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. Author manuscript; available in PMC: 2017 Jun 18.
Published in final edited form as: Support Care Cancer. 2014 Sep 24;23(4):953–965. doi: 10.1007/s00520-014-2443-5

Table 4.

Multiple Linear Regression Analyses for Interleukin 1R2 (IL1R2) Haplotype A2 (HapA2) and Tumor Necrosis Factor Alpha (TNFA) rs1800629 to Predict Low to High State Anxiety (n=231)

Predictor of Low to High State Anxiety β Coefficient Standard Error 95% CI t p-value
IL1R2 HapA2 genotype 3.014 1.380 .294, 5.735 2.18 .030
Age −.968 .314 −1.587, −.349 −3.08 .002
Functional status −2.210 .573 −3.338, −1.081 −3.86 <.001
Overall model fit: F(9, 221) = 4.45, p <.0001 R2 = .1534
TNFA rs1800629 −3.679 1.462 −6.560, −.797 −2.52 .013
Age −1.031 .312 −1.647, −.415 −3.30 .001
Functional status −2.070 .574 −3.202, −.939 −3.61 <.001
Overall model fit: F(9, 221) = 4.65, p <.0001 R2 = .1592

For this model, the first three principle components identified from the analysis of ancestry informative markers as well as self-reported race/ethnicity (White, Asian/Pacific Islander, Black, Hispanic/Mixed Ethnic Background/Other) were retained to adjust for potential confounding due to race or ethnicity (data not shown). Predictors evaluated in the model included genotype (IL1R2 HapA2: composed of IL1R2 rs4141134 [rare “C” allele], rs11674595 [common “T” allele], and rs7570441 [common “G” allele]; and TNFA rs1800629: GG versus GA+AA), age (in 5-year increments), and functional status (Karnofsky Performance Status score, in 10-point increments).