Department of Molecular and Functional Genomics, Geisinger Medical Center, Danville, Pa.
Department of Molecular and Functional Genomics, Geisinger Medical Center, Danville, Pa.
J Vasc Surg Venous Lymphat Disord. 2022 Mar;10(2):382-389.e2. doi: 10.1016/j.jvsv.2021.07.007. Epub 2021 Aug 3.
The present study sought to determine whether protein-truncating variants (PTVs) in PIEZO1 and CASZ1 genes, previously shown to be associated with varicose veins, were associated with an altered risk of varicose veins.
An exome sequence database of 131,918 participants from the Geisinger MyCode Community Health Initiative was used to identify individuals with genetic variants in the PIEZO1 or CASZ1 gene. Clinical phenotypes, including varicose vein diagnoses, were determined by analysis of the electronic health record data.
We identified 12,531 individuals (9.5%) with a diagnosis of varicose veins. Exome sequence data identified 92 PIEZO1 PTVs in 305 heterozygous carriers. PIEZO1 PTVs were significantly enriched in those with varicose vein (0.37% of cases vs 0.22% of controls; odds ratio [OR], 1.7; P = .0010). Nearly all varicose vein cases were associated with frameshift or stop-gain PTVs (OR, 3.0 for stop-gain [P = .0001]; OR, 2.9 for frameshift variants [P < .0001]). In the varicose vein cases, the PTV carriers were more likely to have an encounter with a vascular surgeon (62.5% for PTV carriers; 36.9% for noncarriers; P = .0003) and more likely to have received vein ablation therapy (OR, 6.9; P < .0001). No association was found between PIEZO1 PTVs and lymphedema, and no association was found for rare missense variants in PIEZO1 with varicose veins. PTVs in CASZ1 were extremely rare (16 total carriers), with none identified in those with varicose vein.
Rare PTVs in PIEZO1 but not CASZ1 were associated with varicose veins and the need for vein ablation therapy. These results have demonstrated that PTVs in the PIEZO1 gene are rare but represent strong genetic risk factors for varicose veins and the need for vein ablation therapy. These results have also identified a potential biologic mechanism and target for the development of novel therapies.
本研究旨在确定先前与静脉曲张相关的 PIEZO1 和 CASZ1 基因中的蛋白截断变异(PTV)是否与静脉曲张风险的改变有关。
利用来自 Geisinger MyCode 社区健康倡议的 131918 名参与者的外显子组序列数据库,鉴定出 PIEZO1 或 CASZ1 基因中存在遗传变异的个体。通过电子健康记录数据分析确定临床表型,包括静脉曲张的诊断。
我们确定了 12531 名(9.5%)静脉曲张诊断患者。外显子组数据在 305 名杂合携带者中鉴定出 92 个 PIEZO1 PTV。PIEZO1 PTV 在静脉曲张患者中明显富集(0.37%的病例vs 0.22%的对照;比值比[OR],1.7;P =.0010)。几乎所有静脉曲张病例均与移码或无义 PTV 相关(无义 PTV 的 OR 为 3.0[P =.0001];移码变异的 OR 为 2.9[P <.0001])。在静脉曲张病例中,PTV 携带者更有可能接受血管外科医生的治疗(PTV 携带者为 62.5%;非携带者为 36.9%;P =.0003),并且更有可能接受静脉消融治疗(OR,6.9;P <.0001)。在 PIEZO1 中未发现 PTV 与淋巴水肿之间存在关联,并且 PIEZO1 中的罕见错义变异与静脉曲张之间也未发现关联。CASZ1 中的 PTV 极为罕见(共有 16 名携带者),静脉曲张患者中未发现 PTV。
PIEZO1 中的罕见 PTV 与静脉曲张和静脉消融治疗的需要有关,但 CASZ1 中的 PTV 则不然。这些结果表明,PIEZO1 基因中的 PTV 虽然罕见,但却是静脉曲张和静脉消融治疗的重要遗传风险因素。这些结果还确定了一种潜在的生物学机制和新疗法的开发靶点。