Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Clin Genet. 2022 Sep;102(3):191-200. doi: 10.1111/cge.14176. Epub 2022 Jul 4.
The study describes all patients in Denmark with vascular Ehlers-Danlos syndrome (vEDS). Carriers of pathogenic or likely pathogenic COL3A1 variants were retrospectively identified through registries and specialized clinics. Medical records were reviewed for vascular- or organ ruptures and invasive procedures performed. Identified families were divided by variant type (null, splice, and missense) and familial phenotypes (severe or attenuated). Families in which at least one carrier has suffered a major event before the age of 30 were classified as severe, whereas families in which at least three carriers had reached the age of 40 without a major event were classified as attenuated. Eighty-seven persons (59 still alive) from 25 families were included with a mean observation time of 44 years. Sixty-seven percent of patients could be subclassified in a familial phenotype. Thirty-one major events were observed. Eleven complications in 172 invasive procedures were recorded. No fatal complications to elective surgery were observed. The type of COL3A1 variant did not reliably predict phenotype, but a pattern of intrafamilial consistency emerged with some families showing an attenuated form of vEDS. Elective medical procedures appear to be safer than previously thought, although data only allow for conclusions regarding individuals from families with the attenuated form of vEDS.
该研究描述了丹麦所有患有血管型埃勒斯-当洛斯综合征(vEDS)的患者。通过注册中心和专门诊所,回顾性地确定了携带致病性或可能致病性 COL3A1 变异的患者。对血管或器官破裂以及进行的侵入性操作的医疗记录进行了审查。根据变异类型(无义、剪接和错义)和家族表型(严重或轻度)对确定的家族进行了分类。如果至少有一名携带者在 30 岁之前发生过重大事件,则将家族归类为严重,而如果至少有三名携带者在 40 岁之前没有发生重大事件,则将家族归类为轻度。共纳入了 25 个家族的 87 人(59 人仍存活),平均观察时间为 44 年。67%的患者可以按家族表型进一步分类。观察到 31 次重大事件。在 172 次侵入性操作中记录到 11 次并发症。择期手术未发生致命性并发症。COL3A1 变异类型不能可靠地预测表型,但在某些家族中出现了一致的轻度 vEDS 模式。择期医疗程序似乎比以前认为的更安全,尽管数据仅允许对具有轻度 vEDS 形式的家族的个体得出结论。