Articles tagged with Autism
A recent study by the University of Cambridge found that autistic individuals have a higher risk of chronic mental and physical health conditions. They also report lower quality healthcare experiences, including difficulties with symptom description and sense overload.
Infants diagnosed with autism spectrum disorder at 24 months had differences in visual processing areas of the brain apparent at 6 months old. These early changes could affect further brain development and play a role in ASD symptoms.
Researchers have identified unique differences in the visual systems of infants who later develop autism, which are associated with inherited genetic factors. These differences in brain structure and function precede the appearance of autistic symptoms and are related to the severity of autism traits in older siblings.
A study led by Tel Aviv University researchers reveals a common mechanism underlying genetic mutations associated with autism, schizophrenia, and other neurological disorders. The discovery points to an experimental drug developed by the team as a potential treatment for these conditions.
A study analyzing reviews of therapeutic interventions found that certain types of early therapies can promote communication and social interactions in young children with autism. However, the quality of evidence was often limited, leaving families to navigate different approaches.
A study published in Current Biology observed toddlers with autism achieving joint attention during toy play with parents at typical levels. Children with autism also used hand-following cues to follow their parent's attention into joint attention.
The study reveals that the YWHAZ gene can alter neuronal development, leading to behavioral alterations in response to novelty. The team identified key neurotransmitter alterations involved in behavior and found that using fluoxetine and quinpirole can reduce social behavior alterations.
A recent study found that 78.3% of autistic adults in Pennsylvania reported receiving or intending to get a COVID-19 vaccine, compared to 42% of overall adults. The research identified key factors driving vaccine acceptance and hesitancy, such as feelings of increased loneliness and concerns about vaccine safety.
Researchers used gene therapy to recover the TCF4 gene's function in human brain tissue, rescuing neural structure and function in brain organoids. The study offers promising insights into treating neurological disorders like autism spectrum disorders and schizophrenia.
A study led by Kobe University researchers found that idiopathic autism is caused by epigenetic abnormalities in hematopoietic cells, leading to immune dysregulation and brain-gut axis disorders. The study used BTBR mice as a model and identified histone deacetylase HDAC1 as a common mechanism underlying these pathologies.
A new study of over 111,000 adolescents aged 11-17 found that autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (ADHD) significantly increased the risk of self-harm. Additionally, school absence was also associated with a three-fold higher risk of self-harm. These findings suggest that early identification and...
Scientists at Gladstone Institutes have discovered that reducing protein tau levels soon after birth can prevent autism and epilepsy in an experimental model. The study pinpointed the crucial brain cells where tau levels must be reduced to avoid these problems, and showed that lowering tau is still effective when initiated after birth.
A new study published in Frontiers in Behavioral Neuroscience reveals that nine out of ten autistic women in France have suffered sexual violence, with most victims being assaulted multiple times at a young age. The findings highlight the need for improved prevention and care programs to address this vulnerable population.
A new study found a bi-directional relationship between gastrointestinal issues and internalized symptoms in children with autism, highlighting the importance of the gut-brain axis. The research aims to develop personalized treatments for individuals with autism experiencing gastrointestinal problems.
Researchers found no widespread systematic measurement bias in the Autism Diagnostic Observation Schedule (ADOS-2) across race and sex. However, the study suggests potential underdetection of autism in certain groups, warranting further research to improve diagnosis accuracy.
A new study examines factors associated with COVID-19 vaccine hesitancy and uptake in the autism community, revealing that early skepticism waned over time. The majority of caregivers eventually received the vaccine following FDA approval. Firmly held vaccine-hesitant beliefs influenced a minority of autism spectrum disorder caregivers.
A preclinical study suggests that astrocyte abnormalities may contribute to repetitive behaviors and memory deficits in autism spectrum disorders. Researchers grew human astrocytes from patients with ASD and transplanted them into healthy mice, which developed repetitive behaviors but not social deficits.
A new report highlights the intersection of autism, poverty, and non-white race/ethnicity, revealing increased rates of health concerns and care challenges. Autistic children living in lower-income households and those who are BIPOC disproportionately experience poor health outcomes.
A new review found that Autistic women face significant challenges in breastfeeding, despite being motivated to do so. The lack of understanding of their needs and limited support from healthcare professionals exacerbate these issues.
Researchers at Shinshu University have elucidated a new molecular mechanism controlling the survival of cerebral nerve cells. Neurexin regulates cerebellar granule cell survival independently of synapses, playing a crucial role in neurodevelopmental disorders such as autism and schizophrenia.
Researchers analyzed prenatal MRI scans of children later diagnosed with autism and found significant differences in brain structures at 25 weeks' gestation. These differences may be a strong biomarker for predicting ASD emergence, with the insular lobe showing increased volume.
A genetic disease in children, CHARGE syndrome causes intellectual disability, attention deficit disorder, and autism. The INRS team is studying the gene's impact on brain development to identify potential treatments.
A Synapsy study has identified a new neural pathway involved in social interaction, distinct from the traditional reward system. This discovery may hold key to understanding and treating autism spectrum disorders.
A long-term study of FXTAS carriers has identified key indicators of disease progression, including cognitive decline and motor symptoms. Researchers hope to develop a validated tracking tool to monitor premutation carriers and patients with FXTAS.
A landmark study found that autistic individuals think as quickly and rationally as non-autistic people, challenging the idea that autism is a mental processing disorder. The research suggests that certain fundamental processes are more similar between autistic and non-autistic individuals than previously thought.
Research identifies genetic variants associated with reduced grey matter volume in brain regions linked to schizophrenia and autism spectrum disorders. The study suggests a potential new target for treating severe mental illnesses by targeting the IL-6 gene.
This year's Experimental Biology 2022 meeting features groundbreaking studies on COVID-19 vaccine-associated symptoms in non-menstruating people, a plant compound showing promise for alleviating food allergies, and the potential of omega-3s to boost immunotherapy's cancer-fighting power. Researchers also explore the safety of using CBD...
A new study funded by the NIH found that amygdala overgrowth in autism spectrum disorder begins between 6-12 months of age, suggesting early intervention may be effective in reducing symptoms. The study also identified distinct brain growth patterns in infants with Fragile X syndrome.
Researchers found that babies who later develop autism show overgrowth of the amygdala between six and 12 months, prior to behavioral symptoms. This finding suggests a potential link between early sensory processing problems and amygdala enlargement.
A team of scientists discovered that a disrupted circadian clock gene may contribute to the development of autism spectrum disorder. The study found that deleting the Bmal1 gene in mice led to autistic-like behaviors and cerebellar dysfunction, which were alleviated by mTORC1 inhibition.
A study of 383 extremely preterm babies found that most had neurodevelopmental disorders and/or other diagnoses during childhood. The children were referred for habilitation services and had a range of additional diagnoses, including asthma and short stature.
Researchers have identified 79 ASD-associated genes and found that many of them alter behavior in fruit flies, providing functional evidence for their consequences. The study also uncovered a new form of rare disease due to the GLRA2 gene, highlighting the importance of de novo genetic variants in autism.
Researchers found that over half of autistic people were considered vulnerable adults, but only a quarter received reasonable adjustments. Autistic defendants often experienced meltdowns and stress due to lack of understanding from law enforcement and courts.
Researchers have developed a new approach to studying brain activity, allowing for longer-term studies and improved understanding of neural traffic jams. The new cranial window system uses surgical glue and a tiny glass window to capture high-quality blood flow imaging and stable electrical recordings.
A new early screening tool for autism has been found to be extremely accurate in identifying young children on the autism spectrum. The tool, developed by La Trobe University researchers, detects over 3 years earlier than traditional testing and has already been used in 11 countries.
Scientists developed a powerful new tool called Giraffe to improve genomic research by leveraging global genetic diversity. The tool allows for the use of a diverse pangenome reference point, enabling faster and more sensitive comparisons of short-read human genome sequences.
Researchers observed that chandelier cells, which regulate cortical circuit activity, communicate with other neurons shortly after birth, influencing brain development. This interaction is crucial for normal brain function and may be disrupted in neurological disorders.
In a breakthrough discovery, microglia have been found to play a crucial role in forming critical synapses in the brain, particularly in chandelier cells. This finding suggests that immune cells may not only remove unwanted connections but also nurture their formation, which is essential for cognitive functioning.
The March issues of American Psychiatric Association journals focus on the genomics of psychopathology, exploring its relationship with various mental illnesses. Research highlights unique genetic patterns among individuals who die by suicide using violent means.
The Phase 1b/2a clinical trial found that AB-2004 lowered blood and urinary levels of gut-derived metabolites and improved irritability and anxiety in adolescents with Autism Spectrum Disorder. The study's results support the potential of AB-2004 as a novel therapeutic approach for treating co-occurring conditions associated with ASD.
The collaboration aims to prepare professionals to support school-aged students with autism spectrum disorder and related disabilities. Full scholarships will be awarded to 24 graduate students starting in Fall 2022.
The SynGAP Research Fund has developed a pre-screening tool to identify potential SYNGAP1 patients through a free online survey. The partnership with Probably Genetic aims to screen undiagnosed patients and provide them with genetic testing resources, ultimately advancing treatment development for SYNGAP1.
A recent study identified specific RNA biomarkers linked to gastrointestinal symptoms in children with autism. The findings could lead to the development of personalized treatments to ease the pain of these individuals. The research has implications for precision medicine, enabling healthcare providers to track medication effectiveness...
Researchers found that blocking an overactive signaling pathway during the first five weeks of life prevents autism symptoms from developing in mice. The study suggests that targeting this critical period could lead to a potential cure for autism.
A recent online survey found that pandemic-related school closures have a disproportionate negative impact on students with autism. The study reveals differences in the psychological impact of the pandemic on neurotypical and autistic children, highlighting the need for alternative ways to support autistic children's educational goals.
Researchers at UC Davis MIND Institute found a novel gene linked to autism spectrum disorder in newborns. The study analyzed DNA methylation signatures in the placenta, which reflected fetal brain development and early autism diagnosis.
A UMass Amherst researcher has received a $3 million grant to study the complex interplay of risk factors for autism, including early life exposure to environmental pollutants and genetic susceptibility. The study aims to better understand how multiple pollutants and the folate system are associated with autistic traits.
A systematic review and meta-analysis of 27 studies found that individuals with autism spectrum disorder and attention-deficit/hyperactivity disorder have an increased risk of mortality. The study suggests that understanding the underlying reasons for these associations could lead to targeted strategies to prevent avoidable deaths.
A recent study conducted by researchers at the University of Kansas has analyzed the cost of two commonly used interventions for students with autism spectrum disorder. The results showed that implementing emerging or ineffective interventions can consume valuable resources without promising positive outcomes. The study's goal was to p...
Prenatal exposure to industrial toxin TCDD may cause long-term damage to brain circuits and potentially lead to neurodevelopmental disorders like autism and ADHD. Researchers found that pharmacological manipulation can restore microglia function, suggesting a possible therapeutic avenue for these disorders.
Researchers at Lancaster University have identified a genetic change that impacts insulin signaling and glucose metabolism in the brain, which may lead to effective drug treatments for autism. The study found that individuals with a specific DNA deletion are more likely to develop neurodevelopmental disorders, including autism.
A study by UC Davis MIND Institute researchers found that autistic children have distinct amygdala changes, with larger volumes associated with traditional anxiety and smaller volumes linked to autism-distinct anxieties. The study used brain scans of 71 autistic and 55 non-autistic children between ages 2-12.
Researchers found that 30% of fetuses who later developed ASD had heart, kidney, and head anomalies detected during routine prenatal ultrasounds. These anomalies were more common in girls and linked to the severity of ASD. The study suggests that doctors can use these signs to evaluate the probability of a child being born with ASD.
A team of scientists has identified hundreds of new genomic loci associated with brain structure, shedding light on how the human brain is shaped. The study used genetically informed brain atlases to uncover the largest number of genetic variants linked to cortex size and thickness.
A study in rats found that mothers with sleep apnea during pregnancy may have an increased risk of their male offspring developing autism-like behaviors, including impaired cognitive and social function. The findings suggest a potential mechanism for the link between maternal sleep apnea and neurodevelopmental disorders.
A study by University of Otago researchers has found that young Autistic people in Aotearoa have significantly lower rates of criminal justice system interactions compared to those without Autism. However, if charged, Autistic young people were more likely to face serious and violent offence charges.
Researchers used 3D mini-brain models to study the effects of three autism risk genes on neural formation and development. The study found that despite unique molecular mechanisms, the genes converged on affecting specific types of neurons, suggesting potential therapeutic targets for autism treatment.
A new study of over 84,000 children found a significant association between screen time at age 1 and the presence or absence of an autism spectrum disorder diagnosis at age 3. The research suggests that early exposure to screens may be a potential risk factor for developing autism.
Gene-environment interactions play a crucial role in the development of autism symptoms, according to a new study by UNIGE researchers. By inhibiting Trpv4 and inducing massive inflammation, scientists observed neuronal hyperexcitability, which disrupted communication channels and led to social avoidance behaviors.
Researchers at Flinders University found that autistic individuals with eating disorders also report higher weight and shape concerns, suggesting a unique combination of symptoms. The study highlights the need for best-practice guidelines to address co-occurring autism and eating disorders in treatment.