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阿尔茨海默病患者大脑中线粒体DNA缺失水平的显著变化。

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.

作者信息

Corral-Debrinski M, Horton T, Lott M T, Shoffner J M, McKee A C, Beal M F, Graham B H, Wallace D C

机构信息

Department of Genetics and Molecular Medicine, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

Genomics. 1994 Sep 15;23(2):471-6. doi: 10.1006/geno.1994.1525.

Abstract

Levels of the common 4977 nucleotide pair (np) mitochondrial DNA (mtDNA) deletion (mtDNA4977) were quantitated in the cortex, putamen, and cerebellum of patients with Alzheimer disease (AD) and compared to age-matched controls. Although cerebellum deletion levels were comparably low in AD patients and controls of all ages, cortical deletion levels were clearly different. The levels of mtDNA deletions in control brains started low, but rose markedly after age 75, while those of AD patients started high and declined to low levels by age 80. Choosing age 75 to arbitrarily delineate between younger and older subjects, younger patients had 15 times more mtDNA deletions than younger controls, while older patients had one-fifth the deletion level of older controls. Younger AD patients also had fourfold more deletions than older AD patients. These results support the hypothesis that OXPHOS defects resulting from somatic mtDNA mutations may play a role in AD pathophysiology.

摘要

对阿尔茨海默病(AD)患者的皮质、壳核和小脑中常见的4977个核苷酸对(np)线粒体DNA(mtDNA)缺失(mtDNA4977)水平进行了定量,并与年龄匹配的对照组进行了比较。尽管在所有年龄段的AD患者和对照组中,小脑的缺失水平相对较低,但皮质的缺失水平明显不同。对照组大脑中的mtDNA缺失水平开始时较低,但在75岁后显著上升,而AD患者的mtDNA缺失水平开始时较高,并在80岁时降至低水平。选择75岁作为区分年轻和老年受试者的任意界限,年轻患者的mtDNA缺失比年轻对照组多15倍,而老年患者的缺失水平是老年对照组的五分之一。年轻的AD患者的缺失也比老年AD患者多四倍。这些结果支持了这样的假设,即体细胞mtDNA突变导致的氧化磷酸化缺陷可能在AD的病理生理学中起作用。

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