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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Pharmacogenet Genomics. 2020 Dec;30(9):208–211. doi: 10.1097/FPC.0000000000000412

Table 1.

Participant characteristics overall and stratified by SLCO1B1 T/T versus C-carrier genotypes

Characteristic All
(n = 379)
SLCO1B1 T/T
(n = 259; 68%)
SCLO1B1 C/T or C/C
(n = 120; 32%)
ap-value
Male sex 193* (51%) 138 (53%) 55 (46%) 0.166
Age started atorvastatin (years) 56.9 ± 10.8 56.9 ± 10.8 57.0 ± 10.9 0.940
Atorvastatin dose (mg) 22.3 ± 18.0 22.7 ± 18.4 21.6 ± 17.2 0.588
Coronary artery disease 77 (20%) 58 (22%) 19 (16%) 0.140
Myocardial infarction 55 (15%) 39 (15%) 16 (13%) 0.658
Hypertension 181 (48%) 119 (46%) 62 (52%) 0.300
Smoker 115 (30%) 78 (30%) 37 (31%) 0.888
Family history of heart disease 171 (45%) 126 (49%) 45 (38%) 0.043
Hypothyroidism 42 (11%) 27 (10%) 15 (13%) 0.549
Heavy alcohol consumption 5 (1.3%) 4 (1.5%) 1 (0.8%) 1.000
Obesity 64 (17%) 44 (17%) 20 (17%) 0.938
Kidney disease 9 (2.4%) 6 (2.3%) 3 (2.5%) 1.000
Diabetes 59 (16%) 42 (16%) 17 (14%) 0.609
Family history of muscle disease 27 (7.1%) 14 (5.4%) 13 (11%) 0.056
Metabolic muscle disease 10 (2.6%) 7 (2.7%) 3 (2.5%) 1.000
Inflammatory muscle disease 26 (6.9%) 20 (7.7%) 6 (5%) 0.330
Liver disease 10 (2.6%) 7 (2.7%) 3 (2.5%) 1.000
Discontinued atorvastatin due to SAMS 233 (61%) 158 (61%) 75 (63%) 0.781
Discontinued atorvastatin due to elevated CK 55 (15%) 38 (15%) 17 (14%) 0.897
a

Continuous variables are presented as mean ± standard deviation and compared between the two SLCO1B1 genotype groups by the student’s t-test. Categorical variables are presented as counts (%) and compared between the two SLCO1B1 genotype groups with the chi-square or Fisher’s exact test where necessary. Bolded values are for p < 0.05.

*

Sex was undisclosed for one participant.

CK = creatine kinase; SAMS = statin-associated muscle symptoms; SLCO1B1 = solute carrier organic anion transporter family member 1B1