REFINEMENT OF THE MODIFIED-RELATIVE-DOSE-RESPONSE TEST AS A METHOD FOR ASSESSING VITAMIN-A STATUS IN A FIELD SETTING - EXPERIENCE WITH INDONESIAN CHILDREN

The modified-relative-dose-response (MRDR) test, which has been used e xtensively throughout the world for assessing vitamin A status, has be en simplified. The major methodologic change resulting from the curren t studies in Indonesia is the use of graded standard doses of 3,4-dide hydroretinyl acetate (DRA) based on the age range of the population of interest. Instead of a dose of 0.35 mu mol/kg body wt, standard doses of 5.3 mu mol for children younger than 6 y, 7.0 mu mol for children between 6 and 12 y of age, and 8.8 mu mol for adults and children > 12 y of age are suggested for field use. The acceptable time between adm inistering the oral dose and obtaining a blood sample was validated as being 4-7 h in a group of children (n = 84) by taking two blood sampl es per child between 3 and 7 h after dosing with DRA. Furthermore, DRA in vitamin E-containing corn oil, with or without the addition of 4.6 mmol all-rac-alpha-tocopheryl acetate/L, was found to be stable for g reater than or equal to 18 mo at 2 degrees C and at -20 degrees C, but not at 22 degrees C or at 37 degrees C. When DRA was stored in amber glass vials, stability was affected more by temperature than by exposu re to room light. In keeping with earlier studies in adults, the ratio of 3,4-didehydro-retinol to retinol tends to be independent of body w eight. Indeed, slower growing children tie, those with a lower weight- for-age) may have a somewhat better vitamin A status than their heavie r counterparts.