The journey to a Parkinson's disease diagnosis can be lengthy and uncertain, especially when a person has other chronic (long-term) conditions or is taking medications that may complicate identifying the source of motor symptoms. To make an accurate diagnosis, physicians rely on understanding how symptoms evolve over time and in what order and by ruling out other possible causes
A neurologist, particularly one specializing in movement disorders, often plays a key role in this process. Receiving a diagnosis from such a specialist can help reduce the risk of misdiagnosis.
Parkinson’s disease and other forms of parkinsonism result from the gradual loss of dopamine-producing neurons in the brain. Dopamine, a neurotransmitter (chemical messenger), is essential for transmitting signals between nerve cells, which helps regulate movement, motivation, reward, and mood. When dopamine levels drop, communication between the brain regions that control movement becomes disrupted. This can lead to symptoms including:
Parkinson’s disease is the most common type of parkinsonism, accounting for around 80 percent of cases. Read more about types of parkinsonism.
Diagnosing parkinsonism is the first step, which requires the presence of bradykinesia along with either rest tremor (tremor when muscles are relaxed) or muscle rigidity. After confirming parkinsonism, a neurologist evaluates whether Parkinson’s disease is the likely cause.
Factors that suggest a Parkinson’s disease diagnosis include:
Factors that may suggest other conditions include:
Other considerations that might lead a neurologist to explore different diagnoses include:
Given these various factors, it may take time for a doctor to confirm a Parkinson’s diagnosis, as they need to observe how symptoms respond to medications and evolve over time.
Various tests can support a Parkinson’s diagnosis or help rule out other conditions.
The doctor will take a thorough history, asking about symptoms over time, family medical history, previous head traumas, any medications you take, and possible exposures to toxins. This comprehensive history can reveal risk factors that either increase suspicion of Parkinson’s or suggest other diagnoses.
A neurological exam assesses mental function, mood, and physical signs like muscle strength, reflexes, and coordination. The doctor may ask you to perform movements to assess slowness, rigidity, or balance. They might also check your ability to feel sensations by using tools like a tuning fork or testing hot and cold items on different parts of your body.
You may be asked to sniff strongly scented materials and asked to identify the odors. Loss of the sense of smell is a very common early symptom in people with Parkinson’s and may begin years before motor symptoms.
Since Parkinson’s disease responds better to certain medications, the neurologist is likely to prescribe levodopa/carbidopa to find out whether it helps your symptoms. The neurologist may inject you with the drug at the office and observe changes to your symptoms while you wait. They may also prescribe a longer course of oral levodopa/carbidopa for two months or more and ask you to report whether and how symptoms change. If symptoms improve, it suggests Parkinson’s is more likely.
DaTscan, an imaging method approved by the U.S. Food and Drug Administration (FDA), can help neurologists visualize dopamine-producing cells in the brain. DaTscan can help differentiate parkinsonism from essential tremor. DaTscan involves an intravenous (IV) injection of a radioactive tracer into the bloodstream that binds to dopamine-producing cells, allowing a special camera to detect abnormal dopamine function.
Although DaTscan is not definitive for diagnosing Parkinson’s, it can support the diagnosis. Potential side effects include:
If a Parkinson’s diagnosis is in question, a neurologist may order an imaging scan to check for problems with the structure of the brain. Imaging scans sometimes used include magnetic resonance imaging (MRI), functional MRI (fMRI), or positron emission tomography (PET).
Around 10 percent to 15 percent of Parkinson’s cases are thought to be directly caused by a genetic mutation (variation) inherited from parents. If the doctor suspects a genetic form of Parkinson’s, especially in early-onset cases, they may order blood tests to check for specific genetic markers. Blood tests can also be used to rule out other conditions that might mimic Parkinson’s, like certain thyroid or metabolic disorders.
The process of ruling out similar conditions is known as differential diagnosis. Parkinson’s has symptoms in common with conditions including Alzheimer’s disease, frontotemporal dementia, and Huntington’s disease. Certain medications, such as antipsychotics, can also cause symptoms similar to those of Parkinson’s disease, a form known as drug-induced parkinsonism.
Other conditions that may cause parkinsonism include:
A doctor might quickly rule out some conditions based on your medical history and simple blood tests. Others may require more time and repeat testing to confirm or exclude. Coexisting conditions can complicate the diagnosis, potentially leading to multiple diagnoses over time.
MyParkinsonsTeam is the social network for people with Parkinson’s disease and their loved ones. On MyParkinsonsTeam, more than 105,000 members come together to ask questions, give advice, and share their stories with others who understand life with Parkinson’s disease.
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I fall down a lot my mother dyed in a nursing home and she had Parkenson and a form of denentia. She died in januarry 1997.. i was diagnosed in 1920. I am 82 yrs old and this month i started Assisted… read more
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