Your nerves carry messages and information from your brain and spinal cord to your muscles and organs, coordinating your movements and bodily functions. As Parkinson’s disease progresses, it causes nervous system function to decline, making movement and bodily functions difficult. The exact causes of Parkinson’s disease are still unclear. However, research has identified several physical, genetic, and environmental factors that can contribute to the neurodegeneration associated with this condition.
Brain & Body Risk Factors
Parkinson’s disease is marked by lower levels of chemicals messengers, or neurotransmitters, which are responsible for the symptoms of this condition. Additionally, people with Parksinson’s may have unusual clumps of protein deposits in their brain, known as Lewy bodies.
Reduced Dopamine Levels
The neurodegeneration that characterizes Parkinson’s disease starts in the brain, in an area known as the substantia nigra, located in the middle of the brain. Small clusters of nerve cells, or neurons, in this area stop functioning properly and die. The neurons in the substantia nigra normally produce an important neurotransmitter known as dopamine. Dopamine is responsible for transmitting signals to parts of your brain that control your muscles and ensure smooth and coordinated movements. The loss of neurons in the substantia nigra leads to low dopamine levels in your brain. This weakens communication between your brain and your muscles and affects your movements. As a result, the primary symptoms of Parkinson’s disease are typically muscle and movement-related issues, such as tremors in your limbs, slow movements, and muscle rigidity. Symptoms typically start appearing when approximately 50% of the dopamine neurons are depleted. As more neurons are lost, the condition gets progressively worse, until the brain is unable to control movement at all. Parkinson’s disease is therefore classified as a movement disorder and primarily treated with dopamine therapy.
Reduced Norepinephrine Levels
Parkinson’s disease is also typified by low levels of another neurotransmitter, known as norepinephrine. This happens due to a loss of nerve endings that produce this chemical. Norepinephrine plays an important role in the sympathetic nervous system; it is the primary chemical messenger for this system. This system is responsible for several autonomic body functions, such as digestion, blood pressure, heart rate, and even breathing. Low norepinephrine levels are the cause of the non-movement-related symptoms of Parkinson’s disease. These can include fatigue, slower digestion, and a sudden drop in blood pressure upon standing from a seated or lying-down position.
Accumulated Lewy Bodies
People with Parkinson’s disease may have substances in their brain cells known as Lewy bodies, which are unusual clumps of a protein called alpha-synuclein. This protein is clumped in a way that can’t be broken down. Lewy bodies are microscopic markers of Parkinson’s disease. People with the symptoms of Parkinson’s disease who don’t have Lewy bodies in their brain are sometimes diagnosed with parkinsonism. Parkinsonism is an umbrella term for the movement-related symptoms of Parkinson’s disease, stemming from various causes. Lewy bodies and alpha-synuclein are a major area of focus for researchers of Parkinson’s disease. People with Parkinson’s disease also tend to have abnormal clumps of misshapen alpha-synuclein proteins in their intestines, suggesting that there may be a connection between Parkinson’s disease and gut health.
Family History & Genetics
Researchers have been able to identify certain genetic mutations that can increase the risk of developing Parkinson’s disease. These are the two types of Parkinson’s disease, from a genetic standpoint:
Hereditary Parkinson’s disease: Roughly 15% of all cases of Parkinson’s disease are inherited. In these cases, mutations in certain genes are passed down through families and increase the individual’s risk of developing this condition. Sporadic Parkinson’s disease: On the other hand, cases in which people don’t have a family history of Parkinson’s disease are referred to as sporadic cases. These cases are in fact the majority. Scientists have found that alterations in certain genes may also play a role in sporadic cases, in addition to other environmental and lifestyle-related factors.
However, the role that these genetic mutations play in the development of the condition hasn’t been fully understood yet.
Lifestyle Risk Factors
Apart from genetic factors, certain environmental and lifestyle-related factors may also increase your chances of developing Parkinson’s disease and contribute to the progression of the condition:
Vitamin D deficiency, as this nutrient plays an important role in maintaining brain health. Meat cooked at high temperatures, which can release cancerous compounds that may also cause Parkinson’s. Exposure to air pollution may cause inflammation in the brain and trigger the accumulation of alpha-synuclein deposits in the brain, sometimes from childhood. Exposure to pesticides can cause several biological reactions in the brain that lead to the damage and death of dopamine-producing neurons. Exposure to trichloroethylene (TCE), a chemical compound used in some household cleaning products, dry cleaning, and industrial degreasing. Industrial sites may release this compound into the environment. Exposure to heavy metals such as manganese in industrial settings; the greater the exposure, the greater the chances of developing symptoms associated with Parkinson’s disease. Head injuries, which can contribute to the loss of dopamine, especially in people who have been exposed to pesticides.
On the plus side, caffeine intake may help reduce your risk of developing Parkinson’s disease.
