How to Test for Suspected Parkinson's Disease
The diagnosis of Parkinson's disease is primarily clinical, based on identifying bradykinesia plus either resting tremor or rigidity, with neurologist confirmation required; when the clinical picture is unclear, obtain MRI brain first to exclude structural causes, followed by I-123 ioflupane SPECT/CT (DaTscan) to differentiate true Parkinsonian syndromes from mimics like essential tremor or drug-induced parkinsonism. 1
Initial Clinical Assessment
Essential Motor Features to Document
Bradykinesia is mandatory - this slowness of movement must be present for diagnosis and affects fine motor tasks (buttoning clothes, writing), gross motor activities (walking, turning), facial expressions, and speech. 1
Plus at least one of the following cardinal signs:
- Resting tremor - typically 4-6 Hz, present at rest and diminishing with action 1, 2
- Rigidity - assess by passively moving the patient's limbs while instructing complete relaxation, testing both upper and lower extremities through full range of motion at varying speeds 1
- Postural instability - though this typically appears later in disease progression 1
Technique for Detecting Rigidity
- Have the patient relax completely while you passively move their limbs through full range of motion 1
- Compare sides for asymmetry, as PD typically presents asymmetrically 1
- Note constant resistance throughout movement (lead-pipe rigidity) or ratchet-like jerky resistance when combined with tremor (cogwheel phenomenon) 1
- Use activation maneuvers - ask the patient to open and close the opposite hand while testing for rigidity, as this often brings out subtle rigidity that might otherwise be missed 1, 3
Red Flags Suggesting Alternative Diagnoses
- Early severe autonomic dysfunction, cerebellar signs, or pyramidal signs suggest Multiple System Atrophy rather than PD 1
- Vertical gaze palsy, especially downward indicates Progressive Supranuclear Palsy 1
- Asymmetric rigidity with alien hand phenomenon points to Corticobasal Syndrome 1
- Ataxia suggests an alternative parkinsonian syndrome 1
Diagnostic Testing Algorithm
Step 1: Exclude Secondary Causes
- Medication history - rule out drug-induced parkinsonism from antipsychotics, antiemetics, or other dopamine-blocking agents 1, 3
- For patients under 50 years old, exclude Wilson's disease by measuring serum ceruloplasmin, 24-hour urinary copper excretion, and performing slit-lamp examination for Kayser-Fleischer rings 1
- Thyroid function tests (TSH, free T4) to exclude hyperthyroidism 1
- Metabolic screening including blood glucose, calcium-phosphorus metabolism, and serum bilirubin 1
Step 2: Structural Imaging
- MRI brain without contrast is mandatory as the first imaging study - this is the optimal modality due to superior soft-tissue characterization and sensitivity to iron deposition 1, 4
- MRI rules out structural lesions, vascular disease, hydrocephalus, or focal abnormalities that could explain parkinsonism 1
- Common pitfall: Never skip structural imaging before ordering functional imaging; structural causes must be excluded first 1
- MRI is often normal in early PD, which is expected and does not exclude the diagnosis 1
Step 3: Functional Imaging (When Diagnosis Remains Uncertain)
I-123 ioflupane SPECT/CT (DaTscan) is the definitive test when clinical diagnosis is uncertain after history, examination, and MRI 1, 3, 4
How DaTscan works: The radiotracer binds to presynaptic dopamine transporters in the striatum, visualizing dopaminergic neuronal loss 1
Interpretation:
- Abnormal scan (decreased striatal uptake, typically progressing from posterior putamen to anterior caudate) confirms dopamine-deficient parkinsonian syndrome 1, 4
- Normal scan essentially excludes Parkinsonian syndromes and supports diagnoses of essential tremor, drug-induced tremor, or psychogenic parkinsonism 1, 3, 4
Key limitation: DaTscan cannot differentiate among specific Parkinsonian syndromes (PD vs. MSA vs. PSP vs. CBD) - all show abnormal dopaminergic depletion 1
Step 4: Additional Imaging for Atypical Features
- FDG-PET/CT can help differentiate Progressive Supranuclear Palsy from idiopathic PD by showing characteristic hypometabolism in medial frontal and anterior cingulate cortices, striatum, and midbrain 1, 4
- Do not order amyloid PET/CT or tau PET/CT - there is no evidence supporting their use in evaluating parkinsonian syndromes 1
Specialist Referral
- General neurologists or movement disorder specialists must confirm the diagnosis because correctly diagnosing a parkinsonian syndrome on clinical features alone is challenging 1
- Specialist involvement is critical to avoid missing atypical parkinsonian syndromes (PSP, MSA, CBD) that have different prognoses and treatment responses 1
- Imaging studies require proper interpretation in clinical context, another reason for neurologist involvement 1
Assessment Tools for Disease Severity
- Unified Parkinson's Disease Rating Scale (UPDRS) is the standard clinical assessment tool, consisting of four parts: mentation, activities of daily living, motor examination, and complications of therapy 1, 5
- The Movement Disorder Society-UPDRS (MDS-UPDRS) is a newer version with improved evaluation of non-motor aspects, freezing of gait, and tremor subtypes 1
Common Diagnostic Pitfalls to Avoid
- Failure to have the patient completely relax during rigidity testing leads to false positives from voluntary muscle contraction 1
- Not using activation maneuvers may cause you to miss subtle rigidity 1, 3
- Confusing spasticity with rigidity - spasticity is velocity-dependent (increases with faster stretching) while rigidity shows constant resistance throughout movement 1
- Ordering functional imaging before structural imaging - always obtain MRI first 1
- Assuming a normal MRI excludes PD - MRI is often normal in early PD but is essential to exclude alternative diagnoses 1