Disentangling Heterogeneity in Alzheimer's Disease and Related Dementias Using Data-Driven Methods

被引:110
作者
Habes, Mohamad [1 ,2 ,3 ,6 ,9 ]
Grothe, Michel J. [10 ,11 ,12 ,13 ]
Tunc, Birkan [4 ,7 ,8 ]
McMillan, Corey [3 ,5 ]
Wolk, David A. [3 ,6 ]
Davatzikos, Christos [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Ctr Biomed Image Comp & Analyt, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Radiol, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Penn Frontotemporal Degenerat Ctr, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Ctr Adv Med, Penn Memory Ctr, Philadelphia, PA 19104 USA
[7] Childrens Hosp Philadelphia, Ctr Autism Res, Philadelphia, PA 19104 USA
[8] Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA
[9] Univ Texas Hlth Sci Ctr San Antonio, Glenn Biggs Inst Neurodegenerat Disorders, Biggs Inst Neuroimaging Core, San Antonio, TX 78229 USA
[10] German Ctr Neurodegenerat Dis, Rostock, Germany
[11] Univ Seville, Serv Neurolo & Neurofisiol Clin, Unidad Trastornos Movimiento, Hos Univ Virgen Rocio,Inst Biomed Sevilla,CSIC, Seville, Spain
[12] Univ Gothenburg, Wallenberg Ctr Mol & Translat Med, Gothenburg, Sweden
[13] Univ Gothenburg, Dept Psychiat & Neurochem, Gothenburg, Sweden
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Brain aging; Clustering; Frontotemporal dementia; Heterogeneity; Lewy body dementias; Machine learning; MRI; Neuroimaging; PET; MILD COGNITIVE IMPAIRMENT; PARKINSONS-DISEASE; LEWY BODIES; BEHAVIORAL VARIANT; FRONTOTEMPORAL DEMENTIA; BRAIN ATROPHY; ANATOMICAL SUBTYPES; CEREBROSPINAL-FLUID; DISTINCT SUBTYPES; DEFINED SUBTYPES;
D O I
10.1016/j.biopsych.2020.01.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain aging is a complex process that includes atrophy, vascular injury, and a variety of age-associated neurodegenerative pathologies, together determining an individual's course of cognitive decline. While Alzheimer's disease and related dementias contribute to the heterogeneity of brain aging, these conditions themselves are also heterogeneous in their clinical presentation, progression, and pattern of neural injury. We reviewed studies that leveraged data-driven approaches to examining heterogeneity in Alzheimer's disease and related dementias, with a principal focus on neuroimaging studies exploring subtypes of regional neurodegeneration patterns. Over the past decade, the steadily increasing wealth of clinical, neuroimaging, and molecular biomarker information collected within large-scale observational cohort studies has allowed for a richer understanding of the variability of disease expression within the aging and Alzheimer's disease and related dementias continuum. Moreover, the availability of these large-scale datasets has supported the development and increasing application of clustering techniques for studying disease heterogeneity in a data-driven manner. In particular, data-driven studies have led to new discoveries of previously unappreciated disease subtypes characterized by distinct neuroimaging patterns of regional neurodegeneration, which are paralleled by heterogeneous profiles of pathological, clinical, and molecular biomarker characteristics. Incorporating these findings into novel frameworks for more differentiated disease stratification holds great promise for improving individualized diagnosis and prognosis of expected clinical progression, and provides opportunities for development of precision medicine approaches for therapeutic intervention. We conclude with an account of the principal challenges associated with datadriven heterogeneity analyses and outline avenues for future developments in the field.
引用
收藏
页码:70 / 82
页数:13
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