Heald Brandie, Rigelsky Christina, Moran Rocio, LaGuardia Lisa, O'Malley Margaret, Burke Carol A, Zahka Kenneth
Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio.
Sanford R Weiss Center for Hereditary Colorectal Cancer Neoplasia, Cleveland Clinic, Cleveland, Ohio.
Am J Med Genet A. 2015 Aug;167A(8):1758-62. doi: 10.1002/ajmg.a.37093. Epub 2015 Apr 30.
Hereditary hemorrhagic telangiectasia (HHT) is characterized by abnormal vascular structures that may present as epistaxis, telangiectasias, and/or arteriovenous malformations. The genes associated with HHT (ACVRL1, ENG, and SMAD4) are members of the TGFβ pathway. Other syndromes associated with abnormalities in TGFβ signaling include Marfan syndrome, Loeys-Dietz syndrome and related disorders. These disorders have aortic disease as a prominent finding. While there are case reports of patients with HHT and aortopathy (dilatation/aneurysm, dissection, and rupture), this has not been systematically investigated. We conducted a retrospective chart review to determine the prevalence of aortopathy in an HHT cohort. Patients from a single institution were identified who met the Curacao Criteria for a clinical diagnosis of HHT and/or had a mutation in ACVRL1, ENG, or SMAD4 and underwent echocardiogram. Two-dimensional echocardiograms were reviewed by a single pediatric cardiologist, and data were collected on demographics, genotype, HHT features, aortic root measurements, past medical history, and family history. Z scores and nomograms were utilized to identify abnormal results. Twenty-six patients from 15 families (one ACVRL1, four ENG, eight SMAD4, and two clinical diagnoses) were included in the analysis. Aortopathy was found in 6/26 (23%) patients; all had SMAD4 mutations. In our cohort, 6/16 (38%) SMAD4 mutation carriers had evidence of aortopathy. These data suggest that aortopathy could be part of the spectrum of SMAD4-induced HHT manifestations. Routine aortic imaging, including measurements of the aorta, should be considered in patients with SMAD4 mutations to allow for appropriate medical and surgical recommendations.
遗传性出血性毛细血管扩张症(HHT)的特征是血管结构异常,可表现为鼻出血、毛细血管扩张和/或动静脉畸形。与HHT相关的基因(ACVRL1、ENG和SMAD4)是转化生长因子β(TGFβ)信号通路的成员。其他与TGFβ信号异常相关的综合征包括马凡综合征、洛伊迪茨综合征及相关疾病。这些疾病以主动脉病变为突出表现。虽然有HHT患者合并主动脉病变(扩张/动脉瘤、夹层和破裂)的病例报告,但尚未进行系统研究。我们进行了一项回顾性病历审查,以确定HHT队列中主动脉病变的患病率。从单一机构中识别出符合HHT临床诊断库拉索标准和/或ACVRL1、ENG或SMAD4基因发生突变并接受超声心动图检查的患者。由一名儿科心脏病专家对二维超声心动图进行审查,并收集有关人口统计学、基因型、HHT特征、主动脉根部测量、既往病史和家族史的数据。使用Z评分和列线图来识别异常结果。分析纳入了来自15个家庭的26名患者(1例ACVRL1突变、4例ENG突变、8例SMAD4突变和2例临床诊断)。在6/26(23%)的患者中发现了主动脉病变;所有患者均为SMAD4突变。在我们的队列中,6/16(38%)的SMAD4突变携带者有主动脉病变的证据。这些数据表明,主动脉病变可能是SMAD4诱导的HHT表现谱的一部分。对于SMAD4突变患者,应考虑进行包括主动脉测量在内的常规主动脉成像,以便给出适当的医学和手术建议。