Genetics and Underlying Pathology of Dementia

被引:43
作者
Ferencz, Beata [1 ,2 ]
Gerritsen, Lotte [3 ,4 ]
机构
[1] Karolinska Inst, ARC, Stockholm, Sweden
[2] Stockholm Univ, S-10691 Stockholm, Sweden
[3] VU Med Ctr Amsterdam, Dept Psychiat, Stockholm, Sweden
[4] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Genetics; Dementia; Alzheimer's disease; Lewy body dementia; Vascular dementia; Frontotemporal lobar degeneration; FRONTOTEMPORAL LOBAR DEGENERATION; GENOME-WIDE ASSOCIATION; ONSET ALZHEIMER-DISEASE; COMPLEMENT RECEPTOR 1; AMYLOID-BETA PEPTIDE; LEWY BODY DEMENTIA; VASCULAR DEMENTIA; PARKINSONS-DISEASE; COMMON VARIANTS; IDENTIFIES VARIANTS;
D O I
10.1007/s11065-014-9276-3
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
As the population steadily ages, dementia, in all its forms, remains a great societal challenge. Yet, our knowledge of their etiology remains rather limited. To this end, genetic studies can give us insight into the underlying mechanisms that lead to the development of dementia, potentially facilitating treatments in the future. In this review we cover the most recent genetic risk factors associated with the onset of the four most common dementia types today, including Alzheimer's disease (AD), Vascular Dementia (VaD), Frontotemporal Lobar Degeneration (FTLD) and Lewy Body Dementia (LBD). Moreover, we discuss the overlap in major underlying pathologies of dementia derived from their genetic associations. While all four dementia types appear to involve genes associated with tau-pathology and neuroinflammation only LBD, AD and VaD appear to involve amyloid genes while LBD and FTLD share alpha synuclein genes. Together these findings suggest that some of the dementias may exist along a spectrum and demonstrates the necessity to conduct large-scale studies pinpointing the etiology of the dementias and potential gene and environment interactions that may influence their development.
引用
收藏
页码:113 / 124
页数:12
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