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柳氮磺胺吡啶诱导的粒细胞缺乏症与人类白细胞抗原基因座相关。

Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.

机构信息

Department of Medical Sciences, Clinical Pharmacology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.

Uppsala Clinical Research Center and Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

Clin Pharmacol Ther. 2018 May;103(5):843-853. doi: 10.1002/cpt.805. Epub 2017 Sep 28.

Abstract

Agranulocytosis is a serious, although rare, adverse reaction to sulfasalazine, which is used to treat inflammatory joint and bowel disease. We performed a genome-wide association study comprising 9,380,034 polymorphisms and 180 HLA alleles in 36 cases of sulfasalazine-induced agranulocytosis and 5,170 population controls. Sulfasalazine-induced agranulocytosis was significantly associated with the HLA region on chromosome 6. The top hit (rs9266634) was located close to HLA-B, odds ratio (OR) 5.36 (95% confidence interval (CI) (2.97, 9.69) P = 2.55 × 10 ). We HLA-sequenced a second cohort consisting of 40 cases and 142 treated controls, and confirmed significant associations with HLA-B08:01, OR = 2.25 (95% CI (1.02, 4.97) P = 0.0439), in particular the HLA-B08:01 haplotype HLA-DQB102:01-DRB103:01-B08:01-C07:01, OR = 3.79 (95% CI (1.63, 8.80) P = 0.0019), and with HLA-A31:01, OR = 4.81 (95% CI (1.52, 15.26) P = 0.0077). The number needed to test for HLA-B08:01 and HLA-A31:01 to avoid one case was estimated to be 1,500. We suggest that intensified monitoring or alternative treatment should be considered for known carriers of HLA-B08:01 or HLA-A*31:01.

摘要

粒细胞缺乏症是一种严重的不良反应,虽然罕见,但对柳氮磺胺吡啶(用于治疗炎症性关节和肠道疾病)。我们进行了一项全基因组关联研究,该研究包括 36 例柳氮磺胺吡啶诱导的粒细胞缺乏症和 5170 名人群对照的 938 万个多态性和 180 个 HLA 等位基因。柳氮磺胺吡啶诱导的粒细胞缺乏症与 6 号染色体上的 HLA 区域显著相关。最高命中(rs9266634)位于 HLA-B 附近,优势比(OR)为 5.36(95%置信区间(CI)(2.97,9.69)P=2.55×10)。我们对包括 40 例和 142 例治疗对照的第二个队列进行了 HLA 测序,并证实与 HLA-B08:01 显著相关,OR=2.25(95%CI(1.02,4.97)P=0.0439),特别是 HLA-B08:01 单倍型 HLA-DQB102:01-DRB103:01-B08:01-C07:01,OR=3.79(95%CI(1.63,8.80)P=0.0019),以及与 HLA-A31:01 显著相关,OR=4.81(95%CI(1.52,15.26)P=0.0077)。为避免发生一例病例,估计检测 HLA-B08:01 和 HLA-A31:01 的人数需要 1500 人。我们建议,对于已知 HLA-B08:01 或 HLA-A*31:01 携带者,应考虑加强监测或替代治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da83/5947520/4e71fc988b05/CPT-103-843-g001.jpg

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