The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age
Abstract
We have examined the role of somatic mitochondrial DNA (mtDNA) mutations in human ageing by quantitating the accumulation of the common 4977 nucleotide pair (np) deletion (mtDNA4977) in the cortex, putamen and cerebellum. A significant increase in the mtDNA4977 deletion was seen in elderly individuals. In the cortex, the deleted to total mtDNA ratio ranged from 0.00023 to 0.012 in 67-77 year old brains and up to 0.034 in subjects over 80. In the putamen, the deletion level ranged from 0.0016 to 0.010 in 67 to 77 years old up to 0.12 in individuals over the age of 80. The cerebellum remained relatively devoid of mtDNA deletions. Similar changes were observed with a different 7436 np deletion. These changes suggest that somatic mtDNA deletions might contribute to the neurological impairment often associated with ageing.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Evidence indicates age-related mtDNA changes do in fact occur within the human brain.”
From Brain aging, Alzheimer's disease, and mitochondria (2011) · cites this paper as [115]
In the citing paper
“Levels of a 5-kilobase deletion that particularly affects mtDNA COX genes increase with age [115].”
From Brain aging, Alzheimer's disease, and mitochondria (2011) · cites this paper as [115]
Citations
Cites
Biometry: The Principles and Practice of Statistics in Biological Research
Sokal, R. R., & Rohlf, F. J. (1969) · Cited by 20,963
Mirra, S. S., Heyman, A., McKeel, D., Sumi, S. M., Crain, B. J., Brownlee, L. M., Vogel, F. S., Hughes, J. P., Belle, G. V., Berg, L., et al. (1991) · Neurology · doi:10.1212/wnl.41.4.479 · Cited by 4,961
Normal oxidative damage to mitochondrial and nuclear DNA is extensive.
Richter, C., Park, J. W., & Ames, B. N. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.17.6465 · Cited by 1,730
Evans, D. A. (1989) · JAMA · doi:10.1001/jama.262.18.2551 · Cited by 1,627
Diseases of the mitochondrial DNA
Wallace, D. C. (1992) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.61.070192.005523 · Cited by 1,319
Self-citationMitochondrial Genetics: A Paradigm for Aging and Degenerative Diseases?
Wallace, D. C. (1992) · Science · doi:10.1126/science.1533953 · Cited by 1,262
Self-citationEvans, D. A. (1989) · JAMA · doi:10.1001/jama.1989.03430180093036 · Cited by 1,226
Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases
Linnane, A., Ozawa, T., Marzuki, S., & Tanaka, M. (1989) · The Lancet · doi:10.1016/s0140-6736(89)92145-4 · Cited by 983
Detection of a specific mitochondrial DNA deletion in tissues of older humans
Cortopassi, G. A., & Arnheim, N. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.23.6927 · Cited by 788
Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing
Trounce, I., Byrne, E., & Marzuki, S. (1989) · The Lancet · doi:10.1016/s0140-6736(89)92143-0 · Cited by 730
Research works printed but not linked: 4
- Muller-Hocker, J. Cytochrome-c-oxidase deficient cardiomyocytes in the human heart. Am. J. Pathol. 134, 1167–1173 (1989).
- Chawluk, J.B., Alavi, A. & Jamieson, D.G. Changes in local cerebral glucose metabolism with normal ageing: the effect of cardiovascular and systemic health factors. J. Cereb. Blood Flow Metab. 7, S411 (1987).
- Morris, J.C. & McManus, D.Q. The neurology of ageing: Normal versus pathological changes. Geriatrics 46, 47–54 (1991).
- Harman, D. in Free radical ageing and degenerative diseases. (eds Johson J.E., Jr. et al.) 3–49 (Alan R. Liss, New York, 1986).
Cited by
Sorted by citations
Items 801–888 of 888
ALEXEYEV, M. F., LeDoux, S. P., & Wilson, G. L. (2006) · Elsevier eBooks · doi:10.1016/b978-012369391-4/50042-4 · Cited by 1
Pathogenesis of Parkinson’s disease: iron and mitochondrial DNA deletion
Mizuno, Y., Mochizuki, H., Nishi, K., Ikebe, S., Hattori, N., & Hattori-Nakagawa, Y. (1993) · Key topics in brain research · doi:10.1007/978-3-7091-9322-8_10 · Cited by 1
The Control of Ageing and Mitochondria
Lestienne, P. P., & Véziers, J. (1999) · Springer eBooks · doi:10.1007/978-3-642-59884-5_17
Mitochondrial Diseases and Aging
Wallace, D. C., Lott, M. T., Trounce, I. A., Brown, M. D., Huoponen, K., Krawiecki, N., & Shoffner, J. M. (1995) · Progress in cell research · doi:10.1016/b978-0-444-82235-2.50046-1
Self-citationSelected Age-Related Disorders
Behl, C., & Ziegler, C. (2013) · SpringerBriefs in molecular medicine · doi:10.1007/978-3-642-45179-9_4
Mitochondrial Involvement in Neurodegeneration and Aging
Pickrell, A. M. (2012)
Molecular Biological Analyses and Molecular Pathology in Clinical Chemistry
Lo, Y. M. D., Lam, C., & Wong, I. H. N. (2000) · Wiley eBooks · doi:10.1002/9780470027318.a0534
Quantitative transcriptional analysis of aging C. elegansPreprint
David-Rus, D. (2012) · arXiv (Cornell University) · doi:10.48550/arxiv.1212.1920
Mitochondriale DNA des Menschen
Wissinger, B. (2008) · Springer eBooks · doi:10.1007/978-3-540-69414-4_5
Mitochondrial dysfunction in ageing and degenerative disease
Wredenberg, A. (2007) · Figshare
Models of mitochondrial disease
Liolitsa, D., & Hanna, M. G. (2002) · International review of neurobiology · doi:10.1016/s0074-7742(02)53016-6
Navidi, W. C., Tavaré, S., & Arnheim, N. (2003) · Lecture notes-monograph series · doi:10.1214/lnms/1215091146
Hewakapuge, S. (2009) · Victoria University Research Repository (Victoria University)
A study of mitochondrial biogenesis in the rodent nervous system
Desai, R. A. (2015) · UCL Discovery (University College London)
Reichmann, H., Janetzky, B., & Seibel, P. (1996) · Springer eBooks · doi:10.1007/978-3-642-61017-2_4
Chapter 6 Pathophysiology of Mitochondrial Disease as Illuminated by Animal Models
Wallace, D. (2002) · Blue books of practical neurology · doi:10.1016/s1877-3419(09)70065-0
Casadesús, G., Shukitt‐Hale, B., Smith, M. A., Stellwagen, H. M., & Joseph, J. A. (2002) · Springer eBooks · doi:10.1007/978-1-4615-1067-3_6
Progressive models of Parkinson's disease : behavioural and neurochemical analyses
Alvarsson, A. (2015) · Figshare
Chapter 4 Genetic Abnormalities in Amyotrophic Lateral Sclerosis
Kasarskis, E. J., & Clair, D. K. S. (1999) · Advances in cell aging and gerontology · doi:10.1016/s1566-3124(08)60024-3
Mitochondrial genome consensus sequence for the South African Khoi–San population
Mouton, C. (2003) · Boloka Institutional Repository (North-west University)
Age‐related dysfunction of the cellular powerplants
Bečanović, K., & Leavitt, B. R. (2006) · Clinical Genetics · doi:10.1111/j.1399-0004.2006.0699_2.x
Interrelationship of aging and mitochondrial DNA deletion in luteinized granulosa cells
Kim, N. H., Lee, S. K., Jang, B. W., & Lee, D. H. (2010) · Korean Journal of Obstetrics & Gynecology · doi:10.5468/kjog.2010.53.9.816
How mtDNA mutations cause aging
Choi, C. Q. (2004) · Genome biology · doi:10.1186/gb-spotlight-20050718-01
INDUCTION OF MITOCHONDRIAL DNA DELETION BY IONIZING RADIATION IN HUMAN LUNG FIBROBLAST IMR-90 CELLS
Eom, H. S., Jung, U., Park, H.-R., & Jo, S. (2009) · Journal of Radiation Protection and Research
Mitochondrial Dysfunction, Aging, and Huntington’s Disease
Beal, M. F. (1994) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4684-9203-3_11
Effects of H2O2 Treatment of Mouse B82 Cells on mtDNA Amounts and Respiratory Function
Natsume, M., Iwamuro, Y., Tanaka, M., Itoi, C., Murakami, H., & Hayashi, J. (2006) · International Journal of Sport and Health Science · doi:10.5432/ijshs.4.628
Mitochondrial DNA mutations. Brain developmental and ageing consequences, and possible treatments
Ross, J. M. (2012) · Figshare
Accumulation de mutations de l’ADN mitochondrial chez la souris : un modèle idéal de vieillissement
Rötig, A. (2004) · médecine/sciences · doi:10.1051/medsci/20042010847
Heteroplasmy in mammal mitochondrial deoxyribonucleic acid
Viramontes, F. (2011) · doi:10.71781/3750
Aging, Energy and Alzheimer’s Disease
Bowling, A. C., & Beal, M. F. (1981) · Springer eBooks · doi:10.1007/978-3-662-01135-5_21
Parallelized Sequence Comparison of Human and Naked Mole Rat for Aging Studies
Vidya, A., Venugopal, K. R., & Patnaik, L. M. (2014) · ePrints@Bangalore University (Bangalore University)
Aging and Gene Expression in the Primate
Fraser, B. B., Khaitovich, P., Plotkin, J. B., & Eisen, M. B. (2005)
Genotypic Selection of Age-Related DNA Rearrangements by PCR
Wong, A., & Cortopassi, G. A. (1999) · Springer eBooks · doi:10.1007/978-3-642-59916-3_1
mtDNA Mutations in Brain Aging and Neurodegeneration
Krishnan, K. J., & Reeve, A. K. (2011) · Springer eBooks · doi:10.1007/978-0-85729-701-3_5
Mitochondrial Mutations in Parkinson's Disease and Dystonias
Simon, D. K. (2003) · Elsevier eBooks · doi:10.1016/b978-012566652-7/50043-5
Silva, D. S. B. S. (2015) · Americanae (AECID Library)
The influence of aging on oocyte quality and the importance of mitochondria
Trull, K. (2014) · Digital Repository Service (Northeastern University) · doi:10.17760/d20005089
Ballinger, S. W. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.08.079
Mitochondrial involvement in neuronal cell death
Gray, J. J. (2014) · Digital Commons - DU (University of Denver)
Bayliss, J. A. (2017) · Figshare · doi:10.4225/03/58b8c4bc41e03
Aus der Neurologischen Klinik und Poliklinik der Ludwig
München, M.-U., & Dieterich, M. (2011)
A model for mitochondrial disease associated with rearrangements of the mitochondrial genome
Glasssmith, L. L. (1998) · Enlighten: Theses (The University of Glasgow)
Rucz, K. (2008) · Orvosi Hetilap · doi:10.1556/oh.2008.28335
Oxidative Stress, Cerebral Aging and Longevity
Ceballos-Picot, I. (1997) · Neuroscience intelligence unit · doi:10.1007/978-3-662-22516-5_4
The mitochondrial protein profile changes during the aging process
Mao, L. (2005) · DepositOnce · doi:10.14279/depositonce-1067
Influence of caloric restriction and exercise on mitochondrial quality control in skeletal muscle
Hattori, S., & Akimoto, T. (2015) · 体力科學 · doi:10.7600/jspfsm.64.389
mitochondrial morphology, instability of mtDNA and senescence
Kato, A., Kurashima, K., Chae, M. S., Sawada, S., Hatakeyama, S., Tanaka, S., & Inoue, H. (2010)
Clinical and genotypic aspects of mitochondrial disease
Gorman, G. S. (2015)
A characterization of deficits associated with loss of NCB5OR in the mouse brain
Stroh, M. A. (2016) · KU ScholarWorks (The University of Kansas)
The Role of p38 MAPK in Protein Homeostasis and Aging
Ryan, S. M. (2016) · Digital Commons - DU (University of Denver)
Quarles, E. K. (2017) · ResearchWorks at the University of Washington (University of Washington)
Mitochondrial Dysfunction in Aging and Neurodegeneration
Walia, V., & Garg, M. (2018) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/978-1-5225-5282-6.ch004
Chiang, S. (2019) · The Sydney eScholarship Repository (The University of Sydney)
de Grey, A. D. N. J., & Rae, M. J. (2019) · Springer eBooks · doi:10.1007/978-3-319-69892-2_436-1
Bacman, S. R., & Moraes, C. T. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819656-4.00018-8
Meier-Ruge, W. A., Bertoni–Freddari, C., & Fattoretti, P. (2004) · Springer eBooks · doi:10.1007/978-3-642-18741-4_5
Mitochondrial DNA in sensitive forensic analysis.
Nilsson, M. E. (2011) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
de Grey, A. D. N. J., & Rae, M. J. (2021) · Springer eBooks · doi:10.1007/978-3-030-22009-9_436
Viscomi, C. F., & Zeviani, M. (2019) · Springer eBooks · doi:10.1007/978-3-030-05517-2_22
Mann, D. M. A. (1997) · Springer eBooks · doi:10.1007/978-1-4615-6001-2_4
Mitochondriale DNA des Menschen
Wissinger, B. (2003) · Springer eBooks · doi:10.1007/978-3-662-07588-3_4
Role of microglia in myelin turnover
Safaiyan, S. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5727
Charakterisierung von Peroxiredoxin 2 im zentralen Nervensystem bei Multipler Sklerose
Winkler, D. A. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8882
Mitochondrial Dysfunction in Aging and Neurodegeneration
Walia, V., & Garg, M. (2022) · IGI Global eBooks · doi:10.4018/978-1-6684-5295-0.ch016
Conclusions and Future Directions
Hisama, F. M., Martin, G. M., & Weissman, S. M. (2003) · CRC Press eBooks · doi:10.1201/9780203911709.pt4
de Grey, A. D. N. J., & Rae, M. J. (2021) · Springer eBooks · doi:10.1007/978-3-319-69892-2_436-2
Rommy von Bernhardi, M., Flores, B., & Nakanishi, H. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1429-6_13
Molecular Biological Analyses and Molecular Pathology in Clinical Chemistry
Lo, Y. M. D., Wong, I. H. N., Tsui, N. B. Y., & Lam, C. (2009) · Wiley eBooks · doi:10.1002/9780470027318.a0534.pub2
Mitophagy and mitohormetics: promising antiaging strategy
Lin, C. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90235-9.00001-x
Pathophysiology of Brain Aging: A Brief Account on Molecular Changes
Chikkanarayanappa, V., & Gangadharappa, H. (2015) · JOURNAL OF CLINICAL AND BIOMEDICAL SCIENCES · doi:10.58739/jcbs/v05i2.11
Kamfar, S., Alaei, F., Zaferani, R., & Zeinali, V. (2022) · Iranian Journal of Blood and Cancer · doi:10.58209/ijbc.14.4.104
Noncoding RNAs and RNA Epigenetics in Brain Aging
Sugai-Munson, A., Simon, C., Graves, O. K., McKay, T. B., & Li, H. (2025) · RNA technologies · doi:10.1007/978-3-031-91072-2_10
Xue, X., Liu, Y., Wu, Z., Huang, A., Cai, Y., & Xu, E. (2025) · Research Square · doi:10.21203/rs.3.rs-7423787/v1
Emerging therapeutic approaches in neurobiology of type 2 diabetes
Kumar, U., Garg, S., Shrivastav, A., Sharma, B., Arora, B., Sahu, B., & Gupta, M. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-32848-0.00023-6
Billard, P. (2021) · theses.fr (ABES) · doi:10.70675/7d145f6az2700z4c8bzad56z3286d493fb31
65Chapter 4 The power of mitochondrial DNA: when nuclear DNA isn’t enough
Sharma, J., Bansal, P., Duhan, P., Goyal, S., Raj, M., & Sangwan, S. (2026) · De Gruyter eBooks · doi:10.1515/9783112219799-004
The Genetic and Epigenetic Mechanisms of mtDNA in Regulation of Inflammation and Metabolism
Zhang, Y., 郑言江, Duan, H., & Li, Y. (2026) · The FASEB Journal · doi:10.1096/fj.202600927r
Chromatin signaling in aging and cellular senescence
Gagné, L. M., Couteau, F., & Mallette, F. A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-19001-8.00018-0
The impact of aging, sex, and exercise on brain mitochondria
Zhang, J., Darley-Usmar, V. M., & Li, Y. (2026) · Frontiers in Aging · doi:10.3389/fragi.2026.1920914
Mitochondrial DNA in Cardiovascular Disease
Koller, A., & Weißensteiner, H. (2026) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2026.121952
The role of telomerase in brain during ageing and under dietary restriction
Czapiewski, R. (2013)
Application of Molecular Biology Techniques on Forensic Sciences
Seubwai, W., & Khunkitti, W. (2014) · Srinagarind Medical Journal (SMJ) - ศรีนครินทร์เวชสาร
Metadata
- Authors
- Corral-Debrinski, M., Horton, T., Lott, M. T., Shoffner, J. M., Flint Beal, M., & Wallace, D. C.
- Affiliations
- Emory University (US)
- Venue
- Nature Genetics
- Published
- 1992-12
- Volume
- 2
- Issue
- 4
- Pages
- 324-329
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1973851166
- Cited by
- 890
- References
- 43
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 19 · 2023: 12 · 2022: 25 · 2021: 19 · 2020: 23 · 2019: 36 · 2018: 21 · 2017: 28 · 2016: 21 · 2015: 32 · 2014: 23 · 2013: 32 · 2012: 24
- FWCI
- 10.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- mitochondrial DNA deletions, somatic mtDNA mutations, human aging, brain aging, cerebral cortex, putamen, cerebellum, regional variation, neurological deficit
- MeSH terms
- Adult, Aged, Aged, 80 and over, Aging, Base Sequence, Brain, DNA Damage, DNA, Mitochondrial, Female, Humans, Male, Molecular Sequence Data, Oxidative Phosphorylation, Tissue Distribution, Sequence Deletion
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review