Table 2.

GP lbα genotypes and CHD



All*

Whites

African Americans
Genotype
CHD, no.
Non-CHD, no.
RH (95% CI)
CHD, no.
Non-CHD, no.
RH (95% CI)
CHD, no.
Non-CHD, no.
RH (95% CI)
BC+BB   61   50   1.6 (0.8-3.2)   26   31   1.1 (0.4-2.6)   35   19   5.6 (1.2-26.6)  
CC   239   279   &   206   219   &   33   60   &  
CD+DD
 
45
 
30
 
1.8 (0.87-3.6)
 
33
 
25
 
1.4 (0.8-3.1)
 
12
 
5
 
21.7 (4.3-108.8)
 


All*

Whites

African Americans
Genotype
CHD, no.
Non-CHD, no.
RH (95% CI)
CHD, no.
Non-CHD, no.
RH (95% CI)
CHD, no.
Non-CHD, no.
RH (95% CI)
BC+BB   61   50   1.6 (0.8-3.2)   26   31   1.1 (0.4-2.6)   35   19   5.6 (1.2-26.6)  
CC   239   279   &   206   219   &   33   60   &  
CD+DD
 
45
 
30
 
1.8 (0.87-3.6)
 
33
 
25
 
1.4 (0.8-3.1)
 
12
 
5
 
21.7 (4.3-108.8)
 

RH (95% CI) indicates relative hazard (95% confidence interval), adjusted for age, sex, race, hypertension, diabetes mellitus, total cholesterol, HDL-C, smoking, and alcohol intake; &, reference value in calculation of adjusted relative hazard.

P values calculated for the comparison of GP lbα genotypes against incident CHD status. P is computed by adjusting the effects of age, sex, and race for all subjects, and by adjusting the effects of age and sex for whites and African Americans. In African Americans, P = .014 for CC versus BC+BB and P = .0001 for CC versus CD+DD.

*

P = .101.

P = .871.

P < .0001.

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