Ropper A H, Williams R S
Neurology. 1980 Jun;30(6):639-44. doi: 10.1212/wnl.30.6.639.
In patients with Down syndrome, senile plaques and neurofibrillary tangles accumulate in the cortex at an earlier age than in persons of normal karyotype. We studied 20 Down syndrome patients dying after age 30 (average age, 49); all had neocortical plaques and tangles, but only 3 of 20 had been demented. In 12 cases (average age, 53), tissue was available for quantitative study of plaque and tangle densities and estimation of cell loss in the hippocampus. Although at least 8 of these 12 cases had plaque and tangle densities comparable to those previously reported in demented old people, only 1 had dementia. The regional distribution of plaques and tangles in the hippocampus of these Down cases differed from the pattern in senile dementia. Although Alzheimer-like dementia occurs in Down disease, it is less prevalent than the plethoric plaques and tangles in the cortex.
在唐氏综合征患者中,与核型正常的人相比,老年斑和神经原纤维缠结在皮质中的积累年龄更早。我们研究了20名30岁以后死亡的唐氏综合征患者(平均年龄49岁);所有人都有新皮质斑和缠结,但20人中只有3人患有痴呆症。在12例(平均年龄53岁)中,有组织可用于对斑块和缠结密度进行定量研究,并估计海马体中的细胞损失。尽管这12例中至少有8例的斑块和缠结密度与先前报道的老年痴呆患者相当,但只有1例患有痴呆症。这些唐氏病例海马体中斑块和缠结的区域分布与老年痴呆症的模式不同。虽然唐氏病中会出现类似阿尔茨海默病的痴呆症,但它的患病率低于皮质中过多的斑块和缠结。