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Cellular and Molecular Neurobiology

, Volume 36, Issue 6, pp 981–988 | Cite as

A Polymorphism Within the 3′UTR of NLRP3 is Associated with Susceptibility for Ischemic Stroke in Chinese Population

  • Zhansheng Zhu
  • Jing Yan
  • Chunsong Geng
  • Dagang Wang
  • Chaoyang Li
  • Shuai Feng
  • Huiping Wang
Original Research

Abstract

Stroke was regarded as a severe disorder with high morbidity and high mortality worldwide, ischemic stroke (IS) accounts for 85 to 90 % of new increased stroke cases. Partial mechanisms were elucidated by genetic factors including genomic instability such as single nucleotide polymorphism (SNP). Previous reports demonstrated that inflammation was involved in IS, NLRP3 [nucleotide-binding domain (NOD)-like receptor protein 3], acting as a specific inflammatory gene, however, its function and influence on IS was not well clarified. In this study, a case–control study including 1102 IS patients and 1610 healthy controls was conducted to investigate the association between IS susceptibility with a SNP (rs10754558) in 3′UTR of NLRP3. Logistic regression analysis showed that the heterozygote and the homozygote GG confer a significantly increased risk of CRC after controlling for other covariates (adjusted OR = 1.52, 95 % C.I. 1.19–1.97, P = 0.002; adjusted OR = 2.22, 95 % C.I. 2.18–3.67, P < 0.001, respectively). Carriage of G allele was associated with a greatly increased risk of developing the disease (OR = 1.69, 95 % C.I. 1.31–1.83, P < 0.001). Stratification analysis found that hypertension had interaction with rs10754558 to modulate IS risk. Further in vitro assay revealed that rs10754558 can affect mRNA level of NLRP3, suggesting its possible functional significance. Our data suggested that genetic polymorphisms in NLRP3 may influence IS risk in Chinese population. Replication of our studies in other populations and further functional studies are required for complete comprehension of the roles of NLRP3 polymorphisms in IS risk.

Keywords

Ischemic Stroke NLRP3 rs10754558 3′UTR 

Notes

Acknowledgments

This study is supported by grants from Natural Science Foundation of China (No. 81502428), Natural Science Foundation of Jiangsu Province (No. BK20140222, No. 15KJB310024, No. BK20150220), Xuzhou Medical College scientific research fund for talents (No. D2015018 to Zhansheng Zhu, and No. D2015019 to Huiping Wang).

Compliance with Ethical Standards

Conflict of Interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  • Zhansheng Zhu
    • 1
  • Jing Yan
    • 2
  • Chunsong Geng
    • 3
  • Dagang Wang
    • 4
  • Chaoyang Li
    • 5
  • Shuai Feng
    • 6
  • Huiping Wang
    • 7
  1. 1.Department of PathologyXuzhou Medical CollegeXuzhouPeople’s Republic of China
  2. 2.Center of EmergencyThe Affiliated Hospital of Xuzhou Medical CollegeXuzhouPeople’s Republic of China
  3. 3.Department of LaboratorySuzhou Kowloon Hospital Shanghai Jiao Tong University School of MedicineSuzhouPeople’s Republic of China
  4. 4.Department of LaboratoryBeijing 302 Military Hospital of ChinaBeijingPeople’s Republic of China
  5. 5.Department of Gastrointestinal SurgeryThe Affiliated Hospital of Xuzhou Medical CollegeXuzhouPeople’s Republic of China
  6. 6.Department of Respiratory DiseasesThe Affiliated Hospital of Xuzhou Medical CollegeXuzhouPeople’s Republic of China
  7. 7.Department of GeneticsXuzhou Medical CollegeXuzhouPeople’s Republic of China

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