

 
Reviewed by John M. Grohol, Psy.D. on May 19, 2010
A provocative theory on the effect of strategies used to cope with stress may explain mental and physical health variations among ethnic groups.
When people are under chronic stress, they tend to smoke, drink, use drugs and overeat to help cope. These behaviors trigger a biological cascade that helps prevent depression, but they also contribute to a host of physical problems that eventually contribute to early death.
University of Michigan social scientist James S. Jackson and colleagues discuss the hypothesis in an article published in the American Journal of Public Health.
The theory helps explain a longtime epidemiological puzzle: why African-Americans have worse physical health than whites but better psychiatric health.
Read in Full:Â http://psychcentral.com/news/2010/05/19/coping-strategies-help-mental-harm-physical-health/13932.html
 
ScienceDaily (May 19, 2010) — A newly published study reported that children with new/recent onset epilepsy have significantly slowed expansion of white matter volume compared to healthy children over a two year interval. The reduced white matter volume may affect brain connectivity and influence cognition.
Results of this study conducted by researchers from the University of Wisconsin School of Medicine and Public Health are now available online and will appear in the July issue of Epilepsia, a journal published by Wiley-Blackwell on behalf of the International League Against Epilepsy.
Epilepsy, a common nervous system disorder, frequently develops in early childhood and causes recurrent seizures. Seizures can range from mild staring spells to major convulsions. According to the Epilepsy Foundation there are 326,000 children under the age of 15 with epilepsy in the U.S. More than 45,000 new cases of epilepsy are diagnosed in children each year.
A research team, led by Bruce Hermann, Ph.D., investigated the neurodevelopmental changes in brain structure in children with new or recent-onset epilepsy. Thirty-four healthy children (control group) and 38 with new/recent onset epilepsy were enrolled in the study. The epilepsy group contained 21 children with localization-related epilepsy and 17 with idiopathic generalized epilepsy. Children in both groups had a mean age of 12.9 years and underwent magnetic resonance imaging (MRI) at baseline and 2 years later.
At the 2 year follow-up, seizure frequency was evaluated. During the prior year, 53% of children with epilepsy were seizure free; 34% reported only one seizure. In the remaining children with epilepsy, 5% reported monthly, 5% weekly, and 3% daily seizures.
“Our study determined that children with new or recent-onset epilepsy exhibited an altered brain development pattern characterized by delayed age-appropriate increase in white matter volume,” said Dr. Hermann. The research team found that total cerebral white matter volume increased significantly in the healthy control group over the 2-year period. However, the epilepsy group did not show significant change in white matter volume in the total cerebrum and across all lobes — the difference from normal controls being most pronounced in the frontal lobes.
Researchers suspect that the delayed white matter volume increase in children with epilepsy may affect cognitive development by reducing brain connectivity. With altered brain development, children with epilepsy may also experience impaired executive function — mental tasks such as organizing, planning, and paying attention which are commonly reported in people with epilepsy.
“Research into the symmetry between patterns of cognitive change and age-appropriate brain development remains to be addressed in childhood epilepsy,” concluded Dr. Hermann. “Further exploration of how subtle neurodevelopmental alterations in brain development affect cognition is needed. Longer term follow-up is also needed to determine whether this finding represents a temporary delay in brain development versus a fixed difference.”
Journal Reference:
- Bruce P. Hermann, Kevin Dabbs, Tara Becker, Jana E. Jones, Adan Myers y Gutierrez, Gary Wendt, Monica A. Koehn, Raj Sheth, Michael Seidenberg. Brain development in children with new onset epilepsy: A prospective controlled cohort investigation. Epilepsia, 2010; DOI: 10.1111/j.1528-1167.2010.02563.x
http://www.sciencedaily.com/releases/2010/05/100519081554.htm
 
ScienceDaily (May 19, 2010) — A newly published study reported that children with new/recent onset epilepsy have significantly slowed expansion of white matter volume compared to healthy children over a two year interval. The reduced white matter volume may affect brain connectivity and influence cognition.
Results of this study conducted by researchers from the University of Wisconsin School of Medicine and Public Health are now available online and will appear in the July issue of Epilepsia, a journal published by Wiley-Blackwell on behalf of the International League Against Epilepsy.
Epilepsy, a common nervous system disorder, frequently develops in early childhood and causes recurrent seizures. Seizures can range from mild staring spells to major convulsions. According to the Epilepsy Foundation there are 326,000 children under the age of 15 with epilepsy in the U.S. More than 45,000 new cases of epilepsy are diagnosed in children each year.
A research team, led by Bruce Hermann, Ph.D., investigated the neurodevelopmental changes in brain structure in children with new or recent-onset epilepsy. Thirty-four healthy children (control group) and 38 with new/recent onset epilepsy were enrolled in the study. The epilepsy group contained 21 children with localization-related epilepsy and 17 with idiopathic generalized epilepsy. Children in both groups had a mean age of 12.9 years and underwent magnetic resonance imaging (MRI) at baseline and 2 years later.
At the 2 year follow-up, seizure frequency was evaluated. During the prior year, 53% of children with epilepsy were seizure free; 34% reported only one seizure. In the remaining children with epilepsy, 5% reported monthly, 5% weekly, and 3% daily seizures.
“Our study determined that children with new or recent-onset epilepsy exhibited an altered brain development pattern characterized by delayed age-appropriate increase in white matter volume,” said Dr. Hermann. The research team found that total cerebral white matter volume increased significantly in the healthy control group over the 2-year period. However, the epilepsy group did not show significant change in white matter volume in the total cerebrum and across all lobes — the difference from normal controls being most pronounced in the frontal lobes.
Researchers suspect that the delayed white matter volume increase in children with epilepsy may affect cognitive development by reducing brain connectivity. With altered brain development, children with epilepsy may also experience impaired executive function — mental tasks such as organizing, planning, and paying attention which are commonly reported in people with epilepsy.
“Research into the symmetry between patterns of cognitive change and age-appropriate brain development remains to be addressed in childhood epilepsy,” concluded Dr. Hermann. “Further exploration of how subtle neurodevelopmental alterations in brain development affect cognition is needed. Longer term follow-up is also needed to determine whether this finding represents a temporary delay in brain development versus a fixed difference.”
Journal Reference:
- Bruce P. Hermann, Kevin Dabbs, Tara Becker, Jana E. Jones, Adan Myers y Gutierrez, Gary Wendt, Monica A. Koehn, Raj Sheth, Michael Seidenberg. Brain development in children with new onset epilepsy: A prospective controlled cohort investigation. Epilepsia, 2010; DOI: 10.1111/j.1528-1167.2010.02563.x
http://www.sciencedaily.com/releases/2010/05/100519081554.htm
 
Article Date: 19 May 2010 – 2:00 PDT
A Swedish investigation has compared choir singing and group discussion in irritable bowel syndrome in the current issue of Psychotherapy and Psychosomatics.
Singing in a choir is very popular in the Nordic countries. This activity has been associated with increased longevity, and it induces feelings of relaxation and energy. Several studies have shown beneficial psychological and/or biological effects of singing. A study has shown that a singing lesson (practicing singing individually) is associated with increases in relaxation, energy and joy, as well as an elevated oxytocin concentration in serum. Low levels of oxytocin have been observed in irritable bowel syndrome (IBS) in adults. IBS is a common gastrointestinal disorder that is influenced by psychological factors. Merely talking to IBS patients about difficult matters may influence endocrine functions of importance to the symptoms. Group-based information events, including group talk as well as behavioural therapy, have been shown to be of some benefit compared to the distribution of written IBS information. Repeated stress responses correspond to reactions that are needed in energy mobilisation. At the same time, anabolic/regenerative processes in the body are inhibited. Anabolic/regenerative processes are reflected for instance in the blood concentration of testosterone. Recently, it has been shown that fluctuations in the ‘free’ blood concentration (not bound to proteins in the blood) of testosterone are closely mirrored in saliva. The anabolic/regenerative activities are of central importance to our ability to withstand adverse effects of long-lasting stress. Accordingly, processes that stimulate anabolic/regenerative processes may reduce the effects of stress. Advertisements for subjects with a verified IBS diagnosis were made in a daily newspaper and in the patient union journal. It was explained before the start that the participants would be randomly allocated either to a choir group meeting or an information/discussion group meeting, in both cases once a week for a year. The choir group met once a week, starting in May 2006 and ending in May 2007. A professional music teacher and music therapist served as the group’s paid leader. The information group also met once a week during the initial stage, but after half a year the frequency of the meetings was reduced to 3 per month. Participants in both groups received information pamphlets (7 books) ‘living with IBS’. After 6 months, there were 16 participants in both groups (corresponding to 56 and 57% in the choir and information groups, respectively). After 12 months, there were 13 participants in the choir (46%) and 14 (52%) in the information group. Saliva sampling took place before the start, and then 6, 9 and 12 months afterwards. On each test occasion, saliva specimens were collected upon awakening, half an hour later, at the end of the working day, before the event (choir and information respectively), after the event, and finally at bedtime (i.e. 6 samples in total). The saliva testosterone concentration was assessed by means of the Spectria RIA (a coated-tube immunoassay for testosterone; Orion Diagnostica Oy, Spoo, Finland).
The ANOVA of saliva testosterone showed a significant time effect, but no difference in means between the groups. In addition, there was a strong 2-way interaction illustrating that the variations in the choir group were significantly more pronounced than those in the information group (F group = 1.36, p = 0.26; F time = 4.06 p = 0.01; F interaction (group X time) = 5.22, p = 0.003). Gender-separated analyses and exclusion of 4 female participants below the age of 50 years (premenopausal ages) made no difference to the results. Saliva testosterone concentration during the waking hours of the day from the choir singers showed an increase after 6 months, when compared to before the interventions. The most likely interpretation is that the highly significant peak in the choir group after 6 months is associated with the intervention itself.
The findings of this study have to be replicated in larger studies. Despite the study’s weaknesses there is a clear indication that choir singing once a week induces a state of stimulated regeneration during the first half-year in IBS patients, but that in this particular case this effect did not last until the end of the year.
 
Article Date: 19 May 2010 – 2:00 PDT
A Swedish investigation has compared choir singing and group discussion in irritable bowel syndrome in the current issue of Psychotherapy and Psychosomatics.
Singing in a choir is very popular in the Nordic countries. This activity has been associated with increased longevity, and it induces feelings of relaxation and energy. Several studies have shown beneficial psychological and/or biological effects of singing. A study has shown that a singing lesson (practicing singing individually) is associated with increases in relaxation, energy and joy, as well as an elevated oxytocin concentration in serum. Low levels of oxytocin have been observed in irritable bowel syndrome (IBS) in adults. IBS is a common gastrointestinal disorder that is influenced by psychological factors. Merely talking to IBS patients about difficult matters may influence endocrine functions of importance to the symptoms. Group-based information events, including group talk as well as behavioural therapy, have been shown to be of some benefit compared to the distribution of written IBS information. Repeated stress responses correspond to reactions that are needed in energy mobilisation. At the same time, anabolic/regenerative processes in the body are inhibited. Anabolic/regenerative processes are reflected for instance in the blood concentration of testosterone. Recently, it has been shown that fluctuations in the ‘free’ blood concentration (not bound to proteins in the blood) of testosterone are closely mirrored in saliva. The anabolic/regenerative activities are of central importance to our ability to withstand adverse effects of long-lasting stress. Accordingly, processes that stimulate anabolic/regenerative processes may reduce the effects of stress. Advertisements for subjects with a verified IBS diagnosis were made in a daily newspaper and in the patient union journal. It was explained before the start that the participants would be randomly allocated either to a choir group meeting or an information/discussion group meeting, in both cases once a week for a year. The choir group met once a week, starting in May 2006 and ending in May 2007. A professional music teacher and music therapist served as the group’s paid leader. The information group also met once a week during the initial stage, but after half a year the frequency of the meetings was reduced to 3 per month. Participants in both groups received information pamphlets (7 books) ‘living with IBS’. After 6 months, there were 16 participants in both groups (corresponding to 56 and 57% in the choir and information groups, respectively). After 12 months, there were 13 participants in the choir (46%) and 14 (52%) in the information group. Saliva sampling took place before the start, and then 6, 9 and 12 months afterwards. On each test occasion, saliva specimens were collected upon awakening, half an hour later, at the end of the working day, before the event (choir and information respectively), after the event, and finally at bedtime (i.e. 6 samples in total). The saliva testosterone concentration was assessed by means of the Spectria RIA (a coated-tube immunoassay for testosterone; Orion Diagnostica Oy, Spoo, Finland).
The ANOVA of saliva testosterone showed a significant time effect, but no difference in means between the groups. In addition, there was a strong 2-way interaction illustrating that the variations in the choir group were significantly more pronounced than those in the information group (F group = 1.36, p = 0.26; F time = 4.06 p = 0.01; F interaction (group X time) = 5.22, p = 0.003). Gender-separated analyses and exclusion of 4 female participants below the age of 50 years (premenopausal ages) made no difference to the results. Saliva testosterone concentration during the waking hours of the day from the choir singers showed an increase after 6 months, when compared to before the interventions. The most likely interpretation is that the highly significant peak in the choir group after 6 months is associated with the intervention itself.
The findings of this study have to be replicated in larger studies. Despite the study’s weaknesses there is a clear indication that choir singing once a week induces a state of stimulated regeneration during the first half-year in IBS patients, but that in this particular case this effect did not last until the end of the year.
 
Article Date: 19 May 2010 – 2:00 PDT
This study formulates the hypothesis that rufinamide, a drug so far used against epilepsy, may also be effective in bipolar disorder, depressive and anxiety disorders, panic disorder and obsessive-compulsive disorder, eating disorders, and substance use disorders. It is just an hypothesis based on two cases that needs to be confirmed by specific studies.
Rufinamide is a triazole derivative indicated in the USA for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in children 4 years and older and adults. Rufinamide has activity in the maximal electroshock model and the pentylenetetrazol test, although the ED 50 (median effective dose) is an order of magnitude higher in the pentylenetetrazol test, and in a wide range of other animal models, including seizures induced by GABA-A receptor antagonists, and models of neocortical epilepsy. Based on in vitro studies, the principal mechanism of action of rufinamide is considered to be the modulation of the activity of sodium channels and, in particular, prolongation of the inactive state of the sodium channel. Rufinamide has a low degree of protein binding (34%), and its half-life is approximately 6 – 10 h, which has led to its recommended twice-daily administration. The most commonly observed adverse experiences seen in association with rufinamide and at a higher frequency than in placebo-treated patients are headache, dizziness, fatigue, somnolence and nausea. This study reports on 2 cases where the off-label use of rufinamide led to marked clinical improvements in patients with complicated psychiatric histories.
The first patient was a woman with bipolar disorder and multiple psychiatric comorbidities (panic disorder, obsessive-compulsive disorder, eating disorder), who had been extraordinarily refractory to treatment and had failed countless pharmacological and nonpharmacological treatment attempts, including ECT. In the context of progressive worsening of her condition, rufinamide 400 mg 1 tablet twice daily was added to her complicated pharmacological regimen, leading to a marked clinical improvement. The patient reported a marked improvement in depressive and obsessive symptoms, a reduction in anxiety and panic attacks, and a significant mood stabilization and reduction in mood swings. The dose was subsequently adjusted to 800 mg twice daily and the patient’s improvement persisted over the following 2 months.
The second patient was another woman with bipolar disorder and multiple psychiatric and medical comorbidities (panic disorder, alcohol abuse, chronic pain) who also had been extraordinarily refractory to treatment and had failed countless pharmacological and nonpharmacological treatment attempts. In the context of an acute worsening of her condition, rufinamide 400 mg 1 tablet twice daily was added to her pharmacological regimen, leading to a very rapid (within days) clinical improvement. The patient reported a marked improvement in depressive and anxiety symptoms, significant mood stabilization and reduction in mood swings, and a reduction in craving for alcohol and binge eating.
These 2 cases are highly suggestive of potent therapeutic effects of rufinamide and its metabolites with respect to bipolar disorder, depressive and anxiety disorders, panic disorder and obsessive-compulsive disorder, eating disorders, and substance use disorders. Since these are just anecdotal reports of off-label uses of rufinamide in highly refractory cases, the Authors cannot rule out the possibility that these marked clinical changes were due to nonspecific effects or to the concomitant treatments, which seemed ineffective prior to rufinamide treatment initiation. On the other hand, these observations may merit further investigation of the potential therapeutic benefits of this antiepileptic drug.
 
Article Date: 19 May 2010 – 2:00 PDT
This study formulates the hypothesis that rufinamide, a drug so far used against epilepsy, may also be effective in bipolar disorder, depressive and anxiety disorders, panic disorder and obsessive-compulsive disorder, eating disorders, and substance use disorders. It is just an hypothesis based on two cases that needs to be confirmed by specific studies.
Rufinamide is a triazole derivative indicated in the USA for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in children 4 years and older and adults. Rufinamide has activity in the maximal electroshock model and the pentylenetetrazol test, although the ED 50 (median effective dose) is an order of magnitude higher in the pentylenetetrazol test, and in a wide range of other animal models, including seizures induced by GABA-A receptor antagonists, and models of neocortical epilepsy. Based on in vitro studies, the principal mechanism of action of rufinamide is considered to be the modulation of the activity of sodium channels and, in particular, prolongation of the inactive state of the sodium channel. Rufinamide has a low degree of protein binding (34%), and its half-life is approximately 6 – 10 h, which has led to its recommended twice-daily administration. The most commonly observed adverse experiences seen in association with rufinamide and at a higher frequency than in placebo-treated patients are headache, dizziness, fatigue, somnolence and nausea. This study reports on 2 cases where the off-label use of rufinamide led to marked clinical improvements in patients with complicated psychiatric histories.
The first patient was a woman with bipolar disorder and multiple psychiatric comorbidities (panic disorder, obsessive-compulsive disorder, eating disorder), who had been extraordinarily refractory to treatment and had failed countless pharmacological and nonpharmacological treatment attempts, including ECT. In the context of progressive worsening of her condition, rufinamide 400 mg 1 tablet twice daily was added to her complicated pharmacological regimen, leading to a marked clinical improvement. The patient reported a marked improvement in depressive and obsessive symptoms, a reduction in anxiety and panic attacks, and a significant mood stabilization and reduction in mood swings. The dose was subsequently adjusted to 800 mg twice daily and the patient’s improvement persisted over the following 2 months.
The second patient was another woman with bipolar disorder and multiple psychiatric and medical comorbidities (panic disorder, alcohol abuse, chronic pain) who also had been extraordinarily refractory to treatment and had failed countless pharmacological and nonpharmacological treatment attempts. In the context of an acute worsening of her condition, rufinamide 400 mg 1 tablet twice daily was added to her pharmacological regimen, leading to a very rapid (within days) clinical improvement. The patient reported a marked improvement in depressive and anxiety symptoms, significant mood stabilization and reduction in mood swings, and a reduction in craving for alcohol and binge eating.
These 2 cases are highly suggestive of potent therapeutic effects of rufinamide and its metabolites with respect to bipolar disorder, depressive and anxiety disorders, panic disorder and obsessive-compulsive disorder, eating disorders, and substance use disorders. Since these are just anecdotal reports of off-label uses of rufinamide in highly refractory cases, the Authors cannot rule out the possibility that these marked clinical changes were due to nonspecific effects or to the concomitant treatments, which seemed ineffective prior to rufinamide treatment initiation. On the other hand, these observations may merit further investigation of the potential therapeutic benefits of this antiepileptic drug.
 
ScienceDaily (May 18, 2010) — Tourette syndrome, a neurological disorder characterized by tics like grimacing, blinking and vocalizations, is normally treated in children and teens with one of several antipsychotic medications. But such drugs usually don’t eliminate all the tics, and worse, they can often have side effects, acting as sedatives, causing weight gain and impairing cognitive function.
Now, a multisite study led by a UCLA researcher has developed an effective, non-medication treatment for children and adolescents with Tourette’s and related tic disorders that has shown improvement similar to that found in recent anti-tic medication studies.
Lead study author John Piacentini, a UCLA professor of psychiatry and his colleagues at seven sites around the nation found that a specialized form of behavior therapy called comprehensive behavioral intervention for tics, or CBIT, significantly reduced chronic tics and tic-related problems in children and adolescents.
Almost 53 percent of children receiving CBIT were rated as significantly improved, compared with 19 percent of those receiving a comparison treatment, and the degree of improvement with CBIT was similar to that found in recent anti-tic medication studies.
The study appears in the May 19 issue of the Journal of the American Medical Association (JAMA).
Tourette syndrome, which affects approximately six out of every 1,000 children and adolescents, is a chronic neurological disorder characterized by motor and vocal tics, including eye blinking, facial grimacing, head jerking, throat clearing, sniffing and grunting. Although the repetition of curse words is often portrayed as the defining feature of the syndrome, cursing is an uncommon symptom and is not required for diagnosis of the disorder.
“Besides its physical manifestations, Tourette syndrome can cause a number of other problems,” Piacentini said. “It is often associated with other psychiatric problems, difficulties in school, work and social functioning, and, in severe cases, can be disabling.
“Historically, Tourette syndrome has been treated with antipsychotic medications, which reduce tics but are associated with side effects that often limit their usefulness in children. So the development of an effective non-medication treatment for children with this disorder is a major therapeutic advance,” he said.
CBIT is built on the observation that tics are preceded by unwanted feelings or sensations which in turn are temporarily relieved by the tics. In this treatment, children learned to recognize when a tic was about to occur and to engage in a voluntary action incompatible with the tic until the unwanted sensation passed.
In addition, parents were taught how to promote these management strategies in their children and to minimize stressful situations in their children’s environments associated with tic worsening.
In the multisite study, 126 children between the ages of 9 and 17 with moderate to severe Tourette syndrome or Chronic Tic Disorder were randomly assigned to CBIT or to a supportive counseling and education program about Tourette syndrome. Approximately one-third of the children entered the study on a stable dose of anti-tic medication.
The study showed that CBIT resulted in a significantly greater reduction in tic severity and tic-related problems than the supportive counseling. Almost 53 percent of children receiving CBIT were rated as significantly improved, compared with 19 percent of those receiving the comparison treatment.
The degree of improvement with CBIT was similar to that found in recent anti-tic medication studies. Benefits were observed in both children who were on a tic medication and children not on medication. Adverse treatment effects, including tic worsening, were rare in both CBIT and supportive counseling. Treatment gains for CBIT were maintained over time, with 87 percent of available responders showing continued benefits six months after treatment had ended.
“The fact that CBIT works about as well as the standard medications for tics but without the negative side effects greatly expands the available treatment options for chronic tic disorders,” said Susanna Chang, a UCLA assistant professor of psychiatry and a study author. “Importantly, CBIT also emphasizes the development of skills that foster autonomy and empowerment, allowing for patients and their families to take a more active role in treatment than previously indicated.”
Piacentini noted that additional studies are underway using neuroimaging and other neuroscientific techniques to examine the brain mechanisms underlying how CBIT might work. In addition, investigators are currently working with the Tourette Syndrome Association and the U.S. Centers for Disease Control and Prevention to teach CBIT to clinicians who treat children with tic disorders and to develop new versions of CBIT for use with younger children and by nurses and other health care professionals.
Other authors on the study included Douglas Woods, of the University of Wisconsin-Milwaukee; Lawrence Scahill and James Dziura, of Yale University; Sabine Wilhelm and Thilo Deckersbach, of Massachusetts General Hospital/Harvard Medical School; Alan Peterson, of the University of Texas Health Science Center; Dr. John Walkup and Golda Ginsburg, of the Johns Hopkins Medical Institutions and Weil-Cornell Medical School; and Sue Levi-Pearl, of the Tourette Syndrome Association.
The study was funded by the National Institutes of Health. The authors report no conflict of interest.
![]()
Story Source:
Adapted from materials provided by University of California – Los Angeles. Original article written by Mark Wheeler.
Journal Reference:
- John Piacentini; Douglas W. Woods; Lawrence Scahill; Sabine Wilhelm; Alan L. Peterson; Susanna Chang; Golda S. Ginsburg; Thilo Deckersbach; James Dziura; Sue Levi-Pearl; John T. Walkup. Behavior Therapy for Children With Tourette Disorder: A Randomized Controlled Trial. JAMA, 2010; 303 (19): 1929-1937 [link]
Source: http://www.sciencedaily.com/releases/2010/05/100518180930.htm
Â
 
ScienceDaily (May 18, 2010) — Tourette syndrome, a neurological disorder characterized by tics like grimacing, blinking and vocalizations, is normally treated in children and teens with one of several antipsychotic medications. But such drugs usually don’t eliminate all the tics, and worse, they can often have side effects, acting as sedatives, causing weight gain and impairing cognitive function.
Now, a multisite study led by a UCLA researcher has developed an effective, non-medication treatment for children and adolescents with Tourette’s and related tic disorders that has shown improvement similar to that found in recent anti-tic medication studies.
Lead study author John Piacentini, a UCLA professor of psychiatry and his colleagues at seven sites around the nation found that a specialized form of behavior therapy called comprehensive behavioral intervention for tics, or CBIT, significantly reduced chronic tics and tic-related problems in children and adolescents.
Almost 53 percent of children receiving CBIT were rated as significantly improved, compared with 19 percent of those receiving a comparison treatment, and the degree of improvement with CBIT was similar to that found in recent anti-tic medication studies.
The study appears in the May 19 issue of the Journal of the American Medical Association (JAMA).
Tourette syndrome, which affects approximately six out of every 1,000 children and adolescents, is a chronic neurological disorder characterized by motor and vocal tics, including eye blinking, facial grimacing, head jerking, throat clearing, sniffing and grunting. Although the repetition of curse words is often portrayed as the defining feature of the syndrome, cursing is an uncommon symptom and is not required for diagnosis of the disorder.
“Besides its physical manifestations, Tourette syndrome can cause a number of other problems,” Piacentini said. “It is often associated with other psychiatric problems, difficulties in school, work and social functioning, and, in severe cases, can be disabling.
“Historically, Tourette syndrome has been treated with antipsychotic medications, which reduce tics but are associated with side effects that often limit their usefulness in children. So the development of an effective non-medication treatment for children with this disorder is a major therapeutic advance,” he said.
CBIT is built on the observation that tics are preceded by unwanted feelings or sensations which in turn are temporarily relieved by the tics. In this treatment, children learned to recognize when a tic was about to occur and to engage in a voluntary action incompatible with the tic until the unwanted sensation passed.
In addition, parents were taught how to promote these management strategies in their children and to minimize stressful situations in their children’s environments associated with tic worsening.
In the multisite study, 126 children between the ages of 9 and 17 with moderate to severe Tourette syndrome or Chronic Tic Disorder were randomly assigned to CBIT or to a supportive counseling and education program about Tourette syndrome. Approximately one-third of the children entered the study on a stable dose of anti-tic medication.
The study showed that CBIT resulted in a significantly greater reduction in tic severity and tic-related problems than the supportive counseling. Almost 53 percent of children receiving CBIT were rated as significantly improved, compared with 19 percent of those receiving the comparison treatment.
The degree of improvement with CBIT was similar to that found in recent anti-tic medication studies. Benefits were observed in both children who were on a tic medication and children not on medication. Adverse treatment effects, including tic worsening, were rare in both CBIT and supportive counseling. Treatment gains for CBIT were maintained over time, with 87 percent of available responders showing continued benefits six months after treatment had ended.
“The fact that CBIT works about as well as the standard medications for tics but without the negative side effects greatly expands the available treatment options for chronic tic disorders,” said Susanna Chang, a UCLA assistant professor of psychiatry and a study author. “Importantly, CBIT also emphasizes the development of skills that foster autonomy and empowerment, allowing for patients and their families to take a more active role in treatment than previously indicated.”
Piacentini noted that additional studies are underway using neuroimaging and other neuroscientific techniques to examine the brain mechanisms underlying how CBIT might work. In addition, investigators are currently working with the Tourette Syndrome Association and the U.S. Centers for Disease Control and Prevention to teach CBIT to clinicians who treat children with tic disorders and to develop new versions of CBIT for use with younger children and by nurses and other health care professionals.
Other authors on the study included Douglas Woods, of the University of Wisconsin-Milwaukee; Lawrence Scahill and James Dziura, of Yale University; Sabine Wilhelm and Thilo Deckersbach, of Massachusetts General Hospital/Harvard Medical School; Alan Peterson, of the University of Texas Health Science Center; Dr. John Walkup and Golda Ginsburg, of the Johns Hopkins Medical Institutions and Weil-Cornell Medical School; and Sue Levi-Pearl, of the Tourette Syndrome Association.
The study was funded by the National Institutes of Health. The authors report no conflict of interest.
![]()
Story Source:
Adapted from materials provided by University of California – Los Angeles. Original article written by Mark Wheeler.
Journal Reference:
- John Piacentini; Douglas W. Woods; Lawrence Scahill; Sabine Wilhelm; Alan L. Peterson; Susanna Chang; Golda S. Ginsburg; Thilo Deckersbach; James Dziura; Sue Levi-Pearl; John T. Walkup. Behavior Therapy for Children With Tourette Disorder: A Randomized Controlled Trial. JAMA, 2010; 303 (19): 1929-1937 [link]
Source: http://www.sciencedaily.com/releases/2010/05/100518180930.htm
Â
 
Gary McKinnon is hoping to avoid U.S. prosecution for hacking by approaching the new coalition government
Britain’s new government is giving fresh consideration to a hacker’s plea to postpone an upcoming court hearing in a long-running bid to avoid a U.S. trial that could send him to prison for decades.
The U.K.’s Home Office, which oversees criminal justice affairs, is reviewing a letter from lawyers for Gary McKinnon, who was charged in the U.S. in 2002 for breaking into military and government computers.
McKinnon is scheduled for a judicial review hearing in the High Court on May 25 and 26 on the basis of his diagnosis of Asperger’s syndrome, a neurological disorder related to autism characterized by deficiencies in social interaction.
Theresa May, the new home secretary from the Conservative party, is expected to issue a response “as soon as possible,” according to a Home Office spokesman.
“The Home Secretary has received a letter from Gary McKinnon’s legal team asking her to agree to an adjournment of the Judicial Review in light of further representations,” according to a Home Office statement.
McKinnon’s case has risen in profile over the last couple of years, with celebrities, along with politicians, voicing their support for him.
The recent change in government could help his cause. Some members of the U.K.’s new coalition government have been highly critical of the circumstances of McKinnon’s case.
Last year, David Cameron — now Britain’s prime minister — criticized the extradition treaty McKinnon was subject to. Nick Clegg, the Liberal Democrat’s leader who is deputy prime minister, said last year he opposed extraditing McKinnon given his medical condition.
The U.K. government approved McKinnon’s extradition in 2006, but his lawyers undertook a series of court maneuvers that have kept him from being extradited.
McKinnon had asked to be prosecuted in the U.K., but the request was denied on the basis that U.S. authorities wanted jurisdiction over the case and because most of the witnesses are in the U.S.
McKinnon was indicted by the U.S. District Court for the Eastern District of Virginia in 2002 for hacking into 97 military and NASA computers between February 2001 and March 2002. He could face up to 60 years in prison.
McKinnon has remained free in the U.K. but isn’t allowed to use a computer. He has publicly admitted to hacking the computers using a program called “RemotelyAnywhere,” a remote access tool.
McKinnon has said that many of the computer systems still had their default passwords — considered a poor security practice — and that other passwords were easy to obtain.
McKinnon, who went by the name “Solo,” contends he was merely searching for proof of the existence UFOs and didn’t harm the systems. The U.S. military contends that McKinnon deleted critical files from its computers, which hampered its efforts after the Sept. 11, 2001, terrorist attacks.
Source:Â http://www.itworld.com/legal/108187/new-british-government-considers-mckinnons-appeal
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Theresa May halts Gary McKinnon’s legal battle against extradition to America
Gary McKinnon has received a double boost in his five year battle against being extradited to America to face computer hacking charges.
By Christopher Hope, Whitehall Editor
Published: 3:19PM BST 20 May 2010
The Home Office said on Thursday that Home Secretary Theresa May had decided to halt the legal process so she could re-examine impact of extradition on Mr McKinnon’s health.
The coalition Government also confirmed in its formal agreement it would conduct a comprehensive review of the controversial extradition treaty under which Mr McKinnon was set to be extradited.
Mr McKinnon, 44, who suffers from a form of autism, is challenging a US bid to extradite him on charges of hacking into highly sensitive military computers eight years ago.
He had been on the verge of being extradited earlier this year after the-then Home Secretary Alan Johnson ruled he should go, despite evidence that he was suicidal.
However, the move was postponed after a judge found that it was “arguable†that extraditing him could violate his human rights.
The Home Office said Mrs May would re-examine the medical evidence for herself to decide whether Mr McKinnon should be extradited.
A spokesman said: “The Home Secretary has considered the proposal from Gary McKinnon’s legal team and has agreed an adjournment should be sought. An application to the court is being made today.â€
An adjournment was granted on the case late on Thursday by a judge in the High Court who has asked for an update by the end of July.
Karen Todner, Mr McKinnon’s solicitor, said Mrs May wanted to have “appropriate time†to consider the issues after receiving a request from Mrs Todner.
She said: “I hope this may be a signal of a more compassionate and caring Home Secretary and one that is willing to defend the rights of our citizens.”
Janis Sharp, Gary McKinnon’s mother, said: “We are grateful that the new Home Secretary has agreed to reconsider Gary’s case and we await Mrs May’s decision with great hope that Gary may still have a future.
“Gary is still terrified and undergoing a state of ongoing heightened stress but today’s news gives us hope, at last, that his ordeal may soon be over.
“We need it to be over and totally believe that the new coalition will keep their promises and allow Gary to be tried in his own country.”
Isabella Sankey, a spokesman from campaign group Liberty which has been campaigning for Mr McKinnon, said she welcomed the decision for a “pause for thought†in Mr McKinnon’s extradition battle.
She said: “We hope this might lead to a new approach to extradition that combines international cooperation with justice and compassion.
“This is yet another early test for the coalition parties to honour in government what they promised in opposition.â€
Mark Lever, chief executive of the National Autistic Society, said: “Both David Cameron and Nick Clegg have previously spoken out in concern for Gary, and now is their opportunity to take action.
“We heard with relief that Theresa May has agreed to put legal proceedings on hold in order to reconsider Gary’s case once more, and wait in hope that she will be in the position to make the decision Gary and his family so desperately need to hear.”
Last year Mr Johnson had refused to halt McKinnon’s removal, saying he was “of the firm view†that extradition would not be incompatible with his human rights, and “extradition to the United States must proceed forthwithâ€.
Mr McKinnon was accused in 2002 of using his home computer to hack into 97 American military and Nasa computers, causing damage that the US government claims will cost more than $700,000 dollars (£425,000) to repair.
He admits breaching the systems but denies causing damage and claims he was looking for evidence of UFOs. If he is found guilty he faces spending years
Separately the Government said in its coalition agreement that it would review the workings of the 2003 Extradition treaty. It said: “We will review the operation of the Extradition Act – and the US/UK extradition treaty – to make sure it is even-handed.â€
Before the election, the Tories had said they wanted to renegotiate the treaty amid claims it was “one-sided” while the Liberal Democrats – including deputy Prime Minister Nick Clegg – said extraditing Mr McKinnon would be a “travesty of justice”.
A source close to Mr Clegg said today: “Nick has always taken a keen interest in the case but this was a decision by the Home Secretary.”
Critics have long claimed the treaty made it easier for US authorities to extradite Britons to America. Others have complained that it has been used by American authorities to target white collar criminals.
The controversial case has now been considered by six home secretaries.
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Previous Updates
Gary McKinnon Updates: US Prosecution Of McKinnon ‘Spiteful’, Says Ex-Top-Cop
McKinnon’s Mum Fights For Civil Liberties In Parliamentary Run(Includes Outcome Update)
Gary McKinnon Updates: Janis Sharp To Battle Straw
Gary McKinnon Updates: New Court Date In Extradition Marathon
Gary McKinnon Updates: Charlie Mckinnon On His Son’s Fight Against US Extradition
Gary McKinnon Updates: Death Threats
Gary McKinnon Updates: Pentagon Hacker Wins Delay Of Extradition To U.S.
Gary McKinnon Updates: New Hope on Extradition
Gary McKinnon Updates: Gary McKinnon’s Mother In Tears After Snub From Alan Johnson
Gary McKinnon Updates: Computer Hacker Gary McKinnon Loses Fight To Stand Trial In UK
GaryMcKinnon Updates: Verdict on Extradition to be Announced This Week
Gary McKinnon Updates: Protestors Challenge McKinnon Extradition/American Civil Liberties Union Attacks David Miliband over UK/US Extradition Treaty
Updates(Includes New Petition): Gary McKinnon Loses Appeal Against Extradition To The U.S.
Updates: Gary McKinnon’s Impending Extradition Must Be Stopped/No Pity From US

