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Gender differences in the association of syndecan-4 with myocardial infarction: The population-based Tromsø Study
Marit D Solbu1, Svein O Kolset2, Trond G Jenssen3
1Section of Nephrology, University Hospital of North Norway, Tromsø, Norway; Metabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway.
Insights
Increased serum syndecan-4 levels are linked to myocardial infarction (MI) risk, particularly in women. This finding suggests syndecan-4 may serve as a potential biomarker for coronary heart disease, warranting further clinical investigation.
Area of Science:
- Cardiovascular research
- Endothelial biology
- Biomarker discovery
Background:
- Cardiovascular disease (CVD) is a leading cause of death, with known gender-specific differences in its development.
- The endothelial glycocalyx is crucial for vascular integrity; its shedding indicates endothelial dysfunction and early atherosclerosis.
- Syndecan-1 and -4 are key glycocalyx components, with elevated serum levels signaling glycocalyx damage.
Purpose of the Study:
- To investigate the association between serum syndecan-1 and -4 levels and the risk of myocardial infarction (MI), ischemic stroke, and all-cause mortality in a general population.
- To explore potential gender differences in these associations.
Main Methods:
- A case-cohort study design was employed, including 1495 participants from the Tromsø Study (2001-02).
- Serum levels of syndecan-1 and -4 were measured.
- Multivariable Cox regression models assessed hazard ratios, adjusting for cardiovascular risk factors and urinary albumin-creatinine ratio (ACR).
Main Results:
- Syndecan-4 was independently associated with incident MI (HR 1.32 per 10 ng/mL increase), but not with ischemic stroke or mortality.
- The association between syndecan-4 and MI was stronger in women than in men, with borderline significant interaction by sex.
- Serum syndecan-1 levels showed no association with any of the studied endpoints.
Conclusions:
- Elevated serum syndecan-4 is associated with an increased risk of myocardial infarction, especially in women.
- This finding suggests a potential role for endothelial glycocalyx shedding, as indicated by syndecan-4, in the pathogenesis of coronary heart disease in women.
- Further research is needed to evaluate syndecan-4 as a clinical risk marker for cardiovascular events.
Background And Aims:
Cardiovascular disease is a common cause of morbidity and mortality, with gender differences in pathophysiology. The endothelial glycocalyx maintains vascular integrity, and glycocalyx shedding reflects endothelial dysfunction and early atherosclerosis. Syndecan-1 and -4 are components of the glycocalyx, and increased serum levels indicate glycocalyx damage. We hypothesised that increased serum syndecan-1 and -4 were independently associated with myocardial infarction (MI), ischaemic stroke and all-cause mortality in men and women from a general population.
Methods:
Using a case-cohort design, we included 1495 participants from the Tromsø Study 2001-02. Syndecan-1 and -4 were measured in serum. Baseline variables also included age, gender, cardiovascular risk factors and urinary albumin-creatinine ratio (ACR). Hazard ratios were assessed using multivariable Cox regression models.
Results:
Between baseline in 2001-02 and December 2007 fatal or non-fatal MI was experienced by 328 and ischaemic stroke by 191 subjects, and 423 participants died. Syndecan-4 was independently associated with MI (hazard ratio per 10 ng/mL increase 1.32; 95% confidence interval 1.06-1.63), but not ischaemic stroke and mortality, and the associations were unchanged by adjustment for urinary ACR. Interaction between syndecan-4 and sex was borderline significant, and in gender-specific analysis, syndecan-4 was associated with MI in women only. Syndecan-1 was not associated with any endpoint.
Conclusions:
Syndecan-4 was associated with incident MI, and the association was stronger in women than in men. This suggests a link between endothelial glycocalyx shedding and coronary heart disease in women. Use of syndecan-4 as a risk marker in clinical setting needs further investigation.
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