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The results are presented in table 5 for model adjusted with 2-h glucose levels, but the results were essentially similar when the model was adjusted for fasting plasma glucose instead.
We studied the effect of obesity, smoking and alcohol abuse in a multivariate model adjusted with the effect of age (continuous variable), sex and organism (S. Aureus, Str. Pneumoniae, β-hl str., or E. coli).
In this model (adjusted with age), the median levels of PCT were 6.7 ng/mL (range 0.56 to 85) in recipients without hepatic dysfunction and 8.7 ng/mL (range 1.13 to 45) in recipients with hepatic dysfunction.
The association of DRS with miR-144 or NRF2 levels was analyzed using a linear mixed effect model adjusted with exposure conditions as fixed effects and with participants as a random effect.
After constructing a model adjusted with propensity scores, mild and severe hypoglycemia still demonstrated higher hazard ratios (HRs) for cardiovascular diseases (HR 2.09 [95% CI 1.63 2.67]), all-cause hospitalization (2.51 [2.00–3.16]), and total mortality (2.48 [1.41 4.38]).
Obesity and smoking also remained independent risk factors for case fatality when their effect was studied together in a multivariate model adjusted with the effect of alcohol abuse, age (continuos variable), sex and causative organism.
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We can distinguish between global models, adjusted with experimental tests, and local models, based on the constitutive equations for materials.
* P-value and OR (95% CI) were calculated with the use of logistic regression models, adjusted with sex and age.
The models adjusted with survival in this work attempts to answer the next two questions: a) what is the fraction of sample which will survive (in this study, survive is equivalent to not dropout) past a certain time?
The multivariate Cox's regression models adjusted with conventional prognostic markers demonstrate that carrying any of the three promoter variants is an independent prognostic factor, with approximately two-fold increased risk of death or distant metastasis for the carriers (Table 2).
Model 4: Model 2 adjusted with subsequent advanced CKD after hospital discharge as a time-varying covariate.
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