Skip to main content
. Author manuscript; available in PMC: 2011 Feb 1.
Published in final edited form as: Cancer Res. 2010 Feb 9;70(4):1496–1504. doi: 10.1158/0008-5472.CAN-09-3264

Table 2.

Association between RXRA and VDR genes and metachronous colorectal neoplasia.

Any metachronous Proximal metachronous Distal metachronous
neoplasia neoplasia neoplasia
OR 95%CI OR 95%CI OR 95%CI
RXRA
PC1 1.01 (0.96–1.05) 1.01 (0.97–1.06) 0.97 (0.93–1.03)
PC2 0.90 (0.83–0.99) 0.88 (0.80–0.97) 1.01 (0.91–1.12)
PC3 1.12 (1.00–1.25) 1.10 (0.98–1.24) 1.03 (0.91–1.17)
PC41 1.09 (0.94–1.28) 1.10 (0.94–1.30) 1.15 (0.96–1.38)
LRT p-value2 0.04 0.03 0.49
VDR
PC1 0.98 (0.93–1.03) 1.00 (0.95–1.06) 1.00 (0.94–1.06)
PC2 0.97 (0.92–1.02) 0.96 (0.91–1.02) 1.00 (0.93–1.06)
PC3 1.03 (0.95–1.10) 0.99 (0.92–1.07) 1.06 (0.98–1.16)
PC4 0.96 (0.88–1.04) 0.94 (0.86–1.03) 0.97 (0.98–1.16)
PC5 1.06 (0.93–1.19) 1.02 (0.89–1.16) 1.02 (0.88–1.18)
PC6 1.13 (0.99–1.30) 1.14 (0.99–1.31) 1.01 (0.86–1.17)
PC7 1.03 (0.89–1.20) 1.00 (0.85–1.16) 0.97 (0.82–1.15)
PC81 1.19 (1.02–1.40) 1.21 (1.02–1.43) 0.98 (0.81–1.17)
LRT p-value2 0.11 0.18 0.96
1

An 80% explained-variance threshold is used for including principal components (PC) in the model.

2

P-value for each model is from a likelihood ratio test (LRT) with degrees of freedom equal to the number of principal components.

HHS Vulnerability Disclosure