Dr. Litvan Webinar on CBD – Notes

What a shame that this CurePSP webinar with such an expert as Dr. Irene Litvan was held at 6:30am California time with very little advance notice.  I was able to get up in time and noticed one other local support group member on the call.  There was a ten-minute delay in getting started (due to technical problems).  Judging by the few questions that were asked, I don’t think that many people participated in the webinar.

My key takeaway from today’s webinar with Dr. Litvan is that there are three common clinical presentations of CBD:

  • corticobasal syndrome
  • frontotemporal dementia presentation
  • progressive aphasia

Here are the details Dr. Litvan shared on the three presentations:

#1 – corticobasal syndrome:  symptoms are unilateral; parkinsonism (slowness, stiffness); ideomotor apraxia (ie, difficulty using a limb not due to motor of sensory problems); myoclonus (jerky movements); dystonic posture (abnormal posture/contracture); alien limb syndrome (feeling of limb as alien); levitation (uncontrolled elevation of limb); sensory neglect (unaware of sensation only when there is double stimulation).

If presentation #1 includes bilateral parkinsonism, rather than unilateral parkinsonism (which is more common), then the survival time is shorter.

#2 – frontotemporal dementia (FTD) presentation:  the primary symptom is frontal dementia (executive, frontal behavioral and language disturbances).  May or may not have bilateral parkinsonism.

Presentation #2 has a shorter survival time.

#3 – progressive aphasia:  language problems.

Unfortunately, Dr. Litvan did not describe the third presentation at all nor did she give the percentage prevalence of these three common forms.  (Or, if she did, I missed it!)  You’ll have to refer to the notes from Dr. Boeve’s presentation for that.  PPA (primary progressive aphasia) was one of the four disorders Dr. Boeve addressed in his webinar.
One other item mentioned briefly was the use of transcranial ultrasound in Europe (but not in the US) for aiding in the diagnosis of CBD.

In some ways, Dr. Litvan’s presentation was an excerpt of Dr. Boeve’s webinar from several months ago.

If you listened to today’s webinar, please let me know your key takeaways and if your understanding of the three clinical presentations is different from mine (described above).

My notes from Dr. Litvan’s presentation and the very short Q&A follow.  [Editor’s Note:  The webinar recording is no longer on the CurePSP website.]

Robin

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10/18/20 Webinar
Hosted by CurePSP
Challenges in CBD Management
Irene Litvan, MD, Director, Division of Movement Disorders, University of Louisville, Louisville, KY

Topics addressed in today’s presentation
* Diagnostic Challenges
* Pathogenesis (Cause/s)
* Treatment

CBD Diagnostic Challenges:
* Varied clinical presentations
* No markers for the disease (no blood test)
* Clinical presentations do not always correspond to underlying CBD brain lesions

Early and accurate diagnosis is important for:
* appropriate management
* prognosis
* clinical research

CBD Epidemiologic Aspects
* Underdiagnosed (25-48%).  Fewer than half who have the disease are diagnosed as having it during life.
* Diagnosis:  at half course of the disease
* There are no epidemiologic studies
* Togasaki & Tanner estimated that
(a) 4-6% of patients with parkinsonism have CBD
(b) incidence:  0.6 – 0.9 new patients per 100,000 each year
(c) prevalence:  4.9 – 7.3 per 100,000
* Sources:  Litvan et al, 1996; Wenning et al 1998; Litvan et al 2000; Togasaki and Tanner, 2000

CBD usually has a combination of:
* cognitive features (such as language) and/or
* motor features (such as dystonia or parkinsonism)
* underlying brain lesions of aggregated tau protein.  (This protein is a problem in AD and PSP.)

Classically, CBD presents with the corticobasal syndrome unilaterally:
* parkinsonism (slowness, stiffness)
* ideomotor apraxia (ie, difficulty using a limb not due to motor of sensory problems)
* myoclonus (jerky movements)
* dystonic posture (abnormal posture/contracture)
* alien limb syndrome (feeling of limb as alien)
* levitation (uncontrolled elevation of limb)
* sensory neglect (unaware of sensation only when there is double stimulation)

Underlying brain lesions are heterogeneous in the corticobasal syndrome (CBS):
* 36 people presented with CBS while only 18 had CBD.  6 had PSP; 4 had AD; 3 had CJD; 3 had non-specific changes; 1 had Pick, 1 had Pick/AD.
* Source:  Boeve paper

[Robin’s note:  I will try to find this article.  The one I’ve seen on 36 Mayo cases is on the neuropsychiatric features and all 36 had CBD.]

Alzheimer Disease presenting with CBD:
* visuomotor disturbances
* ideomotor apraxia
* intermanual conflict
* action myoclonus
* left dystonia
* left alien limb syndrome
* aphasia (including difficulty naming objects)
* clock drawing shows hemi-neglect on the right side (of the brain).  So nearly all 12 numbers are on the right side of the clock.  Usually hemi-neglect is on the left side.
* brain autopsy showed:  AD with lesions on one side; this is a rare presentation of AD
* Source:  Chand et al 2006

CBS with underlying TDP-43 proteinopathy with progranulin mutations
* Described by:  Guerreiro et al 2008; Le Ber et al 2008; Lopez de Munain et al 2008; Kelley et al 2007; Spina et al 2007

We need to know the underlying disease in order to find treatments

Clinical diagnoses in 32 consecutive autopsied cases at the Mayo Clinic with brain CBD pathology:
* Initial Clinical Diagnosis:  10 CBD (31%); 6 atypical PD; 2 PSP; 4 Primary progressive aphasia; 6 dementia/AD; 1 DLB; 1 Marchiafava-Bignami disease; 1 Multiple sclerosis; 1 Stroke
* Final Clinical Diagnosis:  18 CBD (50%); 7 PSP (22%); 4 Primary progressive aphasia; 1 AD; 1 DLB; 1 Marchiafava-Bignami disease
* Source:  Boeve et al 2000

[Robin’s note:  I will try to find this article.]

CBD with a frontotemporal dementia (FTD) presentation:
* dementia (executive, frontal behavioral and language disturbances)
* may or may not have bilateral parkinsonism
* Sources:  Bergeron et al 1998; Wenning et al 1998; Litvan et al 1999; Grimes et al 1999

Chart from Murray et al, Neurology 2007;6k:1274-1283 (UPenn study):
Only a few had the final clinical diagnosis of CBD yet the chief complaints were classic CBD (unilateral problems)

CBD presentation matters because survival is different for each presentation.  Shorter survival in CBD when presenting with dementia and/or bilateral parkinsonism.

In summary, diagnostic challenges are:
* No diagnostic biological markers.  Diagnosis still relies on clinical features, confirmed by pathology.
* CBD presents with various clinical presentations including CBS, FTD, and primary progressive aphasia
* The underlying brain lesions of the CBS vary and include CBD, PSP, Alzheimer Disease, FTD, progranulin mutations and Creutzfeld-Jakob Disease

Lab tests that can help some with diagnosis:
* brain MRI in CBD:  might be able to see unilateral atrophy
* transcranial ultrasound:  used in Europe; might help with diagnosis

What goes wrong in the brains of those with CBD?
* Tau aggregates in neurons and glia.
* Astrocytic plaque is indicative of CBD.
* Some key terms:  NFT, tufted astrocyte; threads; coiled body; astrocytic plaque.

Tau is important for the brain cell structure.  In CBD, tau collects in insoluble forms.

What triggers tau to change in CBD?
We don’t really know but question whether the following factors may play a role — genetics; mitochondrial abnormalities (oxidative stress); dietary/environmental toxicants; inflammation; gene/environment combination

What do we know about genetics?
* CBD is very weakly hereditary
* No highly penetrant tau mutations are found
* CBD is associated with H1 haplotypes and H1 hyplotype variants.  Also true in PSP.
* ? Genetic predisposition CBD

From looking at H1/H1, H1/H2, and H2/H2 at PSP, CBD, and in controls, we conclude:
* H1/H1 genotype is (nearly) necessary but far from sufficient for CBD or PSP to develop
H1/H1:  88% of PSP; 84% of CBD; 60% of controls
* Predisposition triggered by other factors of relative rare mutation with low penetrance?
* ? H2/H2 is protective
H2/H2:  0% in PSP; CBD of CBD

Defined tau mutations give rise to tauopathies presenting with PSP/CBD clinical and pathological phenotype.  Example:  PPND (FTDP-17 with N279-K mutation).  Seen in Mr. Wszolek, a Mayo patient.

What do we know about mitochondrial abnormalities and oxidative injury?
* Impaired activity of Complex I of the mitochondrial respiratory chain
* Oxidative stress in CBD.  Cells die.

What do we know about inflammation?
* Activated microglia in the brain in CBD.  Can see this in people who have died and in living people.
* Sources:  Ishizawa and Dickson 2001; Gerhard et al 2004; Henkel et al 2004)

Hypothesized pathways to cell death in CBD and PSP:
* H1 haplotype variants:  do these lead to tau dysfunction?
* Inflammation:  does this lead to tau inclusions, which causes cell death, which leads to more inflammation

CBD Treatment Challenges:
* Difficulties in accurately diagnosing patients during life
* Difficulty in slowing disease progression when the cause is unknown
* Symptomatic treatments have limited efficacy.  We can improve the quality of life.

Symptomatic RX:
Dystonia (limbs) — botox
Dystonia (neck) — botox (avoid when antecollis)
Speech problems — speech therapy; communication aids
Myoclonus — clonazepam, piracetam, valproate
Belpharospasm — botox
Walking — PT; weighted walker
Patient and family support — social services; laymen associations; support RX

In summary:
* CBD has various clinical presentations:  CBS, progressive aphasia (language problem), frontal dementia
* The underlying brain lesions corresponding to these presentations are not always CBD
* Telltale signs (such as focal signs) are present in mid-phase of the disease
* More research is needed to identify:
(a) better ways to diagnose CBD during life;
(b) causes contributing to development;
(c) specific ways to slow the progression of the disease

Questions & Answers:  (all questions were answered by Dr. Litvan)

BRAIN DONATION

In response to someone noting that they’ve made arrangements for brain donation and to someone else to donated her mother’s brain upon death, Dr. Litvan said:  “Thank you for donating your brain!”

RESEARCH

Q:  What are some centers that are studying this disease?

A:  Mayo, UPenn, UCSF

Q:  Are there any known causes?

A:  There is a genetic susceptibility for those with the H1 genotype.  There is a study going on in PSP as to the causes, but not in CBD.  We aren’t studying this in CBD due to the diagnostic challenges.

Q:  Any hope on the horizon for developing biomarkers?

A:  There are multiple groups trying to search for this.  One group is trying to label the protein tau with a PET scan.  This would help with the diagnosis and at least to differentiate from other disorders.  There are a lot of researchers involved.  Of course we want more researchers to be involved and more money.

ABOUT THE THREE PRESENTATIONS AND SYMPTOMS

Q:  Are there typical symptoms to expect as disease progresses?

A:  It depends on the form of the disease.  If the disease presents in a unilateral way, the disease may affect the other side of the body.  If the disease presents with dementia, the disease may affect both sides of the body.

Usually memory is not a major issue in this disease.

Q:  Will dementia appear?

A:  It can happen that dementia never appears.

Q:  Alien limb.

A:  Usually the arms are more effected than the legs.

Q:  My sister has language problems.  What guess can you make about her survival time?

A:  Forms that have speech problems progress slowly.  Those with CBS have a survival time of 5-8 years.

Q:  In PSP, there are two common forms.  Do you guess that the same two forms appear in CBD?

A:  Yes, this is exactly what I said.  There are three forms in CBD.

Q:  Are itching and constipation part of CBD?

A:  Itching is not part of CBD.  Constipation is part of many neurodegenerative diseases.

ABOUT TREATMENTS

Q:  If CBD presents as AD, can AD drugs help?

A:  We don’t have AD drugs that can help with CBD symptoms.

Q:  Would CBD patients benefit from DBS (deep brain stimulation)?

A:  No.  People with PD who get DBS do improve because they respond to dopamine medication.  If you don’t respond to levodopa/carbidopa, then you won’t respond to DBS.

CBS and PSP listed in “Frontotemporal Disorders” booklet (NIH)

PSP and CBD folks –

A great new publication, Frontotemporal Disorders: Information for Patients, Families and Caregivers,has just been released by the National Institute on Aging and NIH.  It is free and available by download or in hardcopy via the following link:  [Editor’s note: link modified in 2017]

www.nia.nih.gov/alzheimers/publication/frontotemporal-disorders/introduction

Jennifer Merrilees, RN, from UCSF’s MAC, assisted in the creation of this booklet along with people from Northwestern University and the Association for Frontotemporal Dementias.

I’ve copied below some excerpts that are on terminology, CBS, and PSP.  I especially liked the terminology section (“FTD? FTLD? Understanding Terms”) and the section on symptoms (with a breakdown by type of symptom — behavioral, language, emotional, and movement).  Of course not all of the symptoms listed occur in each disorder nor in each person with a given disorder.

Robin

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www.nia.nih.gov/alzheimers/publication/frontotemporal-disorders/introduction

Excerpts from

Frontotemporal Disorders: Information for Patients, Families, and Caregivers
NIA and NIH
Published October 2010

FTD? FTLD? Understanding Terms
One of the challenges shared by patients, families, clinicians, and researchers is confusion about how to classify and label frontotemporal disorders. A diagnosis by one doctor may be called something else by a second, and the same condition or syndrome referred to by another name by a pathologist who examines the brain after death.

For many years, scientists and physicians used the term frontotemporal dementia (FTD) to describe this group of illnesses. After  further research, FTD is now understood to be just one of several possible variations and is more precisely called behavioral variant frontotemporal dementia, or bvFTD.

This booklet uses the term frontotemporal disorders to refer to changes in behavior and thinking that are caused by underlying brain diseases collectively called frontotemporal lobar degeneration (FTLD). FTLD is not a single brain disease but rather a family of neurodegenerative diseases, any one of which can cause a frontotemporal disorder (see “Causes,” page 11). Frontotemporal disorders are diagnosed by physicians and psychologists based on a person’s symptoms. FTLD can be identified definitively only by brain autopsy after death.

Types of Frontotemporal Disorders
Frontotemporal disorders can be grouped into three types, defined by the earliest symptoms physicians identify when they examine patients.

• Progressive behavior/personality decline—characterized by changes in personality, behavior, emotions, and judgment (e.g., behavioral variant frontotemporal dementia).

• Progressive language decline—marked by early changes in language ability, including speaking, understanding, reading, and writing (e.g., primary progressive aphasia).

• Progressive motor decline—characterized by various difficulties with physical movement, including shaking, difficulty walking, frequent falls, and poor coordination.

Types of Frontotemporal Disorders
Diagnostic Terms and Main Early Symptoms
Progressive Motor Decline

Corticobasal syndrome (CBS)
• Muscle rigidity
• Difficulty closing buttons, operating simple appliances
• Language or spatial orientation problems

Progressive supranuclear palsy (PSP)
• Progressive problems with balance and walking
• Slow movement, falling, body stiffness
• Restricted eye movements

FTD with parkinsonism
• Movement problems similar to Parkinson’s disease, such as slowed movement and stiffness
• Changes in behavior or language

FTD with amyotrophic lateral sclerosis (FTD-ALS)
• Combination of FTD and ALS (Lou Gehrig’s disease)
• Changes in behavior and/or language
• Muscle weakness, shrinkage, jerking

Movement Disorders
Two rare neurological disorders associated with FTLD, corticobasal syndrome (CBS) and progressive supranuclear palsy (PSP), occur when the nerves attached to muscles malfunction and cause problems with movement. The disorders may affect thinking and language abilities, too.

CBS is caused by corticobasal degeneration—gradual atrophy and loss of nerve cells in specific parts of the brain. This degeneration causes progressive loss of movement and muscle rigidity, typically beginning around age 60. Symptoms may appear first on one side of the body, but eventually both sides are affected. Occasionally, a person with CBS first has language problems or trouble orienting objects in space and later develops movement symptoms.

PSP causes serious problems with balance and walking. People with the disorder typically move slowly, fall, and have body stiffness, especially in the neck and upper body—symptoms similar to those of Parkinson’s disease. A hallmark sign of PSP is trouble with eye movements, such as involuntary closing of the eyelids, difficulty opening and closing the eyes, trouble looking way up and way down, and limited blinking. These symptoms may give the face a fixed stare. Behavior problems can also develop.

Other movement-related frontotemporal disorders include frontotemporal dementia with parkinsonism and  frontotemporal dementia with amyotrophic lateral sclerosis (FTD-ALS).

Frontotemporal dementia with parkinsonism is an inherited disease caused by a genetic mutation. Symptoms include movement problems similar to those of Parkinson’s disease, such as slowed movement, stiffness, and balance problems, and changes in behavior or language.

FTD-ALS is a combination of bvFTD and ALS, commonly called Lou Gehrig’s disease. Symptoms include the behavioral and/or language changes seen in bvFTD as well as the muscle weakness, shrinking, and jerking seen in ALS. Symptoms of either disease may appear first, with other symptoms developing over time. Mutations in certain genes have been found in some patients with FTD-ALS.

Confusing symptoms
Carol had a tingling sensation and numbness in her upper right arm. Then her arm became stiff. She had to change from cursive handwriting to printing. Carol, 61, told her doctor that she had trouble getting her thoughts out and  described her speech as “stumbling.” She had increasing trouble talking but could still understand others. Eventually, she was diagnosed with CBS.

Trouble with walking
For a year and a half, John had trouble walking and fell several times. He also had trouble concentrating. He couldn’t read because the words merged together on the page. John, 73, also seemed less interested in social activities and projects around the house. His wife noticed that he was more irritable than usual and sometimes said  uncharacteristically inappropriate things. John’s primary care doctor did several tests, then referred him to a  neurologist, who diagnosed PSP.

Common Symptoms
Symptoms of frontotemporal disorders vary from person to person and from one stage of the disease to the next as different parts of the frontal and temporal lobes are affected. In general, changes in the frontal lobe are associated with behavioral symptoms, while changes in the temporal lobe lead to language and emotional disorders.

Symptoms are often misunderstood. Family members and friends may think that a person is misbehaving, leading to anger and conflict. For example, a person with bvFTD may neglect personal hygiene or start shoplifting. It is important to understand that people with these disorders cannot control their behaviors and other symptoms.

Behavioral Symptoms
• Problems with executive functioning—Problems with planning and sequencing (thinking through which steps come first, second, third, and so on), prioritizing (doing more important activities first and less important activities last), multitasking (shifting from one activity to another as needed), and self-monitoring and correcting behavior.

• Perseveration—A tendency to repeat the same activity or to say the same word over and over, even when it no longer makes sense.

• Social disinhibition—Acting impulsively without considering how others perceive the behavior. For example, a person might hum at a business meeting or laugh at a funeral.

• Compulsive eating—Gorging on food, especially starchy foods like bread and cookies. People may take food from other people’s plates.

• Utilization behavior—Difficulty resisting impulses to use or touch objects that one can see and reach. For example, a person picks up the telephone receiver while walking past it when the phone is not ringing and the person does not intend to place a call.

Language Symptoms
• Aphasia—A language disorder in which the ability to use or understand words is impaired but the physical ability to speak properly is normal.

• Dysarthria—A language disorder in which the physical ability to speak properly is impaired (e.g., slurring) but the message is normal.

Emotional Symptoms
• Apathy—A lack of interest, drive, or initiative. Apathy is often confused with depression, but people with apathy may
not be sad. They often have trouble starting activities but can participate if others do the planning.

• Emotional changes—Emotions are flat, exaggerated, or improper. Emotions may seem completely disconnected from a situation or are expressed at the wrong times or in the wrong circumstances. For example, a person may laugh at sad news.

• Social-interpersonal changes—Difficulty “reading” social signals, such as facial expressions, and understanding personal relationships. People may lack empathy—the ability to understand how others are feeling—making them seem indifferent, uncaring, or selfish. For example, the person may show no emotional reaction to illnesses or accidents that occur to family members.

• Changes in insight—An inability to understand changes in one’s condition and how they affect others. This lack of awareness is hard for caregivers to deal with because the person may reject efforts to help.

Movement Symptoms
• Dystonia—Abnormal postures of the hands or feet. A limb may be bent stiffly or not used when performing activities that are normally done with two hands.

• Gait disorder—Abnormalities in walking, such as walking with a shuffle, sometimes with frequent falls.

• Tremor—Shakiness, usually of the hands.

• Clumsiness—Dropping of small objects or difficulty manipulating small items like buttons or screws.

Managing Movement Problems
No treatment can slow down or stop frontotemporal-related movement disorders, though medications and physical and occupational therapy may provide modest relief.

For people with corticobasal syndrome (CBS), movement difficulties are sometimes treated with medications for depression, Alzheimer’s disease, or Parkinson’s disease. But these medicines do not often lead to much  improvement. Physical and occupational therapy can help a person with CBS move more easily. Speech therapy may delay the worsening of language symptoms.

For people with progressive supranuclear palsy (PSP), sometimes Parkinson’s disease drugs provide temporary relief for slowness, stiffness, and balance problems. Although physical therapy generally does not help, exercises can keep the joints limber, and weighted walking aids—such as a walker with sandbags over the lower front rung—can help maintain balance. Speech, vision, and swallowing difficulties usually do not respond to any drug treatment. Antidepressants have shown modest success. For people with trouble looking up or down, bifocals or special glasses called prisms are sometimes prescribed. …

For any movement disorder caused by FTLD, a team of experts can help patients and their families address difficult medical and caregiving issues. Physicians, nurses, social workers, and physical, occupational, and speech therapists who are familiar with frontotemporal disorders can ensure that people with movement disorders get appropriate medical treatment and that their caregivers can help them live as well as possible.

Caring for a Person with a Frontotemporal Disorder
In addition to managing the medical and day-to-day care of people with frontotemporal disorders, caregivers can face a host of other challenges. These challenges may include changing family relationships, loss of work, poor health, decisions about long-term care, and end-of-life concerns.

Family Issues
People with frontotemporal disorders and their families often must cope with changing relationships, especially as symptoms get worse. …

Work Issues
Frontotemporal disorders disrupt basic work skills, such as organizing, planning, and following through on tasks. Activities that were easy before the illness began might take much longer or become impossible. People lose their jobs because they can no longer perform them. As a result, the caregiver might need to take a second job to make ends meet—or reduce hours or even quit work to provide care and run the household.

Caregiver Health and Support
Caring for someone with a frontotemporal disorder can be very hard, both physically and emotionally. To stay healthy, caregivers can do the following:

• Get regular health care.

• Ask family and friends for help with child care, errands, and other tasks.

• Spend time doing enjoyable activities, away from the demands of caregiving. Arrange for respite care—short-term caregiving services that give the regular caregiver a break—or take the person to an adult day care center, a safe, supervised environment for adults with dementia or other disabilities.

• Join a support group for caregivers of people with frontotemporal disorders. Such groups allow caregivers to learn coping strategies and share feelings with others in the same position.

The organizations listed in the Resources section of this book (starting on page 27) can help with information about caregiver services and support.

Long-Term Care
For many caregivers, there comes a point when they can no longer take care of the person with a frontotemporal disorder without help. The caregiving demands are simply too great, perhaps requiring around-the-clock care. As the disease progresses, caregivers may want to get home health care services or look for a residential care facility, such  as a group home, assisted living facility, or nursing home. The decision to move the person with a frontotemporal disorder to a care facility can be difficult, but it can also give caregivers peace of mind to know that the person is safe
and getting good care.

End-of-Life Concerns
People with frontotemporal disorders typically live 6 to 8 years with their conditions, sometimes longer, sometimes less. Most people die of problems related to advanced disease. For example, as movement skills decline, a person can have trouble swallowing, leading to aspiration pneumonia, in which food or fluid gets into the lungs and causes infection. People with balance problems may fall and seriously injure themselves.

It is difficult, but important, to plan for the end of life. Legal documents, such as a will and durable powers of attorney for health care and finances, should be created or updated as soon as possible after a diagnosis of bvFTD, PPA, or a related disorder. Early on, many people can understand and participate in legal decisions. But as their illness progresses, it becomes harder to make such decisions.

A physician who knows about frontotemporal disorders can help determine the person’s mental capacity. An attorney who specializes in elder law, disabilities, or estate planning can provide legal advice, prepare documents, and make financial arrangements for the caregiving spouse or partner and dependent children. If necessary, the person’s access to finances can be reduced or eliminated.

Resources

Federal Government

National Institute on Aging
www.nia.nih.gov/Frontotemporal

National Institute of Neurological Disorders and Stroke
www.ninds.nih.gov

MedlinePlus
www.medlineplus.gov

Organizations

Association for Frontotemporal Dementias
www.ftd-picks.org

ALS Association
www.alsa.org

CurePSP
www.curepsp.org

National Aphasia Association
www.aphasia.org

WE MOVE
www.wemove.org

Caregiver Services

Eldercare Locator
www.eldercare.gov

Family Caregiver Alliance
www.caregiver.org

National Academy of Elder Law Attorneys, Inc.
www.naela.org

Caregiver Support

FTD Support Forum
www.ftdsupportforum.com

PPA Support Group
www.groups.yahoo.com/group/PPA-support

Well Spouse Association
www.wellspouse.org

Diagnosis, Treatment, and Research Centers  [many are listed, including…]

University of California, San Francisco
Memory and Aging Center
San Francisco, CA
1-415-476-6880
www.memory.ucsf.edu/ftd

Article on Stress and CBD (in new CBD Newsletter)

CBD folks –

The long-time owner of the Washington Wizards NBA basketball franchise was Abe Pollin. He died in late 2009. His clinical diagnosis was CBD, and I heard from someone who is in the PSP community in the Washington, D.C. area that the diagnosis was confirmed upon brain autopsy.

Irene Litvan, MD, is one of this country’s leading experts on CBD. Several years ago she started the Litvan Neurological Research Foundation, named in memory of her father. Abe Pollin donated to LNRF, which led to the creation of the Center of Excellence in Corticobasal Degeneration. This COE is presented located at the University of Louisville in KY, which is where Dr. Litvan currently works.

The Center is working to establish its own website — cbdcenter.org (under construction).

I was digging around on the web tonight and found that the Center has published its inaugural newsletter in Spring 2010. Here’s a link to that newsletter:
http://www.litvanfoundation.com/images/ … 202010.pdf

There are interesting articles on:
* the Center’s creation
* profile of Abe Pollin
* CBD diagnostic criteria being reformulated
* profile of Dr. Irene Litvan
* stress and CBD
* fall prevention

The remainder of this post is a copy of the “Stress and Corticobasal Degeneration” article.

Robin

Stress and Corticobasal Degeneration
CBD Newsletter
Volume 1, Issue 1, Spring 2010
The Center of Excellence in Corticobasal Degeneration

It’s no secret that your mental state can have an effect on your physical well-being. Dealing with the effects of a disease like CBD, either as a patient or as a caregiver, is a very real and perfectly rational cause of stress, but too much stress can have a severe negative effect on your health. This article explores the nature of stress and suggests some methods of reducing its impact on your life.

What is Stress?
Stress is your body’s natural response to a threat. When you are faced with a physical threat, your body releases hormones and adrenaline that help you prepare to either fight the threat, or flee from it. Most commonly, when we refer to “stress” in our daily lives, we are not referring to a physical threat, but rather some perceived psychological or emotional threat. The illness of yourself or a loved one is a typical cause of psychological stress.

In small doses, stress can be beneficial, it can help you to overcome challenges and to excel by increasing your performance capacity. If stress continues for too long, however, it can begin to have a severe toll on your body, in fact chronic stress disrupts nearly every system in your body! Typical effects of chronic stress include pain, heart disease, liver problems, digestive problems, sleep disturbances, and autoimmune diseases, among others.

Stress & CBD
In terms of corticobasal degeneration, increased stress is a normal reaction whether you are the pa-tient diagnosed with the disease or the spouse or loved one caring for a family member with the diagnosis. CBD is a chronic and debilitating disease for which we do not know a cause or an effective course of treatment. You would be very unique if the presence of CBD in your life, in any capacity, didn’t cause you stress.

Because of the lack of knowledge about CBD, its chronic nature, and the level of care needed to maintain patients diagnosed with the disease, CBD-caused stress very typically drifts from the “normal” stress range into the “unhealthy” stress range. So, what can you do to prevent a CBD induced stress overload?

Fighting CBD Stress
Like a gladiator heading to the arena, the first order of business in dealing with CBD stress is to arm yourself appropriately. In the fight against CBD induced stress, the weapon of choice is knowledge.

Yes, its true that very little is known about the causes of CBD or how to treat the disease or even prevent symptoms, but as a patient or as a caregiver, you should still arm yourself with the best knowledge available. Learning all you can about the progression of disease symptoms, while sobering, can help reduce anxiety over what the future will bring. Learning about adaptive devices and techniques that can help CBD patients retain their independence can ease feelings of helplessness and reduce caregiver strain. In general, the more you know, the better prepared you will be to deal with the future, and the better prepared you feel, the less stress you will experience.

Another key way to reduce stress is to build a strong support group. The more friends and family members you know you can count on, the less stressed you will feel. Some of us are blessed with good support networks, others not so much. If you find yourself dealing with your situation on your own, then its time to reach out for help. Old friends, co-workers, family members you haven’t talked to for a while, all can be good general sources of support.

For CBD patients and their caregivers, a number of support groups exist or are being formed that can put you in contact with other patients and caregivers who are dealing with the same issues. Regardless of the form your support group takes, it is a very important tool in reducing your stress load.

Other ways to reduce stress or better prepare your body to deal with the effects of stress include exercise, yoga, meditation, and deep breathing exercises. These activities help our bodies to initiate a relaxation response, the opposite of a stress response.

If you feel that you are slipping into despair or depression, seek out the help of a trained therapist.

For more information on decreasing stress, a number of books have been published on the subject and can be found at your local library, book store or online outlet.

The Center of Excellence in Corticobasal Degeneration is committed to helping patients, their families, and caregivers deal with stress due to CBD. In the near future we will be providing support groups and stress-related work-shops in the Louisville, KY area, as well as coordinating with other providers of similar services throughout the United States to assist individuals in finding re-sources near their location.

Please visit www.cbdcenter.org for more details.

PSP and CBD public service announcement

Check out this short public service announcement for PSP and CBD:

www.youtube.com/watch?v=qEBxqOFojUU&t=4s

The audio quality is not as good as it is on Sean Donnelly’s webpage.  He’s the volunteer who produced the video:

www.seandonnelly.com/psp/psp_0428.wmv

It may be a tear-jerker for many of you.

I know the couple in the first set — “from vitality to lethargy.”  It’s Ed Plowman with his wife Rose.  Ed is a member of the PSP Forum, who has joined our local caregiver support group meetings in the past (when visiting the west coast).

The third set — “from active to debilitated” — is my dad and me.

The set of photos for “ability to see/ability to walk” are of Den Reichardt, local group member Sharon’s husband.

On the “Hope” page there’s another photo of my dad and me (to the right of “Hope”), a photo of my dad alone (below “Hope”), and a photo of Den in the lower right.

If you or your family members appear in any of these photos, please let me know!

A volunteer put together this PSA for CurePSP earlier in the year.  CurePSP finalized permissions and its Board approved it back in June.  I just received word that it’s OK to circulate the link.  Surprising that it’s not on the CurePSP website.  And I certainly haven’t seen it on TV.  (I’d be floored if I did!)

Robin

Ocular Issues – DLB, PSP, CBS

This medical journal article reviews ocular motility issues in aging and dementia, and includes PSP, CBS, and DLB among others (AD, PD, FTLD, CJD).

Here’s a link to the abstract:

Ocular Motility of Aging and Dementia
Pelak VS.
Current Neurology and Neuroscience Reports.
2010 Aug 10. [Epub ahead of print] PubMed ID#: 20697981

I’ve copied below a few excerpts related to three disorders within Brain Support Network — PSP, CBS, and DLB.

Robin


Excerpts from:
Ocular Motility of Aging and Dementia
Pelak VS.
Current Neurology and Neuroscience Reports.
2010 Aug 10. [Epub ahead of print] PubMed ID#: 20697981

Dementia with Lewy Bodies

Ocular Motility Dysfunction
Systematic study of eye movements in DLB has been very limited. … Reflexive saccades are impaired in DLB, with increased latencies and antisaccades errors. Vertical and horizontal supranuclear palsies are rare but have been described. Balint syndrome may be prominent because of involvement of the biparietal cortex.

Visual Symptoms
Visual hallucinations are the most common visual complaint, but reading difficulties, difficulty focusing, and other visual complaints similar to those in both AD and PD…may occur.

Corticobasal Syndrome

Ocular Motility Dysfunction
The most prominent disturbance is increased saccade latency, which is greater for saccades toward the direction of limb apraxia and correlates with limb apraxia scores. On examination, some patients may use head thrusts to improve horizontal saccades. Convergence insufficiency and a high number of errors on the antisaccade test also may be observed. Vertical and horizontal gaze palsies and/or ocular misalignment may occur, but rarely to the significant extent seen, for example, in PSP.

Visual Symptoms
Patients may report difficulty reading, likely
because of problems moving their eyes from word to word and from line to line in the presence of severely increased saccade latency. If ocular misalignment or convergence insufficiency is present, patients will report diplopia.

Progressive Supranuclear Palsy

Ocular Motility Dysfunction
The diagnostic ocular motility hallmark is
limitation of vertical gaze, usually downgaze
before upgaze. Involvement of horizontal gaze typically follows. Supranuclear gaze palsies may appear months or years after the onset of other neurologic symptoms, and they usually are preceded by marked slowing of voluntary vertical saccades. Horizontal saccades also may be markedly abnormal with decreased saccade amplitude and velocity, whereas latency often is normal. Saccadic gain and smooth pursuit gain are significantly decreased… An increased frequency of square wave jerks is seen in 60% of PSP patients, and these are readily notable during fixation.

Visual Symptoms
Difficulty reading is an especially prominent
complaint because of the downgaze palsy. Diplopia is relatively uncommon because the gaze palsy usually is symmetric. Blurred vision and eye discomfort occur, and these symptoms more likely are related to decreased blink rate and inadequate tear production than to ocular motility disturbances; however, fixation instability and impaired convergence also may contribute.