Table 2.
Populations | Risk allele frequency |
Plasma Lp(a) levels (mg/dl) | Risk of CHD | Ref. | |||
---|---|---|---|---|---|---|---|
β (95% CI)† | p-value |
Variance explained (%) |
Odds ratio (95% CI) |
p-value | |||
Diabetic patients | 0.07 | 1.28 (1.08–1.48) | 4.6 × 10−39 | 3–4 | 0.94 (0.69–1.28) | 0.36 | [23] |
General populations | 0.07 | 1.08 (1.02–1.13) | 3.6 × 10−166 | 25 | 1.47 (1.35–1.60) | 3.6 × 10−15 | [4] |
‡p-value for heterogeneity | – | – | 0.06 | – | – | 0.006 | – |
Regression coefficients were estimated as each one copy effect of a risk allele (G-allele) for 1-standard deviation log-transformed Lp(a).
The p-value was tested for heterogeneity in the association of single nucleotide polymorphism rs10455872 with plasma Lp(a) levels and risk of CHD between the diabetic and general populations.
CHD: Coronary heart disease; Lp(a): Lipoprotein(a).