Université de Paris, AP-HP, Hôpital Bichat-Claude Bernard, Département de génétique, UMR1152, INSERM, Paris, France.
Université de Paris, AP-HP, Hôpital Bichat-Claude Bernard, Service de pneumologie B, UMR1152, INSERM, Paris, France.
J Heart Lung Transplant. 2022 Sep;41(9):1207-1209. doi: 10.1016/j.healun.2022.06.012. Epub 2022 Jun 19.
Almost 25% of patients with pulmonary fibrosis referred for lung transplantation have a germline rare variant of a telomere-related gene. Acquired TERT promoter mutations may counterbalanced the germline defect and reduce the risk of hematological complications in this population. In a series of 34 patients with a germline telomere-related gene mutation who underwent lung transplantation, 12 (35%) patients had at least 1 acquired TERT promoter mutation. Six patients presented myelodysplasia before lung transplantation, with no difference between patients with and without an acquired TERT promoter mutation. After lung transplantation, myelodysplasia developed in only 1 of 8 patients with an acquired TERT promoter mutation versus 7 of 18 patients without a mutation. Survival did not differ between patients with and without an acquired mutation. The presence of an acquired TERT promoter mutation could be associated with reduced hematological complications after transplantation and with better outcome in telomere-related gene mutation carriers but requires further study.
约 25% 因肺纤维化而接受肺移植的患者存在与端粒相关基因的种系罕见变异。获得性 TERT 启动子突变可能会抵消种系缺陷,并降低该人群发生血液学并发症的风险。在一系列接受肺移植的 34 例存在种系端粒相关基因突变的患者中,有 12 例(35%)患者至少存在 1 种获得性 TERT 启动子突变。6 例患者在肺移植前表现出骨髓增生异常,而有无获得性 TERT 启动子突变的患者之间无差异。肺移植后,仅在 8 例存在获得性 TERT 启动子突变的患者中有 1 例出现骨髓增生异常,而在 18 例无突变的患者中有 7 例出现骨髓增生异常。有无获得性突变的患者的存活率无差异。获得性 TERT 启动子突变的存在可能与移植后血液学并发症减少以及端粒相关基因突变携带者的预后更好相关,但仍需要进一步研究。