S100B Serum Level is Independent of Moderate Alcohol Intoxication

Laura Emine Stollhof1, Udo Obertacke2, David Eschmann2

  • 1Orthopädie und Unfallchirurgie, BG Unfallklinik Tübingen.

Abstract

Insights

Serum S100B levels in healthy volunteers were unaffected by moderate alcohol consumption. This suggests S100B can reliably indicate brain injury even in patients with low to moderate alcohol intoxication.

Area of Science:

  • Neurology
  • Toxicology
  • Biochemistry

Background:

  • Minor head injury (MHI) patients frequently have coexisting alcohol intoxication (up to 50%).
  • Alcohol can alter neurological symptoms, potentially leading to misdiagnosis or delayed treatment in MHI patients.
  • S100B is a proposed biomarker for MHI, but its reliability may be compromised by alcohol's influence on serum levels.

Purpose of the Study:

  • To investigate the relationship between blood ethyl alcohol concentration and serum S100B concentration.
  • To determine if alcohol intoxication affects S100B levels in a controlled experimental setting.
  • To assess the utility of S100B as a biomarker in intoxicated MHI patients.

Main Methods:

  • 58 healthy adult volunteers participated in the study.
  • Blood ethyl alcohol and serum S100B concentrations were measured before and after voluntary alcohol consumption.
  • Automated measuring systems (Cobas e411, Siemens Dimension Vista 1500) were used for sample analysis.

Main Results:

  • Post-consumption blood alcohol levels ranged from 0.23 to 1.92 g/l.
  • Serum S100B levels ranged from 0.021 to 0.115 µg/l (standard < 0.11 µg/l).
  • Pearson correlation (r=0.01181) indicated no significant relationship between alcohol and S100B concentrations; S100B levels were independent of alcohol intake at low to moderate levels.

Conclusions:

  • Moderate alcohol blood concentrations (around 1 g/l) do not significantly alter serum S100B concentrations in healthy individuals.
  • S100B remains a potentially valuable biomarker for detecting brain injury in patients with low to moderate alcohol intoxication.
  • The findings support the use of S100B for selecting MHI patients requiring further diagnostics, irrespective of mild to moderate alcohol influence.

Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess...
186
Serum Studies: Renal Function Tests01:24

Serum Studies: Renal Function Tests

Renal function tests are crucial for assessing kidney health, monitoring disease progression, and evaluating the kidneys' efficiency in waste elimination, fluid balance, and electrolyte regulation. These tests offer critical insights into kidney function, even though routine measurements may appear normal until there is a significant decline in the glomerular filtration rate or GFR. Typically, signs of kidney impairment only become evident when the GFR falls to about 50% of its normal level.
370
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug...
217
Drug Distribution: Plasma Protein Binding01:29

Drug Distribution: Plasma Protein Binding

Drugs predominantly attach to plasma proteins, with only a small percentage remaining unbound. The unbound portion can be calculated as one minus the bound fraction. Acidic drugs form large, inactive complexes by reversibly binding to plasma albumin, which prevents them from diffusing across biological barriers. These drug-protein complexes act as reservoirs for the drugs. As the concentration of unbound drugs decreases, these complexes quickly dissociate to release the free drug, maintaining...
8.6K
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
257
Hypothesis Test for Test of Independence01:16

Hypothesis Test for Test of Independence

The test of independence is a chi-square-based test used to determine whether two variables or factors are independent or dependent. This hypothesis test is used to examine the independence of the variables. One can construct two qualitative survey questions or experiments based on the variables in a contingency table. The goal is to see if the two variables are unrelated (independent) or related (dependent). The null and alternative hypotheses for this test are:
H0: The two variables (factors)...
7.4K