Table 3.
D/R | pT | eGFR | Estimate | SE | Pun | Padj | I2 | N | N SNPs |
---|---|---|---|---|---|---|---|---|---|
combined | 0.0001 | 1year | 0.011 | 0.003 | 4.35×10−5 | 0.001 | 0.0% | 3234 | 6229 |
recipient | 0.0001 | 1year | 0.008 | 0.002 | 8.68×10−5 | 0.005 | 6.2% | 5295 | 6229 |
donor | 0.0001 | 1year | 0.006 | 0.003 | 0.01 | 0.755 | 2.7% | 3564 | 6229 |
donor | 0.1 | 5year | 0.011 | 0.005 | 0.05 | 1 | 35.0% | 2152 | 287016 |
recipient | 0.0001 | 5year | 0.008 | 0.004 | 0.06 | 1 | 0.0% | 2494 | 6229 |
combined | 0.0001 | 5year | 0.008 | 0.005 | 0.11 | 1 | 0.0% | 1930 | 6229 |
recipient | 0.0001 | ∆ | 0.668 | 0.367 | 0.07 | 1 | 0.0% | 2191 | 6229 |
donor | 0.001 | ∆ | -0.348 | 0.358 | 0.33 | 1 | 0.0% | 1904 | 14097 |
combined | 0.001 | ∆ | -0.513 | 0.413 | 0.21 | 1 | 0.0% | 1722 | 14097 |
Meta-analysis results for linear regression of polygenic risk scores vs. eGFR measures. 1/5 year = log10 eGFR at 1/5 year post-transplant. ∆ = change in eGFR between 1 and 5 years post-transplant. Model was adjusted for all available significant clinical covariates and the first eight principal components at each site (see section 2.5 and 3.1). D/R = indicates whether the test was carried out on the recipient, donor or combined donor-recipient genotype. pT = p-value threshold of the calculated polygenic risk score. Estimate = estimated effect size. SE = standard error of the estimate. Pun = uncorrected p-value. Padj=approximate adjusted p-value. I² = the proportion of total variation in study estimates that is due to heterogeneity. N = number of individuals tested. N SNPs = number of SNPs at the given p-value threshold (prior to pruning for linkage disequilibrium).