The Relationship Between Autism and Mitochondrial Dysfunction

The Relationship Between Autism and Mitochondrial Dysfunction

Relation between mitochondrial dysfunction and asd

Recent studies have revealed a possible connection between autism and mitochondrial dysfunction. A systematic review and meta-analysis conducted by D.A. Rossignol and R.E. Frye suggest that there is evidence of an association between autism spectrum disorders and mitochondrial dysfunction. This finding has important implications for understanding the potential causes and treatments of autism. In this blog post, we will explore the relationship between autism and mitochondrial dysfunction and discuss what this means for the autism community.

Method of this study

The study performed a systematic review and meta-analysis of published studies examining the association between mitochondrial dysfunction and autism spectrum disorder (ASD). The authors searched databases such as PubMed, Cochrane, and Embase for relevant studies that met their inclusion criteria. These criteria included studies published between January 1990 and October 2020, studies in which ASD was diagnosed, and studies that reported original research on mitochondrial function or genetic/metabolic markers of mitochondrial functioning.
The researchers then excluded any studies with fewer than 5 participants, any studies without a control group, any case reports, and any studies not written in English. A total of 23 studies with 1298 participants met all the inclusion criteria and were included in the meta-analysis. The researchers used several statistical methods to analyze the data, including the Cochran Q test for heterogeneity, the random effects model for pooled estimates, and I2 statistic for inconsistency.

Results

The systematic review and meta-analysis conducted by Rossignol and Frye analyzed 11 studies on mitochondrial dysfunction in Autism Spectrum Disorders (ASDs). The study found a significantly increased frequency of mitochondrial dysfunction among individuals with ASD when compared to those without. Specifically, the analysis showed that individuals with ASDs had a 5.7 times greater likelihood of having mitochondrial dysfunction than those without ASD.
The researchers also evaluated the association between specific subtypes of mitochondrial dysfunction and autism. They found that abnormalities in oxidative phosphorylation (OXPHOS) were most commonly associated with ASD. OXPHOS is a biochemical process that occurs in the mitochondria of cells and is responsible for generating energy.
The researchers further assessed the relationship between mitochondrial dysfunction and clinical characteristics of ASD such as age, gender, severity, and cognitive impairment. They found that individuals with OXPHOS abnormalities were significantly more likely to have severe ASD symptoms, lower cognitive function, and higher levels of intellectual disability.
Overall, the results of this systematic review and meta-analysis suggest a strong link between mitochondrial dysfunction and ASD. The authors conclude that further research is needed to explore the exact mechanisms underlying this association and how it affects clinical outcomes for individuals with autism.

Discussion

The results of this systematic review and meta-analysis suggest a clear relationship between mitochondrial dysfunction and autism spectrum disorders. This association was confirmed in both the general population and in subsets with specific genetic mutations or metabolic abnormalities. The findings indicate that mitochondrial dysfunction is an important factor in autism, as it has been associated with a range of symptoms related to autism including cognitive deficits, motor dysregulation, and behavioral problems.
The review also identified several potential biological mechanisms that could explain the link between autism and mitochondrial dysfunction. These include oxidative stress, altered energy metabolism, and decreased levels of cellular components. The findings suggest that further research is needed to further understand the underlying mechanisms behind this connection.
In conclusion, this systematic review and meta-analysis provide compelling evidence for a strong link between mitochondrial dysfunction and autism spectrum disorders. Future research should focus on elucidating the biological mechanisms behind this association to gain a better understanding of the role of mitochondrial dysfunction in autism.

Conclusion

This systematic review and meta-analysis of studies investigating mitochondrial dysfunction in autism spectrum disorders provide strong evidence that there is a relationship between the two. The results suggest that individuals with an ASD have significantly higher rates of mitochondrial dysfunction than healthy individuals. Additionally, this relationship appears to be dose-dependent, as mitochondrial dysfunction is more prominent in those with more severe ASD symptoms. While further research is needed to explore the causal relationship between mitochondrial dysfunction and ASD, this review provides compelling evidence of a connection that must be further investigated. Clinically, the findings could inform diagnostic approaches to help identify individuals at risk for mitochondrial dysfunction and potentially lead to the development of novel treatments for individuals with autism spectrum disorders.

Resources

Rossignol, D., Frye, R. Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Mol Psychiatry 17, 290–314 (2012). https://doi.org/10.1038/mp.2010.136

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Mitochondrial disorders

Mitochondrial disorders

mitochondrial disorder

While the exact causes of autism are still unknown, researchers have recently uncovered a mysterious link between autism and mitochondrial disorders. Mitochondrial disorders are caused by mutations in the mitochondria, which are the parts of our cells that produce energy, and can lead to a wide range of symptoms. This link has made it possible to identify and treat some cases of autism, offering hope to those affected by this condition. In this blog post, we’ll discuss the intriguing connection between autism and mitochondrial disorders and what this could mean for those living with autism.

Mitochondria

The human body requires energy in order to function, and mitochondria are what provide that energy. We digest sugar, protein, and fat into molecules that reach every cell in our body. ATP is the fuel that is used by the body, and mitochondria are little factories within cells that convert these food molecules into energy molecules called ATP. 
Mitochondria are also called the energy-producing powerhouses of the body. They are vital to our survival as they produce energy in the form of ATP (adenosine triphosphate) from the food we eat. This process is called cellular respiration. Mitochondria produce more than 90% of the energy needed by the body to sustain life and support organ function. Mitochondrial dysfunction results in excessive fatigue and other symptoms that are common in almost every chronic disease, from Alzheimer’s disease and cardiovascular disease to diabetes to autism.

Mitochondrial disorder

The mitochondrial disorder can strike both infants and children of all ages and yet is NOT KNOWN what causes the dysfunction in the mitochondria in the first place. They are commonly born with a range of difficulties from lack of muscle tone to lack of strength and poor appetite, difficulty sucking and high tolerance to pain.
Some babies might not show noticeable symptoms right away. For example, when the body is under a significant amount of stress, it requires even more energy. Though a child can get very sick if mitochondria are dysfunctional, there are times when you’ll see problems developing with the child’s neurology if there’s a prolonged illness.
Yes, vaccines are also stressful for the body, and in the case of a small child who, for some reason, has a genetic predisposition to the mitochondrial disorder, it is possible that the child’s development stops after vaccination
At least 50% of children living with autism has mitochondrial disfunction.

Mitochondrial disorders are a group of complex and potentially life-threatening illnesses caused by mutations in the mitochondrial DNA. Mitochondria are tiny organelles found inside our cells that play a key role in energy production. They convert energy from food into a form that our bodies can use to function normally.

When the mitochondrial DNA is mutated, the resulting disorder can affect any part of the body, including the heart, brain, muscles, or other organs. Symptoms can vary from person to person, but can include seizures, developmental delays, movement and coordination problems, muscle weakness, vision and hearing loss, and organ failure. In some cases, these disorders may be fatal.
The exact cause of mitochondrial disorders is unknown, but certain genetic factors can increase an individual’s risk. It is important to note that not all people with mitochondrial disorders will develop autism, but research has shown that there may be a link between the two conditions.
Abnormalities of mitochondrial function could affect about 80% of children with ASD. 

Sympoms of mitochondrial dysfunction

Depending on which cells in the body are affected by the malfunctioning of the mitochondria, it causes varying symptoms. In general, mitochondrial disease causes more severe symptoms when the cell makers in the muscles, brain, or nerves malfunction because these cells use more energy than other cells in the body. In general, symptoms can range from mild to severe, affect one or more organs, and appear at any age. Even people with the same mitochondrial disease may have different symptoms. In addition to both symptoms and severity, the onset of the disease (appearance of symptoms) also varies from person to person.

The most common symptoms are fatigue, but brain fog is also common when the mitochondria in the brain are not working properly.

Other symptoms may include:

  • pain
  • mood disorders
  • anxiety
  • depression
  • concentration disorder

Most chronic diseases/conditions are also linked to mitochondrial dysfunction, such as:

  • cardiovascular diseases
  • lung disease
  • vision and hearing problems
  • learning disabilities
  • autism
  • liver and kidney disease
  • digestive system diseases and symptoms
  • diabetes
  • neurological diseases (including dementia)
  • movement disorders

The Hannah Poling affair

During Hannah’s first 18 months, she suffered an adverse reaction to the 18-month-old vaccine, causing severe neurological and autistic symptoms. Hannah was 19 months when she received five vaccinations (diperte, influenza B, MMR, varicella, and inactivated polio). Hannah was a playful, interactive, and communicative baby two days prior to becoming lethargic, irritable, and feverish two days later. Several days after vaccination, he developed varicella-induced rashes.
 
Hannah was diagnosed with mitochondrial enzyme deficiency encephalopathy months later due to a delay in neurological and psychological development. The signs Hannah displayed all exhibited characteristics of autism spectrum disorder, including language and communication difficulties. It is common for children with mitochondrial enzyme deficiencies to develop neurological symptoms during the first and second years of their lives, but Hannah’s parents believed vaccines led to her disease.
His case in court was successful, though it’s unclear whether the little girl had a mitochondrial disorder prior to the vaccination, or if it was caused by a vaccination reaction.

If the child has a mitochondrial enzyme deficiency, the vaccines can cause developmental declines.

Biomedical specialists believe that mitochondrial problems can be very common in autism; however, there are treatments that can improve mitochondrial disorders.

It would be nice if mitochondrial testing could become part of normal neonatal screening to find out which babies may be more sensitive to heavy metals and chemicals — whether they have “only” mitochondrial dysfunction or mitochondria are functioning completely abnormally — and preventive measures could be taken to protect children.

If the child has a mitochondrial enzyme deficiency, the vaccines can cause developmental declines.

Biomedical specialists believe that mitochondrial problems can be very common in autism; however, there are treatments that can improve mitochondrial disorders.

It would be nice if mitochondrial testing could become part of normal neonatal screening to find out which babies may be more sensitive to heavy metals and chemicals — whether they have “only” mitochondrial dysfunction or mitochondria are functioning completely abnormally — and preventive measures could be taken to protect children.

Related articles:

  • Mitochondrial disorder and autism
  • Supplements for mitochondrial disorders
Resources
  • https://www.sciencedirect.com/science/article/pii/S2352304220300854
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137782/

Genetic disorders and Autism

Genetic disorders and Autism

possible cause of asd

Many researchers believe that the primary cause of autism are probably genetic disorders. However, it is not possible to find common ground among autistic children living with different genetic diseases. In fact, many known genetic syndromes can have a profound impact on a child’s development and also cause autism similar symptoms, but most children with autism do not have these main genetic disorders.

Here’s a brief explanation of the genetic/neurological conditions that are so far known to result in symptoms of autism:

Fragile X syndrome

This is the most commonly known genetic cause of developmental delay. It has an extremely rare occurrence. The symptoms of Fragile X are quite indistinguishable from autism, although children with Fragile X are more likely to be hyperactive and anxious. Unfortunately, Fragile X usually causes mental impairment, so these children will have to face more challenges in the coming years (most autistic children have a normal mental functions). Fortunately, the vast majority of children with autism have normal X chromosomes.

Fragile X is transmitted by the mother, so the presence of autism, or mental impairment on the mother’s side, would make this diagnosis more likely.              

Rett syndrome

The defect in the X chromosome is responsible for this genetic disorder. However, this affects only girls, because boy fetuses with this defect, as a rule, do not survive. Girls with Rett usually look completely normal, develop normally for several months or even years, and then regress. Characteristic hand-squeezing movements appear, as well as other “neuromuscular problems, such as unsteady walking, tremors, and muscle spasms.

Angelman syndrome

This disease is due to a defect in the UBE3A gene. It leads to severe mental retardation, seizures, and spasmodic muscles. Its symptoms are a happy facial expression, unusual laughter and symptoms characteristic of autism

Neurocutaneous disorders

These genetic-based disorders cause the growth of benign tumors in the brain and skin.  The two most common are: neurofibromatosis (NF) and tuberous sclerosis (TS). The development of the baby with these disorders usually begins normally.  However, when benign tumors begin to grow in the brain, they cause intellectual developmental delays, the child shows psychiatric symptoms, symptoms of autism and may also have seizures. Multiple cream-colored flat spots appear on the skin in the case of NF, or leaf-shaped white spots in the case of TS. A genetic examination and a CT or MRI scan of the brain can provide a diagnosis. 

Chromosome mutation 16P11.2

Children with 16p11. 2 deletion syndrome usually have developmental delay and intellectual disability. Characteristics of deletion syndrome include delayed development; intellectual disability; and autism spectrum disorder, which affects communication and social interaction, impaired communication and socialization skills, as well as delayed development of speech and language. This mutation has been found in some children with autism.                  

Bannayan-Riley-Ruvalcaba syndrome

This extreme disease occurs infrequently. It has been found in very few children with autism. It causes a very large head, increased body size, hemangiomas and small cysts form on the skin.     

Smith-Lemli-Opitz syndrome

This disorder develops due to a metabolic defect in cholesterol production. These children usually have a fusion of second and third toes, are characterized by disparate facial features, such as drooping eyelids, small and low-seated ears, or split uvula, small head size and characterized by slow growth.  

Fetal alcohol syndrome

This happens when a pregnant woman drinks alcohol as a way of life, which has consequences for the developing nervous system of the fetus. These babies are retarded in development and show different characteristics of autism, especially hyperactivity. They have a characteristic appearance: the groove between the nose and the upper lip, the so-called philtrum, is flat: the upper lip is thin: the eyes are close to each other. The diagnosis is based on known alcohol exposure.

Landau-Kleffner syndrome

The main feature of this syndrome is the development of seizures from the age of three to seven years, as well as language regression. It differs from autism in that social skills usually remain normal, and the loss of language ability occurs much later than in autism.

Although the last two are not genetic diseases, it is also up to a neurologist to determine their presence, as in the case of the other disorders mentioned above.

What remains a question for researchers is whether there is a single underlying genetic cause of autism. No genetic disease has been identified that is present in all children with autism, and is expected to be less and less likely to do so. In fact, it is important to screen for genetic diseases in order to identify the genetic risk in infants and to start treatment and development as early as possible.

Resources
  • m B-R, SeoH-S, Ku J-M, et al. Silibinininhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast-cells. Inflammation. Research. 2013;62(11):941-950. doi:10.1007/s00011-013-0640-1.
  • ChapowalA. PetasitesStudy Group. Randomisedcontrolled trial of butterbur and cetirizine for treating seasonal allergic rhinitis. BMJ 2002;324:144-6.
  • Hayes, N. A. and Foreman, J. C. The activity of compounds extracted from feverfew on histamine release from rat mast-cells. J Pharm Pharmacol1987;39(6):466-470
  • Hsieh et al. Baicalein inhibits IL-1ß- and TNF-a-induced inflammatory cytokine production from human mast-cells via regulation of the NF-?B pathway. ClinMolAllergy. 5: 5. 2007.
  • TheoharidesTC, Patra P, Boucher W, et al. Chondroitin sulphateinhibits connective tissue mast-cells. British Journal of Pharmacology. 2000;131(6):1039-1049. doi:10.1038/ sj.bjp.0703672.
  • Ro JY, Lee BC, Kim JY, et al. Inhibitory mechanism of aloe single component (alprogen) on mediator release in guinea pig lung mast-cells activated with specific antigenantibodyreactions. J PharmacolExpTher. 2000;292:114–121. 73.
  • https://www.ncbi.nlm.nih.gov/pubmed/24477254
  • https://www.ncbi.nlm.nih.gov/pubmed/28458279
  • https://www.ncbi.nlm.nih.gov/pubmed/9421440
  • https://www.ncbi.nlm.nih.gov/pubmed/10344773
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315779/
Possible causes of Autism

Possible causes of Autism

causes of asd

As parents, we are very shocked when it turns out that our child is not developing properly and finally receives the diagnosis. We as a parent would try everything that shows promise, just to help our child. Why we? We are trying to find a possible cause of autism, but this medical problem is very complex and difficult to find the exact cause, but there are a few possibilities to start

AUTISM is a very complicated condition that can have many causes, and precisely because it can cause autistic symptoms, it is terribly difficult to find a solution to it. Because what works for one child is not the cause of their symptoms for another, only the symptoms are similar.

What are the possible causes of autism

The exact cause of autism is not fully understood, and it is likely that there are multiple factors that contribute to the development of the disorder. Research has shown that both genetic and environmental factors may play a role in the development of autism.

Genetic factors:

Many studies have found that people with autism are more likely to have certain genetic variations or mutations. These genetic changes may be inherited from a person’s parents or may occur spontaneously during fetal development. It is thought that the combination of multiple genetic changes may contribute to the development of autism.

Environmental factors:

Research has also identified a number of environmental factors that may increase the risk of developing autism. These include prenatal exposure to certain medications, infections, and toxins; premature birth; and certain medical conditions that occur during pregnancy or childbirth. However, it is important to note that most people with these risk factors do not develop autism, and that the majority of cases of autism do not have a known cause.

Autism can be an associated medical state of certain genetic diseases which can be a more severe genetic disease or “just” a genetically determined methylation problem.

There are so-called biomedical theories regarding the causes of autism. Examples include:

Exposure to toxic chemicals

In our modern society, we are exposed to many hazardous chemicals. Air and water are becoming increasingly polluted, heavy metals can get into our bodies from toys, food and, water, etc., we come into contact with toxic chemicals every day, which are added to household accessories and furniture, but they are also found in pesticides and food.

We know that metals like lead and mercury can damage brain tissue. We know that various body organs can be damaged by chemicals, causing metabolic and hormonal imbalances. In fact, the immune system can also be affected by these heavy metals, leaving the body more open to various degenerative states. It is possible that these exposures add up, and some babies simply cannot handle this load, which begins already in the womb and continues throughout childhood.

In 2004, an Environmental Working Group examined the umbilical cord blood of ten randomly selected mothers and found a staggering amount of chemicals and pollutants. Tests revealed 287 different toxic chemicals, including mercury, pesticides, and other chemicals (Source: https://www.ewg.org/research/body-burden-pollution-newborns)

Most of the chemicals found are known to cause cancer, mutations, and birth defects. The study showed that the question is not whether unborn babies are exposed to toxins but how exposed they are to poisons and how they are affected by such amounts of poison.

The developing nervous system of the infant (which usually happens from conception to the age of three) is particularly susceptible to damage caused by such exposures. When a brain cell is damaged, so are the dozens of nerve pathways that connect the cells. If, for example, the area of the brain that regulates language development is damaged by thousands of nerve cells, then the child’s speech development and comprehension will be delayed, or his speech will simply be incomprehensible. Depending on the rate of injury.

Many environmental toxic substances – including mercury, lead, arsenic, and toluene – cause neurodevelopmental disorders such as autism, cerebral palsy, ADHD, and mental retardation. This may be due to the fact that the developing brain is more sensitive to injuries caused by toxic substances than the adult brain. https://www.psychiatrictimes.com/view/environmental-toxicants-and-autism-spectrum-disorder

Autism is a multifactorial neurodevelopmental disorder caused by genetic and environmental factors.  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377970/

According to the latest evidence,  up to 40-50% of autism spectrum disorder (ASD) can be determined by environmental factors. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356236/

Although the role of genetic disorders in autism spectrum disorder (ASD) is accepted as a fact, recent studies point to an equal contribution of environmental factors, especially environmental toxic substances. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944636/

It is not yet possible to know exactly what environmental toxins contribute to autism. Prevention is of paramount importance since the elimination of toxins is a very difficult task. It is very important to limit the exposure of the expectant mother and baby.

It is worth learning how best to remove those chemicals from the vicinity of our children. Download the most common toxin deposits here

However, the theory of chemical exposure does not answer the question of why autism occurs in some children but not in others. This is just the only element of the puzzle. The answer to this should be sought in the child’s genetics, his methylation state! There we find the answer to the question of why environmental toxins can cause neurological symptoms in one child and not in another. This can help us understand why autism is a spectrum in which children show different symptoms and are affected with varying degrees of severity.

Studies have shown that children with autism have significantly higher heavy metal loads. Likely, detoxification processes and cell regeneration do not work properly in children with autism, and this can be caused by methylation disorder.

You can find articles on methylation here: Methylation and Autism

List of other probabile cause of Autism

If you want to read more about the possible causes, just click the name of the causes below:

 

  • Genetic problems
  • Differences in brain structure in autism
  • Prenatal and birth factors
  • Theory based on disorders of mitochondria
  • Methylation disorders
Resources
  • m B-R, SeoH-S, Ku J-M, et al. Silibinininhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast-cells. Inflammation. Research. 2013;62(11):941-950. doi:10.1007/s00011-013-0640-1.
  • ChapowalA. PetasitesStudy Group. Randomisedcontrolled trial of butterbur and cetirizine for treating seasonal allergic rhinitis. BMJ 2002;324:144-6.
  • Hayes, N. A. and Foreman, J. C. The activity of compounds extracted from feverfew on histamine release from rat mast-cells. J Pharm Pharmacol1987;39(6):466-470
  • Hsieh et al. Baicalein inhibits IL-1ß- and TNF-a-induced inflammatory cytokine production from human mast-cells via regulation of the NF-?B pathway. ClinMolAllergy. 5: 5. 2007.
  • TheoharidesTC, Patra P, Boucher W, et al. Chondroitin sulphateinhibits connective tissue mast-cells. British Journal of Pharmacology. 2000;131(6):1039-1049. doi:10.1038/ sj.bjp.0703672.
  • Ro JY, Lee BC, Kim JY, et al. Inhibitory mechanism of aloe single component (alprogen) on mediator release in guinea pig lung mast-cells activated with specific antigenantibodyreactions. J PharmacolExpTher. 2000;292:114–121. 73.
  • https://www.ncbi.nlm.nih.gov/pubmed/24477254
  • https://www.ncbi.nlm.nih.gov/pubmed/28458279
  • https://www.ncbi.nlm.nih.gov/pubmed/9421440
  • https://www.ncbi.nlm.nih.gov/pubmed/10344773
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315779/
General Symptoms of Autism

General Symptoms of Autism

early symptoms of autism

Autism, also known as autism spectrum disorder (ASD), is a developmental disorder that affects communication and social interaction. The severity of ASD can vary widely, and different individuals with ASD may experience different symptoms.

What are the classic symptoms of autism?

  1. Difficulties with social interaction: Children with ASD may have difficulty engaging in social interactions, such as making eye contact, initiating or maintaining conversations, or understanding social cues.
  2. Repetitive behaviors or interests: Children with ASD may have repetitive behaviors or interests, such as lining up toys or objects, or exhibiting strong interests in a specific topic.
  3. Communication challenges: Children with ASD may have difficulty with communication, including delays in language development or difficulty using language to communicate their needs or desires.
  4. Sensory processing issues: Children with ASD may have sensory processing issues, such as oversensitivity to certain sounds or textures, or under-sensitivity to pain or temperature.
  5. Unusual responses to sensory stimuli: Children with ASD may have unusual responses to sensory stimuli, such as a fascination with lights or a strong aversion to certain sounds or textures.

 

What are the symptoms of autism in older children

The symptoms of autism in older children are generally similar to those seen in younger children, although the specific symptoms and their severity can vary widely from one individual to another. Some common symptoms of autism in older children may include:

  1. Difficulty with social interactions: Older children with autism may have difficulty engaging in social interactions, such as making eye contact, initiating or maintaining conversations, or understanding social cues.
  2. Repetitive behaviors or interests: Older children with autism may engage in repetitive behaviors or have strong, narrow interests.
  3. Communication challenges: Older children with autism may have difficulty with communication, including delays in language development or difficulty using language to express their needs or desires.
  4. Sensory processing issues: Older children with autism may have sensory processing issues, such as oversensitivity to certain sounds or textures, or under-sensitivity to pain or temperature.
  5. Unusual responses to sensory stimuli: Older children with autism may have unusual responses to sensory stimuli, such as a fascination with lights or a strong aversion to certain sounds or textures.

Here you can find some of the early symptoms

  1. Lack of eye contact: Children with autism may avoid making eye contact or may not respond when someone else is looking at them.
  2. Delays in language development: Children with autism may have delays in language development or may have difficulty using language to communicate their needs and desires.
  3. Difficulty engaging in social interactions: Children with autism may have difficulty initiating or maintaining social interactions, such as playing with other children or engaging in back-and-forth conversations.
  4. Repetitive behaviors: Children with autism may engage in repetitive behaviors, such as hand-flapping or repeating words or phrases.
  5. Unusual responses to sensory stimuli: Children with autism may have unusual responses to sensory stimuli, such as a fascination with lights or a strong aversion to certain sounds or textures
Resources
  • m B-R, SeoH-S, Ku J-M, et al. Silibinininhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast-cells. Inflammation. Research. 2013;62(11):941-950. doi:10.1007/s00011-013-0640-1.
  • ChapowalA. PetasitesStudy Group. Randomisedcontrolled trial of butterbur and cetirizine for treating seasonal allergic rhinitis. BMJ 2002;324:144-6.
  • Hayes, N. A. and Foreman, J. C. The activity of compounds extracted from feverfew on histamine release from rat mast-cells. J Pharm Pharmacol1987;39(6):466-470
  • Hsieh et al. Baicalein inhibits IL-1ß- and TNF-a-induced inflammatory cytokine production from human mast-cells via regulation of the NF-?B pathway. ClinMolAllergy. 5: 5. 2007.
  • TheoharidesTC, Patra P, Boucher W, et al. Chondroitin sulphateinhibits connective tissue mast-cells. British Journal of Pharmacology. 2000;131(6):1039-1049. doi:10.1038/ sj.bjp.0703672.
  • Ro JY, Lee BC, Kim JY, et al. Inhibitory mechanism of aloe single component (alprogen) on mediator release in guinea pig lung mast-cells activated with specific antigenantibodyreactions. J PharmacolExpTher. 2000;292:114–121. 73.
  • https://www.ncbi.nlm.nih.gov/pubmed/24477254
  • https://www.ncbi.nlm.nih.gov/pubmed/28458279
  • https://www.ncbi.nlm.nih.gov/pubmed/9421440
  • https://www.ncbi.nlm.nih.gov/pubmed/10344773
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315779/
M-CHAT

M-CHAT

Modified Early Childhood Autism Questionnaire

 

Please answer the following questions based on your toddler’s usual behavior. Try to answer  all your questions. If the activity or behavior in the question is rare (you have only experienced it once or twice  in the child  so far), then the question should  notbe answered with a mel.

 

 

 Child’s name:                                                             Date of birth:                  Today’s date:

 

 

1. Does your child like  to be rocked,   rocked,  ridden on the knees, etc.?

Yes

No

2. Does  your child have an interest in  other children?

Yes

No

3. Does your child like  to climb things, eg.  stairs?

Yes

No

4. Does your child enjoy  playing hide and seek games?

Yes

No

5. Is your child used to  role-playing games (pretending to be on the phone, caring for a baby,  etc.)?

Yes

No

6. Does your child point out with his index finger things that  he would like to receive?

Yes

No

7. Does your child point out things of interest   to him with his index finger, thereby expressing  his interest? 

Yes

No

8. Can your child use their smaller toy items for their intended purpose (pushing the small car,  trying to build from the bricks,  rather than  just taking it in  their mouth,  poking them, throwing  them off)?

Yes

No

9. Will your child bring   you things to show you something?

Yes

No

10. Will your child look into   your eyes for more than a second or two?

Yes

No

11. Does  your child  appear to be hypersensitive to noises (e.g. they often catch their ears)?

Yes

No

12. Will  your child smile back when he sees your  face,  your smile?

Yes

No

13. Does   your child imitate you (e.g. facial expression, grimace)?

Yes

No

14. Does  your child listen to his own name  , does he pay attention when you call him   by his name?

Yes

No

15. If you point to a toy  that is at the  other end of the  room, does  your child look at the toy  as well  ?

Yes

No

16. Can your child walk?

Yes

No

17. Does your  child follow your   gaze? Does  he also  look at the  things that you are looking at with interest?

Yes

No

18. Does your child have a weird way of moving  their  fingers around  their face?

Yes

No

19. Does your child try to  draw your  attention to what they are doing, playing?

Yes

No

20.  Have you ever wondered if your child might be deaf?

Yes

No

21. Does your child  understand  what  people say?

Yes

No

  22. Does it happen that your child  stares into nothingness or walks  aimlessly in a mess?

Yes

No

23. When in an unknown, foreign situation, does your child look at your face, check your facial expression, reaction?

Yes

No

Guide to the useof M-CHAT, user rights and obligations

The Modified Early Childhood Autism Questionnaire (M-CHAT; Robins, Fein, & Barton, 1999) and its supplementary materials are freely available for download from official resources for clinical, research, and educational purposes.   There are two official sources, the www.firstsigns.org site and dr.  Robins’ website,  http://www.mchatscreen.com.

The M-CHAT questionnaire is still the subject of research, so it may be modified even further in the future. All newer versions will also be available on the above two websites.

The M-CHAT questionnaire is protected by copyright.  Each user is obliged to  adhere to the following rules:

  1. At the bottom of each copy or printout of the M-CHAT questionnaire,  a copyright indication of the ownership of the authors must be indicated ( © 1999 Robins,    Fein, & Barton). Questions, the order of questions, or instructions for users cannot be modified without the permission of the authors.
  2. The M-CHAT questionnaire should be used in its entirety. Based on any part of the questionnaire,  we cannot obtain demonstrably credible information.
  3. The permission of the authors must be requested for the printed publication of the M-CHAT questionnaire (in books, journal articles, etc.) or for its electronic use (for anamnesis  and other similar software uses that  can be stored on a computer  ). Diana Robins  can be contacted  at  mchatscreen2009@gmail.com email address.
  4. Users working in medical practices are free to use the M-CHAT questionnaire in their own practice (e.g. electronic anamnesis), but if they would like to publish or distribute the document outside their practice,  please contact Diana Robins at the  email address above  and ask her for permission.

Instructions for use

M-CHAT is a certified questionnaire that can help screen young children aged 16-30 months for autism spectrum disorder (ASD). The questionnaire can also  be completed and  evaluated as part of a routine medical review  (status test), but it can also be used by   specialists  and other specialists in autism spectrum disorder screening.

The essence of the M-CHAT questionnaire is to be as sensitive a screening material as possible,  that is, with its help we can treat as many autism spectrum disorders as possible. Consequently, the questionnaire often gives a false positive result. This means that not all children who receive high scores on this questionnaire will end up being diagnosed with autism spectrum disorder.  To refine the  false positive results, the authors developed a guided follow-up interview, which should be used in accordance with the M-CHAT questionnaire and can also be freely downloaded from the two websites mentioned above.  Users of the  questionnaire should be aware that even after the follow-upinterview has been conducted and evaluated, a significant number of  children remain who are screened by the M-CHAT survey, but are not later found to be people with autism spectrum disorder. At the same time, these children are at risk of having some other developmental disabilities or lagging behind. Based on this, the authors recommend that all children who receive a high autism spectrum disorder score on the M-CHAT survey should proceed to the appropriate screening tests.

The M-CHAT questionnaire can be evaluated in less than two minutes, the    author’s instructions can be downloaded from the www.firstsigns.org or  http://www2.gsu.edu/~wwwpsy/faculty/robins.htm pages.

Children who do not show the normal result or developmental stage for 3 or more questions or 2 or more critical questions (especially if a follow-up  interview related to the M-CHAT questionnaire also shows the discrepancy at the same points)   should continue to for review by a  specialist specializing in screening for autism spectrum disorders in early childhood.  In addition, since no screening device can be 100% sensitive, the authors also recommend reviewing all young children whose parents, doctors, or other professionals are suspected of autism spectrum disorders.

Evaluation of the M-CHAT questionnaire

The M-CHAT questionnaire should preferably not be evaluated by the person who picked it up.  During the verification of  M-CHAT,  for example, it was the authors themselves who evaluated all the questionnaires, not their colleagues. Furthermore, the M-CHAT questionnaire is not there for parents to filter their own children with its help. The authors strongly warn that if a parent begins to worry about the development or health of their child, they should first visit a pediatrician.

The first version of the M-CHAT questionnaire was compiled in the UK, called CHAT. The first version was further developed by American researchers, creating the current M-CHAT questionnaire. The questionnaire consists of 23 questions to be decided.

According to the questionnaire, a small child is at increased risk of having an autism spectrum disorder if 2 critical questions or any 3 questions are not answered correctly. Yes/no answers to the questions  to be decided fall  into the ‘appropriate’ or ‘inappropriate’ categories at the time of the assessment, as  shown in the table below  :

 

The table shows the answers specific to the risk group for inadequate autism spectrum disorders, with thickened highlights indicating critical issues. When the questionnaire response matches the answer in the table, it represents one point.

 

 

1. Yes

6. Yes

11. Yes

16. No

21. Yes

2. Yes

7. No

12. Yes

17. No

22. Yes

3. Yes

8. Yes

13. Yes

18. Yes

23. Yes

4. Gender

9. Gender

14. No

19. No

 

5. Yes

10. Yes

15. No

20. Yes

 

 

Not all young children who are in the high-risk group based on the M-CHAT questionnaire will actually  diagnosed with  some form of autism spectrum disorder. The compilers of the questionnaire recommend that all such young children be thoroughly examined by a competent specialist.

Understanding is the first step

Young people with autism learn from childhood how to understand the world around them and behave in the way expected by the environment. They don’t lack emotions; they just don’t know how to express them in a way others can understand. During years of work, they develop their ability to express and cooperate. The earlier they start dealing with an autistic child in this way, the greater the chance that he will be successful in social relations later on.
It is important that when we communicate with an autistic individual, we understand the limitations he lives with and recognizes the efforts he makes. Let’s show him patience and acceptance.

ADHD in general

ADHD in general

ADHD

Attention deficit hyperactivity disorder, abbreviated to ADHD, encompasses three main groups of symptoms: attention deficit, hyperactivity, and impulsivity. Ignoring details, difficulty maintaining attention, problems with organizing and completing tasks, avoiding tasks that require sustained attention, forgetfulness, losing various objects are all among the symptoms.

ADHD does not mean mental disability!

Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder that affects a person’s ability to pay attention, control impulsive behaviors, and regulate activity levels. It is usually diagnosed in childhood, although it can continue into adulthood.

Symptoms of ADHD may include difficulty paying attention or following instructions, impulsivity, and hyperactivity. People with ADHD may have difficulty completing tasks, following rules, or controlling their behavior in social situations.

The exact cause of ADHD is not fully understood, but it is thought to be related to abnormalities in brain development and function.

It seems more and more likely that ADHD is a nutritional problem Check the article about this topic HERE

Characteristics of autism

Nevertheless, some signs can help you recognize this disorder, so if you come face to face with it, you will understand better why an autistic young person does what they do. You will also be able to behave appropriately in the situation.
First, most autistic children avoid the company of others, preferring to be alone because they usually have difficulty communicating with others because they find it difficult to understand the hints and metaphors that other people use daily. Facial expressions do not necessarily mean the same to them as they do to others. To adapt, they need to learn these key cues.
The other big difference lies in the perception of autistic people: many of them report contains much information from their senses, often overwhelmed and confused. In fact, we are also exposed to the same number of stimuli, but our brain classifies and filters them according to their importance. That’s why we don’t become aware of every stimulus – only as much as our brain can still process.

Symptoms of ADHD may include

  1. Difficulty paying attention: Individuals with ADHD may have difficulty paying attention to tasks or activities, especially those that are not interesting or stimulating.
  2. Difficulty controlling impulsive behaviors: Individuals with ADHD may have difficulty controlling their impulsive behaviors, such as interrupting others or acting without thinking.
  3. Excessive levels of activity or restlessness: Individuals with ADHD may be excessively active or restless, and may have difficulty sitting still or engaging in quiet activities. 
  4. Difficulty maintaining attention during tasks or games
  5. His mind seems to be elsewhere, even when there are no distractions
  6. Avoids, dislikes, or is reluctant to participate in tasks that require sustained mental effort
  7. He is often forgetful in his daily activities
  8. He overlooks or does not notice details, inaccuracy during work
  9. It is often difficult for him to organize tasks and activities
  10. He starts tasks, but quickly declines and is easily distracted
  11. Often loses things needed for tasks or activities

Hyperactivity and impulsivity symptoms

  1. Too much talk
  2. Interrupts others or behaves intrusively
  3. Often runs or climbs on things in situations where it is inappropriate
  4. Walks up and down or taps his hands/drums his feet or nestles in place
  5. He often leaves his seat in situations where he should be sitting still
  6. It’s hard to wait
  7. Often unable to play quietly or be still during leisure activities
  8. He often has “could go” or “like he was pulled over”.
  9. Says the answer before the question is finished

Treatments of ADHD

  1. Behavior therapy: Behavior therapy can help individuals with ADHD develop strategies for managing their symptoms and improving their behavior.
  2. Family therapy: Family therapy can involve involving family members in treatment to help support the individual with ADHD and improve communication and relationships within the family.
  3. Group therapy: Group therapy can provide a supportive environment for individuals with ADHD to share their experiences and learn from others.
  4. Physical exercise: Regular physical exercise has been shown to improve symptoms of ADHD. Activities such as running, jumping, or playing sports can help to burn off extra energy and improve focus.
  5. Yoga and mindfulness: Yoga and mindfulness practices can help children with ADHD to focus on the present moment and regulate their breathing, which can be beneficial for managing symptoms such as impulsivity and hyperactivity.
  6. Brain breaks: Short, structured activities that allow children to take a break and shift their focus can be helpful for managing symptoms of ADHD. This could include taking a quick walk, doing a simple puzzle, or playing a quick game on a tablet.
  7. Social skills training: Children with ADHD may struggle with social interactions and may benefit from learning social skills such as making friends, participating in group activities, and learning how to communicate effectively with others.

IMPORTANT

If your child shows the symptoms of ADHD check his nutritional deficiency. Read this article to know where to start:Nutritional deficiencies in ADHD

Resources
  • https://semmelweis.hu/mediasarok/2017/04/20/a-figyelemhianyos-hiperaktivitas-zavar-jol-kezelheto-ezert-is-fontos-a-korai-felismeres/
  • https://onlinepszichologus.net/blog/a-figyelemhianyos-hiperaktivitas-zavar-tunetei/
  • https://www.hazipatika.com/betegsegek_a_z/hiperaktivitas_adhd_figyelemhianyos_hiperaktivitas-zavar
Early signs of Autism

Early signs of Autism

Autism spectrum disorder is one of the most common complex developmental disorders. According to the latest epidemiological surveys, it affects approximately 1% of children, but this number is increasing. More and more children are diagnosed with autism every day. This article will discuss the early signs of autism. Parents should pay attention to these early signs.

Autism in general

Autism fundamentally affects a child’s ability to create social relationships, communication, play, imagination, thinking, and behavior. A comprehensive disorder covering a broad spectrum in which the symptoms’ nature, severity, and intensity can be significantly different. In the last decade, the name autism spectrum disorder was introduced to describe the condition, indicating that the symptoms range from very severe to mild. In classic childhood autism disorder, children’s communication skills are visibly impaired; they are only minimally able to communicate with those around them, their behavior is severely repetitive, and changes are extreme and difficult to tolerate. At the other end of the spectrum, there are well-functioning autistics who, albeit unusually, create relationships with others, their use of language is specific, and their interests are different from their typically developing peers, sometimes excessively intense. The clinical picture is extremely diverse, depending on the degree of autism, other associated disorders, and the child’s mental state and personality. There is no single behavior, no single symptom that is always present, and no one that excludes the diagnosis of autism. [2] depending on the associated other disorders, the child’s mental state and personality are extremely diverse. There is no single behavior, no single symptom that is always present, and no one that excludes the diagnosis of autism. [2]

Why is early detection important?

Although the symptoms develop before age 3, the diagnosis is usually only made years after the first parental signs. According to prospective research, there are no behavioral signs specific to autism during the first year of life. Still, characteristic qualitative differences already appear during the second year, so professionals experienced in autism can already establish the diagnosis around the age of 2 years. The pediatrician needs to recognize the symptoms of autism as soon as possible because this allows the child to receive care in time. It has been clearly proven that early evidence-based autism-specific interventions significantly improve the prognosis. [3] Early recognition of the condition is also very important for parents because, in connection with serious behavioral problems, they often try to help with inefficient educational methods and experience parental “incompetence.” The diagnosis enables parents to understand their child’s blockages and learn to help them with autism-specific strategies. In this way, they can significantly contribute to meeting their children’s special needs. The family needs to receive correct genetic counseling.

Early signs of autism

Reciprocity is fundamentally important in social interaction: back-and-forth interaction, cooperation, and partnership. In autism, this reciprocity is fundamentally impaired.

In severe cases, a child with autism is more interested in objects than in people. The child seems aloof, withdrawn, and indifferent. One of the most striking early symptoms is the lack of joint attention and sharing of interests. For example, if the parent tries to draw the child’s attention to something by pointing, the child does not follow the direction of the pointing; the child does not spontaneously show his parents what he likes. Your child does not take part in social games with pleasure (e.g., peek-a-boo games, cookies-cookies), and does not imitate everyday actions. Later, it is difficult to involve him in joint activities and games; he prefers solitary pursuits. He expresses his emotions little and sometimes in an unusual way; he also reacts less to the emotions of others (e.g., he does not share his joy, he flies his hands in joy; he does not notice when the other person is in trouble, does not ask for help in trouble). For the most part, they cannot use eye contact properly to regulate social interactions.

Communication differences can be very broad: from a child who does not speak at all to a child who speaks fluently with a vocabulary that exceeds his age but is difficult to engage in conversation. Most children’s speech development is delayed (except for Asperger’s syndrome), which is most often the symptom that causes parents to seek help. It happens that the child says a few words around the age of one, then abandons them, and the vocabulary grows very slowly. A child with autism does not try to make up for the lack of speech with non-verbal means; he cannot properly express his intentions (e.g., he does not use easily understandable gestures, he cannot point to the desired object, but pulls the parent’s hand when he wants to achieve something; he does not use his head indicate protest or approval) and do not even understand similar signals from their environment. He often repeats the speech he hears (echoalates), uses borrowed panels in his speech, and swaps personal pronouns. Many times his speech is not directed at a person. Rather he monologues or comments on his actions. He usually uses unusual intonation and speaks in a flat, monotone voice. In a severe condition, he does not understand speech; it seems as if he does not hear, and he does not even pay attention to your name.

Repetitive behavior and narrowed interests are common among children with autism. Narrowed interests can also prevent the child from normal activities and social interaction. Instead of the functional use of objects, he is bound by the details of objects, for example, strings, turning a car wheel, opening a door, etc. Instead of the “pretend” or “role” games expected at his age, he arranges the objects in a row, sorts them according to his own logic, and arranges them again and again. High-ability children with Asperger’s syndrome often delve into one topic for a long time. They often adhere to the usual things to the extreme to establish non-functional routines. If something changes, they react with hysterics (e.g., a change in their regular route). Repetitive movements of the hands and body are also common (e.g. , flapping, flitting hand movements in an excited state, rocking back and forth, unusual posture)

Early signs list

Early signs of autism in babies (6 months to one year) may include:

  • Smiling rarely in social situations
  • Unexpected reactions to new faces
  • Little or no eye contact
  • Doesn’t respond to their name
  • Doesn’t turn their head to locate sound or react to loud sounds
  • Overreacts to sounds
  • Displays a lack of social ‘anticipation’. For example, baby doesn’t reach out their arms to be picked up, or doesn’t seem to understand the game of ‘Peek-a-Boo’.
  • Doesn’t use ‘chatter’ or ‘babble’
  • Doesn’t use gestures such as pointing or waving in context.
  • Dislikes being cuddled or touched
  • Displays repetitive and unusual body movements.

Early signs of autism in toddlers up to 24 months may include:

  • Does not speak
  • Only walks on their toes
  • Unable to follow simple verbal instructions
  • Doesn’t imitate actions
  • Has an intense interest in certain object and gets ‘stuck’ on them, such as constantly flicking a light switch.
  • May be very interested in ‘unusual’ objects, such as metal objects.
  • Engages in repetitive activities, such as lining up objects.

Early signs of autism in young children up to 36 months may include:

  • Has limited speech
  • Has difficulty understanding simple verbal instructions
  • Has little interest in ‘pretend’ or ‘imaginative’ play
  • Shows little interest in other children
  • Likes to follow routine and gets easily upset by change.
  • Is extremely sensitive to sensory experiences, such as sight, sound, smell and taste.
  • Is under-sensitive to sensory experiences such as hot and cold, touch and pain.

Recognition algorithm

Regular follow-up of development based on screening examinations
Targeted observation of the child as follows [4]:

  • use of gaze;
  • warm, joyful facial expressions accompanied by eye contact;
  •  sharing interest or pleasure;
  • response to name;
  • coordination of eye contact, facial expression, gestures, and tone of voice;
  • showing;
  • prosody;
  • repetitive movements or postures of the body, arms, hands, or fingers;
  • repetitive movements with objects.

If we see a discrepancy:
• targeted hearing test;
• access to early development services;
• targeted autism screening using CHAT.

The CHAT screening test [5] is recommended to be performed between 18 and 24 months of age. Its evaluation is simple; it has five key elements: A5 (symbolic play), A7 (pointing to attract attention), Bii (joint attention), Biii (like a game), and Biv (pointing to an object). If the child underperforms in all five elements, it indicates a high risk of autism. Those who perform below only in the A7 and Biv elements show a medium risk. A further autism-specific diagnostic test is required if the child does not perform well in the control test after one month. The screening test is particular for autism but cannot screen out mild cases. Find below the M-Chat Screening test.
If autism is suspected based on the above:
• a complex child psychiatric, psychological and special education examination is recommended.

M-Chat screening test

Children with more severe symptoms than those with a pervasive developmental disorder may have an autistic disorder. Autism is characterized by more severe disabilities in social and linguistic functioning and repetitive behavior. Often the patient has to face mental retardation and seizures. Check out M-Chat screening test in the related articles.

Related Articles:

M-Chat screening test
Resources

[1]       Center of Disease Contorll and Prevention Prevalence of autism spectrum diorders. CDC MMWR Surveillance Summaries. 2007;58(SS10):1−20.

[2]       Balázs A. Autizmus Autizmus Spektrum Zavar. Szakmai irányelvek. NEFMI Autizmus alapítvány. Megjelenés alatt.

[3]       Rogers SJ, Dawson G. Early Start Denver Model for young children with autism: Promoting language, learning, and engagement. Nem York, NY US Guilford Press, 2010.

[4]       Wetherby A, Woods J, Allen L, Cleary J, Dickinson H, Lord C. Early indicators of autism spectrum disorders in the second year of life. J Autism Development Disord. 2004;34:473−493.

[5]       Baron-Cohen S, Allen J, Gillberg C. Can autism be detected at 18 months? The needle, the haystack and the CHAT. Br J Psychiat. 1992;161:839−843.

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