Division of Allergy and Clinical Immunology, Department of Internal Medicine, University of Michigan, Ann Arbor, Mich; Mary H. Weiser Food Allergy Center, University of Michigan, Ann Arbor, Mich.
Division of Rheumatology, Allergy and Immunology, Department of Internal Medicine, University of North Carolina, Chapel Hill, NC.
J Allergy Clin Immunol. 2021 Nov;148(5):1316-1323. doi: 10.1016/j.jaci.2021.04.013. Epub 2021 Apr 22.
Mastocytosis is a risk factor for Hymenoptera venom anaphylaxis (HVA). Current guidelines recommend measuring tryptase in patients with HVA and that those with mastocytosis pursue lifelong venom immunotherapy (VIT). Available data on HVA and mastocytosis largely derive from European single-center studies, and the prevalence of HVA with and without mastocytosis in the United States is unknown.
We sought to determine the prevalence of HVA and mastocytosis in the United States using an insurance claims database and evaluate the impact of mastocytosis on VIT in patients with HVA in a US cohort.
The IBM Watson Database, consisting of insurance claims from approximately 27 million US patients in 2018, was queried to identify patients with HVA and/or mastocytosis. Furthermore, a retrospective study of 161 patients undergoing VIT between 2015 and 2018 at the University of Michigan was conducted.
In the IBM Watson Database, the prevalence of HVA was 167 per 100,000 (0.167%) and the prevalence of mastocytosis 10 per 100,000 (0.010%) overall and 97 per 100,000 (0.097%) among those with HVA. Mastocytosis showed a 9.7-fold increase among patients with HVA versus the general population. In the U-M cohort, 2.6% of patients with VIT had mastocytosis. Tryptase level did not correlate with venom reaction severity but was higher in patients with systemic VIT reactions.
We observed a lower US HVA prevalence than previously reported. Mastocytosis was more common in US patients with HVA, though at lower rates than previously reported. In patients with VIT there was no correlation between tryptase level and reaction severity.
肥大细胞增多症是蜂类毒液过敏反应(HVA)的一个危险因素。目前的指南建议对 HVA 患者进行类胰蛋白酶检测,且那些患有肥大细胞增多症的患者应进行终身毒液免疫治疗(VIT)。目前关于 HVA 和肥大细胞增多症的可用数据主要来自欧洲单中心研究,而美国 HVA 伴或不伴肥大细胞增多症的患病率尚不清楚。
我们试图利用保险索赔数据库在美国确定 HVA 和肥大细胞增多症的患病率,并在一个美国队列中评估肥大细胞增多症对 HVA 患者 VIT 的影响。
我们使用 IBM Watson 数据库(包含 2018 年约 2700 万美国患者的保险索赔数据)来识别 HVA 和/或肥大细胞增多症患者。此外,我们还对 2015 年至 2018 年期间在密歇根大学接受 VIT 的 161 名患者进行了回顾性研究。
在 IBM Watson 数据库中,HVA 的患病率为 167 例/10 万人(0.167%),肥大细胞增多症的总患病率为 10 例/10 万人(0.010%),HVA 患者中的患病率为 97 例/10 万人(0.097%)。与普通人群相比,HVA 患者中肥大细胞增多症的发病率增加了 9.7 倍。在 U-M 队列中,接受 VIT 的患者中有 2.6%患有肥大细胞增多症。类胰蛋白酶水平与毒液反应严重程度无相关性,但在发生全身性 VIT 反应的患者中水平更高。
与之前报道的相比,我们观察到美国 HVA 的患病率较低。肥大细胞增多症在有 HVA 的美国患者中更为常见,但比率低于之前的报道。在接受 VIT 的患者中,类胰蛋白酶水平与反应严重程度之间无相关性。