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Kennedy's Disease Association

A Public Benefit, Non-Profit Organization

Our Focus Remains on Research, Education and Support

The Kennedy’s Disease Association has worked to educate others about this lesser-known disease and to support clinical research efforts. We distributed information to more than 10,000 neurologists to help them recognize clinical signs and symptoms of Kennedy’s Disease.

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Will my child be born with this DNA defect?

It takes an enormous amount of money to fund research…more than any of us can afford alone, but together, we are capable of great accomplishments. We are searching for available foundation grants, but the process is lengthy. We need researchers to continue their work, and it is only the KDA that makes funding this disease a priority.

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Kennedy’s Disease Knows No Boundaries...

It is passed on from generation to generation in families worldwide. Males generally inherit the disease symptoms and females are the carriers. The defect is in the ‘X’ Chromosome that makes testosterone almost a poison to his body.

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What is Kennedy's Disease?

Kennedy’s Disease (spinal and bulbar muscular atrophy) is an adult-onset “X” linked inherited disease with symptoms usually beginning to appear between the ages of 30 and 50. However, onset has also been reported as early as in the teens and as late as the 60s.

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2013 - Research Updates PDF Print E-mail

Current Research

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June 01, 2013 - Research Update with Dr. Grunseich (Chat room transcript)
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May 28, 2013 - Clenbuterol shows mixed results in pilot trial

An article written by Amy Madsen for MDA’s Quest Magazine describes a pilot trial using Clenbuterol for a treatment for Kennedy’s Disease (SBMA). To read the entire article, follow this link: Clenbuterol Study.

Summary of Trial


Results from a 20-person pilot trial suggest that clenbuterol may improve motor and respiratory function in people with spinal-bulbar muscular atrophy, but safety concerns were raised.

Article Highlights:

  • Treatment with a drug called Clenbuterol was well-tolerated and was correlated with an increase in walking distance and respiratory capacity in a 20-person, open-label pilot study in Italy in people with spinal-bulbar muscular atrophy (SBMA).
  • During the trial, muscle strength did not improve, and an indicator of ongoing muscle damage increased in blood samples.
  • Clenbuterol, which belongs to a class of drugs called beta 2 agonists, is approved in some countries for treatment of asthma or other breathing disorders, but is not approved by the U.S. Food and Drug Administration to treat human conditions or diseases in the United States.
  • Study investigators suggest that additional clinical trials to test the therapeutic potential of Clenbuterol, or similar beta 2 agonist drugs, in people with SBMA may be warranted.
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May 04, 2013 - Research Update with Dr. Merry (Chat room transcript)

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March 22, 2013 - Convenient Diagnosis of SBMA

Abstract: Spinal and bulbar muscular atrophy (SBMA) is a slowly progressive motor neuron disease. Lower and primary sensory neuronopathy is one of the ... www.ajnd.us/files/ajnd1212003.pdf

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March 04, 2013 -Slowing Kennedy’s Disease Progression

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MDA’s Quest Magazine published an interesting article reported by Amy Madsen on some recent research by a member of the Kennedy’s Disease Association’s Scientific Review Board. Dr. La Spada has been instrumental in Kennedy’s Disease research for many years.  While the research opportunity still needs further study and testing, preliminary findings reflect this could be a potential treatment.
Below is the Quest article.
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Arimoclomol Slows Disease Progression

in SBMA Mice


Mice treated with the small-molecule compound improved muscle strength, increased motor neuron survival and boosted production of a motor-neuron support molecule called VEGF
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MDA research grantee Albert La Spada and colleagues have found that treatment with a compound called arimoclomol can help improve muscle function in mice with a disease resembling SBMA.

Article Highlights:
  • An MDA-supported research team has shown that treatment with a small-molecule compound called arimoclomol improved nerve-cell survival, resulting in increased muscle strength and function in mice with a disease resembling spinal-bulbar muscular atrophy (SBMA).
  • Arimoclomol is thought to work by inducing the heat shock response, which helps cells combat exposure to heat or other types of stress.
  • Although still early stage, the findings ultimately could lead to development of arimoclomol or similar compounds as a treatment for SBMA.
by Amy Madsen on March 4, 2013

Mice with a disorder mimicking human spinal-bulbar muscular atrophy (SBMA, or Kennedy disease) that were treated with an experimental therapy called arimoclomol showed improved nerve-cell survival, increased body weight, and better muscle strength and function than mice that didn't receive the treatment.

A small-molecule compound, arimoclomol is thought to work by inducing the heat shock response, in which levels of naturally occurring heat shock proteins (HSPs) increase when cells are exposed to heat or other types of stress.

The findings, which could lead to development of arimoclomol or similar compounds as a treatment for SBMA, were reported online Feb. 7, 2013, in Brain. MDA supported Albert La Spada at the University of California, San Diego, in La Jolla for his contribution to this work. (To read the full report, available for a fee, see Co-Induction of the Heat Shock Response Ameliorates Disease Progression in a Mouse Model of Human Spinal and Bulbar Muscular Atrophy: Implications for Therapy.)

Treatment began after symptom onset
Mice in the study were randomly assigned to two different groups, in which they were treated with 120 milligrams per kilogram of body weight per day of arimoclomol dissolved in drinking water (treatment group) or water alone (control group). Treatment began at 12 months of age, after symptom onset and lasted for six months through late-stage disease.

Results show that treatment with arimoclomol from the time of symptom onset dramatically delayed disease progression. When investigators examined 18-month-old SBMA mice, they found that those treated with arimoclomol:
  • demonstrated significantly improved hind-limb muscle force;
  • had 26.9 percent stronger muscles than did untreated mice;
  • showed a 23-percent improvement in motor unit (a nerve cell and the muscle fibers it activates);
  • had significantly increased muscle weight; and
  • had a 28.4-percent increase over untreated mice in the number of motor neurons that survived.

Mice treated with arimoclomol also had higher levels of a protein called vascular endothelial growth factor (VEGF), a protein that may protect or nourish nerve cells.

Treatment with arimoclomol had no effect on muscle force in mice that didn't have an SBMA-like disorder. This, the investigators noted, suggests that beneficial effects of arimoclomol in the mice are likely due to specific effects of the drug on disease processes, as opposed to indiscriminate improvement of muscle force.

Arimoclomol activated the heat shock response
Several treatment strategies for SBMA have focused on inducing overexpression of heat shock proteins, such as HSP70 and HSP90. (HSPs can function as “chaperones” for other proteins, helping them fold into the right shape, preventing them from forming abnormal clumps and blocking cell death.)

Data from the current study showed that levels of heat shock protein 70 (HSP70) were 2.3 times higher in the spinal cord and three times higher in hind-limb muscles in mice treated with arimoclomol than in mice that didn't receive treatment. 

This upregulation (increase) of the heat shock response by treatment with arimoclomol may have therapeutic potential in the treatment of SBMA, the researchers say.

 



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