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A Controlled Mouse Model for Neonatal Polymicrobial Sepsis
Published on: January 27, 2019
Effect of sepsis syndrome on neonatal protein and energy metabolism
J D Mrozek1, M K Georgieff, B R Blazar
1Infant Pulmonary Research Center, Children's Health Care-St. Paul, Minneapolis, MN, USA.
Insights
Neonatal sepsis triggers a hypermetabolic state, increasing energy expenditure and nitrogen loss. Nutritional support with protein may benefit septic neonates, with inflammatory markers indicating illness severity.
Area of Science:
- Biomedical Science
- Neonatology
- Metabolic Research
Background:
- Sepsis in neonates can significantly disrupt normal physiological processes.
- Understanding the metabolic impact of sepsis is crucial for effective clinical management.
- Inflammatory mediators like TNF-alpha, IL-6, and IL-1 beta are implicated in sepsis-related metabolic alterations.
Purpose of the Study:
- To investigate the effects of septic illness on protein and energy metabolism in neonates.
- To determine if inflammatory markers (TNF-alpha, IL-6, IL-1 beta) correlate with metabolic changes during neonatal sepsis.
Main Methods:
- A study involving 31 infants categorized into septic, sick-nonseptic, healthy-nonseptic, and recovered septic groups.
- Measurements included degree of illness, oxygen consumption, nitrogen balance, urine 3-methylhistidine/creatinine ratio (MeH/Cr), and levels of TNF-alpha, IL-6, IL-1 beta, and C-reactive protein (CRP).
Main Results:
- Increased oxygen consumption and MeH/Cr, with decreased nitrogen balance, were observed as the severity of illness increased.
- Nitrogen balance showed improvement upon recovery from sepsis.
- Elevated levels of IL-6 and CRP were found in septic infants compared to non-septic groups.
Conclusions:
- Neonates with sepsis exhibit a hypermetabolic response characterized by increased nitrogen loss, directly proportional to illness severity.
- The findings suggest that enhanced protein substrate delivery could be nutritionally beneficial for septic neonates.
Objective:
It was our hypothesis that septic illness would alter both protein and energy metabolism in neonates, with elevations of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), and interleukin-1 beta (IL-1 beta) serving as markers for these effects.
Study Design:
A total of 31 infants with suspected sepsis were enrolled into four groups: septic, sick-nonseptic, healthy-nonseptic, and recovered septic infants. Degree of illness, oxygen consumption, nitrogen balance, urine 3-methylhistidine/creatinine (MeH/Cr), and TNF-alpha, IL-6, IL-1 beta, and C-reactive protein (CRP) were measured.
Results:
Oxygen consumption increased, while nitrogen balance decreased and MeH/Cr increased with increasing degree of illness. Nitrogen balance improved on recovery from sepsis. IL-6 and CRP levels were elevated in septic infants compared with sick-nonseptic and healthy infants.
Conclusion:
Neonates experience a hypermetabolic response with increased nitrogen loss during septic illness, proportional to the degree of illness. Increased delivery of protein substrate may be nutritionally advantageous to the septic neonate.
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