MARKED CHANGES IN MITOCHONDRIAL-DNA DELETION LEVELS IN ALZHEIMER BRAINS

被引:254
作者
CORRALDEBRINSKI, M
HORTON, T
LOTT, MT
SHOFFNER, JM
MCKEE, AC
BEAL, MF
GRAHAM, BH
WALLACE, DC
机构
[1] EMORY UNIV,SCH MED,DEPT MOLEC & MED GENET,ATLANTA,GA 30322
[2] EMORY UNIV,SCH MED,DEPT NEUROL,ATLANTA,GA 30322
[3] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[4] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
D O I
10.1006/geno.1994.1525
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Levels of the common 4977 nucleotide pair (np) mitochondrial DNA (mtDNA) deletion (mtDNA(4977)) 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. (C) 1994 Academic Press, Inc.
引用
收藏
页码:471 / 476
页数:6
相关论文
共 24 条
  • [1] DISTRIBUTION OF ALZHEIMER-TYPE PATHOLOGICAL-CHANGES IN NONDEMENTED ELDERLY INDIVIDUALS MATCHES THE PATTERN IN ALZHEIMERS-DISEASE
    ARRIAGADA, PV
    MARZLOFF, K
    HYMAN, BT
    [J]. NEUROLOGY, 1992, 42 (09) : 1681 - 1688
  • [2] MATERNALLY TRANSMITTED DIABETES AND DEAFNESS ASSOCIATED WITH A 10.4 KB MITOCHONDRIAL-DNA DELETION
    BALLINGER, SW
    SHOFFNER, JM
    HEDAYA, EV
    TROUNCE, I
    POLAK, MA
    KOONTZ, DA
    WALLACE, DC
    [J]. NATURE GENETICS, 1992, 1 (01) : 11 - 15
  • [3] GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES
    CORDER, EH
    SAUNDERS, AM
    STRITTMATTER, WJ
    SCHMECHEL, DE
    GASKELL, PC
    SMALL, GW
    ROSES, AD
    HAINES, JL
    PERICAKVANCE, MA
    [J]. SCIENCE, 1993, 261 (5123) : 921 - 923
  • [4] ASSOCIATION OF MITOCHONDRIAL-DNA DAMAGE WITH AGING AND CORONARY ATHEROSCLEROTIC HEART-DISEASE
    CORRALDEBRINSKI, M
    SHOFFNER, JM
    LOTT, MT
    WALLACE, DC
    [J]. MUTATION RESEARCH, 1992, 275 (3-6): : 169 - 180
  • [5] HYPOXEMIA IS ASSOCIATED WITH MITOCHONDRIAL-DNA DAMAGE AND GENE INDUCTION - IMPLICATIONS FOR CARDIAC DISEASE
    CORRALDEBRINSKI, M
    STEPIEN, G
    SHOFFNER, JM
    LOTT, MT
    KANTER, K
    WALLACE, DC
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 266 (13): : 1812 - 1816
  • [6] MITOCHONDRIAL-DNA DELETIONS IN HUMAN BRAIN - REGIONAL VARIABILITY AND INCREASE WITH ADVANCED AGE
    CORRALDEBRINSKI, M
    HORTON, T
    LOTT, MT
    SHOFFNER, JM
    BEAL, MF
    WALLACE, DC
    [J]. NATURE GENETICS, 1992, 2 (04) : 324 - 329
  • [7] A PATTERN OF ACCUMULATION OF A SOMATIC DELETION OF MITOCHONDRIAL-DNA IN AGING HUMAN TISSUES
    CORTOPASSI, GA
    SHIBATA, D
    SOONG, NW
    ARNHEIM, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) : 7370 - 7374
  • [8] DUYCKAERTS C, 1992, METHODS NEUROSCIENCE, V10, P526
  • [9] EVANS DA, 1989, JAMA-J AM MED ASSOC, V262, P2551, DOI 10.1001/jama.1989.03430180093036
  • [10] AGE-DEPENDENT INCREASE IN DELETED MITOCHONDRIAL-DNA IN THE HUMAN HEART - POSSIBLE CONTRIBUTORY FACTOR TO PRESBYCARDIA
    HATTORI, K
    TANAKA, M
    SUGIYAMA, S
    OBAYASHI, T
    ITO, T
    SATAKE, T
    HANAKI, Y
    ASAI, J
    NAGANO, M
    OZAWA, T
    [J]. AMERICAN HEART JOURNAL, 1991, 121 (06) : 1735 - 1742