Table 2.
Renal disease phenotypes following short-term treatment of B6.Pdss2kd/kd missense mutant mice with probucol
Urine albumin (mg/24 h) |
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Group | N | Age at first test | Probucol treatment duration | Pre-treatment test | Post-treatment test | p-Value |
Males | 7 | 102 ± 0.49 | 14.6 ± 1.40 days | 14.40 ± 19.1 | 2.32 ± 1.73 | p < 0.05 |
Females | 12 | 106 ± 1.37 | 13.4 ± 2.36 days | 10.30 ± 7.59 | 5.09 ± 5.10 | p < 0.05 |
ALL | 19 | 104 ± 2.52 | 13.8 ± 2.13 days | 11.46 ± 12.3 | 4.07 ± 4.22 | p < 0.01 |
Elevated 24 h urine albumin levels suggestive of renal glomerular disease in 100-day-old untreated missense mutants (pre-treatment test) were significantly reduced in both males and females following approximately 2 weeks of oral probucol treatment (post-treatment test). Histological nephritis score was also lower following probucol treatment than typical of untreated age-matched missense mutants (Table 1). Non-parametric statistical analysis (Mann–Whitney U-test) of mean urine albumin in treated versus untreated missense mutant groups showed short-term probucol treatment significantly reduced albuminuria (p = 0.01). A trend towards greater reduction in urine albumin was seen in males, with a mean reduction by 71.1% +/− 14.1% in males and 47.1% +/− 27.6% in females (p = 0.07).