1997
DOI: 10.1016/s0899-9007(97)83044-4
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Metabolic response to injury and sepsis: changes in protein metabolism

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Cited by 99 publications
(31 citation statements)
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“…It is thought to be a consequence of malnutrition, liver dysfunction, disturbed protein and albumin synthesis by inflammatory mediators that can directly inhibit transcription of genes responsible for albumin synthesis [34,35]. Trauma and sepsis initiate a cascade of events that lead to accelerated protein degradation, decreased rate of synthesis of selected proteins, and increased amino acid catabolism and nitrogen loss [36]. The results of our studies are similar to the observations of other authors.…”
Section: Discussionsupporting
confidence: 86%
“…It is thought to be a consequence of malnutrition, liver dysfunction, disturbed protein and albumin synthesis by inflammatory mediators that can directly inhibit transcription of genes responsible for albumin synthesis [34,35]. Trauma and sepsis initiate a cascade of events that lead to accelerated protein degradation, decreased rate of synthesis of selected proteins, and increased amino acid catabolism and nitrogen loss [36]. The results of our studies are similar to the observations of other authors.…”
Section: Discussionsupporting
confidence: 86%
“…Another possibility is that high levels of mean fasting glucose during the first weeks after SAH reflect an acute metabolic response, including insulin resistance persisting during the acute ilness. Such a state has been described in other groups of critically ill patients1921 and has been associated with cardiovascular complications and poor clinical outcome previously, but mostly in the long term and in patients who already had abnormalities of glucose metabolism 2224. Although previous studies did not report a relation between DM and SAH occurrence,2527 it is possible that high fasting glucose levels after aneurysmal SAH represent pre-existent, but previously unrecognised, abnormalities in glucose metabolism.…”
Section: Discussionmentioning
confidence: 69%
“…Of the 22 highest abundance plasma proteins, at least 10 proteins vary by at least 25% in the acute phase response, including: albumin, transferrin, fibrinogen, alpha-1-antitrypsin, C3, haptoglobin, ceruloplasmin, C4, factor B, and C9 [19,3]. At least 7 of the remaining 12 high abundance proteins have also been reported to change concentrations in the acute phase response, including: prealbumin [20], alpha-1-acid glycoprotein, alpha-2-macroglobulin [21], apolipoprotein A-1 [22], apolipoprotein B [23], lipoprotein (a) [24], and C8 [25,3].…”
Section: Numerous Abundant Plasma Proteins Are Affected By the Acute mentioning
confidence: 99%