Yusuf Hamzah, Rasheed Amna, Kim Helen, Conrad Miles B, Hetts Steven W
University of California San Francisco School of Medicine, San Francisco, California, USA
Touro College of Medicine, Vallejo, California, USA.
J Neurointerv Surg. 2023 Oct;15(10):1050-1054. doi: 10.1136/jnis-2022-019162. Epub 2022 Sep 22.
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder characterized by recurrent epistaxis (nose bleeds), mucosal telangiectasias (spider veins), and arteriovenous malformations. Although HHT affects all racial groups, few studies have explored racial disparities among patients with HHT.
We performed a retrospective chart review of HHT patients who were seen at a single academic center between July 1, 2014 and January 1, 2022. The primary outcomes of this study were the Epistaxis Severity Score (ESS) and the presence of pulmonary, cerebral, gastrointestinal, spinal, and hepatic arteriovenous malformations (AVMs). We analyzed racial differences using t-tests and analysis of variance (ANOVA) for continuous variables, and chi-squared tests for categorical variables. We then performed multivariable linear and logistic regressions on outcomes.
Our review identified 35 Asian, 6 Black or African American, 72 Hispanic or Latino, and 244 White or Caucasian patients who met the inclusion criteria. Through an analysis of variance model, race/ethnicity was not significantly associated with ESS. Two univariable logistic regression models between race and both pulmonary and brain AVMs showed that race was associated with the incidence of pulmonary AVMs (p<0.01), with Asian patients at a 2.3-fold increased risk of pulmonary AVMs compared with White patients (p=0.03). Race was also associated with the incidence of cerebral AVMs (p<0.01) with Hispanic or Latino patients at a 4.8-fold increased risk compared with White patients (p<0.01).
Patients who identified as Asian may have higher rates of pulmonary AVMs while patients identifying as Hispanic or Latino may have more cerebral AVMs. The correlations may be important for identifying risk factors in certain patient populations.
遗传性出血性毛细血管扩张症(HHT)是一种罕见的常染色体显性疾病,其特征为反复鼻出血(流鼻血)、黏膜毛细血管扩张(蜘蛛状血管)和动静脉畸形。尽管HHT影响所有种族群体,但很少有研究探讨HHT患者之间的种族差异。
我们对2014年7月1日至2022年1月1日期间在单一学术中心就诊的HHT患者进行了回顾性病历审查。本研究的主要结局指标是鼻出血严重程度评分(ESS)以及肺部、脑部、胃肠道、脊柱和肝脏动静脉畸形(AVM)的存在情况。对于连续变量,我们使用t检验和方差分析(ANOVA)分析种族差异;对于分类变量,我们使用卡方检验。然后,我们对结局进行多变量线性和逻辑回归分析。
我们的审查确定了35名亚洲患者、6名黑人或非裔美国患者、72名西班牙裔或拉丁裔患者以及244名白人或高加索患者符合纳入标准。通过方差分析模型,种族/族裔与ESS无显著关联。种族与肺部和脑部AVM的两个单变量逻辑回归模型显示,种族与肺部AVM的发生率相关(p<0.01),亚洲患者发生肺部AVM的风险比白人患者高2.3倍(p=0.03)。种族也与脑部AVM的发生率相关(p<0.01),西班牙裔或拉丁裔患者发生脑部AVM的风险比白人患者高4.8倍(p<0.01)。
自我认定为亚洲人的患者可能有更高的肺部AVM发生率,而自我认定为西班牙裔或拉丁裔的患者可能有更多的脑部AVM。这些相关性对于确定某些患者群体的危险因素可能很重要。