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. 2021 Jul 23;46(12):2132–2139. doi: 10.1038/s41386-021-01097-0

Table 1.

Demographic and clinical characteristics of the COMBINE, PREDICT, and CITA participants included in the pharmacogenomics GWAS.

COMBINE PREDICT CITA
Sample sizes p value
    Total N 498 266 319
    Acamprosate N 223 110 319
    Naltrexone N 199 102
    Placebo only or no pills N 177 54
Age, mean(SD) 45.4 (10.6) 45.2 (8.5) 43.4 (11.6) 0.012
Sex, male N(%) 343 (68.9%) 266 (100%) 204 (64.0%) <0.0001
Age of onset 30.5 (11.9) 30.2 (10.2) 29.6 (12.0) 0.63
Baseline alcohol consumptiona, mean (sd)
    Days since last drinking day 8.0 (5.4) 22.0 (4.3) 19.7 (8.8) <0.0001
    Average number of drinks per drinking day 12.1 (7.4) 21.0 (12.7) 12.0 (8.6) <0.0001
    % Drinking daysb 56.2 (22.8) 82.0 (26.8) 32.2 (28.2) <0.0001
    % heavy drinking days 47.2 (23.8) 79.4 (27.9) 28.6 (26.8) <0.0001
Treatment Outcomes:
 Relapse, N (%) 380 (76.3%) 158 (59.4%) 101 (31.7%) <0.0001
  Relapse in acamprosate subset, N (%) 167 (74.9%) 62 (56.4%) 101 (31.7%) <0.0001
   Relapse in naltrexone subset, N (%) 146 (73.4%) 65 (63.7%) 0.084
 Heavy Relapse, N (%) 338 (67.9%) 142 (53.4%) 84 (26.3%) <0.0001
  Heavy relapse in acamprosate subset, N (%) 144 (64.6%) 56 (50.9%) 84 (26.3%) <0.0001
  Heavy relapse in naltrexone subset, N (%) 127 (63.8%) 57 (55.9%) 0.18

aBaseline alcohol consumption measures are based on 30 days before start of treatment.

b% drinking days = 100 − % days abstinent in the 30 days before start of treatment.