Since the assigned proteins cover only one-sixth of the predicted A. thaliana protein-coding loci, we extended our study by also including predicted phosphorylation sites to achieve better proteome coverage in our analyses, attaining a coverage of 80% of all protein-coding loci in A. thaliana.
The results show that the theoretical error analyses are attained within the range of engineering accuracy.
When the data were analysed by attained age, parity was found to be protective only among carriers over the age of 40 years (HR = 0.44, 95% CI 0.23 to 0.84; p = 0.013; p = 0.048 for the difference in HR between 40 years or less and more than 40 years).
One way sensitivity analyses illustrated PCV13 attained a positive net benefit over PPV23 and over 'no vaccination' in most of the tested scenarios and an acceptable ICER in all tested scenarios.
For cancer sites associated with a statistically significant SIR, we carried out further analyses stratifying by attained age.
Analyses stratified by attained age (≤40 v >40) showed no significant effect modification.
Stratified analyses of highest attained asbestos exposure across cigarette pack years categories are presented in Table 3.
To explore whether BMI had a different impact on prostate cancer in the different age groups, analyses stratified on attained age and age at measurement were performed.
Additionally, we adjusted analyses for highest attained education (basic school/high school, vocational training, higher education, unknown (3.7%)) and disposable income (lowest (1st quarter), middle (2nd-3rd quarter), highest (4th quarter), and unknown (4.1%)) (fully adjusted model).
In the analyses stratified by attained age (Table 4 > -wrap-foot>), the RR of prostate cancer in age 50 59 years for obese men (measured at an average age of 45 years) was 1.58 (95% CI: 1.29 1.94) compared with men with BMI within the 'normal range'.
