D, including the derivation of a conversion factor for calcidiol monohydrate
被引:19
|作者:
Turck, Dominique
Bohn, Torsten
Castenmiller, Jacqueline
de Henauw, Stefaan
Hirsch-Ernst, Karen-Ildico
Knutsen, Helle Katrine
Maciuk, Alexandre
Mangelsdorf, Inge
McArdle, Harry J.
Pentieva, Kristina
Siani, Alfonso
Thies, Frank
Tsabouri, Sophia
Vinceti, Marco
Lanham-New, Susan
Passeri, Giovanni
Craciun, Ionut
Fabiani, Lucia
De Sousa, Rita Ferreira
Martino, Laura
Martinez, Silvia Valtuena
Naska, Androniki
机构:
关键词:
Ergocalciferol;
cholecalciferol;
calcidiol monohydrate;
conversion factor;
tolerable upper intake level;
SERUM 25-HYDROXYVITAMIN D;
ALL-CAUSE MORTALITY;
BONE-MINERAL DENSITY;
RANDOMIZED-CONTROLLED-TRIAL;
J-SHAPED ASSOCIATION;
CARDIOVASCULAR-DISEASE MORTALITY;
DOUBLE-BLIND RCT;
D SUPPLEMENTATION;
POSTMENOPAUSAL WOMEN;
D INSUFFICIENCY;
D O I:
10.2903/j.efsa.2023.8145
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Following two requests from the European Commission (EC), the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver a scientific opinion on the revision of the tolerable upper intake level (UL) for vitamin D and to propose a conversion factor (CF) for calcidiol monohydrate into vitamin D-3 for labelling purposes. Vitamin D refers to ergocalciferol (vitamin D-2), cholecalciferol (vitamin D-3), and calcidiol monohydrate. Systematic reviews of the literature were conducted to assess the relative bioavailability of calcidiol monohydrate versus vitamin D-3 on serum 25(OH)D concentrations, and for priority adverse health effects of excess vitamin D intake, namely persistent hypercalcaemia/hypercalciuria and endpoints related to musculoskeletal health (i.e. falls, bone fractures, bone mass/density and indices thereof). Based on the available evidence, the Panel proposes a CF for calcidiol monohydrates of 2.5 for labelling purposes. Persistent hypercalciuria, which may be an earlier sign of excess vitamin D than persistent hypercalcaemia, is selected as the critical endpoint on which to base the UL for vitamin D. A lowest-observed-adverse-effect-level (LOAEL) of 250 & mu;g/day is identified from two randomised controlled trials in humans, to which an uncertainty factor of 2.5 is applied to account for the absence of a no-observed-adverse-effect-level (NOAEL). A UL of 100 & mu;g vitamin D equivalents (VDE)/day is established for adults (including pregnant and lactating women) and for adolescents aged 11-17 years, as there is no reason to believe that adolescents in the phase of rapid bone formation and growth have a lower tolerance for vitamin D compared to adults. For children aged 1-10 years, a UL of 50 & mu;g VDE/day is established by considering their smaller body size. Based on available intake data, European populations are unlikely to exceed the UL, except for regular users of food supplements containing high doses of vitamin D.
引用
收藏
页数:219
相关论文