Test-Retest Reproducibility of the Relative Dose Response for Vitamin A Status in Guatemalan Adults: Issues of Diagnostic Sensitivity

• Published in: The Journal of nutrition Vol. 120; no. 7; pp. 738 - 744
• Main Authors: Solomons, Noel W., Morrow, Frank D., Vasquez, Alejandrina, Bulux, Jesus, Guerrero, Aura-Marina, Russell, Robert M.
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 01.07.1990; American Society for Nutritional Sciences
• Subjects: Administration, Oral; Adolescent; Adult; Aged; Biological and medical sciences; CARENCE EN VITAMINES; Chromatography, High Pressure Liquid; DEFICIENCIA DE VITAMINAS; Dose-Response Relationship, Drug; ENSAYO; ESTADO NUTRICIONAL; ETAT NUTRITIONNEL; EVALUACION; EVALUATION; Female; FEMME; GUATEMALA; HOMBRES; HOMME; Human physiology applied to population studies and life conditions. Human ecophysiology; Humans; INVESTIGACION; Male; Medical sciences; Middle Aged; MUJERES; NUTRICION; NUTRITION; Nutritional survey. Food supply and nutritional requirement; PLASMA SANGUIN; PLASMA SANGUINEO; PROTEINAS; PROTEINE; RECHERCHE; relative dose response; Reproducibility of Results; RETINOL; retinol binding protein; TESTAGE; vitamin A; Vitamin A - administration & dosage; Vitamin A - blood; Vitamin A Deficiency - diagnosis; Guatemala; retinol; relative dose response; vitamin A; humans; retinol binding protein; Human; Central America; Methodology; Vitamin; Dose activity relation; Retinol; Binding protein; Reproducibility; America; Guatemala; Diagnosis; Measurement method; Nutritional status; Public health
• ISSN: 0022-3166; 1541-6100
• DOI: 10.1093/jn/120.7.738

The relative dose response (RDR) test has been used as a functional measure of whole-body stores of vitamin A in humans. We have examined the reproducibility of the RDR procedure in a population of Guatemalan adult subjects who would be expected to show a moderate prevalence of hypovitaminosis A. Fifty-one subjects were administered a standard RDR test, and the plasma samples were analyzed for retinol, tocopherol, retinol binding protein (RBP) and prealbumin (PAL). Thirty-four of the subjects underwent repeat RDR tests 7 d later. Plasma levels in fasted subjects were as follows: retinol, 1.35 ± 0.30 µmol/L; RBP, 37.8 ± 7.7 mg/L; PAL, 187.0 ± 39.0 mg/L; and tocopherol, 16.6 ± 6.2 µmol/L. RDRs ranged from -35.2% to +63.1%, with a mean of 2.6 ± 10.4%. Overall, we observed poor within-subject reproducibility of the RDR procedure whether expressed numerically or by diagnostic classification. Moreover, in contrast to previous studies in children, we observed fewer positive RDR tests than would be expected for the population studied. Nevertheless, the mean RDR was inversely proportional to fasting retinol levels, thus confirming the validity of the biological basis of the RDR procedure in humans. Because of high intra-individual variability with this test, investigators should be cautious when using the RDR procedure in serial studies to monitor the efficacy of therapeutic interventions or subject compliance to dietary regimens.