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. 2023 Jul 17;153(9):2762–2771. doi: 10.1016/j.tjnut.2023.07.004

TABLE 1.

Selected demographics and plasma retinol concentrations in healthy young people and in subjects with SCD-HbSS before and after vitamin A supplementation1

Healthy (n = 20) SCD-HbSS pre-supplementation (n = 22) SCD-HbSS post-supplementation (n = 21)
Sex, % males 60 59 57
Age, y 14 (9–19) 14 (9–19) 14 (9–19)
Plasma retinol, μmol/L 1.47 (0.87–2.27)2 1.12 (0.46–2.35) 1.24 (0.74–2.37)

SCD-HbSS, sickle cell disease hemoglobin SS type.

1

Subjects were participants in the studies reported by Brownell et al. [6]. Tabulated values are arithmetic mean (range), except for sex, which is reported as percent males. Plasma retinol concentration was calculated as [12C]retinol + [13C]retinol. Values for the healthy group include 19 subjects at 3 d after isotope ingestion and 1 at 5 d. For the SCD-HbSS group before supplementation, values include all 22 subjects at 3 d whereas after supplementation, values are for 20 of the same subjects (with n = 14 at 3 d, 4 at 4 d, 1 at 7 d, and 1 at 8 d). Retinol concentrations were compared between healthy subjects and subjects with SCD-HbSS pre-supplementation using Student’s unpaired t test. Subjects with SCD-HbSS were compared before and after vitamin A supplementation using a mixed effects linear regression model adjusting for hydroxyurea use and including a time × dose interaction term. The Benjamini and Hochberg false discovery rate method was applied with a maximum false discovery rate of 0.05 to derive corrected P values to address the issue of multiple testing.

2

Significant difference between group means using unpaired t test, P < 0.05.