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Other studies have reported that the influence of socioeconomic factors as well as the effect of interventions differs between different diagnostic groups [ 25- 27].
This study was designed to investigate differences in CpG methylation events between different diagnostic groups with a particular emphasis on identifying specific markers related to tumour progression from in situ to invasive cancer.
We found no difference in long time re-employment between different diagnostic groups or between intervention and control groups.
Although we could not find a significant difference in serum 25(OH D levels between different diagnostic groups, we can not rule out the possibility of a type II error, due to modest number of subjects in some of our diagnostic sub-groups.
This pilot study identified that cytokine expression between different diagnostic groups is more sensitive using saliva than in blood samples.
We also performed a direct comparison between different diagnostic groups.
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For the non-psychotic control group, a one-way ANOVA revealed no significant difference between five different diagnostic groups with regard to scores on psychoticism, F 4,102) = 2.113, p = .085, or paranoid ideation, F 4, 102) = 2.148, p = .08.08
Differences in age and cognitive scores between the different diagnostic groups were tested with analysis of variance, and if significant, followed by Bonferroni corrected post hoc tests.
To estimate differences in mean change of the OSS between the different diagnostic groups, a multiple linear regression model with adjustment for prosthesis type, age (≤ 60, 60 70, > 70), sex, and revision state was performed (Tables 4 and 5).
A one-way ANOVA test revealed no significant difference (F 4,90) = 1.41, p = 0.236) in 25(OH D levels between the different diagnostic groups.
We could not find any difference in vitamin D deficiency between patients in different diagnostic groups.
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