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Misclassification bias is also possible because some subjects with a higher POP value but a lower sample volume could be classified in the reference group, or vice versa.
Second, misclassification bias is possible because some subjects with a higher POP value but a lower sample volume could be classified in the reference group, or vice versa.
This is important because some subjects with BRCA1 or BRCA2 mutations may be reluctant to enroll in a trial restricted to mutation carriers, since their genetic status would be known by virtue of their participation.
Moreover, subjects with 20 or more teeth and those with 9 or less teeth were excluded in the models in which denture/bridge use and use of interdental brush/dental floss were used as outcome variables, respectively, because some subjects with 20 or more teeth and those with 9 or less teeth might not need to use denture/bridge and interdental brush/dental floss, respectively.
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The contradiction conclusion in the studies might be due to the influence of diabetes on the relationship of FA serum level and the development of CVD, because some subjects are CVD patients with diabetes; the higher level of FA might mainly be due to the diabetes.
We chose this control group, because subjects with subjective cognitive impairment are not impaired in neuropsychological testing, and accordingly show a normal age-related decrease in cognitive performance.
Finally, because some of the subjects with MODY were related to each other, we sought to account for nonindependence in two ways.
Another meta-analysis was excluded because only subjects with underlying chronic diseases were included.
Because most subjects with longer duration of disease might be older than subjects with shorter disease duration, we adjusted for age at recruitment in these analyses.
Because the subjects with impaired glucose tolerance (IGT) did not differ significantly from individuals with normal glucose tolerance, the author combined individuals with IGT with individuals with normal glucose metabolism and compared them with individuals with diabetes.
Although significantly more common in patients with metabolic syndrome, hypertension and diabetes were not used as covariates because all subjects with hypertension and diabetes were included in our definition of metabolic syndrome.
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