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. Author manuscript; available in PMC: 2015 Oct 1.
Published in final edited form as: Emotion. 2014 May 26;14(5):930–939. doi: 10.1037/a0036835

Table 3.

Summary of the simple-effect analyses decomposing the significant three-way interaction among genotype, stress, and reappraisal in predicting depressive symptoms. High and low values of stress and reappraisal were determined using values +/− 1 SD from the mean.

Stress level Reappraisal level Simple effect result β t-statistic df p-value
Comparing short allele carriers to non-carriers (N = 201)
High High Short-allele carriers did not differ from non-carriers .07 < 1 197 .52
High Low Short-allele carriers reported more depressive symptoms than non-carriers .36 3.21 197 .002
Low High Short-allele carriers did not differ from non-carriers .05 < 1 197 .61
Low Low Short-allele carriers reported fewer depressive symptoms than non-carriers −.40 3.75 197 <.001

Comparing stress levels or reappraisal levels within short-allele carriers (n = 137)
High Reported fewer depressive symptoms when they were high (vs. low) in reappraisal −.39 3.94 133 <.001
Low Reported the same number of depressive symptoms whether they were high or low in reappraisal −.03 < 1 133 .73
High Reported increased depressive symptoms when they were high (vs. low) in stress .38 3.55 133 .001
Low Reported increased depressive symptoms when they were high (vs. low) in stress .76 9.26 133 <.001

Comparing stress levels or reappraisal levels within non-carriers (n = 68)
High Reported the same number of depressive symptoms whether they were high or low in reappraisal −.15 1.02 64 .31
Low Reported fewer depressive symptoms when they were high (vs. low) in reappraisal −.65 4.65 64 <.001
High Reported increased depressive symptoms when they were high (vs. low) in stress .42 3.38 64 .001
Low Reported the same number of depressive symptoms whether they were high or low in stress −.04 < 1 64 .81
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