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Table 5 Percentage change of pharmacodynamic parameters according to SLCO1B1 c.388A > G, SLCO1B1 c.521T > C and SLCO1B3 int7A > G genotypes and SLCO1B1 haplotypes after 12 months of raloxifene treatment in 53 postmenopausal women

From: Organic anion transporting polypeptides OATP1B1 and OATP1B3 and their genetic variants influence the pharmacokinetics and pharmacodynamics of raloxifene

Pharmacodynamic parameter

Δ FN BMD (%)

Δ QUI (%)

Δ OC (%)

  

genotype

SLCO1B1 c.388A > G

SLCO1B1 c.521T > C

SLCO1B3 int7C > G

  
 

AA

−1.1 (1.5)

TT

2.5 (1.1)

CC

−21.0 (3.5)

  
 

AG

3.4 (0.6)

TC

−1.6 (1.4)

non CC

−33.5 (3.5)

  
 

GG

−0.6 (1.1)

      

test/p-value

ANOVA

0.001 a

t-test

0.033

t-test

0.015

  

Pharmacodynamic parameter

Δ FN BMD (%)

Δ CTX (%)

Δ SOS (%)

Δ QUI(%)

haplotype

*1a

*1b

*15

*15

 

0 copies

−0.65 (1.1)

0 copies

−20.7 (6.7)

0 copies

0.2 (0.1)

0 copies

2.4 (1.1)

 

1 copy

3.5 (0.6)

1 copy

−24.7 (5.1)

1 copy

−0.3 (0.2)

1 copy

−1.9 (1.6)

 

2 copies

−2.0 (1.6)

2 copies

−56.9 (10.4)

    

test/p-value test/p-value

ANOVA

0.0002 b

ANOVA

0.039 c

t-test

0.031

t-test

0.03

  1. The values are presented as means (standard errors).
  2. aBonferoni test (ANOVA), p = 0.004 for AA vs. AG, =0.021 for AG vs. GG.
  3. bBonferoni test (ANOVA), p = 0.013 for 0 vs. 1, p = 0.0004 for 1 vs. 2 copies of haplotype*1a.
  4. cBonferoni test (ANOVA), p = 0.035 for 0 vs. 2 copies of haplotype*1b.
  5. Δ FN BMD (%), percentage change of femoral neck bone mineral density; Δ QUI (%), percentage change of quantitative ultrasound index; Δ OC (%), percentage change of osteocalcin; Δ CTX (%), percentage change of serum C-terminal telopeptide fragments of type I collagen; Δ SOS (%), percentage change of heel speed of sound.