Related Experiment Videos
Low plasma selenium concentrations in critically ill children: the interaction effect between inflammation and
Insights
Low plasma selenium in critically ill children is linked to both malnutrition and inflammation. The interaction between these factors is key for understanding selenium status and guiding supplementation decisions.
Area of Science:
- Pediatric Critical Care
- Nutritional Biochemistry
- Clinical Chemistry
Background:
- Low plasma selenium is common in critically ill patients, but its causes (systemic inflammation vs. nutritional deficiency) are unclear.
- Understanding factors associated with low selenium is crucial for managing critically ill children.
Purpose of the Study:
- To determine factors associated with low plasma selenium in critically ill children.
- To investigate the interplay between inflammatory response and nutritional status in selenium levels.
Main Methods:
- Prospective study of 173 critically ill children.
- Measured plasma selenium, C-reactive protein (CRP), and nutritional status.
- Analyzed data using Binomial Generalized Estimating Equations, considering correlations between admission and 5th-day measurements.
Main Results:
- Malnutrition and elevated CRP levels were significantly associated with low plasma selenium.
- A significant interaction was found between malnutrition and CRP levels.
- The impact of malnutrition on low selenium was more pronounced at lower CRP levels (<40 mg/L).
Conclusions:
- The interaction between inflammatory response magnitude and malnutrition significantly affects plasma selenium concentrations.
- Plasma selenium interpretation in critically ill patients requires consideration of both inflammation and nutritional status.
- This interaction is important for decisions regarding selenium supplementation in systemic inflammation.
Introduction:
Low plasma selenium concentrations are frequent in critically ill patients. However, whether this is due to systemic inflammation, a deficient nutritional state or both is still not clear. We aimed to determine the factors associated with low plasma selenium in critically ill children while considering the inflammatory response and nutritional status.
Method:
A prospective study was conducted in 173 children (median age 34 months) with systemic inflammatory response who had plasma selenium concentrations assessed 48 hours after admission and on the 5th day of ICU stay. The normal reference range was 0.58 μmol/L to 1.6 μmol/L. The outcome variable was 'low plasma selenium', which was defined as plasma selenium values below the distribution median during this period. The main explanatory variables were age, malnutrition, sepsis, C-reactive protein (CRP), and clinical severity scores. The data were analyzed using a Binomial Generalized Estimating Equations model, which includes the correlation between admission and 5th day responses.
Results:
Malnutrition and CRP were associated with low plasma selenium. The interaction effect between these two variables was significant. When CRP values were less than or equal to 40 mg/L, malnutrition was associated with low plasma selenium levels (odds ratio (OR) = 3.25, 95% confidence interval (CI) 1.39 to 7.63, P = 0.007; OR = 2.98, 95% CI 1.26 to 7.06, P = 0.013; OR = 2.49, 95% CI 1.01 to 6.17, P = 0.049, for CRP = 10, 20 and 40 mg/L, respectively). This effect decreased as CRP concentrations increased and there was loose significance when CRP values were >40 mg/L. Similarly, the effect of CRP on low plasma selenium was significant for well-nourished patients (OR = 1.13; 95% CI 1.06 to 1.22, P <0.001) but not for the malnourished (OR = 1.03; 95% CI 0.99 to 1.08, P = 0.16).
Conclusions:
There is a significant interaction between the magnitude of the inflammatory response and malnutrition on low plasma selenium. This interaction should be considered when interpreting plasma concentrations as an index of selenium status in patients with systemic inflammation as well as in the decision on selenium supplementation.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Drug Excretion
Serum Studies: Renal Function Tests
Drug Dosing in Renal Diseases: Measurement of Serum Creatinine Concentration and Clearance