Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about PD: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.
PD is a concept in neurodegeneration research. Key relationships include: implicated in, causes, associated with. Associated with DEPRESSION, T2DM, synucleinopathies. Connected to 53 entities in the SciDEX knowledge graph.
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| Name | PD |
| Key Genes/Proteins | 263BP_ALLELE, 265BP_ALLELE, 267BP_ALLELE, 269BP_ALLELE, 271BP_ALLELE, 273BP_ALLELE |
| Related Diseases | AGE |
| Linked Hypotheses | 44 hypotheses |
Knowledge base pages for this entity
graph TD
PD["PD"]
PD -->|"causes"| NEURODEGENERATION["NEURODEGENERATION"]
PD -->|"causes"| DOPAMINERGIC_NEURONS["DOPAMINERGIC_NEURONS"]
PD -->|"contributes to"| synucleinopathies["synucleinopathies"]
PD -->|"causes"| neurodegeneration["neurodegeneration"]
NEUROINFLAMMATION["NEUROINFLAMMATION"] -->|"contributes to"| PD
SNCA["SNCA"] -->|"causes"| PD
LRRK2["LRRK2"] -->|"causes"| PD
GBA1["GBA1"] -->|"causes"| PD
PRKN["PRKN"] -->|"causes"| PD
PINK1["PINK1"] -->|"causes"| PD
PARK7["PARK7"] -->|"causes"| PD
VPS35["VPS35"] -->|"causes"| PD
alpha_synuclein["alpha_synuclein"] -->|"causes"| PD
neurodegeneration -->|"causes"| PD
haploinsufficiency["haploinsufficiency"] -->|"causes"| PD
protein_truncating_variants["protein_truncating_variants"] -->|"causes"| PD| Target | Relation | Type | Str |
|---|---|---|---|
| NEURODEGENERATION | causes | phenotype | 0.87 |
| DOPAMINERGIC_NEURONS | causes | cell_type | 0.87 |
| synucleinopathies | contributes_to | disease | 0.76 |
| neurodegeneration | causes | phenotype | 0.72 |
| DEPRESSION | associated_with | disease | 0.64 |
| T2DM | associated_with | disease | 0.64 |
| PYROPTOSIS | activates | pathway | 0.60 |
| VCP | co_discussed | gene | 0.60 |
| RB1 | activates | gene | 0.60 |
| SIRT1 | activates | gene | 0.60 |
| TFEB | activates | gene | 0.60 |
| TP53 | activates | gene | 0.60 |
| PLP1 | activates | gene | 0.60 |
| SNCA | causes | gene | 0.60 |
| SNCA | expresses | gene | 0.60 |
| TH | activates | gene | 0.60 |
| STING | inhibits | gene | 0.60 |
| STING | causes | gene | 0.60 |
| SNCA | associated_with | gene | 0.60 |
| SOD2 | co_discussed | gene | 0.60 |
| TH | co_discussed | gene | 0.60 |
| PI3K/AKT/MTOR | inhibits | pathway | 0.60 |
| RIPK1 | associated_with | gene | 0.60 |
| RIPK3 | associated_with | gene | 0.60 |
| STING | expresses | gene | 0.60 |
| PINK1 | regulates | gene | 0.60 |
| TNF | inhibits | gene | 0.60 |
| PINK1 | interacts_with | gene | 0.60 |
| ULK1 | regulates | gene | 0.60 |
| ULK1 | targets | gene | 0.60 |
| RAS | co_discussed | gene | 0.60 |
| STING | markers | gene | 0.60 |
| TREM2 | mediates | gene | 0.60 |
| PYROPTOSIS | co_discussed | pathway | 0.60 |
| TREM2 | associated_with | gene | 0.60 |
| TREM2 | co_discussed | gene | 0.60 |
| SOD1 | co_discussed | gene | 0.60 |
| SQSTM1 | interacts_with | gene | 0.60 |
| TH | inhibits | gene | 0.60 |
| ULK1 | co_discussed | gene | 0.60 |
| RAS | activates | gene | 0.60 |
| TLR4 | associated_with | gene | 0.60 |
| SNCA | markers | gene | 0.60 |
| PSEN2 | associated_with | gene | 0.60 |
| PSEN2 | regulates | gene | 0.60 |
| SOD1 | interacts_with | gene | 0.60 |
| SQSTM1 | co_discussed | gene | 0.60 |
| TFEB | expresses | gene | 0.60 |
| TFEB | protects_against | gene | 0.60 |
| VPS35 | interacts_with | gene | 0.60 |
| Source | Relation | Type | Str |
|---|---|---|---|
| 26655867 | was common in | paper | 0.90 |
| GBA1 mutations | increases_risk | gene | 0.90 |
| therapeutics-adenosine-a2a-receptor-antagonists-pd | describes | wiki | 0.90 |
| TNF | associated_with | entity | 0.85 |
| PARKIN | associated_with | entity | 0.85 |
| PINK1 | associated_with | entity | 0.85 |
| SNCA | cross_disease_mechanism_in | gene_or_pathway | 0.84 |
| MAPT | cross_disease_mechanism_in | gene_or_pathway | 0.82 |
| TREM2 | cross_disease_mechanism_in | gene_or_pathway | 0.80 |
| NRF2 | protects_against | entity | 0.80 |
| NLRP3 | associated_with | entity | 0.80 |
| NEUROINFLAMMATION | associated_with | phenotype | 0.79 |
| NLRP3 | cross_disease_mechanism_in | gene_or_pathway | 0.79 |
| PINK1 | cross_disease_mechanism_in | gene_or_pathway | 0.78 |
| TP53 | regulates | gene | 0.75 |
| TBK1 | cross_disease_mechanism_in | gene_or_pathway | 0.73 |
| GBA1 | causes | gene | 0.72 |
| PRKN | causes | gene | 0.72 |
| PINK1 | causes | gene | 0.72 |
| SNCA | causes | gene | 0.72 |
| PARK7 | causes | gene | 0.72 |
| alpha_synuclein | causes | protein | 0.72 |
| neurodegeneration | causes | phenotype | 0.72 |
| VPS35 | causes | gene | 0.72 |
| LRRK2 | causes | gene | 0.72 |
| haploinsufficiency | causes | phenotype | 0.68 |
| protein_truncating_variants | causes | phenotype | 0.68 |
| entities-ltp | associated_with | wiki | 0.65 |
| 269BP_ALLELE | activates | gene | 0.64 |
| 265BP_ALLELE | activates | gene | 0.64 |
| EPS | treats | drug | 0.64 |
| PD_ProS | associated_with | phenotype | 0.64 |
| 267BP_ALLELE | inhibits | gene | 0.64 |
| T2DM | associated_with | disease | 0.64 |
| 271BP_ALLELE | activates | gene | 0.64 |
| AGE | associated_with | phenotype | 0.64 |
| RAC1 | associated_with | gene | 0.60 |
| TPM2 | associated_with | gene | 0.60 |
| ASTROCYTE | expresses | cell_type | 0.60 |
| FTD | expresses | gene | 0.60 |
| PARKINSON DISEASE | regulates | disease | 0.60 |
| PARK7 | co_discussed | gene | 0.60 |
| AD | markers | gene | 0.60 |
| ASTROCYTES | activates | cell_type | 0.60 |
| AD | targets | gene | 0.60 |
| FTD | regulates | gene | 0.60 |
| FRONTOTEMPORAL DEMENTIA | regulates | disease | 0.60 |
| INFLAMMASOME | regulates | pathway | 0.60 |
| NEURONS | targets | cell_type | 0.60 |
| NEURON | targets | cell_type | 0.60 |
Hypotheses where this entity is a therapeutic target
Scientific analyses that reference this entity
neurodegeneration | 2026-04-28 | 17 hypotheses Top: 0.828
neurodegeneration | 2026-04-27 | 0 hypotheses
neurodegeneration | 2026-04-27 | 3 hypotheses Top: 0.626
neurodegeneration | 2026-04-27 | 3 hypotheses Top: 0.626
neurodegeneration | 2026-04-27 | 4 hypotheses Top: 0.662
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. Cost |
|---|---|---|---|---|---|---|---|
| PGC-1α knockout analysis of PV+ interneuron maturation | validation | neurodevelopmental disorders | 0.850 | 0.00 | knockout mice | proposed | N/A |
| Molecular docking analysis of aminophylline binding targets | exploratory | depression | 0.800 | 0.00 | in silico molecular docking | proposed | N/A |
| PV+ interneuron subtype diversification analysis | exploratory | neurodevelopmental disorders | 0.750 | 0.00 | mouse cortical PV+ interneuron | proposed | N/A |
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
|---|---|---|---|---|
| The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Mic [PMID:28930663] | Krasemann S, Madore C, Cialic R, Baufeld | Immunity | 2017 | 1 |
| Enhancing TREM2 expression activates microglia and modestly mitigates tau pathol [PMID:40122810] | ["Chen Kai", "Li Fuyao", "Zhang Shuwen", | Journal of neuroinflammation | 2025 | 0 |
| Isoginkgetin antagonizes ALS pathologies in its animal and patient iPSC models v [PMID:41094045] | Li A, Huang S, Cao SQ, Lin J, Zhao L, Yu | EMBO molecular medicine | 2025 | 0 |
| Enhancing TREM2 expression activates microglia and modestly mitigates tau pathol [PMID:40122810] | ["Chen Kai", "Li Fuyao", "Zhang Shuwen", | Journal of neuroinflammation | 2025 | 0 |
| Interaction between autophagy and the NLRP3 inflammasome in Alzheimer's and Park [PMID:36262883] | Unknown | Frontiers in aging neuroscienc | 2023 | 0 |
| TREM2 interacts with TDP-43 and mediates microglial neuroprotection against TDP- [PMID:34916658] | Xie M, Liu YU, Zhao S, Zhang L, Bosco DB | Nature neuroscience | 2022 | 0 |
| Neurodegeneration and Inflammation-An Interesting Interplay in Parkinson's Disea [PMID:33182554] | Marogianni C, Sokratous M, Dardiotis E, | International journal of molec | 2020 | 0 |
| Neurodegeneration and Inflammation-An Interesting Interplay in Parkinson's Disea [PMID:33182554] | Marogianni C, Sokratous M, Dardiotis E, | International journal of molec | 2020 | 0 |
| PINK1/PARKIN signalling in neurodegeneration and neuroinflammation. [PMID:33168089] | Quinn PMJ, Moreira PI, Ambrósio AF, Alve | Acta neuropathologica communic | 2020 | 0 |
| Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive defi [PMID:30742114] | Unknown | Nature neuroscience | 2019 | 0 |
| NLRP3 inflammasome activation drives tau pathology. [PMID:31748742] | ["Ising C", "Venegas C", "Zhang S", "Sch | Nature | 2019 | 0 |
| Multiple Sclerosis Pathology. [PMID:29358320] | Lassmann H | Cold Spring Harbor perspective | 2018 | 0 |
| Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodeg [PMID:30381407] | Gordon R, Albornoz EA, Christie DC, Lang | Science translational medicine | 2018 | 0 |
| LRRK2 Promotes Tau Accumulation, Aggregation and Release. [PMID:26014385] | Unknown | Molecular neurobiology | 2017 | 0 |
| Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. [PMID:25803835] | Unknown | Nature neuroscience | 2015 | 0 |
| The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease. [PMID:25611507] | ["Pickrell Alicia M", "Youle Richard J"] | Neuron | 2015 | 0 |
| TREM2 variants in Alzheimer's disease. [PMID:23150934] | Rita Guerreiro, Aleksandra Wojtas, Jose | The New England journal of med | 2013 | 0 |
| NLRP3 is activated in Alzheimer's disease and contributes to pathology in APP/PS [PMID:23254930] | Heneka MT, Kummer MP, Stutz A, Delekate | Nature | 2013 | 0 |
| NLRP3 is activated in Alzheimer's disease and contributes to pathology in APP/PS [PMID:23254930] | ["Heneka Michael T", "Kummer Markus P", | Nature | 2013 | 0 |
| Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and A [PMID:18322368] | Unknown | Neuro-degenerative diseases | 2008 | 0 |
Multi-agent debates referencing this entity
active · Rounds: 4 · Score: 0.72 · 2026-04-28
active · Rounds: 4 · Score: 0.67 · 2026-04-28
active · Rounds: 4 · Score: 0.67 · 2026-04-28
active · Rounds: 4 · Score: 0.67 · 2026-04-28
active · Rounds: 4 · Score: 0.67 · 2026-04-28
active · Rounds: 6 · Score: 0.89 · 2026-04-27
closed · Rounds: 4 · Score: 1.00 · 2026-04-26
closed · Rounds: 7 · Score: 0.50 · 2026-04-26
closed · Rounds: 4 · Score: 0.70 · 2026-04-21
closed · Rounds: 4 · Score: 0.50 · 2026-04-20
Hypotheses and analyses mentioning PD in their description or question text
Score: 0.778 · neurodegeneration · 2026-04-16
## Mechanistic Overview SIRT1/PGC-1α Axis Activation to Preserve Mitochondrial Resiliency Against Microbiome-Induced Neu
Score: 0.776 · multi · 2026-04-28
Shared mechanism across ALS, FTD, PD: TBK1 coordinates selective autophagy adaptors and innate immune tone. TBK1 haploin
Score: 0.749 · neuroinflammation · 2026-04-13
## Mechanistic Overview PDE4 Inhibition as Inflammatory Reset for PD Oligodendrocytes starts from the claim that modulat
Score: 0.745 · unknown disease · 2026-04-26
Soluble PDGFRβ (sPDGFRβ) is released into the bloodstream upon pericyte damage, serving as a peripheral indicator of blo
Score: 0.732 · neurodegeneration · 2026-04-16
**Molecular Mechanism and Rationale** The molecular foundation for SMPD1 inhibition in Alzheimer's disease centers on t
Score: 0.710 · neurodegeneration · 2026-04-28
Genetic or pharmacologic NRF2 activation using CDDO-EA or sulforaphane upregulates ARE gene transcription (NQO1, HO-1, G
Score: 0.705 · unknown disease · 2026-04-26
Pericyte loss in Alzheimer's disease leads to proteolytic shedding of PDGFRβ into circulation, providing a blood-accessi
Score: 0.703 · neurodegeneration · 2026-04-16
**Molecular Mechanism and Rationale** The pathogenesis of Parkinson's disease (PD) involves complex interactions betwee
Score: 0.684 · neurodegeneration · 2026-04-02
## Mechanistic Overview Pericyte Contractility Reset via Selective PDGFR-β Agonism starts from the claim that modulating
Score: 0.662 · unknown disease · 2026-04-26
CSF soluble PDGFR-β shedding from pericytes as the earliest detectable molecular event in AD, preceding amyloid/tau path