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Schizophrenia Update - A Free Periodic Newsletter

Series 2, Issue 17 - September 25, 2004

A Summary of Schizophrenia-related News and Events Note: Please forward this newsletter to others who might benefit To Subscribe to the newsletter, enter your email address at: www.schizophrenia.com

To Unsubscribe or change your email address, go to the very bottom of the newsletter and click on the link that says "unsubscribe".

Over 26,000 people who use the Schizophrenia Support Groups out our web site schizophrenia.com - join in today!

Schizophrenia.com is a registered nonprofit organization Letters to the Editor can be sent to the following email address: szwebmaster (at) schizophrenia.com

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TABLE OF CONTENTS

Main News Stories

  1. Misdiagnosis of Schizophrenia - a true story
  2. Stress Hormones Could Play a Role in Schizophrenia
  3. Pressure for Full Disclosure of Drug Trial Results
     
  4. Nasal Spray May Improve Cognition, Memory Loss
  5. New Medicare Rules May Affect You
     
  6. Childhood Schizophrenia and Other Brain Disorders - a public report by the Detroit Free Press
  7. Therapy for Major Disorders Via Telephone Shows Promise
     
  8. Successful Therapy for Cognitive Deficits
     
  9. Job Success Predictors for Schizophrenia Patients
  10. Past Abuse May Be a Common Factor in Psychiatric Disorders
  11. Poor Verbal Memory Linked to Pediatric Schizophrenia
  12. Family Affected by SZ Raises Hope, Awareness, and $$ for Research
  13. Interview with Psychotic Mice Scientists

Selections from the Research Blog

  1. The Safety and Effectiveness of Long-Acting Risperdal
  2. Doctor's Recommendations for Monitoring SZ Patient Health
  3. Low Dose vs High Dose Haldol for First-Episode Schizophrenia

 

 

 

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Advertisement

New Schizophrenia Study - Participate Today!
As one of the largest schizophrenia genetics study ever attempted - this NIMH study needs volunteers who have schizophrenia, as well as their siblings. The National Institute of Mental Health (NIMH) has joined forces with medical schools across the country including UCSD, Harvard, UCLA, Mount Sinai, Univ. of Pennsylvania, Univ. of Washington, and the Univ. of Colorado. Through this collaborative research project we hope to learn more about the genetic basis of schizophrenia. Understanding the genetic components of schizophrenia is crucial to finding out about the risk factors, and heritability of this illness. It may also help us to create more effective treatments, and hopefully, someday, find a cure.

We will not ask you to change your medications in any way. The study lasts about 2 half-days. Participants will be paid for the time spent participating in the study.

For more information please go to: http://www.schizophrenia.com/szresearch.html
 

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Misdiagnosis of Schizophrenia - a true story

For three hellish years this woman was treated for schizophrenia. But a simple blood test could have revealed the real problem. This is a lesson for all - make sure the psychiatrists do the proper medical analysis before you or someone you know is diagnosed with schizophrenia.

A True Story By LUCY LAING

WHEN Kaye Asquith was told she was suffering from schizophrenia, she was a bright young student getting top grades at school. A year later, it was revealed that a terrible mistake had been made. Kaye, now 22, who lives in Barnsley with her mother Janet, 45, a nurse, was suffering from a life threatening brain tumour . . .

MY NIGHTMARE began when I was 14, in the summer of 1995. I'd been a happy person - I loved going to school, had lots of friends and was getting A grades at school. My ambition was to go to university.

But I started feeling miserable and depressed - I didn't want to go out and yet I didn't want to stay inside either. It was as if I was drowning in the middle of the ocean with no one to help me.

I went to see my GP several times but he said I was suffering from depression and gave me antidepressants to take. But they didn't make me feel any better.

My periods also stopped altogether - although I wasn't pregnant. After six months they still hadn't restarted so I went to see my GP again and again he put my problems down to depression.

During the next few months, things got worse. I smashed objects in my room because I felt so angry. My mother Janet was at her wits' end - she didn't know what to do to help me.

I was referred to the Department of Psychiatric Medicine in Barnsley and saw a psychiatric doctor once a week. In the summer of 1997 I was diagnosed as having schizophrenia and I was given a cocktail of medicines to take.

In March 1998, things came to a head. I'd been treated for mental illness and depression for nearly two years but I felt no better.

My mother insisted there must be something physically wrong with me - that I couldn't be schizophrenic. But her protests were brushed aside. I just felt numb inside. Eventually they decided not to section me and I was allowed to go home.

Mum had started sleeping in my bedroom by now - she was so frightened I was going to kill myself. I just wanted to be the happy, bright Kaye again. My weight had ballooned from a size eight to nearly 19st - I was enormous.

Yet my appetite had disappeared. Mum had to force two Weetabix down me at breakfast and persuade me to eat a sandwich at lunchtime, but every mouthful was difficult to swallow.

Mum gave up her job as a seamstress to look after me fulltime because Icouldn't be left on my own.

Finally, in August 1998, Mum had had enough. She could see what a terrible state I was in and knew that the medication I was being given wasn't helping at all.

She wasn't convinced that I had schizophrenia - and she thought the time had come to get some proper answers. She decided that taking a different route might be more beneficial.

So she took me back to the GP and this time demanded that I be referred to a gynaecologist as I hadn't had a period for three years. I was referred to Barnsley Hospital - but this time to a consultant gynaecologist. The first time I saw him, he performed a blood test. The results showed that I had a major hormone imbalance. So he sent me for scans.

The consultant said that the good news was they had found a reason why I was feeling so bad. Then he said that the bad news was that I had a brain tumour.

I ran out of the room sobbing. I thought I was going to die.

I was referred to a specialist at the Royal Hallamshire Hospital in Sheffield where they did more tests and discovered that the tumour wasn't cancerous.

When I saw the consultant he reassured me that he wasn't going to let me die, even though the tumour was lying close to my brain. He said it was the size of a plum and was on my pituitary gland.

This gland lies just below the brain, close to the optic nerve. It is known as the 'master' gland of the body as it controls the functions of many other glands.

The tumour had damaged it so badly that it caused a major hormonal imbalance. That is why I'd been experiencing all the terrible mood swings and depression.

It had also caused the missed periods and weight gain. So I didn't have schizophrenia - and for all those long, dark months I'd been receiving drugs to treat a condition I didn't have.

If the tumour had been left any longer and grown any bigger, it could have killed me.

A test would have revealed the hormone imbalance, a classic sign of a brain tumour like mine. I began daily medication to reduce the size of the tumour and balance my hormone levels.

Within a month I felt much better - more like my old self. Suddenly life seemed worth living again.

Last summer I was working as a holiday representative in Turkey, but while I was there I started to feel unwell again.When I came back, doctors discovered that my tumour is growing again, so I am due to have an operation to remove it. But after eight years I finally feel as though I'm getting my life back on track.

Excerpt Source: London Mail

NOTE: Many disorders - both physical and mental - can include schizophrenia-like symptoms, including thyroid/hormonal disorders, epileptic conditions, brain tumours, dementia, and bipolar disorder. The first step in getting a correct and accurate diagnosis is seeing a good doctor and/or psychiatrist who is familiar with schizophrenia and all the other conditions that show overlapping symptoms. See our FAQ guide - what to do if you think someone may have schizophrenia or a psychiatric disorder - to learn how to find a good doctor, how to communicate essential information about symptoms and ask your questions, and what sort of tests to expect.
 

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Stress Hormones Could Play a Role in Schizophrenia

New research suggests that the over-producuction of stress hormones could be responsible for physical changes to the brain in people with schizophrenia.

In a world-first study of 18 to 24-year-olds at high risk of developing a psychotic illness, researchers at the Melbourne Neuropsychiatry Centre and Orygen Research Centre have found that those who develop schizophrenia have a larger pituitary gland at the base of their brains than those who do not develop the illness.

This was also true for those who developed psychotic depression. Psychotic disorders such as schizophrenia are more likely to become apparent in early adulthood than at any other stage of life.

Melbourne University neuropsychiatry professor Christos Pantelis said the hormone cortisol, which is active in response to stress, could damage the brain.

The find could pave the way for early diagnosis, preventative tactics and new treatments for schizophrenia and other psychotic illnesses.

Professor Christos Pantelis said it suggested that high levels of stress at the beginning of the illness may have an affect on the brain.

"It may be that developing ways to treat the illness early as well as reduce
stress may prevent some of the brain changes," he said.

In the early stages of schizophrenia -- which usually develops in a person's late teens or early 20s -- physical changes occur in the region of the brain responsible for behaviour, memory and emotion.

The researchers are currently examining the levels of stress hormones circulating in the bodies of people with different psychotic illnesses.

The findings were released yesterday at the opening of the Melbourne (Australia) Neuropsychiatry Centre at the Royal Melbourne Hospital. While it was not yet clear if the enlarged pituitary gland was a cause or an effect of the brain changes observed, Professor Pantelis said the onset of psychotic conditions was highly stressful for young people and "they may be more vulnerable to the effects of the stress".

I like the notion of the integration of the psychological (stress) and the biological (pituitary gland).

If the findings on the pituitary gland are confirmed it may be possible to inhibit the production of cortisol and stop its damaging effects. Professor Pantelis hopes the changes seen in the earlier MRI work will also enable researchers to detect changes in the brain at the earliest onset of the condition.

David Castle of the Mental Health Research Institute said the initial findings of the team on the changes to the hippocampus were very important.

"I think all these things are pushing back the frontiers, really, and I like the notion of the integration of the psychological (stress) and the biological (pituitary gland)," he said.

Professor Castle said there was still much to be learnt about schizophrenia, saying the unknown outweighed the known. Professor Pantelis' group, with Orygen, is now planning to look at brain changes that might occur earlier in life in those at high risk of psychotic illness

Source: British Journal of Psychiatry (july, 2004 Issue), The Daily Telegraph (Sydney, Australia) and other news stories.

 

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Pressure for Full Disclosure of Drug Trial Results
 

Currently, there is no law requiring drug companies or other research entities to publish all data from their clinical trials. This can lead to biased reporting, as companies may only make public the most favorable studies. However, due to increasing criticism from patient and physician groups, this may soon come to an end.

For example, a new piece of legislation meant to force total disclosure of research data may make an appearance on Capitol Hill this week. According to the bill, the Institutional Review Board (IRB) would require all studies of new therapies to register their trials in a public database at the National Library of Medicine.

Both patients and physicians have expressed concern over the current policies, which don't require reporting of all study results. The recent focus on side-effects of antidepressants in children (whether SSRIs might raise suicide risks) is one such example of how withholding information might harm consumers.

Some clinicians also feel strongly that they should have access to all data, so they can prescribe therapies with maximum benefit potential and minimum risk. For example, with public disclosure of all study data, doctors might have a better idea of when a medication could work for an "off-label" purpose (i.e., a condition that the medication is not primarily approved for).

Joining the campaign for full disclosure are leading medical journals that publish research studies. Just recently, 12 leading journals (among them the prestigious New England Journal of Medicine and the Journal of the American Medical Association), have announced that they will only publish drug trials from companies that have publicly registered their study and all its results.

"We're tired of only receiving [for publication] studies that the pharmaceutical companies want published," said Catherine DeAngelis, JAMA's (Journal of the American Medical Association) editor-in-chief. "They're hot to tell us about studies that go the right way; we want them to be just as hot to tell us about the studies that don't."

The pharmaceutical giant GlaxoSmithKline is feeling the brunt of this contraversy; a recent high-profile lawsuit from New York Attorney General Eliot Spitzer accused the company of publishing bias with a drug used to treat major depressive disorder in children. GlaxoSmithKline denied the charges, but the company now voluntarily posts results from all trials in a public database.

For the full story, see "New bill targets drug data disclosure" - Sept 8, 2004. Available at http://www.cbsmarketwatch.com

Read a New York Times (http://www.nytimes.com) editorial - "For Honest Reports of Drug Trials" (Sept 11, 2004).

View GlaxoSmithKline's Clinical Trials Register, in which all company trial data is available to the public. (http://ctr.gsk.co.uk/welcome.asp)

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Nasal Spray May Improve Cognition, Memory Loss

Source: Daily Mail (UK)

Doctors have successfully used a nasal spray based on insulin to improve memory for the first time. Men and women who used the spray remembered twice as many test words after two months than those using a dummy spray. They also felt happier, fitter and more self-confident according to the report by Roger Dobson.

This treatment may eventually be used by people with schizophrenia to improve the cognitive deficits that are a common symptom of the disease. New research has shown that verbal memory deficits may be a predictor of childhood-onset schizophrenia, and poor verbal memory has been cited in literature as a specific cognitive loss in schiziophrenia patients.
 

Read a full news article about the spray: Intranasal Insulin May Alleviate Memory Loss in Elderly and Alzheimer's Patients (http://www.pslgroup.com/dg/23e1f2.htm).

 

 

 

 

 

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New Medicare Rules May Affect You

New Medicare drug-benefit rules in the USA may impact You - The Government is Seeking Public Feedback.

The Medicare Modernization Act, enacted last year and taking effect in January 2006, represents a fundamental change in the 40-year-old entitlement program. It creates a $ 400 billion prescription drug benefit for elderly people and some people with disabilities and gives private insurers a huge new role. For the first time, private-sector drug plans will administer the benefit through a competitive model

One big issue for the mental health field is the way the benefit will treat people who quality for both Medicare and Medicaid. Called "dual eligibles," these beneficiaries are thought to number about 6.4 million. Up to 40 percent are estimated to have a serious mental illness such as bipolar disorder or schizophrenia. Currently, only Medicaid carries a prescription drug benefit for them.

Dually eligible beneficiaries will see their drug coverage shift from Medicaid to Medicare over time.

The National Alliance for the Mentally Ill (NAMI), worries that dually eligible beneficiaries could find their drug access more limited than it is now. This could happen if the formularies allowed under Medicare are more restrictive than the drug coverage that beneficiaries could obtain through Medicaid, or if the Medicare formularies fail to include a drug that has been covered through Medicaid.

"NAMI would like to see a continuity-of-care requirement" that would prohibit the new Medicare plans from denying people effective medication as they make the transition from Medicaid, Andrew Sperling, NAMI's director of federal legislation stated recently.

"At the very least, the regulations must ... 'grandfather in' this coverage," states a letter from NAMI to CMS Administrator Mark B. McClellan, M.D., Ph.D.

The notice currently does not contain such a requirement. NAMI will work to see that such a requirement is added and will work to ensure that the new regulations allow the greatest access to the broadest range of treatments for mental illness.

Another big issue for the field involves the way that drug formularies will be devised for the new Medicare plans. The regulations and law allow for health insurers to use Pharmacy and Therapeutics Committees to design their formularies and coverage plans. The committees' composition and authority, and the requirement that they must be independent and free of conflict of interest, are discussed in the notice.

But the regulations don't require the committees to conduct their business in "an open, transparent process with public meetings," according to NAMI. "We'd like to see openness and transparency in the process," Sperling said.

A highlight in the regulations, Sperling said, is CMS's decision to name the U.S. Pharmacopeial Convention, Inc. (USP), of Rockville, Md., to develop model guidelines to be used as a framework for insurers as they design their prescription drug formularies. The guidelines will include therapeutic categories and classes of drugs to be covered.

For more information, see Centers for Medicare & Medicaid Services, at: www.cms.hhs.gov/medicarereform
 

 

 

 

 

 

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Childhood Schizophrenia and Other Brain Disorders - a public report by the Detroit Free Press
 

This month, The Detroit Free Press is starting a three part series on Children in Crisis: Mental Health,". It is an important, but disturbing report - and is valuable reading for families, support groups, and especially public policy makers.

The series is available at www.freep.com/specials

So far, Michigan has settled for a sort of mental health shuffle board. Some kids are lucky enough to have their problems spotted and be referred for managed mental health care. A great many, though, are far less fortunate. They either go un-cared for or are shuffled into juvenile detention, foster care or jails -- all overburdened systems that are ill-equipped to diagnose, let alone care for, children with schizophrenia, bipolar disorder or depression.

Much of the problem is that Michigan is like a dog chasing its tail on this issue. If the state had a method, which it incredibly does not, of accurately counting each child in need, legislators might understand the consequences of
inadequately funding the Department of Community Health. They might even see the danger in the shortage of state-run psychiatric hospitals for young people. Once there were six, now only one.

 

 

 

 

 

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Therapy for Major Disorders Via Telephone Shows Promise

Although treatments for many psychiatric disorders are much improved in the last fifty years, the majority of sufferers still struggle to find something that consistently works for them. For example, in the estimation of Dr. Allen Roses, an academic geneticist from Duke University, only 60% of schizophrenia patients treated with medication respond (Source: "Glaxo chief - our drugs do not work on most patients." The Independent, Dec 8 2003. No details were given as to the type of medication administered, the length of time meds were taken, or other therapies concurrent with medication). If medication alone is still largely hit-or-miss, than it's more important than ever to coordinate community health resources and make all kinds of therapies available. A recent study has brought one such therapy to light - the possibility of recieving counseling sessions by telephone.

In the journal article (published in the Journal of American Medicine), the recovery rates for clinically depressed patients taking anti-depressant drugs were significantly improved by telephone counseling sessions during the week.

600 subjects taking antidepressants were randomly assigned to recieve one of three treatment plans: a normal standard of care (a prescription, instructions, and encouragment to use it properly), telephone management (two phone calls with advice and support concerning the prescription, or phone therapy (up to eight telephone sessions with trained counselors providing targeted behavioral therapy). The results from the telephone therapy group were very encouraging - after 18 months, 80% of these subjects reported that their symptoms were "much improved." 66% of subjects recieving just telephone management reported similar improvement, while only 55% of those just receiving medication said the same.

Although it is not clear how many people might benefit from telephone therapy - the study subjects were all independently motivated to seek treatment, and were medication compliant - primary investigator Dr. Gregory E. Simon is excited by the potential in the results.

"This represents an important change in the way we approach treatment," Dr. Simon said, "not only using the phone, but being persistent, proactive, reaching out to people and finding them where they are. Depression is defined by discouragement; very often they're not going to come to you."
Telephone therapy could have many implications, among them improving medication compliance, supplementing existing medication regimens, and extending the reach of mental health services. Stigma is a huge barrier to therapy, particularly in small or rural communities where remaining anonymous is a challenge. Telephone therapy might offer a more secure, less stigmatizing alternative to people seekign support.

Regular follow-up with phone sessions might also help prevent tragedies such as suicide. According to Joanne Stern, who gave a workshop on suicide prevention (on behalf of SPAN-CA) at the NAMI California annual convention in August, good follow-up care is a key component of prevention. In her experience as a suicide-hotline staffer, suicidal feelings are generally lessened through talk. In her own words, "Talk is the breath of life to someone who's drowning."

For the full article, see "New Therapy on Depression FInds Phone Is Effective" (Aug 25 2004) in the New York Times (http://www.nytimes.com).

For more information on the specific efficacy of psychotherapy in treating schizophrenia, see the following Psychiatric Times article: "Medication-Psychotherapy Combination Most Effective for Schizophrenia" (published in Psychiatric Times, May 1998, Vol XV, Issue 5).

For some supplemental treatments that may be helpful for schizophrenia when combined with medication therapy, see Other Treatments on the schizophrenia.com website (http://www.schizophrenia.com/treatments.htm).

 

 

 

 

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Successful Therapy for Cognitive Deficits

According to new research published in this month's Archives of General Psychiatry, cognitive rehabilitation can lead to major improvements for patients with stable schizophrenia. This is promising news, given the inability of most anti-psychotic medications to consistently or dramatically improve the negative, or social/cognitive, symptoms of schizophrenia.

According to the research team, cognitive therapy is most beneficial to patients with controlled symptoms and reduced relapse risk, but with lingering social and cognitive deficits.

In their study, the team examined the potential benefits of two types of cognitive therapy with a pool of 121 symptomatically-stable schizophrenia/schizoaffective disorder patients. The subjects recieved either "cognitive enhancement therapy," an approach that combines neurocognitive training (via computer programs) with social cognitive group exercises, or "enriched supportive therapy," which uses coping strategies and patient education to improve individual illness management.

After 12 months, results showed that the Cognitive Enhancement Therapy group had major improvements in processing speed and neurocognition (esp. improved verbal memory and some problem-solving skills), and modest improvements in cognitive style, social cognition, and social adjustment. This improvement trend continued over an additional 12 months.

Patients recieving enriched supportive therapy did not show such a dramatic cognitive advance, although there were still measurable neurocognitive and behavioral improvements.

The researchers optimistically concluded: "[t]he cognitive disabilities of schizophrenia do not need to be the persistent deficits described in numerous naturalistic, longitudinal studies. Instead, many of these disabilities are capable of improvement after adequate exposure to cognitive rehabilitation."

For the full story, see "Cognitive rehabilitation shows robust benefits for schizophrenics" Sept 10, 2004. Available at http://www.psychiatrysource.com


Read the published research online:
"Cognitive Enhancement Therapy for Schizophrenia: Effects of a 2-year Randomized Trial on Cognition and Behavior" (Arch Gen Psychiatry, 2004;60:866-876).

Cognitive therapy has shown much promise as a form of psychotherapy for schizophrenia patients. See the articles below for details:

1. Cognitive Therapy for Schizophrenia. (http://www.psychologyinfo.com/schizophrenia/cognitive.htm).

2. Cognitive-Enhancement Therapy - an overview of the basic principles, and how it can be effective in treating schizophrenia. (http://planneohio.org/overview.htm)

3. Computer-Assisted Cognitive Rehabilitation Reduces Negative Symptoms in the Severely Mentally Ill. (http://www.braintrain.com/captains_log/schizophrenia_treament.htm).

 

 

 

 

 

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Job Success Predictors for Schizophrenia Patients

A team from Indiana University-Purdue University Indianapolis suggests that the job performance of schizophrenia patients may be more affected by the extent of their cognitive impairments than on the availability of vocational rehabilitation.

The team interviewed 112 schizophrenia patients enrolled in employment programs, and tested them for verbal learning and memory skills, attention, information processing ability, and executive functioning.

After four months, results showed that patients with higher neuropsychological profile scores had better work behaviors, including work habits, personal presentation, work quality, social skills, cooperativeness, number of hours worked per week, and wages earned.

Jovier Evans, primary investigator for the team, emphasizes that both cognitive ability and vocational support resources essentially contribute to the job success of schizophrenia patients.

"Vocational services seem best equipped to help people get jobs, but do not necessarily help clients in the performance of their duties on the jobs," note Evans et al in the journal Schizophrenia Research.

For the full article, see "Cognitive measures predict schizophrenic job success" (Sep 3 2004) at http://www.psychiatrysource.com

For more information about returning to work after a diagnosis of schizophrenia, please see the following links:

1) Can a person with schizophrenia return to work/school? - information and suggestions for a smooth transition

2) Work-related resources for people with disabilities - on the schizophrenia.com website, under the Recovery and Resources section. Once on the page, scroll down to the Resources for Returning to Work section.

 

 

 

 

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Past Abuse May Be a Common Factor in Psychiatric Disorders

A UK research team reported in the British Journal of Psychiatry (2004:185:220-226) that psychosis is more common among people who have a significant number of traumatizing events in their past. The findings were based on a data analysis the 2nd British National Survey of Psychiatric Morbidity.

The team concluded that such negative social events may play a role in the development of psychotic symptoms. In reality, it's difficult to determine cause and effect - perhaps the characteristics of psychosis bring about traumatizing events as a result, or perhaps people with psychosis report hallucinations they experience as real events.

According to the data, the most common trauma experienced by those with psychosis was sexual abuse, followed by being institutionalized during childhood, running away from home, being homeless, or being taken into local authority care.

However, as there does seem to be some correlation between social trauma and psychosis, healthcare providers should put an emphasis on cognitive-behavioral therapy for these patients to address such early trauma events.

For the full article, please see "Psychosis emerges in people subjected to victimizing events" (Sept 3 2004) at www.psychiatrysource.com
 

 

 

 

 

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Poor Verbal Memory Linked to Pediatric Schizophrenia
 

Recent research from the National Public Health Institute in Finland suggests that childhood-onset schizophrenia appears to be linked to more specific cognitive deficits than adult-onset, which involves more generalized deficits.

Children with early-onset schizophrenia had poorer verbal memory function (according to testing with the California Verbal Learning Test, the Wechsler Memory Scale, and the Weschler Adult Intelligence Scalle) than older people with schizophrenia. The study included a total of 237 schizophrenia patients, ranging in age from 13 to 44 years.

The specific verbal deficits included poorer word recall, poor ability to group words into appropriate categories, and poorer word recognition. However, overal working memory performance (general, not specifically verbal) and IQ measures did not differ significantly based on age of onset.

Researchers also noted that although people who have lived with schizophrenia longer have a more marked cognitive decline overall, this still did not offset the fact that children with schizophrenia performed more poorly on verbal-memory tasks specifically.

The article, recently published in the British Journal of Psychiatry (2004:185:215-219) concludes: "Verbal memory deficits – known to be highly associated with functional outcome in schizophrenia – should particularly be taken into account in the neuropsychological evaluation and efforts at remediation in patients with early-onset disorder."

For the full article, see "Age at schizophrenia onset linked to verbal memory deficits" Sept 8, 2004. Psychiatry Source (http://www.psychiatrysource.com).

Read the published study online - available at http://bjp.rcpsych.org/cgi/content/abstract/185/3/215

For further research on this topic, see the following:

1) Neurocognitive Testing of Patients with Schizophrenia - Why? (available at http://www.astrazeneca.no).

2) Neuropsychological deficits in children associated with increased familial risk for schizophrenia. Available at http://www.pubmed.com

3) Childhood developmental abnormalities in schizophrenia: evidence from high-risk studies. Available at http://www.pubmed.com

 

 

 

 

 

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Family Affected by SZ Raises Hope, Awareness, and $$ for Research

Brandon Staglin had a bright and promising future. As a child, he skipped grades at school, had a perfect GPA, stellar test scores, and a high IQ. As a national merit scholar and with aspirations of being an astronautical engineer at age 18, his descent into schizophrenia was sudden and stunning to him and to those who knew him. Within his first week of showing symptoms, he was picked up by the police for wandering around the town of Lafayette and put in a mental institution.

From the day his parents rushed home from a business trip in Paris to collect their son, the family started down a tumultuous and frightening road together.

"We thought there was a huge mistake," says Brandon's mother, Shari Staglin. "There was confusion, fear. We took him home from the hospital, and I remember him saying there was something wrong with his bed. He kept doing this unusual action with his hand."

Garen Staglin, Brandon's father, agreed. "He couldn't function. He was hearing voices that were tormenting him. He couldn't get rid of incoherent thoughts."

After his initial break in 1990, it appeared that Brandon might beat the odds of his illness, and go on to fulfill all his previous potential. He returned to Dartmouth and graduated in 1993 as an anthropology/engineering science major. Working first as a marketing analyst and then as an astronautical engineer, he planned to get his master's degree in engineering.

In 1996, he had his second major break.

"It was a new manifestation of my disease," said Brandon. "I would hallucinate pain. It started in my upper left forehead. Eventually I was experiencing stabbing pain in my stomach. The pain was so bad that I couldn't walk. I couldn't eat. It felt like a spear was going into my stomach."

Brandon checked into an out-patient psychiatric hospital at UCSF, and battled with his illness. Many times he had to pull himself back from the brink of suicide.

From watching and participating in their son's struggle, the Staglin's were moved to make a major contribution to the schizophrenia community. Through connections in venture capitalism, they initiated the Music Festival for Mental Health in 1994. Most of the $90,000 raised from the event was given to the National Alliance for Research on Schizophrenia and Depression.

Today, the Staglins remain in contact with leading schizophrenia researchers, and have created an international council of scientists on the topic of schizophrenia. Their newest project is to offer a $250,000 grant to an young up-and-coming researcher (under the age of 45) who has a promising breakthrough project planned around schizophrenia.

Other projects funded by the Staglins include an endowed professorship at UCLA, and a pilot program at UCSF that uses software programs to provide intensive therapy training to schizophrenia patients.

Besides their generosity and activism, the Staglins have done much to break down the barriers of stigma. "They have decreased the stigma of mental illness," says Craig Van Dyke, chairman of the UCSF Dept. of Psychiatry. "In telling their story, they are giving other families hope."

The Staglin's continue to stress that they do what they do for their son. Today, 34 year-old Brandon is stable on a regimen of medications. He manages his own illness, setting his watch timer to remind him of his meds, and works independently as a writer and a web designer. But he is still troubled by common banes that affect many schizophrenia patients - emotional flatness that isn't helped by medication, apathy where there once was energy.

"I'm not the dynamo I once was, but I'm feeling warmth again," Brandon says. "I wrote a poem called 'To Live on The Moon.' It's about the sun rising in my mind, about my starting to feel passion again, about starting to feel ambition."

Why did I love to live on the moon?
Cold, remote, desolate
Yet magnificent, claimed one whom I followed
So easy it is to take life hard
So natural to be lost
So long as you don't realize it
Some part of me was talent latent
And I don't think it is now
The sun's limb warms my eyelids
Thaws my hands
Without ice, I'll need new material
The ground is still slippery
How to get up and run
God, can I even remember?

For the full story, please see "A family's journey to madness and back: Son's schizophrenia spurs parents to raise millions for research" (Sept 7 2004). San Francisco Chronicle (http://www.sfgate.com).

To read other stories of hope and success from people with schizophrenia, please see "Success Stories" on the Schizophrenia.com website (http://www.schizophrenia.com/success.html)

 

 

 

 

 

 

 

 

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Interview with Psychotic Mice Scientists

As we've covered before in our Daily Schizophrenia Blog, the recent development of genetically alterred laboratory mice that develop schizophrenia may offer insights into the cause of schizophrenia. Here is a brief interview with one of the researchers involved:

Q: What makes mice psychotic other than the looming presence of an
unfriendly feline.

A: In this case the rodents have genetically engineered mutations in two genes.

Q: How do they know which genes to tweak?

A: The mutations are the same as those found in a Canadian family with a history of schizophrenia. The genes concerned are called NPAS1 and NPAS3.

Q: Who is doing this?

A: Dr Steven McKnight and a team from the University of Texas Southwestern Medical Centre and the Children's Hospital Medical Centre in Cincinnati.

Q: What happened?

A: The mice without a working copy of the genes displayed erratic behaviour. When introduced to other mice, instead of climbing over them and sniffing them, they began darting about, trying to avoid them.

Q: So?

A: When the University of Texas research team examined the brains of the psychotic mice, they found an abnormally low level of a protein called reelin,
important in embryonic development of the brain and brain cell signalling.

Q: What has all this to do with schizophrenia?

A: Studies of people who died with schizophrenia have found reduced levels
of reelin in their brains.

Q: So now schizophrenics know they have something in common with psychotic mice. How can that possibly help them?

A: The link may help pharmaceutical companies come up with better therapies. Schizophrenia is a condition that affects around 24 million people worldwide. They experience disrupted thoughts and behaviour and sometimes delusions.


Source: An excerpt from a story in The Herald, Glasgow, Ireland

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The Safety and Effectiveness of Long-Acting Risperdal

Safety and Efficacy of Long-Acting Risperidone in Schizophrenia: A 12-Week, Multicenter, Open-Label Study in Stable Patients Switched From Typical and Atypical Oral Antipsychotics.

Lindenmayer JP, Eerdekens E, Berry SA, Eerdekens M.
J Clin Psychiatry. 2004 Aug;65(8):1084-1089.

Pharmaceutical companies have recently been touting long-acting injectable medications as the answer to maintaining reliable, consistent levels of medication and helping with preventing relapse through medication compliance in those with schizophrenia. Risperidone has been the first such atypical medication available in such a long-acting injectable form. This study aimed to look at the safety and effectiveness of this type of medication in a clinically stable group of people with schizophrenia. The study involved a 12 week open label, multicenter, exploratory clinical trial, where they collected data from a from clinics, hospitals, and physicians' offices.

Participants with schizophrenia entered a 4 week period where they continued to receive the same dose of their current oral medication (which was Haldol, Seroquel or Zyprexa). They received 25mg of long acting injectable risperodone at baseline and then every 2 weeks, with allowance for the doctor to change the dose upto a certain point. Safety measurements were based on the patient’s self-report, clinical observation, lab reports and physical exams. They measured the effectiveness of the medication based on symptom checklists (PANSS & CGI).

The authors report that long-acting risperidone was well tolerated. Of the 141 patients who completed the study, the most frequently reported adverse events were insomnia (16%), headache (15%), psychosis (11%), and agitation (11%). There was a slight increase in body weight (0.4 kg). 5 patients experienced adverse effects that resulted in the discontinuation of the study and a few experienced serious side effects that that included psychosis and agitation. The authors do not report any significant lab abnormalities or ECG results. They also report that the severities of certain side effects (extrapyramidal symptoms) were reduced during treatment and there were improvements in symptoms of schizophrenia that started during the 4th week and continued through the 12-week period.

Limitations of this study are the open label and lack of a control group. This means that the raters were not blind to the medication the patients were on, and this could have biased their ratings of symptoms. Also, since this study allowed other medications to be used at the same time, it is difficult to parse out the unique contributions of the injectable risperidone while the flexible dose approach used could have also biased the results.

The authors have disclosed financial support from Lilly, Pfizer, Janssen, AstraZeneca, Bristol Myers-Squibb, Repligan & Johnson & Johnson (see article for details

Click here to link to PubMed for this article

 

 

 

 

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Doctor's Recommendations for Monitoring SZ Patient Health

Physical health monitoring of patients with schizophrenia.

Marder SR, Essock SM, Miller AL, Buchanan RW, Casey DE, Davis JM, Kane JM, Lieberman JA, Schooler NR, Covell N, Stroup S, Weissman EM, Wirshing DA, Hall CS, Pogach L, Pi-Sunyer X, Bigger JT Jr, Friedman A, Kleinberg D, Yevich SJ, Davis B, Shon S.
Am J Psychiatry. 2004 Aug;161(8):1334-49.

Individuals with schizophrenia seem to have a 20% shorter life expectancy than the population and have more vulnerability to illnesses such as diabetes, coronary heart disease, hypertension, and emphysema. This could be because of lifestyle choices (eg poor dietary habits, obesity, high rates of smoking, alcohol and street drugs) and side effects from certain antipsychotic medications (prolactin elevation, cataract formation, movement disorders, sexual dysfunction, weight gain, onset of diabetes, increases in plasma lipids, and abnormal ECGs).

A conference was organized by some who believed that the health needs of people with schizophrenia who take antipsychotic medications are not adequately addressed by clinicians in specialty mental health programs or in primary care settings. This Mount Sinai Conference (2002) aimed to develop recommendations for the systematic health monitoring of individuals with schizophrenia for whom antipsychotic medication is prescribed. This was based on a consensus meeting of leading psychiatric and other medical experts who evaluated the existing literature and developed recommendations for physical health monitoring of patients with schizophrenia. They reviewed the following areas: 1) weight gain and obesity; 2) diabetes; 3) hyperlipidemia; 4) prolongation of the QT interval on the ECG; 5) prolactin elevation and related sexual side effects; 6) extrapyramidal side effects, akathisia, and tardive dyskinesia; 7) cataracts; and 8) myocarditis.

Their consensus recommendations were as follows: regular monitoring of body mass index, plasma glucose level, lipid profiles, and signs of prolactin elevation or sexual dysfunction. They recommend that information from monitoring should guide the selection of antipsychotic agents. Specific recommendations were also made for cardiac monitoring of patients who receive medications associated with QT interval prolongation, including thioridazine, mesoridazine, and ziprasidone, and for monitoring for signs of myocarditis in patients treated with clozapine. They suggested that patients who receive both older and newer antipsychotic medications should be examined for extrapyramidal symptoms and tardive dyskinesia and receive regular visual examinations.

It is worthwhile to retrieve this article and look through their specific recommendations (Table 1 in the article). This can help with being well informed during clinical appointments with doctors – especially since the conference recommended that mental health care providers be involved in performing physical health monitoring since not all patients receive such physical health monitoring in their primary care settings.

The consensus meeting on which this article is based did not receive financial support from the pharmaceutical industry. However, individual conference participants have disclosed support from various pharmaceutical companies. See the article for full list.

Click here to link to PubMed for this article

 

 

 

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Low Dose vs High Dose Haldol for First-Episode Schizophrenia

Oosthuizen P, Emsley R, Turner HJ, Keyter N. A randomized, controlled comparison of the efficacy and tolerability of low and high doses of haloperidol in the treatment of first-episode psychosis The International Journal of Neuropsychopharmacology (2004), 7:125–131

This study was conducted to determine which of two doses of haloperidol (Haldol) would be more effective for patients who are new to schizophrenia. In America, we are quick to go to second generation antipsychotics like Risperdal or Zyprexa, but outside of the US, Haldol is still used frequently because of its cost effectiveness and its high potency. People often stay away from Haldol because of the greater risk for side effects like tardive dyskinesia (a movement disorder) and other long term side effects. Also, since Haldol is older and off patent, it is not marketed and can sometimes be forgotten. There are some who argue that the new antipsychotics are only marginal improvements and therefore we are quick to ignore Haldol. Anyways, regardless of the debate, these authors wanted to know if a higher dose of Haldol was better to give or if it would be just as effective but more likely to give side effects.

The authors chose to compare a 2mg per day of Haldol group versus an 8 mg per day group. They came up with those doses based on previous data that suggested that 8 mg was a threshold dose for the initiation of side effects. The authors ultimately found that 2mg and 8mg were equally effective but that the 8mg group did have some higher side effects. One side effect was an increase in prolactin (a hormone that is involved in production of breast milk and in growing breast tissue.) They also showed that both groups had movement disorders (called EPS or parkinsonian movments) but that 8mg was worse than 2mg. They also thought that the 2mg did marginally better on negative symptoms than did the 8mg group.

Overall, this study is interesting because in many situations it is worthwhile, though debatable, to consider starting with Haldol first when someone has new symptoms requiring treatment with an antipsychotic. While it is probably better to try a 2nd generation antipsychotic first when available one can see treatment effects from Haldol. It would be better based on these data to start at 2mg per day than a higher dose though individuals vary such that it may be necessary to start at 5mg daily or higher doses if the psychotic symptoms don’t remit. If you or someone you know is on Haldol, you should not consider changing the dose based on this study but if you have questions you can ask your doctor.

This study was supported by the Medical Research Council of South Africa.

Click here to link to the article on Pubmed

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