Table 5.
Parameter | M(BMI) | M0(BMI) | M(CR_PC) | M0(CR_PC) |
---|---|---|---|---|
σAD2 | 0.063 ± 0.014 | 0.066 | 0.113 ± 0.021 | 0.113 |
σRS2 | 0.092 ± 0.012 | 0.091 | 0.100 ± 0.016 | 0.103 |
α0 | 0.036 ± 0.018 | 0.037 | 0.075 ± 0.023 | 0.077 |
β1 | 0.878 ± 0.046 | 0.880 | 0.967 ± 0.054 | 0.969 |
β2 | 0.057 ± 0.022 | 0.063 | 0.004 ± 0.026 | 0.012 |
β3 | 0.085 ± 0.039 | 0.084 | 0.011 ± 0.046 | 0.010 |
β4 | −0.044 ± 0.016 | (F) 0 | −0.054 ± 0.019 | (F) 0 |
Log(LH) | −325.216 | −328.901 | −414.444 | −418.453 |
LHR (p-value) | 0.006 | 0.005 |
M(BMI) and M(CR_PC) are the general models of BMI and CR_PC variation, respectively. These two models include parameter estimates of the contribution of the fat-related (FM, PLL and SK_PC) covariates and G-C-G haplotype, as well as contribution of the putative additive genetic, σAD2 and environmental, σRS2 factors. M0(BMI) and M0(CR_PC) are the restricted models, in which contribution of the G-C-G haplotype, measured by regression coefficient β4, was neglected (restricted to null). Contribution of fat-related covariates as measured by the regression coefficients, β1, β2, and β3, respectively was allowed; α0: regression intercept. 898 individuals, in whom the M1–M2–M3 haplotypes have been unambiguously reconstructed, were included in this analysis. The restricted models show that despite highly substantial contribution of the fat-related phenotypes to variation of BMI and CR_PC, the contribution of G-C-G haplotype to their respective variations cannot be neglected without significant loss of data fitting, and therefore these models were rejected.