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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Pharmacogenet Genomics. 2013 Nov;23(11):619–623. doi: 10.1097/FPC.0000000000000002

Table 1.

Consent for Pharmacogenomic Testing Across Various Patient Subgroups

Consented to
PG sampling
(n = 1674)
Did not
consent to PG
sampling
(n = 1275)
P
Gender, n (%) 0.04
  Male 1021 (58) 729 (42)
  Female 653 (54) 546 (46)
Race, n (%) 0.07
  White 1214 (58) 882 (42)
  African American 293 (54) 254 (46)
  Hispanic 121 (57) 90 (43)
  Asian 21 (41) 30 (59)
  Other 25 (57) 19 (43)
Age, y, mean (SD) 47.4 (7.9) 47.6 (8.3) 0.71
Baseline HCV RNA, n (%) 0.17
  >600,000 IU/mL 1388 (57) 1032 (43)
  ≤600,000 IU/mL 286 (54) 243 (46)
METAVIR fibrosis score, n (%)* 0.7
  F0 25 (54) 21 (46)
  F1 1160 (58) 857 (42)
  F2 235 (55) 192 (45)
  F3 66 (55) 54 (45)
  F4 112 (58) 80 (42)
Baseline smoking history, n (%) 0.39
  Current smoker 620 (57) 470 (43)
  Ex-smoker 626 (58) 455 (42)
  Non-smoker 390 (54) 327 (46)
History of alcohol abuse, n (%) 153 (58) 109 (42) 0.58
History of depression, n (%) 391 (57) 299 (43) 0.95
History of diabetes, n (%) 112 (57) 85 (43) 0.98
History of hypertension, n (%) 454 (57) 342 (43) 0.86
History of coronary artery disease, n (%) 25 (57) 19 (43) 0.99
*

Missing 76 of those who participated in pharmacogenomic testing and 71 of those who did not.

Missing 38 of those who participated in pharmacogenomic testing and 23 of those who did not.

Abbreviations: PG, pharmacogenomics testing.