Table 2.
RCTs w/o Active Comparator | All RCTs | |||
---|---|---|---|---|
β per SD† Increase | P | β per SD‡ Increase | P | |
Coronary Heart Disease | ||||
LnORCoronary Heart Disease | ||||
Baseline LDLRx | −0.045 | 0.320 | −0.083 | 0.014 |
ΔLDLBaseline-Final | −0.091 | 0.052 | −0.082 | 0.029 |
%ΔLDLBaseline-Final | −0.063 | 0.221 | −0.062 | 0.143 |
ΔLDLControl-Rx | −0.108 | <0.001 | −0.129 | <0.001 |
%ΔLDLControl-Rx | −0.095 | 0.030 | −0.127 | <0.001 |
Trial Duration | 0.011 | 0.813 | 0.052 | 0.237 |
All-cause Mortality | ||||
LnORMortality | ||||
Baseline LDLRx | −0.065 | 0.081 | −0.067 | 0.022 |
ΔLDLBaseline-Final | −0.018 | 0.686 | −0.021 | 0.511 |
%ΔLDLBaseline-Final | 0.020 | 0.581 | 0.002 | 0.941 |
ΔLDLControl-Rx | −0.030 | 0.397 | −0.055 | 0.041 |
%ΔLDLControl-Rx | 0 | 0.993 | −0.030 | 0.297 |
Trial Duration | −0.018 | 0.585 | 0.012 | 0.702 |
Models are univariable, i.e., the β coefficients refer to the relationship with each measure as a single independent variable.
SD (RCTs w/o Active Comparator): Baseline LDLRx = 24 mg/dL; ΔLDLBaseline-Final = 15 mg/dL ; %ΔLDLBaseline-Final = 10%; = ΔLDLControl-Rx = 16 mg/dL ; %ΔLDLControl-Rx = 11%; Trial Duration = 15 months.
SD (All RCTs): Baseline LDLRx = 25 mg/dL; ΔLDLBaseline-Final = 17 mg/dL; %ΔLDLBaseline-Final = 11%; ΔLDLControl-Rx = 17 mg/dL; %ΔLDLControl-Rx = 11%; Trial Duration = 23 months.
Ln = Natural logarithm. OR = Odds Ratio. RCT = Randomized Controlled Trial. SD = Standard Deviation.