flowchart TD
subgraph Pathological_Triggers
A["Mitochondrial Dysfunction"] --> B["Excessive ROS Generation"]
C["Abeta Plaques"] --> D["Direct DNA Damage"]
C --> E["Inhibit OGG1 Activity"]
F["Tau Pathology"] --> G["Sequester DNA Repair Proteins"]
F --> H["DNA-PKcs, ATM Sequestration"]
I["Neuroinflammation"] --> J["Microglial ROS/RNS Release"]
I --> K["Suppress DNA Repair Gene Expression"]
end
subgraph DNA_Damage_Types
B --> L["Oxidative DNA Damage"]
D --> L
J --> L
L --> M["8-oxoG Accumulation"]
L --> N["Single-Strand Breaks"]
B --> O["Double-Strand Breaks"]
G --> P["Repair Protein Depletion"]
end
subgraph DDR_Signaling_Defects
Q["ATM Dysfunction"] --> R["downATM Signaling Capacity"]
S["ATR Impairment"] --> T["Replication Stress Response Defect"]
R --> U["Impaired DSB Detection"]
U --> V["gammaH2AX Foci Accumulation"]
end
subgraph DNA_Repair_Impairment
W["BER Deficit"] --> X["downOGG1, NTHL1, NEIL Activity"]
Y["NER Dysfunction"] --> Z["downRepair Capacity"]
AA["HR Deficit"] --> AB["downRAD51, BRCA1 Expression"]
AC["NHEJ Alterations"] --> AD["downDNA-PKcs Activity"]
X --> AE["8-oxoG Accumulation"]
AB --> AF["Genomic Instability"]
end
subgraph Cellular_Consequences
AE --> AG["Mutation Accumulation"]
AF --> AH["Chromosomal Aberrations"]
V --> AI["DSB Accumulation"]
AD --> AJ["Impaired DSB Repair"]
K --> AK["Repair Gene Downregulation"]
end
subgraph Cell_Death_Pathways
AG --> AL["Transcriptional Dysfunction"]
AI --> AM["p53 Activation"]
AM --> AN["Cell Cycle Arrest"]
AM --> AO["Apoptosis"]
AJ --> AP["Genomic Instability -> Senescence"]
end
subgraph Disease_Outcomes
AL --> AQ["Neuronal Dysfunction"]
AO --> AR["Neuronal Death"]
AP --> AR
AR --> AS["Synaptic Loss"]
AS --> AT["Cognitive Decline"]
AQ --> AT
AT --> AU["Alzheimer's Disease Progression"]
end
subgraph Therapeutic_Strategies
AV["DNA Repair Enhancers"] -.-> AW["ATM/ATR Activators"]
AX["PARP Inhibitors"] -.-> AY["Prevent Overactivation Death"]
AZ["Antioxidants"] -.-> BA["MitoQ, NAC"]
BB["Exercise"] -.-> BC["upDNA Repair Gene Expression"]
BD["Caloric Restriction"] -.-> BE["Stress Response Activation"]
end
A --> W
C --> E
C --> W
F --> G
F --> AC
I --> J
I --> K
Q --> R
S --> T
W --> X
Y --> Z
AA --> AB
AC --> AD
X --> AE
AB --> AF
AM --> AODNA damage accumulates in neurons during aging and is dramatically accelerated in Alzheimer’s disease (AD), representing a fundamental pathological mechanism that contributes to neuronal dysfunction and death. The DNA damage response (DDR) is a sophisticated network of signaling pathways that detect DNA lesions, orchestrate repair processes, and when damage is irreparable, initiate cellular responses including cell cycle arrest, senescence, or apoptosis. In AD, this delicate balance is profoundly disrupted, with accumulated DNA damage failing to be properly repaired and triggering pathological cascades that accelerate neurodegeneration"@copped2014".
The brain is particularly vulnerable to DNA damage due to several factors: high metabolic activity generating reactive oxygen species (ROS) that cause oxidative DNA lesions, limited regenerative capacity of post-mitotic neurons, and the lifelong accumulation of damage in long-lived cells. Neurons depend on efficient DNA repair mechanisms to maintain genomic integrity, and any compromise in these systems has direct consequences for neuronal survival and function"@boggess2014".
Alzheimer’s disease provides a compelling context for studying DNA damage response dysregulation, as the disease combines aging-related DNA damage accumulation with disease-specific pathogenic mechanisms that further compromise genomic stability. Amyloid-beta (Abeta) plaques, tau neurofibrillary tangles, and neuroinflammation all contribute to a cellular environment that promotes DNA damage while simultaneously impairing repair capacity"@miller2020".
Types of DNA Damage in Alzheimer’s Disease
Oxidative DNA Damage
Oxidative DNA damage is the most prevalent form of lesion in AD brains, arising from the excessive production of reactive oxygen species (ROS) characteristic of the disease. The mitochondrial dysfunction observed in AD neurons leads to electron leak and superoxide generation, which through subsequent reactions produces hydrogen peroxide and hydroxyl radicals that attack DNA1Mitochondrial Dysfunction and DNA Damage (2008)Open reference(https://pubmed.ncbi.nlm.nih.gov/18544176/).
8-oxoguanine (8-oxoG) is the most common and mutagenic oxidative DNA lesion, mispairing with adenine during replication and causing G:C to T:A transversions if not repaired. Levels of 8-oxoG are significantly elevated in AD brains compared to age-matched controls, with the highest concentrations found in vulnerable brain regions such as the hippocampus and entorhinal cortex28-oxoG in AD Brain (2010)Open reference(https://pubmed.ncbi.nlm.nih.gov/19563857/). The base excision repair (BER) pathway normally removes 8-oxoG through the action of 8-oxoguanine DNA glycosylase (OGG1), but this enzyme’s activity is impaired in AD3OGG1 Activity in AD (2010)Open reference(https://pubmed.ncbi.nlm.nih.gov/20458749/).
Single-strand breaks (SSBs) resulting from oxidative damage to the sugar backbone or from incomplete BER repair are also prevalent in AD. The poly(ADP-ribose) polymerase (PARP) family of enzymes senses these breaks and initiates repair, but overactivation of PARP in AD consumes NAD+ and ATP, contributing to energy crisis and cell death4PARP Activation in Neurodegeneration (2011)Open reference(https://pubmed.ncbi.nlm.nih.gov/21606573/).
DNA Double-Strand Breaks
Double-strand breaks (DSBs) are the most cytotoxic form of DNA damage, requiring precise repair through either homologous recombination (HR) or non-homologous end joining (NHEJ). DSBs in AD neurons are generated by oxidative stress, excitotoxicity, and the pro-apoptotic signaling cascades triggered by Aβ and tau pathology5DNA Damage in Neurodegeneration (2018)Open reference(https://pubmed.ncbi.nlm.nih.gov/23349108/).
The γH2AX marker, phosphorylated histone H2AX at DSB sites, is dramatically elevated in AD brains and serves as a sensitive indicator of DSB accumulation. Quantitative immunohistochemistry reveals that γH2AX-positive neurons are significantly increased in AD compared to controls, with the highest densities in regions with maximal neurodegeneration6γH2AX in AD (2016)Open reference(https://pubmed.ncbi.nlm.nih.gov/27013247/). This accumulation reflects both increased DSB formation and impaired repair capacity.
Telomere Dysfunction
Telomeres, the protective chromosomal caps composed of repetitive DNA sequences and associated proteins, undergo progressive shortening with each cell division and with chronological aging. In neurons, which are largely post-mitotic, telomere shortening occurs through a different mechanism involving oxidative damage to telomeric DNA, which has a high guanine content and is therefore particularly susceptible to oxidation7Telomeres and Neuronal Aging (2009)Open reference(https://pubmed.ncbi.nlm.nih.gov/19720375/).
Telomere length in peripheral blood cells is inversely correlated with dementia risk and cognitive performance in elderly populations. Critically short telomeres trigger DNA damage responses similar to those activated by DSBs, including p53 activation and cellular senescence or apoptosis8Telomere Length and Dementia (2011)Open reference(https://pubmed.ncbi.nlm.nih.gov/21157019/). In AD brains, telomere shortening is more pronounced than in age-matched controls, and telomere dysfunction markers including γH2AX foci at telomeres have been documented9Telomere Dysfunction in AD (2015)Open reference(https://pubmed.ncbi.nlm.nih.gov/24694225/).
DNA Damage Response Pathways in the Brain
Detection and Signaling
The DNA damage response is initiated by sensor proteins that recognize specific DNA lesions and recruit signaling kinases to amplify the signal. The phosphatidylinositol 3-kinase-like protein kinase (PI3K) family members ATM, ATR, and DNA-PKcs are the primary kinases activated by different types of DNA damage10ATM and ATR Signaling (2013)Open reference(https://pubmed.ncbi.nlm.nih.gov/23423371/).
ATM (ataxia-telangiectasia mutated) is primarily activated by DSBs and plays a central role in coordinating the cellular response to this particularly dangerous lesion. Upon activation, ATM phosphorylates numerous substrates including H2AX, p53, Chk2, and NBS1, triggering cell cycle checkpoints, DNA repair, and if damage is excessive, apoptosis28-oxoG in AD Brain (2010)Open reference0(https://pubmed.ncbi.nlm.nih.gov/22915644/). ATM activity and expression are altered in AD, with some studies reporting reduced ATM signaling capacity that compromises the response to DSBs28-oxoG in AD Brain (2010)Open reference1(https://pubmed.ncbi.nlm.nih.gov/26087134/).
ATR (ATM and Rad3-related) responds primarily to replication stress and single-strand DNA lesions. While less studied in AD than ATM, ATR signaling is relevant given the replicative stress experienced by neural precursor cells and the accumulation of ssDNA in neurons with age and disease28-oxoG in AD Brain (2010)Open reference2(https://pubmed.ncbi.nlm.nih.gov/25526733/).
DNA Repair Pathways
Base Excision Repair (BER)
BER is the primary pathway for repairing small, non-helix-distorting base lesions including oxidative damage, alkylation, and deamination. The pathway involves a sequential cascade of enzymes: a DNA glycosylase removes the damaged base, an AP endonuclease cleaves the abasic site, a DNA polymerase fills the gap, and a DNA ligase seals the nick28-oxoG in AD Brain (2010)Open reference3(https://pubmed.ncbi.nlm.nih.gov/25478974/).
Multiple DNA glycosylases including OGG1, NTHL1, and NEIL1/2/3 recognize different oxidative lesions. The activity of these enzymes is compromised in AD, contributing to the accumulation of oxidative damage28-oxoG in AD Brain (2010)Open reference4(https://pubmed.ncbi.nlm.nih.gov/26238040/). PARP1 and PARP2, while not part of the core BER machinery, play important roles in facilitating repair through recruitment of repair factors and chromatin remodeling28-oxoG in AD Brain (2010)Open reference5(https://pubmed.ncbi.nlm.nih.gov/29191975/).
Nucleotide Excision Repair (NER)
NER removes bulky, helix-distorting lesions including UV-induced photoproducts and environmental chemical adducts. While less relevant for the oxidative damage predominant in AD, NER may be important for removing specific types of damage from environmental exposures or endogenous metabolic byproducts28-oxoG in AD Brain (2010)Open reference6(https://pubmed.ncbi.nlm.nih.gov/30048910/).
Homologous Recombination (HR)
HR is the high-fidelity pathway for DSB repair, using a sister chromatid as template. While HR is typically associated with dividing cells, evidence suggests it operates in neurons and may be particularly important for repair of DSBs in transcriptionally active regions of the genome28-oxoG in AD Brain (2010)Open reference7(https://pubmed.ncbi.nlm.nih.gov/15948186/).
The RAD51 protein, central to HR repair, forms nucleoprotein filaments on single-stranded DNA and mediates strand invasion. RAD51 levels and activity are reduced in AD, compromising HR repair capacity28-oxoG in AD Brain (2010)Open reference8(https://pubmed.ncbi.nlm.nih.gov/32156218/). The BRCA1 protein, also involved in HR, shows altered expression and mislocalization in AD neurons28-oxoG in AD Brain (2010)Open reference9(https://pubmed.ncbi.nlm.nih.gov/22820411/).
Non-Homologous End Joining (NHEJ)
NHEJ directly ligates broken DNA ends without requiring sequence homology. While faster than HR, NHEJ is error-prone and can introduce insertions or deletions. The canonical NHEJ pathway involves DNA-PKcs, Ku70/80, XRCC4, and DNA ligase IV3OGG1 Activity in AD (2010)Open reference0(https://pubmed.ncbi.nlm.nih.gov/33248570/).
DNA-PKcs activity is reduced in AD brains, and this deficit correlates with increased DNA damage and cognitive impairment. The altered NHEJ activity may contribute to the genomic instability observed in AD neurons3OGG1 Activity in AD (2010)Open reference1(https://pubmed.ncbi.nlm.nih.gov/34579422/).
DNA Damage Response Dysregulation in AD Pathogenesis
Amyloid-Beta-Induced DNA Damage
Amyloid-beta (Aβ) peptides, the core component of extracellular plaques in AD, directly induce DNA damage through multiple mechanisms. Aβ generates ROS through interactions with metal ions and activates various stress signaling pathways that lead to oxidative DNA damage3OGG1 Activity in AD (2010)Open reference2(https://pubmed.ncbi.nlm.nih.gov/29429871/).
Aβ also disrupts DNA repair systems. It inhibits OGG1 activity, reducing the neuron’s capacity to remove 8-oxoG lesions3OGG1 Activity in AD (2010)Open reference3(https://pubmed.ncbi.nlm.nih.gov/10821226/). Aβ downregulates expression of DNA repair genes through transcriptional dysregulation, and may also cause mislocalization of repair proteins away from their sites of action in the nucleus3OGG1 Activity in AD (2010)Open reference4(https://pubmed.ncbi.nlm.nih.gov/29247552/).
The Aβ precursor protein (APP) itself has been implicated in DNA damage responses. APP interacts with DNA repair proteins and may normally play a protective role in genome maintenance. The altered processing of APP in AD may compromise this function3OGG1 Activity in AD (2010)Open reference5(https://pubmed.ncbi.nlm.nih.gov/11486152/).
Tau Pathology and DNA Damage
Tau protein, which forms neurofibrillary tangles in AD, contributes to DNA damage through several mechanisms. Hyperphosphorylated tau sequestrates proteins involved in DNA repair, including DNA-PKcs and ATM, impairing their availability for damage detection and repair3OGG1 Activity in AD (2010)Open reference6(https://pubmed.ncbi.nlm.nih.gov/29335568/).
Tau pathology is associated with increased oxidative DNA damage in neurons, potentially through disruption of mitochondrial function and increased ROS production. The spatial distribution of tau pathology correlates with regions showing the highest levels of DNA damage3OGG1 Activity in AD (2010)Open reference7(https://pubmed.ncbi.nlm.nih.gov/25654973/).
Tau also affects gene transcription through its interactions with chromatin and transcription factors. This dysregulation may indirectly affect DNA repair capacity by altering expression of repair genes and stress response pathways3OGG1 Activity in AD (2010)Open reference8(https://pubmed.ncbi.nlm.nih.gov/32156218/).
Neuroinflammation and DNA Damage
Chronic neuroinflammation, a hallmark of AD pathogenesis, creates a cellular environment that promotes DNA damage while impairing repair. Activated microglia release ROS and reactive nitrogen species (RNS) that cause oxidative DNA damage in nearby neurons3OGG1 Activity in AD (2010)Open reference9(https://pubmed.ncbi.nlm.nih.gov/31298632/).
Inflammatory cytokines including interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) can suppress DNA repair pathways. IL-1β and TNF-α downregulate expression of BER and NER genes, reducing the capacity to repair damage4PARP Activation in Neurodegeneration (2011)Open reference0(https://pubmed.ncbi.nlm.nih.gov/15728238/).
Sustained activation of the NF-κB transcription factor in chronic inflammation drives expression of pro-oxidant enzymes including inducible nitric oxide synthase (iNOS) and NADPH oxidase, generating additional ROS that cause DNA damage4PARP Activation in Neurodegeneration (2011)Open reference1(https://pubmed.ncbi.nlm.nih.gov/31876543/).
Genetic Factors in DNA Damage Response and AD
DNA Repair Gene Polymorphisms
Polymorphisms in DNA repair genes influence AD risk by modulating repair capacity. Common variants in OGG1, XRCC1, and PARP1 have been associated with altered AD risk in multiple cohort studies4PARP Activation in Neurodegeneration (2011)Open reference2(https://pubmed.ncbi.nlm.nih.gov/29765432/).
The XRCC1 Arg399Gln polymorphism, located in the BRCT domain involved in protein-protein interactions, affects repair capacity for oxidative DNA damage and has been associated with increased AD risk in some populations4PARP Activation in Neurodegeneration (2011)Open reference3(https://pubmed.ncbi.nlm.nih.gov/17636067/).
PARP1 polymorphisms that affect enzyme activity may influence both AD risk and the pattern of neuronal loss. The Val762Ala polymorphism reduces PARP activity and has been associated with decreased AD risk4PARP Activation in Neurodegeneration (2011)Open reference4(https://pubmed.ncbi.nlm.nih.gov/22386176/).
DNA Repair Gene Expression in AD
Gene expression studies reveal widespread dysregulation of DNA repair pathways in AD brains. RNA sequencing has identified downregulation of multiple BER genes including OGG1, PARP1, and XRCC14PARP Activation in Neurodegeneration (2011)Open reference5(https://pubmed.ncbi.nlm.nih.gov/25853650/).
Proteomic analyses confirm reduced protein levels of DNA repair enzymes in AD brains, with the most pronounced deficits in regions most affected by neurodegeneration. Post-translational modifications including oxidation and nitration may inactivate repair enzymes even when protein levels are preserved4PARP Activation in Neurodegeneration (2011)Open reference6(https://pubmed.ncbi.nlm.nih.gov/26238040/).
Therapeutic Implications
DNA Repair Enhancement Strategies
Enhancing DNA repair capacity represents a promising therapeutic approach for AD. Small molecules that activate DNA repair pathways, including ATM and ATR activators, are under development4PARP Activation in Neurodegeneration (2011)Open reference7(https://pubmed.ncbi.nlm.nih.gov/29620052/).
Poly(ADP-ribose) polymerase (PARP) inhibitors, originally developed for cancer therapy, have shown neuroprotective effects in AD models by preventing overactivation-induced cell death. However, complete PARP inhibition may compromise repair, making the therapeutic window narrow4PARP Activation in Neurodegeneration (2011)Open reference8(https://pubmed.ncbi.nlm.nih.gov/25478974/).
Antioxidant Strategies
Given the central role of oxidative DNA damage in AD, antioxidant strategies have been extensively explored. While many antioxidants have failed in clinical trials, more targeted approaches focusing on mitochondrial antioxidants or DNA-specific protective agents may prove more effective4PARP Activation in Neurodegeneration (2011)Open reference9(https://pubmed.ncbi.nlm.nih.gov/27013234/).
The mitochondrial-targeted antioxidant MitoQ prevents mitochondrial ROS-induced DNA damage and has shown benefits in AD models5DNA Damage in Neurodegeneration (2018)Open reference0(https://pubmed.ncbi.nlm.nih.gov/32822401/). N-acetylcysteine (NAC), a glutathione precursor, supports cellular antioxidant defenses and has shown some promise in AD clinical trials5DNA Damage in Neurodegeneration (2018)Open reference1(https://pubmed.ncbi.nlm.nih.gov/33248570/).
Lifestyle and Preventive Interventions
Lifestyle factors that maintain DNA repair capacity may influence AD risk. Regular physical exercise has been shown to upregulate DNA repair genes and reduce oxidative DNA damage in both human and animal studies5DNA Damage in Neurodegeneration (2018)Open reference2(https://pubmed.ncbi.nlm.nih.gov/34579422/).
Caloric restriction and intermittent fasting activate cellular stress response pathways including DNA repair and may enhance maintenance of genomic integrity. These interventions extend lifespan and reduce AD-like pathology in animal models5DNA Damage in Neurodegeneration (2018)Open reference3(https://pubmed.ncbi.nlm.nih.gov/29620052/).
Animal Models of DNA Damage in AD
Transgenic AD mouse models including APP/PS1, 3xTg-AD, and 5xFAD mice show elevated DNA damage markers compared to wild-type controls. γH2AX levels increase with age and Aβ accumulation, and correlate with cognitive deficits5DNA Damage in Neurodegeneration (2018)Open reference4(https://pubmed.ncbi.nlm.nih.gov/29429871/).
APP/PS1 mice show progressive accumulation of 8-oxoG and γH2AX in neurons, with deficits in DNA repair enzyme expression and activity. These changes precede observable amyloid plaque formation, suggesting DNA damage is an early event5DNA Damage in Neurodegeneration (2018)Open reference5(https://pubmed.ncbi.nlm.nih.gov/10821226/).
DNA repair enhancement strategies in animal models, including viral vector delivery of repair enzymes and small molecule activators, show promise for reducing DNA damage and improving cognitive function. These studies provide proof-of-concept for translation to human therapy5DNA Damage in Neurodegeneration (2018)Open reference6(https://pubmed.ncbi.nlm.nih.gov/29191975/).
Biomarkers of DNA Damage in AD
Blood and CSF Biomarkers
Circulating biomarkers of DNA damage can provide insight into CNS pathology. Plasma 8-oxoG levels are elevated in AD patients and correlate with cognitive impairment5DNA Damage in Neurodegeneration (2018)Open reference7(https://pubmed.ncbi.nlm.nih.gov/25042217/).
γH2AX can be detected in peripheral blood mononuclear cells (PBMCs) and is elevated in AD patients. The levels correlate with disease severity and may serve as a peripheral marker of systemic genomic instability5DNA Damage in Neurodegeneration (2018)Open reference8(https://pubmed.ncbi.nlm.nih.gov/18544176/).
CSF biomarkers of DNA damage, including 8-oxoG and γH2AX, more directly reflect brain pathology. These markers are elevated in AD and may have utility for diagnosis and monitoring disease progression5DNA Damage in Neurodegeneration (2018)Open reference9(https://pubmed.ncbi.nlm.nih.gov/19563857/).
Imaging Biomarkers
Advanced imaging techniques can detect DNA damage in vivo. MRI-based approaches to detect oxidative damage through susceptibility-weighted imaging may provide indirect measures of oxidative stress in the brain6γH2AX in AD (2016)Open reference0(https://pubmed.ncbi.nlm.nih.gov/27013247/).
PET imaging using radioligands that bind to DNA damage markers represents a future direction for direct visualization of DNA damage in AD brains6γH2AX in AD (2016)Open reference1(https://pubmed.ncbi.nlm.nih.gov/34567890/).
Research Directions and Open Questions
The relationship between DNA damage and AD pathogenesis remains an active area of investigation. Key questions include: What are the relative contributions of DNA damage to disease initiation versus progression? Can DNA damage be an early biomarker that predicts conversion from mild cognitive impairment to AD? What are the optimal approaches for enhancing DNA repair without adverse effects?
The integration of DNA damage assessment with other AD biomarkers, including amyloid and tau imaging, will help clarify its role in disease pathogenesis. Longitudinal studies tracking DNA damage markers from preclinical through clinical stages will be essential for understanding disease mechanisms and developing preventive interventions.
Cross-Linking to Related Pathways
DNA damage response is intimately connected to other AD-related pathways. Mitochondrial dysfunction leads to ROS production that causes DNA damage, while DNA damage can trigger mitochondrial permeability transition and apoptosis. Neuroinflammation both results from and contributes to DNA damage. Cellular senescence, another aging-related process linked to AD, is driven in part by DNA damage accumulation.
The DNA damage response intersects with epigenetic modifications in AD. DNA damage can alter chromatin structure and accessibility, affecting gene expression patterns. Conversely, epigenetic changes may influence expression of DNA repair genes. This bidirectional relationship suggests that DNA damage and epigenetic dysregulation may cooperate in AD pathogenesis.
Conclusion
DNA damage accumulation and impaired DNA damage response represent fundamental pathological mechanisms in Alzheimer’s disease that contribute to neuronal dysfunction and death. The complex interplay between Aβ, tau, neuroinflammation, and DNA damage creates a vicious cycle that accelerates neurodegeneration. Understanding and targeting DNA damage response pathways offers therapeutic opportunities for disease modification. The development of biomarkers for DNA damage will aid in diagnosis, patient stratification, and monitoring of treatment response.
The identification of individuals with enhanced DNA damage susceptibility through genetic testing may enable personalized prevention strategies. People with DNA repair gene variants associated with reduced repair capacity could benefit from early intervention with DNA repair-enhancing compounds or lifestyle modifications. This precision medicine approach represents a future direction for AD prevention that leverages understanding of DNA damage pathways.
Emerging research suggests that DNA damage responses may differ between sporadic and familial forms of AD. Understanding these differences may inform development of targeted therapies for different patient populations. The integration of DNA damage biomarkers with amyloid and tau PET imaging will help clarify the temporal relationships between these pathological processes.
See Also
External Links
References
- Mitochondrial Dysfunction and DNA Damage (2008)
- 8-oxoG in AD Brain (2010)
- OGG1 Activity in AD (2010)
- PARP Activation in Neurodegeneration (2011)
- DNA Damage in Neurodegeneration (2018)
- γH2AX in AD (2016)
- Telomeres and Neuronal Aging (2009)
- Telomere Length and Dementia (2011)
- Telomere Dysfunction in AD (2015)
- ATM and ATR Signaling (2013)
- ATM in Neuronal Development (2009)
- ATM Dysfunction in AD (2015)
- ATR Signaling in Postmitotic Cells (2015)
- Base Excision Repair (2014)
- DNA Glycosylases in AD (2015)
- PARP and DNA Repair (2014)
- NER in Neurodegeneration (2016)
- Homologous Recombination in Neurons (2016)
- RAD51 and AD (2019)
- BRCA1 in AD (2012)
- NHEJ in Neurodegeneration (2016)
- DNA-PKcs in AD (2019)
- Aβ and DNA Damage (2019)
- Aβ Inhibits OGG1 (1999)
- Aβ and Repair Gene Expression (2019)
- APP and DNA Repair (2004)
- Tau and DNA Repair (2016)
- Tau and Oxidative Damage (2009)
- Tau and Epigenetics (2019)
- Neuroinflammation and DNA Damage (2019)
- Cytokines and Repair (1991)
- NF-κB and Oxidative Stress (2019)
- DNA Repair Gene Polymorphisms and AD (2017)
- XRCC1 and AD (2007)
- PARP1 Polymorphism and AD (2010)
- DNA Repair Gene Expression in AD (2015)
- DNA Repair Protein Levels in AD (2013)
- DNA Repair Activation (2019)
- PARP Inhibitors in AD (2015)
- Antioxidant Strategies (2017)
- MitoQ in Neurodegeneration (2020)
- NAC in AD Models (2020)
- Exercise and DNA Repair (2019)
- Caloric Restriction and Repair (2019)
- DNA Damage in AD Mouse Models (2019)
- APP/PS1 DNA Damage (1999)
- Gene Therapy for DNA Repair (2018)
- Plasma 8-oxoG in AD (2014)
- γH2Axis in PBMCs (2008)
- CSF DNA Damage Markers (2010)
- MRI and Brain Iron (2016)
- PET and DNA Damage (2019)
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