{"artifact":{"id":"experiment-exp-wiki-experiments-non-motor-symptom-progression-pd","artifact_type":"experiment","entity_ids":null,"title":"Non-Motor Symptom Progression in Parkinson's Disease — Mechanisms and Biomarkers","quality_score":0.675,"created_by":"crosslink-v2","provenance_chain":null,"content_hash":null,"metadata":{"source":{"type":"manual","source_name":"wiki","extracted_by":"backfill_v1","extraction_date":"2026-04-16T01:00:16.902018Z"},"summary":"# Non-Motor Symptom Progression in Parkinson's Disease — Mechanisms and Biomarkers\n## Background and Rationale\nParkinson's disease (PD) is characterized not only by motor dysfunction but also by debilitating non-motor symptoms (NMS) that significantly impact quality of life and often precede motor manifestations by years. This longitudinal clinical study investigates the progression mechanisms of five key NMS: depression, anxiety, REM sleep behavior disorder (RBD), constipation, and hyposmia (lo","entities":{"genes":["REM"],"diseases":["Parkinson's Disease"]},"model_system":"human","_schema_version":1,"experiment_type":"clinical","primary_outcome":"Establish biomarker profiles that predict non-motor symptom progression in PD, achieving >80% accuracy in identifying patients at risk for severe RBD, depression, and autonomic dysfunction within 3 years.","methodology_notes":"Phase 1 (Months 1-6): Recruit 400 PD patients and 100 age-matched controls through movement disorder clinics. Inclusion criteria: diagnosed PD (UK Brain Bank criteria), Hoehn-Yahr stages 1-3, age 45-80. Exclusion: dementia (MoCA<24), major psychiatric disorders, significant comorbidities. Phase 2 (Baseline assessment): Comprehensive NMS evaluation using MDS-UPDRS Part I, NMSS, Beck Depression/Anxiety Inventories, UPSIT olfactory test, Rome IV constipation criteria, and video-polysomnography for RBD. Collect CSF (15mL) and blood samples (30mL) for alpha-synuclein, neurofilament light, inflammatory cytokines analysis using ELISA and electrochemiluminescence. Perform 3T MRI including T1/T2-weighted, DTI, neuromelanin-sensitive sequences, and DaTscan SPECT imaging. Phase 3 (Follow-up, every 6 months for 60 months): Repeat clinical assessments and biomarker collection. Annual neuroimaging studies. Polysomnography repeated at 18-month intervals. Phase 4 (Data analysis): Apply machine learnin","replication_status":"single_study","extraction_metadata":{"backfill_at":"2026-04-16T01:00:16.902023","needs_review":true,"extraction_notes":"Backfilled from wiki source (no PMID 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