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Relationship of Polymorphism of Adhesion Molecules VCAM-1 and ICAM-1 with Preeclampsia
1Department of Obstetrics and Gynecology, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China weijuanbing@163.com.
Insights
Genetic variations in vascular cell adhesion molecule-1 (VCAM-1) are linked to preeclampsia (PE) risk, particularly in severe and late-onset cases. Intercellular adhesion molecule-1 (ICAM-1) gene polymorphisms showed no significant association with preeclampsia in this study.
Area of Science:
- Genetics
- Obstetrics
- Immunology
Background:
- Preeclampsia (PE) is a serious pregnancy complication.
- Adhesion molecules like VCAM-1 and ICAM-1 play roles in vascular function and inflammation.
- Genetic variations may influence susceptibility to PE.
Purpose of the Study:
- To examine the association between VCAM-1 and ICAM-1 gene polymorphisms and the occurrence of preeclampsia.
- To investigate if specific genotypes correlate with early-onset, late-onset, mild, or severe preeclampsia.
Main Methods:
- Genotyping of VCAM-1 (rs3181092) and ICAM-1 (rs5498) polymorphisms using TaqMan assay.
- Case-control study involving 252 PE patients and 200 healthy pregnant women.
- Statistical analysis using SPSS 18.0.
Main Results:
- VCAM-1 rs3181092 AA and AA+AG genotypes were significantly more prevalent in PE patients compared to controls.
- The AA genotype of VCAM-1 was more common in late-onset and severe PE cases.
- No significant association was found between ICAM-1 rs5498 polymorphism and preeclampsia.
Conclusions:
- VCAM-1 rs3181092 polymorphism is associated with preeclampsia development, especially severe and late-onset forms.
- The role of ICAM-1 rs5498 polymorphism in preeclampsia requires further research.
Objective:
To investigate the relationship of polymorphism in vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) with preeclampsia (PE).
Methods:
The present study included 252 patients with PE and 200 healthy pregnant women as control admitted to our hospital from February 2012 to December 2016. Allelic discrimination of the rs5498 polymorphisms from the ICAM-1 gene and rs3181092 from the VCAM-1 gene was assessed using the TaqMan assay. Data was analyzed using SPSS 18.0.
Results:
In PE patients, both ratios of AA and AA+AG genotypes of VCAM-1 were significantly higher than those in the control group, P<0.05. The comparison of genotypes between PE patients with early-onset and late-onset showed that late-onset PE patients had a higher ratio of AA genotype in VCAM-1, P<0.05. Similarly, the ratio of genotype AA in severe PE was significantly higher than that in mild PE patients, P<0.05. However, the distribution of rs5498 polymorphism for ICAM-1 showed no significant difference in the groups.
Conclusion:
Rs3181092 polymorphism of VCAM-1 was associated with occurrence of PE, especially for late-onset and severe PE. However, whether rs5498 polymorphism of ICAM-1was associated with PE needs more investigation.
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