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Marked Changes in Mitochondrial DNA Deletion Levels in Alzheimer Brains
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.
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“which has been described in an AD brain [169,170] in which base deletions correlate with complex IV deficiency in an AD hippocampus [171].”
From Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease (2020) · cites this paper as [169]
In the citing paper
“MtDNA from AD subject brains exhibits excess oxidative damage and deletions [47, 102-105].”
From The Alzheimer’s disease mitochondrial cascade hypothesis: progress and perspectives (2014) · cites this paper as [103]
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Recent developments in the molecular genetics of mitochondrial disorders
Graeber, M. B., & Müller, U. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(97)00295-5 · Cited by 79
The Alzheimer’s Disease Mitochondrial Cascade Hypothesis: A Current Overview
Swerdlow, R. H. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-221286 · Cited by 88
“Multiple studies report AD brain mtDNA accumulates excessive age-related, somatic mtDNA mutations [19, 71–79].”
Fenech, M. F. (2017) · Advances in Nutrition · doi:10.3945/an.117.015610 · Cited by 76
Lezza, A. M. S., Mecocci, P., Cormio, A., Real, M. F., Cherubini, A., Cantatore, P., Senin, U., & Gadaleta, M. N. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.9.1083 · Cited by 72
“The values of mtDNA4977 reported here are comparable to those previously determined by other authors in the brains of healthy subjects (14, 15) and AD patients ( 16 , 17).”
ResultA Role for Mitochondrial DNA Review and Sperm Survival
John, J. C. S., Sakkas, D., & Barratt, C. L. R. (2000) · Journal of Andrology · doi:10.1002/j.1939-4640.2000.tb02093.x · Cited by 73
mtDNA Mutations and Their Role in Aging, Diseases and Forensic Sciences
Zapico, S. C. (2013) · Aging and Disease · doi:10.14336/ad.2013.0400364 · Cited by 78
Neuronal activity and early neurofibrillary tangles in Alzheimer's disease
Hatanpaa, K. J., Brady, D. R., Stoll, J., Rapoport, S. I., & Chandrasekaran, K. (1996) · Annals of Neurology · doi:10.1002/ana.410400310 · Cited by 67
Liu, C.-S., Cheng, W., Lee, C.-C., et al. (2006) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2006.00586.x · Cited by 70
Cellular calcium signaling in the aging brain
Remya, C., Kumar, M., Kesavan, L., Jacob, R. S., Gunasekaran, S., Lakshmi, S., Sadasivan, C., & Omkumar, R. V. (2017) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2017.11.008 · Cited by 65
A comprehensive overview of mitochondrial DNA 4977-bp deletion in cancer studies
Yusoff, A. A. M., Abdullah, W. S. W., Khair, S. Z. N. M., & Radzak, S. M. A. (2019) · Oncology Reviews · doi:10.4081/oncol.2019.409 · Cited by 66
Cottrell, D. A., & Turnbull, D. M. (2000) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/00075197-200011000-00009 · Cited by 64
Mitochondrial DNA deletions in Alzheimer's brains: A review
Phillips, N., Simpkins, J. W., & Roby, R. K. (2013) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2013.04.508 · Cited by 62
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Weidling, I. W., & Swerdlow, R. H. (2019) · Biology · doi:10.3390/biology8020039 · Cited by 59
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BackgroundDysregulation of energy metabolism in Alzheimer's disease
Yuan, Y., Zhao, G., & Zhao, Y. (2024) · Journal of Neurology · doi:10.1007/s00415-024-12800-8 · Cited by 74
The Frequency of Point Mutations in Mitochondrial DNA Is Elevated in the Alzheimer's Brain
Chang, S.-W., Zhang, D., Chung, H. D., & Zassenhaus, H. P. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2885 · Cited by 58
Yowe, D. L., & Ames, B. N. (1998) · Gene · doi:10.1016/s0378-1119(97)00628-8 · Cited by 59
Mutations that affect mitochondrial functions and their association with neurodegenerative diseases
Dhillon, V. S., & Fenech, M. F. (2013) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2013.09.001 · Cited by 61
“A common deletion (4977 base-pair) in mtDNA (mtDNA) is observed in a normal ageing brain, but an even higher level of accumulation of mtDNA is present in mitochondria isolated from brain tissue specimens of AD patients [103].”
BackgroundMitochondria, Cognitive Impairment, and Alzheimer's Disease
Mancuso, M., Calsolaro, V., Orsucci, D., Carlesi, C., Choub, A., Piazza, S., & Siciliano, G. (2009) · International Journal of Alzheimer s Disease · doi:10.4061/2009/951548 · Cited by 58
“The mtDNA “common deletion” has been reported to be elevated about 15-fold in AD brains [60].”
BackgroundWong, M.-L., O'Kirwan, F., HANNESTAD, J., Irizarry, K. J. L., Elashoff, D. A., & Licinio, J. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001470 · Cited by 58
Is mitochondrial DNA depletion involved in Alzheimer's disease?
Rodríguez-Santiago, B., Casademont, J., & Nunes, V. (2001) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200629 · Cited by 57
Age-Related Mitochondrial DNA Deletions
Kang, C., Kristal, B. S., & Yu, B. P. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00204-9 · Cited by 57
A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders
Schipper, H. M., & Song, W. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16035400 · Cited by 57
“stress and mitochondrial insufficiency in AD brain are evidenced by (i) a relative abundance of mtDNA deletions and mis-sense mutations [3,4] which correlate with levels of free radical damage [5] (ii) deficiencies in Kreb cycle enzymes and components of the electron transport chain [6]; (iii) altered mitochondrial mo…”
BackgroundMitochondrial Cascade Hypothesis of Alzheimer's Disease: Myth or Reality?
Mancuso, M., Coppedè, F., Murri, L., & Siciliano, G. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1761 · Cited by 56
“The mtDNA “common deletion,” for instance, has been observed to be elevated about 15-fold in AD brains (19).”
Nomiyama, T., Tanaka, Y., Hattori, N., Nishimaki, K., Nagasaka, K., Kawamori, R., & Ohta, S. (2002) · Diabetologia · doi:10.1007/s00125-002-0893-7 · Cited by 55
“Somatic mtDNA mutations not only accumulate during normal ageing [10] but also in various diseases associated with the enhancement of ROS, for example, cancer [11], coronary atherosclerotic heart disease [12] and neurodegenerative diseases [13, 14, 15].”
BackgroundMitochondrial Dysfunction in Neurodegenerative Disorders and Ageing
Turner, C., & Schapira, A. H. V. (2001) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-1249-3_19 · Cited by 56
Heme oxygenase-1 in Alzheimer disease: a tribute to Moussa Youdim
Schipper, H. M. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-010-0436-1 · Cited by 55
“Oxidative stress, pathological iron deposition and mitochondrial deficits (bioenergy failure) have been consistently demonstrated in AD-affected neural tissues ( Corral-Debrinski et al. 1994; Reichmann and Riederer 1994 ;B eal1995; Gibson et al. 1998; Tanno et al. 1998; Mattson 2002; Schipper 2004a).”
BackgroundO'Connell, M., McClure, N., & Lewis, S. E. M. (2002) · Human Reproduction · doi:10.1093/humrep/17.6.1571 · Cited by 55
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BackgroundResultThe complicated nature of somatic mtDNA mutations in aging
Sanchez-Contreras, M., & Kennedy, S. R. (2022) · Frontiers in Aging · doi:10.3389/fragi.2021.805126 · Cited by 60
“Several studies have noted highly elevated levels of reactive oxygen species (ROS) and damaged mtDNA bases in Alzheimer’s disease (AD) brains and elevated levels of deletions and point mutations in several brain regions that frequently correlate with the loss of Complex IV activity (Corral-Debrinski et al., 1994; Lin…”
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Fukuyama, R., Hatanpaa, K. J., Rapoport, S. I., & Chandrasekaran, K. (1996) · Brain Research · doi:10.1016/0006-8993(95)01517-5 · Cited by 53
HIV-associated dementia, mitochondrial dysfunction, and oxidative stress
Valcour, V., & Shiramizu, B. (2004) · Mitochondrion · doi:10.1016/j.mito.2004.05.009 · Cited by 52
Goethem, G. V., Martin, J., & Broeckhoven, C. V. (2003) · NeuroMolecular Medicine · doi:10.1385/nmm:3:3:129 · Cited by 53
“It is noteworthy that Alzheimer’s disease was not present on neuropatholog ical examination in patients with a high proportion of mtDNAdeletions in several parts of cerebral cortex (Suomalainen et al., 1997; Moslemi et al., 1999), refuting earlier speculation on the role of mtDNA deletions in Alzheimer’s disease ( Cor…”
BackgroundLiu, C.-Y., Lee, C.-F., & Wei, Y.-H. (2009) · Journal of the Formosan Medical Association · doi:10.1016/s0929-6646(09)60380-6 · Cited by 52
Čater, M., & Bombek, L. K. (2022) · Antioxidants · doi:10.3390/antiox11081473 · Cited by 55
“Moreover, an increased frequency of mitochondrial genomic deletions in brain samples has been associated with Huntington’s disease and Alzheimer’s disease [68,69].”
BackgroundBONDY, S., & Sharman, E. H. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2006.12.014 · Cited by 49
O’Connell, M., McClure, N., Powell, L. A., et al. (2003) · Fertility and Sterility · doi:10.1016/s0015-0282(02)04827-6 · Cited by 50
Kleinle, S., WIESMANN, U. N., Superti‐Furga, A., et al. (1997) · Human Genetics · doi:10.1007/s004390050567 · Cited by 49
Neuropathology of synuclein aggregates
Duda, J. E., Lee, V. M. ‐., & Trojanowski, J. Q. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20000715)61:2 · Cited by 263
Cwerman-Thibault, H., Augustin, S., Ellouze, S., Sahel, J.-A., & Corral-Debrinski, M. (2014) · Comptes Rendus. Biologies · doi:10.1016/j.crvi.2013.11.011 · Cited by 49
Self-citationMitochondrial DNA Sequence Variation Associated with Dementia and Cognitive Function in the Elderly
Tranah, G. J., The Health, A. A. B. C. S., Nalls, M. A., Katzman, S. M., Yokoyama, J. S., Lam, E. T., Zhao, Y., Mooney, S. D., Thomas, F., Newman, A. B., et al. (2012) · Journal of Alzheimer s Disease · doi:10.3233/jad-2012-120466 · Cited by 50
Golomb, B. A., Kwon, E. K., Koperski, S., & Evans, M. A. (2009) · Drug Safety · doi:10.2165/00002018-200932080-00004 · Cited by 48
Nie, H., Shu, H.-Y., Vartak, R. S., Milstein, A. C., Mo, Y., Hu, X., Fang, H., Shen, L., Ding, Z., Lü, J., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067953 · Cited by 45
“The mitochondrial common deletion has attracted tremendous interests as it is associate with several sporadic diseases including myopathies, Alzheimer disease, Pearson’ s syndrome, photoaging of the skin, Kearns-Sayre syndrome (KSS) and chronic progressive external ophthalmoplegia (CPEO) [5,13,15–19].”
BackgroundGenetic basis of Alzheimer's dementia: role of mtDNA mutations
Grazina, M. M., Pratas, J., Silva, F., Oliveira, S. A., Santana, I. J., & Oliveira, C. R. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00225.x · Cited by 47
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COTTRELL, D. A., Blakely, E. L., Borthwick, G. M., Johnson, M. A., Taylor, G. A., Brierley, E. J., Ince, P. G., & Turnbull, D. M. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06647.x · Cited by 45
Carter, C. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.12.003 · Cited by 44
Mitochondrial Alterations and Neuropsychiatric Disorders
Marazziti, D., Baroni, S., Picchetti, M., Landi, P., Silvestri, S., Vatteroni, E., & Dell’Osso, M. C. (2011) · Current Medicinal Chemistry · doi:10.2174/092986711797379221 · Cited by 45
Amyloid precursor protein‐mediated mitochondrial regulation and Alzheimer's disease
Lopez Sanchez, M. I. G., van Wijngaarden, P., & Trounce, I. A. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14554 · Cited by 45
“…abnormalities in Alzheimer’s disease, including increased mtDNA oxidative damage (reviewed by Santos et al., 2013), pathogenic mtDNA deletions (Corral-Debrinski et al., 1994; Hamblet and Castora, 1997), altered mtDNA methylation (Blanch et al., 2016) and mtDNA gene expression perturbations…”
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Hamblet, N. S., & Castora, F. J. (1997) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(97)00158-9 · Cited by 44
8OHdG levels in brain do not indicate oxidative DNA damage in Alzheimer's disease
Koppele, J. M. T., Lucassen, P. J., Sakkee, A. N., Asten, J. G. V., Ravid, R., Swaab, D. F., & van Bezooijen, C. F. A. (1996) · Neurobiology of Aging · doi:10.1016/s0197-4580(96)00165-0 · Cited by 44
Mitochondrial Dysfunctions: A Thread Sewing Together Alzheimer’s Disease, Diabetes, and Obesity
Rigotto, G., & Basso, E. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7210892 · Cited by 45
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BackgroundDamage in Mitochondrial DNA Associated with Parkinson's Disease
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“…and is a prominent hallmark of Alzheimer’s disease (AD) (Anglade et al., 1997, Blass et al., 2002, Castellani et al., 2002, Chinopoulos et al., 1999, Corral-Debrinski et al., 1994, Coskun et al., 2010, de la Monte et al., 2000, Dragicevic et al., 2010, Eckert et al., 2003, Gibson et al., 2000,…”
BackgroundDNA Damage and Impairment of DNA Repair in Alzheimer's Disease
Obulesu, M., & Rao, D. M. (2010) · International Journal of Neuroscience · doi:10.3109/00207450903411133 · Cited by 43
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Williams, R. S. (2000) · Circulation Research · doi:10.1161/01.res.86.9.915 · Cited by 38
Spina, E., Ferrari, R. R., Pellegrini, E., Colombo, M. M., Poloni, T. E., Guaita, A., & Davin, A. (2025) · Cells · doi:10.3390/cells14030229 · Cited by 45
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Perry, G. L., Nunomura, A., Cash, A., Taddeo, M. A., Hirai, K., Aliev, G., Ávila, J., Wataya, T., Shimohama, S., Atwood, C., et al. (2002) · Journal of neural transmission. Supplementum · doi:10.1007/978-3-7091-6139-5_7 · Cited by 38
H. Swerdlow, R. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211798072535 · Cited by 35
“While some studies conclude there are no differences in either mutational burden or distribution, others report unique quantitative or qualitative signatures [45, 46, 47, 48, 49, 89, 90, 91, 92, 93].”
BackgroundAccelerated aging and aging process in the brain
Исаев, Н. К., Генрихс, Е. Е., Оборина, М. В., & Stelmashook, E. V. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2017-0051 · Cited by 36
“, 2015), accompanied by intensive accelerated accumulation of mitochondrial DNA (mtDNA) mutations in neurons ( Corral-Debrinski et al., 1994).”
BackgroundLewis, S. E. M., Paro, R., Borriello, L., Simon, L., Robinson, L., Dincer, Z., Riedel, G., Battista, N., & Maccarrone, M. (2012) · International Journal of Andrology · doi:10.1111/j.1365-2605.2012.01259.x · Cited by 36
mtDNA Maintenance and Alterations in the Pathogenesis of Neurodegenerative Diseases
Shang, D., Huang, M., Wang, B., Yan, X., Wu, Z., & Zhang, X. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220810114644 · Cited by 44
“Earlier quantitative PCR studies found that a common deletion of mtDNA Δ4977 occurs in AD and accumulates up to 15-fold with age in the frontal cortex [107].”
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Webb, M., & Sideris, D. P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207580 · Cited by 36
Energetic depression caused by mitochondrial dysfunction
Gellerich, F. N., Trumbeckaitė, S., Müller, T., Deschauer, M., Chen, Y., Gizatullina, Z. Z., & Zierz, S. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009885.34498.e6 · Cited by 34
Mitochondrial Function and Alzheimer’s Disease
Ojaimi, J., & Byrne, E. (2001) · Neurosignals · doi:10.1159/000046890 · Cited by 32
Role of diffuse low-level heteroplasmy of mitochondrial DNA in Alzheimer’s disease neurodegeneration
Casoli, T., Spazzafumo, L., Stefano, G. D., & Conti, F. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00142 · Cited by 31
“The levels of mtDNA 4977-bp deletion are increased in AD brains during the early stages of the disease compared to controls and decline later, probably due to the death of the affected cells (Corral-Debrinski et al., 1994).”
BackgroundVisioli, F., Ingram, A., Beckman, J. S., Magnusson, K. R., & Hagen, T. M. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.12.008 · Cited by 31
Boosting mitochondrial health to counteract neurodegeneration
Burtscher, J., Romani, M., Bernardo, G., Popa, T., Ziviani, E., Hummel, F. C., Sorrentino, V., & Millet, G. P. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102289 · Cited by 36
“, 2014b) Mitochondrial DNA deletion linked to OXPHOS defects in AD cortex (Corral-Debrinski et al., 1994) Association between HtrA2 protease mutation and AD and specific protease activity of HtrA2 increased in AD patients (Westerlund et al.”
BackgroundParkinson's disease and mitochondrial gene variations: A review
Andalib, S., Vafaee, M. S., & GJEDDE, A. H. (2014) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2014.07.067 · Cited by 32
Dementia, stroke and migraine — Some common pathological mechanisms
Sas, K., Párdutz, Á., Toldi, J., & Vécsei, L. (2010) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2010.08.001 · Cited by 30
Loss of intraventricular fluid melatonin can explain the neuropathology of Alzheimer's disease
MAURIZI, C. P. (1997) · Medical Hypotheses · doi:10.1016/s0306-9877(97)90220-6 · Cited by 30
Mitochondrial dynamic changes in health and genetic diseases
Chen, L., Winger, A. J., & Knowlton, A. A. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3663-y · Cited by 31
“In a clinic study with AD patients, markedly increased level of mtDNA deletions has been found [93] Table 1.”
Mitochondrial DNA Mutations and Mitochondrial Dysfunction in Epilepsy
Cock, H. R., & Schapira, A. H. V. (1999) · Epilepsia · doi:10.1111/j.1528-1157.1999.tb00897.x · Cited by 29
“In addition to the study of diseases associated with mtDNA mutations, interest in recent years has also begun to focus on the role of mitochondria in a range of acquired degenerative diseases including Parkinson’s (3, Huntington’s (6), and Alzheimer’s (7).”
BackgroundMani, S., Wasnik, S., Shandilya, C., Srivastava, V., Khan, S., & Singh, K. K. (2025) · Frontiers in Aging · doi:10.3389/fragi.2025.1615764 · Cited by 33
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Norambuena, A., Sun, X., Wallrabe, H. K., Cao, R., Sun, N., Pardo, E., Shivange, N., Wang, D. B., Post, L. A., Ferris, H. A., et al. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105737 · Cited by 25
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Mancuso, M., Siciliano, G., Filosto, M., & Murri, L. (2006) · Journal of Alzheimer s Disease · doi:10.3233/jad-2006-9203 · Cited by 28
“The mtDNA “common deletion”, for instance, has been observed to be elevated about 15-fold in AD brains [12].”
Will antioxidants fulfill their expectations for the treatment of Alzheimer disease?
Rottkamp, C. A., Nunomura, A., Hirai, K., Sayre, L. M., Perry, G. L., & Smith, M. A. (2000) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(00)00124-x · Cited by 27
Pandora's Box: mitochondrial defects in ischaemic heart disease and stroke
Andalib, S., Divani, A. A., Michel, T. M., Høilund‐Carlsen, P. F., Vafaee, M. S., & GJEDDE, A. H. (2017) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2017.5 · Cited by 25
A unifying hypothesis of Alzheimer's disease. II. Pathophysiological processes
Heininger, K. (1999) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/(sici)1099-1077(199912)14:8 · Cited by 27
Precision mitochondrial medicine
Chinnery, P. F. (2022) · Cambridge Prisms Precision Medicine · doi:10.1017/pcm.2022.8 · Cited by 24
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BackgroundHsiao, C., Peng, T., Peng, A. C., Reiter, R. J., Tanaka, M., Lai, Y., & Jou, M. (2012) · Journal of Pineal Research · doi:10.1111/jpi.12004 · Cited by 24
“For instance, the mtDNA ‘common deletion’, that is, the mtDNA 4977 bp deletion, increases 15-fold in AD brain [60].”
BackgroundIs there a primary role of the mitochondrial genome in Alzheimer’s disease?
Mancuso, M., Calsolaro, V., Orsucci, D., Siciliano, G., & Murri, L. (2009) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-009-9239-1 · Cited by 24
Fekete, M., Jarecsny, T., Lehoczki, A., Major, D., Fazekas‐Pongor, V., Csípő, T., Lipécz, Á., Szappanos, Á., Pázmándi, E. M., Varga, P., et al. (2025) · Nutrients · doi:10.3390/nu17243929 · Cited by 28
Astrocyte- and Microglia-Specific Mitochondrial DNA Deletions Levels in Sporadic Alzheimer’s Disease
Strobel, S., Grünblatt, E., Heinsen, H., Riederer, P. F., Espach, T., Meder, M., & Monoranu, C. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180661 · Cited by 23
“Some authors foundadistinctaccumulationinbrainsofADpatientsyoungerthan75andadecreaseinADindividu-alsabovetheageof75,comparedwithcontrols [20].”
Mitochondrially-Targeted Therapeutic Strategies for Alzheimer’s Disease
Onyango, I. G., Bennett, J. P., & Stokin, G. B. (2021) · Current Alzheimer Research · doi:10.2174/1567205018666211208125855 · Cited by 22
“Transplantation of these cells into AD animal models induces mitochondrial biogenesis and reverses cognitive defects and extends lifespan [131-133].”
Essa, H., Peyton, L., Hasan, W., León, B. E., & Choi, D. (2022) · Cells · doi:10.3390/cells11020286 · Cited by 25
“Previously quantitative PCR evaluation indicated deletion in frontal cortex in age associated manner [75], and a prominent 15-fold rise of this type of deletion in AD patients younger than 75 years of age [76].”
BackgroundKösel, S., Egensperger, R., Schnopp, N. M., & Graeber, M. B. (1997) · Movement Disorders · doi:10.1002/mds.870120504 · Cited by 23
Sprason, C., Tucker, T., & Clancy, D. J. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1359638 · Cited by 23
Mitochondrial ribosomal protein genes connected with Alzheimer’s and tellurite toxicity
Giudice, L. D., Alifano, P., Calcagnile, M., Schiavi, E. D., Bertapelle, C., Aletta, M., & Pontieri, P. (2022) · Mitochondrion · doi:10.1016/j.mito.2022.02.006 · Cited by 21
Proteostasis impairment and ALS
Lambert-Smith, I. A., Saunders, D. N., & Yerbury, J. J. (2022) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2022.06.001 · Cited by 19
Mendes‐Silva, A. P., Nikolova, Y. S., Rajji, T. K., Kennedy, J. L., Diniz, B. S., Gonçalves, V. F., & Vieira, É. L. M. (2024) · Journal of Affective Disorders · doi:10.1016/j.jad.2024.06.092 · Cited by 19
Dani, S. U., Dani, M. A. C., & Simpson, A. J. G. (2003) · Medical Hypotheses · doi:10.1016/s0306-9877(03)00105-1 · Cited by 19
Neuron-Specific Mitochondrial DNA Deletion Levels in Sporadic Alzheimer´s Disease
Gerschütz, A., Heinsen, H., Grünblatt, E., Wagner, A., Bartl, J., Meißner, C., Fallgatter, A. J., Al‐Sarraj, S., Troakes, C., Ferrer, I., et al. (2013) · Current Alzheimer Research · doi:10.2174/15672050113106660166 · Cited by 18
The mitochondrial genome and mitochondrial muscle disorders
Schaefer, A. M. (2001) · Current Opinion in Pharmacology · doi:10.1016/s1471-4892(01)00051-0 · Cited by 19
Somatic mutations in mitochondria: the chicken or the egg?
Ospelt, C., & Gay, S. (2005) · Arthritis Research & Therapy · doi:10.1186/ar1809 · Cited by 18
“Furthermore, it was suggested that mtDNA mutations are involved in the development of cardiac disease [4] and neurodegenerative disorders such as Alzheimer’s disease [5].”
BackgroundCardiovascular aging: the mitochondrial influence
Sagar, S., & Gustafsson, Å. B. (2023) · The Journal of Cardiovascular Aging · doi:10.20517/jca.2023.22 · Cited by 18
Metadata
- Authors
- Corral-Debrinski, M., Horton, T., Lott, M. T., Shoffner, J. M., McKee, A. C., Beal, M. F., Graham, B. H., & Wallace, D. C.
- Affiliations
- Harvard University (US)
- Venue
- Genomics
- Publisher
- Elsevier BV
- Published
- 1994-09
- Volume
- 23
- Issue
- 2
- Pages
- 471-476
- ISSN
- 0888-7543 (ISSN-L)
- OpenAlex
- W2060626022
- Cited by
- 309
- References
- 0
- Citations by year
- 2026: 8 · 2025: 6 · 2024: 11 · 2023: 8 · 2022: 24 · 2021: 6 · 2020: 15 · 2019: 13 · 2018: 13 · 2017: 8 · 2016: 4 · 2015: 9 · 2014: 8 · 2013: 13 · 2012: 10
- FWCI
- 2.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Genomics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5f32ca009329-02)
- National Institute on Aging (P30AG010130, 1P30AG10130)
- National Cancer Institute (CA09329)
- National Center for Research Resources (M01-RR00039, M01RR000039)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- mitochondrial DNA deletions, Alzheimer's disease, somatic mtDNA mutations, brain aging, cortical mitochondria, putamen, cerebellum
- MeSH terms
- Age Factors, Aged, Aged, 80 and over, Alzheimer Disease, Cerebellum, Cerebral Cortex, DNA Damage, DNA, Mitochondrial, Female, Humans, Male, Middle Aged, Oxidative Phosphorylation, Putamen, Tissue Distribution, Sequence Deletion
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