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Published on: August 9, 2013
Low creatine kinase is associated with a high population incidence of fainting
Lizzy M Brewster1, Gideon Mairuhu, Karin Ganzeboom
1Department of Internal Medicine, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands. l.m.brewster@amc.uva.nl
Insights
Low creatine kinase (CK) activity is linked to a significantly higher risk of fainting. This study suggests low CK may be a new risk factor for vasovagal syncope.
Area of Science:
- Cardiovascular Physiology
- Metabolic Enzyme Function
- Neurology
Background:
- Vasovagal syncope involves vasoconstrictor capacity, skeletal muscle tone, and renal sodium retention.
- Energy-intensive processes like muscle contractility and ion transport rely on enzymes such as creatine kinase (CK).
- A hypothesis posits that reduced CK activity may increase fainting risk.
Purpose of the Study:
- To investigate the association between vasovagal syncope and low serum creatine kinase (CK) activity.
- To explore CK as a potential risk factor for fainting.
Main Methods:
- An observational study included 442 participants aged 34-60 from a general population sample.
- Fainting history was collected while investigators were blinded to CK levels.
- The primary outcome measured was the lifetime cumulative incidence of vasovagal syncope in relation to serum CK levels.
Main Results:
- Individuals with low CK exhibited a 73% greater occurrence of fainting compared to those with high-normal CK (39% vs. 22%).
- The association between low CK and fainting was statistically significant (P = 0.0005).
- This finding remained consistent across recurrent fainters and in both men and women.
Conclusions:
- Low creatine kinase (CK) activity is significantly associated with an increased incidence of vasovagal syncope in the general population.
- The biological plausibility is supported by CK's role in muscle contractility and salt retention.
- Low CK activity emerges as a potential novel risk factor for vasovagal syncope.
Objective:
Vasoconstrictor capacity, skeletal muscle tone, and renal sodium retention are involved in the pathogenesis of fainting. As muscle contractility and ion transport are highly energy-demanding processes, we hypothesized that a low activity of the energy-generating enzyme creatine kinase (CK) is associated with a higher risk of fainting. The aim of this observational study was to explore the association of vasovagal syncope with low CK.
Methods:
A random sample of 1,000 subjects aged 34-60 years was drawn from the general population, with 442 subjects eventually included in the study. Data on fainting history were collected with the investigators blinded to participants' CK level. We prepared this report according to the "Strengthening the Reporting of Observational Studies in Epidemiology" (STROBE) statement. The main outcome was the lifetime cumulative incidence of vasovagal syncope in subjects with low versus high-normal serum CK after a 3 days rest.
Results:
The proportion of fainters within the high CK group was 29 out of 130 (22%) versus 121 out of 312 (39%) in the low CK group; a 73% greater occurrence of fainting with low CK (P = 0.0005). This finding was consistent across recurrent fainters, and in men and women.
Interpretation:
Low CK is associated with a 73% higher incidence of fainting in a random population sample. The association is biologically plausible, as CK enhances cardiovascular and skeletal muscle contractility and salt retention. The presented data suggest that low CK activity is a potential new risk factor for vasovagal syncope.
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