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. 2019 May 2;14(5):e0216407. doi: 10.1371/journal.pone.0216407

Table 2. Regression models of the relationship between somatic instability (SI) in DNA observed in blood and saliva and the estimated progenitor allele length in blood (ePAL) and the age at sampling (Ages).

Model Source Adjusted r2 p Parameter Coefficient Standard error t-statistic p
Model 3:
log(SI) = β+ β1 log(ePAL) + β2(Ages) + β3 log(ePAL) * (Ages) + βlog(ePAL)2 + β5(Ages)2
n = 38 individuals
Blood 0.859 <0.001 Intercept β0 -28.054 6.599 -4.251 <0.001
log(ePAL) β1 21.444 4.404 4.869 <0.001
Ages β2 0.179 0.077 2.314 0.027
log(ePAL) * Ages β3 -0.049 0.024 -2.012 0.053
log(ePAL)2 β4 -3.825 0.744 -5.139 <0.001
Ages2 β5 -0.001 0.000 -2.543 0.016
Saliva 0.717 <0.001 Intercept β0 -27.687 8.743 -3.167 0.003
log(ePAL) β1 20.471 5.834 3.509 0.001
Ages β2 0.224 0.102 2.196 0.035
log(ePAL) * Ages β3 -0.068 0.032 -2.120 0.042
log(ePAL)2 β4 -3.493 0.986 -3.542 0.001
Ages β5 -0.001 0.000 -2.080 0.046

The table shows the squared coefficient of correlation (r2) and statistical significance (p) for each tissue, and the coefficient, standard error, t-statistic and statistical significance (p) associated with each parameter in the model. The number of individuals used in the analysis is indicated (n).