What is Stiff Person Syndrome?

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Stiff person syndrome (SPS) is a rare neurological disorder that is characterized by stiffness and muscle spasms in the trunk and limbs. These symptoms can vary in severity and may be accompanied by other neurological features, such as difficulty speaking, difficulty swallowing, and loss of balance. The stiffness and spasms are often triggered by external stimuli, such as loud noises or sudden movements, and can be very painful and distressing for the person with SPS.

 

What causes Stiff Person Syndrome?

The exact cause of stiff person syndrome (SPS) is not well understood. It is thought to be caused by an autoimmune response, in which the body's immune system mistakenly attacks the nervous system. This results in the destruction of a specific type of nerve cell called gamma-aminobutyric acid (GABA)ergic neurons, which are responsible for transmitting inhibitory signals in the nervous system. As a result of this destruction, the nervous system becomes hyperactive and susceptible to muscle spasms and stiffness.

SPS is often associated with other autoimmune disorders, such as type 1 diabetes and thyroid disease. In some cases, SPS may be triggered by an infection or other immune-related event. However, the specific mechanisms that lead to the development of SPS are not well understood, and further research is needed to fully understand the causes of this disorder.

 

What are the symptoms associated with Stiff Person Syndrome?

The symptoms of stiff person syndrome vary in severity and may affect different people in different ways. In general, the symptoms of SPS are characterized by stiffness and muscle spasms in the trunk and limbs. These symptoms may be accompanied by other neurological features, such as difficulty speaking, difficulty swallowing, and loss of balance.

The stiffness and spasms associated with SPS may be triggered by external stimuli, such as loud noises or sudden movements. They can be very painful and distressing for the person with SPS, and may interfere with their ability to move and perform daily activities.

In addition to stiffness and spasms, people with SPS may experience other symptoms, such as fatigue, anxiety, and depression. They may also have difficulty sleeping, due to the discomfort and pain caused by the stiffness and spasms.

The symptoms of SPS may come and go, with periods of relative stability followed by sudden exacerbations of the symptoms. In some cases, the symptoms may gradually worsen over time, leading to increasing disability and difficulty performing daily activities.

 

How is Stiff Person Syndrome diagnosed?

The diagnosis of stiff person syndrome (SPS) can be challenging, as the symptoms may be similar to those of other neurological disorders. A thorough medical evaluation is necessary to rule out other possible causes of the symptoms.

The first step in the diagnosis of SPS is a detailed medical history, in which the healthcare provider will ask about the person's symptoms, medical history, and any other relevant information. The provider will also perform a physical examination, looking for signs of muscle stiffness and spasms, as well as other neurological abnormalities.

In addition to the medical history and physical examination, the healthcare provider may order several tests to help confirm the diagnosis of SPS. These may include:

  • Neurological testing: This may include a variety of tests, such as electromyography (EMG) and nerve conduction studies, to assess the function of the nervous system.
  • Imaging studies: Imaging studies, such as magnetic resonance imaging (MRI) or computed tomography (CT) scans, may be used to look for abnormalities in the brain or spinal cord.
  • Laboratory tests: Blood tests may be done to look for evidence of an autoimmune disorder, as well as to rule out other possible causes of the symptoms.

If the healthcare provider suspects that the person has SPS, they may refer them to a neurologist, who is a specialist in disorders of the nervous system. The neurologist may conduct additional testing and work with the person to develop a treatment plan.

In some cases, it may be necessary to rule out other possible causes of the symptoms before a definitive diagnosis of SPS can be made. This may involve further testing and evaluation by a team of healthcare providers with expertise in SPS and other neurological disorders.

 

How is Stiff Person Syndrome treated?

The treatment of stiff person syndrome (SPS) is often complex and may involve a combination of medications, physical therapy, and other supportive measures. The specific treatment plan will depend on the person's symptoms and needs, and may be adjusted over time as the person's condition changes.

Medications are often an important part of the treatment of SPS. The goal of medication therapy is to reduce muscle stiffness and spasms, as well as to suppress the autoimmune response that is thought to be responsible for the symptoms of SPS.

The most commonly used medications for SPS are GABAergic drugs, such as diazepam and baclofen, which help to reduce muscle spasms and stiffness. Other medications, such as immunosuppressants and intravenous immunoglobulin (IVIg), may be used to suppress the autoimmune response that is thought to be responsible for the symptoms of SPS.

In addition to medications, physical therapy is an important part of the treatment of SPS. Physical therapy can help to improve flexibility, range of motion, and strength, and can also help to manage muscle spasms and pain. Physical therapists may use a variety of techniques, such as stretching exercises, massage, and heat or cold therapy, to help alleviate symptoms. They may also teach the person with SPS how to use assistive devices, such as canes or walkers, to help improve their mobility and independence.

Other supportive measures may also be helpful in the treatment of SPS. These may include counseling and support groups, which can help the person with SPS to cope with the emotional and psychological challenges of living with a chronic disorder.

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SPS is a complex and often debilitating disorder. It is important for people with SPS to work closely with their healthcare provider and physical therapist to develop a treatment plan that is tailored to their needs. With appropriate treatment, many people with SPS are able to manage their symptoms and maintain a good quality of life.

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