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. Author manuscript; available in PMC: 2007 Dec 10.
Published in final edited form as: Nicotine Tob Res. 2007 Dec;9(12):1251–1257. doi: 10.1080/14622200701705027

Table 3.

Smoking cessation outcomes by treatment condition and DRD2 Taq1A genotype.

Percent abstinent (number of subjects/sample)
Treatment condition DRD2 Taq1A genotype Assessment of abstinence Study 1 (N=431)* Study 2 (N=291) Pooled data (N=722)*
Bupropion A1/A1 or A1/A2 End of treatment 25.7 (26/101) 44.4 (28/63) 32.9 (54/164)
Placebo 25.3 (20/79) 25.8 (17/66) 25.5 (37/145)
Bupropion A2/A2 29.5 (38/129) 45.2 (33/73) 35.2 (71/202)
Placebo 12.1 (14/116) 19.1 (17/89) 15.1 (31/205)
Bupropion A1/A1 or A1/A2 6 months 20.8 (21/101) 23.8 (15/63) 22.0 (36/164)
Placebo 12.7 (10/79) 27.3 (18/66) 19.3 (28/145)
Bupropion A2/A2 20.9 (27/129) 37.0 (27/73) 26.7 (54/202)
Placebo 10.3 (12/116) 14.6 (13/89) 12.2 (25/205)
Bupropion A1/A1 or A1/A2 12 months 11.9 (12/101) 17.5 (11/63) 14.0 (23/164)
Placebo 8.9 (7/79) 18.2 (12/66) 13.1 (19/145)
Bupropion A2/A2 14.7 (19/129) 19.2 (14/73) 16.3 (33/202)
Placebo 8.6 (10/116) 13.5 (12/89) 10.7 (22/205)

Note. Frequencies for participants at both study sites who reported continuous abstinence with biochemically verified 7-day point prevalence, grouped by treatment condition using intention-to-treat criteria and DRD2 Taq1A genotype.

a

Smoking outcomes data missing on 6 individuals in Study 1 (3 each for the A1/A1 or A1/A2 group, and for the A2/A2 group).