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. 2017 Oct 27;7:14212. doi: 10.1038/s41598-017-14152-y

Table 4.

Multiple Logistic regression between CHD with FBG, PBG and HbA1c.

CHD P value. Exp(B) 95% C.I.for EXP(B)
Lower Upper
Model 1 (FBG) Age <0.001 1.029 1.015 1.043
Gender <0.001 2.813 2.083 3.799
SBP 0.032 1.011 1.001 1.021
histrory of Af 0.028 0.515 0.284 0.932
HDL 0.035 0.634 0.415 0.968
Lp(a) <0.001 1.001 1.000 1.001
FBG 0.008 1.155 1.039 1.284
Model 2 (PBG) age 0.001 1.025 1.010 1.039
Gender <0.001 3.179 2.357 4.287
Lp(a) 0.003 1.001 1.000 1.001
PBG <0.001 1.098 1.051 1.147
Model 3 (HbA1c) Age <0.001 1.028 1.014 1.042
Gender <0.001 2.809 2.079 3.795
SBP 0.033 1.011 1.001 1.021
histrory of Af 0.025 0.507 0.280 0.918
HDL 0.045 0.647 0.423 0.990
Lp(a) <0.001 1.001 1.000 1.001
HbA1c 0.002 1.239 1.078 1.424
Model 4 (FBG, PBG, HbA1c) Age 0.001 1.024 1.010 1.039
Gender <0.001 3.139 2.326 4.236
Lp(a) 0.002 1.001 1.000 1.001
PBG <0.001 1.096 1.050 1.145

Multiple logistic regression was performed to identify risk factors associated with the CHD. In model 1, only fasting plasma glucose (FPG) was taken into account as glycemic parameter with other variables. In model 2, only postprandial blood glucose (PBG) was taken into account as glycemic parameter with other variables.In model 3, only HbA1c was taken into account as glycemic parameter with other variables. In model 4, FPG, PBG and HbA1c were all taken into account as glycemic parameters with other variables. Exp, exponential; B, coefficient; CI, confidence interval.