Disorders of Telomere Length.

IF 11.6
NEJM evidence Pub Date : 2026-07-01 Epub Date: 2026-06-23 DOI:10.1056/EVIDra2600012
Kristen E Schratz, Mary Armanios
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Abstract

AbstractRecent discoveries have uncovered roles for telomere length, at both short and long extremes, as a driver of inherited disease risk in children and adults. For short telomere length the predominant phenotype is degenerative, with immunodeficiency, bone marrow failure, and pulmonary disease being most common. Short telomere syndrome genetics inform clinical decisions and have transformed understanding of the etiology, natural history, and treatment of common diseases such as idiopathic pulmonary fibrosis. At the other extreme, ultra-long telomere length predisposes to neoplasia including lympho- and myeloproliferative disease. Individuals with mutations that lengthen telomeres may show features of youthfulness such as delayed hair graying but paradoxically are at risk for benign and malignant neoplasia, which are associated with aging. Their earliest events are traceable in the blood as premature onset of clonal hematopoiesis which shows complete penetrance with aging. Here, we review the genetic basis, pathophysiology, and contrasting phenotypes of Mendelian short and long telomere syndromes, emphasizing how they inform clinical decisions as well as our understanding of the fundamentals of aging and cancer.

端粒长度紊乱。
最近的发现揭示了端粒长度在儿童和成人中作为遗传性疾病风险驱动因素的作用,无论是短端粒还是长端粒。端粒长度短的主要表型是退行性,免疫缺陷,骨髓衰竭和肺部疾病是最常见的。短端粒综合征遗传学为临床决策提供信息,并改变了对病因、自然史和常见疾病(如特发性肺纤维化)治疗的理解。在另一个极端,超长的端粒长度易患肿瘤,包括淋巴和骨髓增生性疾病。具有端粒延长突变的个体可能表现出年轻的特征,如头发变白延迟,但矛盾的是,患与衰老相关的良性和恶性肿瘤的风险较高。它们最早的事件可追溯到血液中克隆造血的过早发作,这显示出与衰老完全外显。在这里,我们回顾了孟德尔短端粒综合征和长端粒综合征的遗传基础、病理生理学和对比表型,强调它们如何告知临床决策以及我们对衰老和癌症基本原理的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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