Roles of Single Nucleotide Polymorphisms in the SLC6A2 Gene in the Risk of Vasovagal Syncope Among Children in Eastern China: A Case‐Control Study
Polymorphisms in the SLC6A2 gene, particularly rs2242446, may increase the risk of VVS in children. Further research is needed to validate these findings and explore therapeutic interventions targeting the norepinephrine system.
Authors
- Haizhao Zhao
- Meng Li (ORCID: https://orcid.org/0000-0003-2123-2444)
- Minmin Wang (ORCID: https://orcid.org/0000-0003-3213-2481)
- Xiaoyue Liu (ORCID: https://orcid.org/0000-0003-2808-6339)
- Qingyu Kong (ORCID: https://orcid.org/0000-0003-2853-0241)
- Cuifen Zhao (ORCID: https://orcid.org/0000-0002-7274-8371)
- Baomin Li
Institutions
- Qilu Hospital of Shandong University (CN)
Publication Details
- Journal
- Health Science Reports
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1002/hsr2.70585
- Primary Topic
- Cardiovascular Syncope and Autonomic Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Shandong Province