The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery
- PMID: 32581188
- PMCID: PMC8049143
- DOI: 10.5551/jat.56333
The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery
Abstract
Aim: Deep vein thrombosis (DVT) is a common complication of orthopedic surgery. Multiple lines of evidence indicate that genetic factors play an important role in the development of DVT following orthopedic surgery (DVTFOS). Recent evidence suggested that the solute carrier family 44 member 2 (SLC44A) gene may contribute to the risk of DVT. In this study, we aimed to investigate the associations of SLC44A2 and DVTFOS in Chinese Han individuals.
Methods: In the study, 2,655 subjects, including 689 DVTFOS patients and 1,966 controls, were recruited. Eighteen SNPs were genotyped in the study. Genetic association analyses were performed at both the single marker and haplotype levels. Bioinformatics analyses were conducted to predict the functional consequences of significant SNPs.
Results: SNP rs2288904 of SLC44A2 was identified as being significantly associated with DVTFOS (P = 0.0003, OR [95%CI] = 1.28[1.12-1.46]). Allelic analyses showed that the G allele of this SNP significantly elevated the risks of DVTFOS, which was replicated in the genotypic association analyses. Moreover, a two-SNP haplotype, including rs2288904, was found to be strongly correlated with the risk of DVTFOS (P = 4.15×10-11). Widespread effects in the expression quantitative trait loci were identified for rs2288904 in multiple tissues.
Conclusion: In summary, our results provide further supportive evidence of the association of SLC44A2 with the risk of DVTFOS, which also provide clues for understanding the important roles of the SLC44A2 gene in the pathogenesis of DVTFOS and in the development of preventive strategies.
Keywords: Case–control study; Deep vein thrombosis; Genetic association; SLC44A2; Single nucleotide polymorphisms.
Conflict of interest statement
All authors declare that they have no conflict of interest.
Figures





Similar articles
-
Evaluation of relationship between KEAP1 gene and genetic susceptibility of deep vein thrombosis after orthopedic surgery in Han Chinese population.J Thromb Thrombolysis. 2021 Apr;51(3):617-624. doi: 10.1007/s11239-020-02216-2. J Thromb Thrombolysis. 2021. PMID: 32770279
-
Activated αIIbβ3 on platelets mediates flow-dependent NETosis via SLC44A2.Elife. 2020 Apr 21;9:e53353. doi: 10.7554/eLife.53353. Elife. 2020. PMID: 32314961 Free PMC article.
-
Genetic effects of BDKRB2 and KNG1 on deep venous thrombosis after orthopedic surgery and the potential mediator.Sci Rep. 2018 Nov 26;8(1):17332. doi: 10.1038/s41598-018-34868-9. Sci Rep. 2018. PMID: 30478260 Free PMC article.
-
Deep vein thrombosis after major orthopedic surgery in Taiwan: A prospective cross-sectional study and literature review.J Formos Med Assoc. 2022 Aug;121(8):1541-1549. doi: 10.1016/j.jfma.2021.12.027. Epub 2022 Jan 13. J Formos Med Assoc. 2022. PMID: 35033412 Review.
-
Lessons from genome-wide association studies in venous thrombosis.J Thromb Haemost. 2011 Jul;9 Suppl 1:258-64. doi: 10.1111/j.1538-7836.2011.04311.x. J Thromb Haemost. 2011. PMID: 21781262 Review.
Cited by
-
Diagnostic and prognostic potential of long non-coding RNA NORAD in patients with acute deep vein thrombosis and its role in endothelial cell function.Thromb J. 2024 Jan 2;22(1):3. doi: 10.1186/s12959-023-00575-3. Thromb J. 2024. PMID: 38167080 Free PMC article.
-
Platelet-Neutrophil Crosstalk in Thrombosis.Int J Mol Sci. 2023 Jan 9;24(2):1266. doi: 10.3390/ijms24021266. Int J Mol Sci. 2023. PMID: 36674781 Free PMC article. Review.
References
-
- Neglen P, Thrasher TL and Raju S: Venous outflow obstruction: An underestimated contributor to chronic venous disease. J Vasc Surg, 2003; 38: 879-885 - PubMed
-
- Souto JC, Almasy L, Borrell M, Blanco-Vaca F, Mateo J, Soria JM, Coll I, Felices R, Stone W, Fontcuberta J and Blangero J: Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia. Am J Hum Genet, 2000; 67: 1452-1459 - PMC - PubMed
-
- Larsen TB, Sorensen HT, Skytthe A, Johnsen SP, Vaupel JW and Christensen K: Major genetic susceptibility for venous thromboembolism in men: a study of Danish twins. Epidemiology, 2003; 14: 328-332 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical