Gwinn-Hardy Katrina
Division of Intramural Research, Neurogenetics Laboratories, National Institute of Neurological Disease and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
Mov Disord. 2002 Jul;17(4):645-56. doi: 10.1002/mds.10173.
Parkinson's disease (PD) was noted to have a familial component as early as 1880 (Leroux, 1880). More recently, the discovery of several genetic factors influencing parkinsonism has emphasized the importance of heredity in PD. The clinical spectrum of familial parkinsonism is wide; it includes not only PD, but also dementia with Lewy bodies (DLB), progressive supranuclear palsy (PSP), essential tremor, and other disorders. In the general population, it is likely that PD results from combined genetic and environmental factors, most of which are not yet known. The discovery of causal mutations in the gene for alpha-synuclein, parkin, and of genetic linkages to chromosomes 2p4, 4p5, and three loci on 1q6-8 have revolutionized PD research. This review focuses on recent progress in the Mendelian genetics of PD and those diseases in which parkinsonism is a prominent feature, and considers how these discoveries modify our beliefs regarding the etiology and pathogenesis of these disorders.
早在1880年(勒鲁,1880年)就有人指出帕金森病(PD)存在家族性因素。最近,几种影响帕金森症的遗传因素的发现凸显了遗传在帕金森病中的重要性。家族性帕金森症的临床谱很广;它不仅包括帕金森病,还包括路易体痴呆(DLB)、进行性核上性麻痹(PSP)、特发性震颤和其他疾病。在一般人群中,帕金森病可能是由遗传和环境因素共同导致的,其中大多数因素尚不清楚。α-突触核蛋白、帕金基因中因果突变的发现,以及与2p4、4p5染色体和1q6 - 8上三个基因座的遗传连锁关系,彻底改变了帕金森病的研究。本综述重点关注帕金森病孟德尔遗传学以及以帕金森症为突出特征的那些疾病的最新进展,并思考这些发现如何改变我们对这些疾病病因和发病机制的认识。