Chinese Journal of Contemporary Neurology and Neurosurgery ›› 2026, Vol. 26 ›› Issue (2): 169-178. doi: 10.3969/j.issn.1672-6731.2026.02.008

• Dementia-associated Cognitive Impairment • Previous Articles    

Progress on frontotemporal dementia

XU Yu-xuan1, NAN Hai-tian1, CHU Min1, WU Li-yong1,2   

  1. 1 Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China;
    2 National Clinical Research Center for Geriatric Diseases, Beijing 100853, China
  • Received:2026-01-13 Published:2026-03-12
  • Supported by:
    This study was supported by Key International Cooperation Program of the National Natural Science Foundation of China (No. W2511084), the National Natural Science Foundation of China for Young Scientists (No. 82401665), and Beijing Natural Science Foundation (No. 7242067).

额颞叶痴呆研究进展

徐语萱1, 南海天1, 褚敏1, 武力勇1,2   

  1. 1 100053 北京, 首都医科大学宣武医院神经内科;
    2 100853 北京, 国家老年疾病临床医学研究中心
  • 通讯作者: 武力勇,Email:wmywly@hotmail.com
  • 基金资助:
    国家自然科学基金重点国际(地区)合作项目(项目编号:W2511084);国家自然科学基金青年科学基金项目(项目编号:82401665);北京市自然科学基金资助项目(项目编号:7242067)

Abstract: Frontotemporal dementia (FTD) is the second most common type of early-onset dementia after Alzheimer's disease (AD), severely impairing patients' quality of life and increasing the burden of family care. Currently, there is a lack of reliable biomarkers for its diagnosis, and reliance on clinical manifestations is prone to misdiagnosis and missed diagnosis. Additionally, there are no approved specific treatments for FTD, and the efficacy of existing therapeutic treatments remains limited. With the deepening research on the genetic mechanisms of FTD, the diagnostic and therapeutic treatments based on this have significant application prospects. This study systematically summarizes research findings in the fields of genetic mechanism, pathological classification, diagnosis and therapeutic treatments of FTD in recent years, aiming to provide a reference for comprehensive understanding of disease's pathogenesis and clinical characteristics, and to lay a foundation for exploring novel diagnostic and therapeutic strategies.

Key words: Frontotemporal dementia, Genes, Mutation, Biomarkers, Transcranial magnetic stimulation, Electric stimulation therapy, Review

摘要: 额颞叶痴呆是仅次于阿尔茨海默病的常见早发型痴呆,严重影响患者生活质量并带来沉重家庭和社会负担。目前疾病诊断主要依靠临床症状,缺乏可靠的生物学标志物,易漏诊或误诊,亦无针对性疾病修饰治疗,现有治疗方法效果有限。随着额颞叶痴呆遗传学机制研究的深入,以此为基础的诊断与治疗手段应用前景广阔,本文系统梳理额颞叶痴呆的遗传学机制、病理分型、诊断与治疗进展,旨在为深入理解疾病的本质特征提供理论依据,并为探索早期诊断与有效治疗的创新策略指引方向。

关键词: 额颞叶痴呆, 基因, 突变, 生物标记, 经颅磁刺激, 电刺激疗法, 综述

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