Skip to main content
. 2010 Aug 31;103(7):1025–1033. doi: 10.1038/sj.bjc.6605846

Table 2. p-AMPK status in colorectal cancer and patient mortality.

    Colorectal cancer-specific mortality
Overall mortality
AMPK status Total N Deaths/ person-years Univariate HR (95% CI) Multivariate stage-matched HR (95% CI) Deaths/ person-years Univariate HR (95% CI) Multivariate stage-matched HR (95% CI)
p-AMPK (−) 309 86/2164 1 (referent) 1 (referent) 125/2164 1 (referent) 1 (referent)
p-AMPK (+) 409 108/2952 0.84 (0.61–1.17) 0.95 (0.71–1.28) 181/2952 1.08 (0.84–1.39) 1.12 (0.89–1.42)

Abbreviations: BMI=body mass index; CI=confidence interval; HR=hazard ratio; CIMP=CpG island methylator phenotype; FASN=fatty acid synthase; MSI=microsatellite instability; p-AMPK=phosphorylated AMP-activated protein kinase.

The multivariate, stage-matched (stratified) Cox model initially included sex, age at diagnosis, year of diagnosis, BMI, family history of colorectal cancer, tumour location, tumour grade, tumour border, CIMP, MSI, LINE-1 methylation, BRAF, KRAS, PIK3CA, TP53 and FASN. A backward stepwise elimination with a threshold of P=0.20 was used to select variables in the final model. Stage adjustment (I, IIA, IIB, IIIA, IIIB, IIIC, IV, unknown) was done using the ‘strata’ option in the SAS ‘proc phreg’ command.