医学
血栓形成
天冬酰胺酶
血栓性
内科学
肿瘤科
因素五莱顿
静脉血栓形成
白血病
免疫学
淋巴细胞白血病
作者
Covida Mootoosamy,Maria Kondyli,Sophie Annaelle Serfaty,David-Étienne Tremblay,Vincent Gagné,Maïté Ribère,Caroline Laverdière,Jean‐Marie Leclerc,Daniel Sinnett,Thai Hoa Tran,Maja Krajinović
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2023-03-01
卷期号:24 (4): 199-206
标识
DOI:10.2217/pgs-2022-0164
摘要
Aim: We previously conducted exome-wide association study in acute lymphoblastic leukemia patients and identified association of five SNPs with asparaginase-related thrombosis. Here we aimed to replicate these findings in an independent patient cohort and through analyses in vitro. Patients & methods: SNPs located in IL16, MYBBP1A, PKD2L1, RIN3 and MPEG1 genes were analyzed in patients receiving Dana-Farber Cancer Institute acute lymphoblastic leukemia treatment protocols 05-001 and 11-001. Thrombophilia-related variations were also analysed. Results: IL16 rs11556218 conferred higher risk of thrombosis and higher in vitro sensitivity to asparaginase. The association was modulated by the treatment protocol, risk group and immunophenotype. A crosstalk between factor V Leiden, non-O blood groups and higher risk of thrombosis was also seen. Conclusion: IL16 and factor V Leiden variations are implicated in asparaginase-related thrombosis.
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