Friday, February 28, 2020

Brain Scans Reveal a New Schizophrenia Type That Almost Looks Like a 'Healthy' Brain

Not all people with schizophrenia show the same abnormal brain structure, a new study has found.

Scanning the brains of over 300 schizophrenia patients, researchers now think they've identified two neuroanatomical subtypes of this mysterious neurological disorder; one of them has never been detected before, according to the team.


Today, the neurobiology of schizophrenia is poorly understood, but historically, it's been linked to a reduction in grey matter volume, the type of brain tissue that contains the main body of neurons.

This is a typical pattern of the disease that keeps popping up in research, but while the majority of patients in this new study also showed these deficits, a large chunk had surprisingly healthy grey matter levels.

"Numerous other studies have shown that people with schizophrenia have significantly smaller volumes of brain tissue than healthy controls," explains radiologist Christos Davatzikos from the University of Pennsylvania.

"However, for at least a third of patients we looked at, this was not the case at all - their brains were almost completely normal."

The only thing that stood out was an increase in basal ganglia volume, the part of the brain primarily responsible for motor control. Although schizophrenia is a disorder of the mind that interferes with the consistent processing of reality, it can also lead to physical problems like slow movements and tics.

But these brain patterns are not exactly in line with the current consensus on schizophrenia. In fact, the idea of 'neuroanatomical heterogeneity' - where some people may show brain deficits while others don't - has only recently been considered.


"These results challenge the conventional notion that brain volume loss is a general feature of schizophrenia," the authors conclude.

Using machine learning, the team analysed the brain scans of 307 schizophrenia patients and 364 healthy controls, categorising them into neuroanatomical subtypes.

In total, nearly 40 percent of the participants with schizophrenia did not show the typical pattern of reduced grey matter. In some cases, they actually showed more brain volume in the middle of the brain, in a part called the striatum.

No clear explanation could be found for the results - not medication, age, or any other demographic factors.

"This is where we are puzzled right now," Davatzikos says.

"We don't know. What we do know is that studies that are putting all schizophrenia patients in one group, when seeking associations with response to treatment or clinical measures, might not be using the best approach."

Patients that fell into either brain subtype had experienced similar levels of symptoms and were medicated at roughly the same dose. Previous research has linked reduced cortical volumes to antipsychotic drugs, but the researchers did not detect such differences between the two subtypes.

The team notes that brain differences between the subtypes could still be influenced by the consequences of taking medication, for example, higher treatment resistance in subtype 1 compared to subtype 2, whose cortical volumes did not appear to be reduced. But other aspects - such as no difference in symptom severity - don't seem to support this explanation.


Other recent studies have also hinted at a more diverse presentation of schizophrenia in the brain; given how variable symptoms of schizophrenia can be, and how few people respond to treatment, this idea that one size does not fit all is not without merit.

But connecting these symptoms to patterns in the brain has proved extremely difficult, especially since animal models aren't useful in a disorder that is largely diagnosed through self-reporting.
"The main message is that the biological underpinnings of schizophrenia - and actually many other neuropsychiatric disorders - are quite heterogeneous," Davatzikos told ScienceAlert.

The latest classification of schizophrenia in the DSM-V categorises the condition as a spectrum based on symptoms alone, having moved away from behavioural subtypes such as paranoid and catatonic.

But Davatzikos thinks that observations of neural diversity in such disorders could ultimately take diagnostic categories much further.

"In the future, we're not going to be saying, 'This patient has schizophrenia,' We're going to be saying, 'This patient has this subtype' or 'this abnormal pattern,' rather than having a wide umbrella under which everyone is categorised."

We'll have to wait for even more research in the neuroanatomy of various disorders to see whether such a categorisation goal is attainable.

The study was published in Brain.


This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.     

https://gscrochetdesigns.blogspot.com. one can see my crochet creations  
https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes    
https://kneereplacement-stickclub.blogspot.com. for info on knee replacement
 

Labels: , , , , , , , , , , ,

Tuesday, December 11, 2018

Smartphones, tablets could change children's brain structures

Children who spend more than seven hours a day on screens like smartphones and video games experience "premature thinning of the cortex," according to a new and ongoing study.
 
The study plans to follow more than 11,000 adolescents for a decade to see how childhood experiences impact the brain.

The first findings from the study is already available. By scanning brains of 4,500 participants, researchers found that children who use smartphones, tablets and video games more than seven hours a day showed premature thinning of cortex.

"That's typically thought to be a maturational process. So what we could expect to see later is happening a little bit earlier," said a Dr.  working on the project when interviewed .

Dr. said it is still early to tell whether the change was caused by the screen time, and whether or not it is a bad thing. "It won't be until we follow them over time that we will see if there are outcomes that are associated with the differences that we're seeing in this single snapshot," she said.

Early results from the study also showed that as little as two hours of screen time daily could negatively affect children: Those who have more than two hours of screen time a day got lower scores on tests focused on thinking and language skills.

As Dr. noted, a full picture of the screen-time effects won't be possible until years down the line, when the study is complete. 

THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES.                                                                                                                                                                                                                                                                                        PS- THOSE INTERESTED IN RECIPES ARE FREE TO  VIEW MY BLOG-                                                                                           https://gseasyrecipes.blogspot.com/                                                                                                                                                                             FOR INFO ABOUT KNEE REPLACEMENT, YOU CAN VIEW MY BLOG-                                                                                                                             https:// kneereplacement-stickclub.blogspot.com/                                                                                       FOR CROCHET DESIGNS                                                                                                                                                                                                                                 https://gscrochetdesigns.blogspot.com 

Labels: , , , , , , , , , , , ,

Wednesday, September 13, 2017

CAUSES OF SOCIAL ANXIETY DISORDER

Labels: , , , , ,

Monday, December 26, 2016

Dysfunction in brain structure may cause Huntington's disease

Dysfunction of a group of brain structures critical for movement and impulse control may be behind Huntington's disease, according to a new study that could lead to a therapy for the currently incurable disorder.
 
Scientists at Northwestern University in the US identified a link between Huntington's disease and dysfunction of the sub-thalamic nucleus, a component of the basal ganglia, a group of brain structures critical for movement and impulse control. Huntington's disease is characterised by the progressive loss of nerve cells in the brain and affects about one in 10,000 people. This fatal disorder is caused by a hereditary defect in a single gene.

"Although the genetic basis of the disease is well established, why the mutation leads to the expression of symptoms and loss of brain tissue remains poorly understood," said Mark Bevan, professor of physiology at Northwestern University Feinberg School of Medicine. The debilitating symptoms of Huntington's disease typically manifest in adulthood and involve loss of motor and cognitive function, depression and personality changes.

From the point of onset, symptoms develop and intensify over the following 10 to 25 years until death, typically due to complications associated with the disease.

"While research into Huntington's disease has focused on other parts of the basal ganglia, the sub-thalamic nucleus has been largely overlooked," said Bevan.


"This is surprising because patients with Huntington's disease have fewer nerve cells in the sub-thalamic nucleus. People who have suffered damage to the sub-thalamic nucleus exhibit excessive movement and impulsive behaviour, similar to patients with Huntington's disease," he said.

Using mice genetically engineered to carry the Huntington's disease gene, scientists discovered the electrical activity of the subthalamic nucleus was lost.

Impaired subthalamic activity was caused by anomalous receptor signalling, leading to defective energy metabolism and accumulation of damaging oxidants.


The researchers also found abnormalities in the sub-thalamic nucleus occur earlier than in other brain regions, and that sub-thalamic nucleus nerve cells progressively degenerate as the mice age, mirroring the human pathology of
Huntington's disease. "Our findings suggest early problems in the sub-thalamic


nucleus not only contribute to the symptoms of Huntington's disease, but are also likely to impair the processing capacity and health of other brain structures, more traditionally associated with the disease," Bevan said.


Currently, there is no cure for Huntington's disease; treatment can only alleviate some of the symptoms. A better understanding of aberrant brain receptor signalling that leads to nerve cell dysfunction could reveal a target for therapy, researchers said. 

The study was published in the journal eLife.

this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.

https://gscrochetdesigns.blogspot.com. one can see my crochet creations
https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes 
https://kneereplacement-stickclub.blogspot.com. for info on knee replacement

Labels: , , , , , , , , , , ,