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男孩在床上

NEURODEVELOPMENTAL DISORDERS

"I am different, not less."   -Dr. Temple Grandin

An increasing number of children (currently up to 1 out of every 44 in the U.S.) are identified as autistic [1].

Challenges of Autism

Autism is a spectrum of neurodevelopmental conditions that can present in many ways. Core signs include unique behaviors and obstacles to communication or social interaction.

 

Some with autism are incredibly gifted, yet speaking or interacting with others is nearly impossible. Others struggle with hyperactivity or expressing emotions. When family or friends show them love and care, they are unable to respond positively, which can unfortunately lead to strained relationships.

There is no approved medical treatment for the core symptoms of autism, and not everyone feels there should be. PS128 has helped many people manage some of the challenges that come with being autistic, as well as showing significant benefits in multiple clinical studies. Some of these results are described below.

Image by MI PHAM

Studies

Autism - PS128 Early vs. Late intervention

Autism - PS128 Early vs. Late intervention
(Taiwan, 2023)

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Study Summary

  • Type: randomized, placebo-controlled, parallel, double-blinded
  • Location: MacKay Memorial Hospital, Taipei, Taiwan
  • Participants: 86 individuals with ASD, ages 2.5-7, male and female
This was a double-blind, randomized, parallel, placebo-controlled study with two stages of interventions, each lasting 2 months. In the first stage, eligible subjects were randomly allocated into either a probiotic group or placebo group using treatment codes (V1). After completing the first 2-month intervention (V2), all subjects received the second 2-month intervention of probiotic capsules. After finishing the two stages of the 4-month trial period, the subjects completed their participation.

Results

Anxiety, depression, and other autism-related behaviors were improved in earlier treatment of PS128.

The Achenbach System of Empirically-Based Assessment (ASEBA) comprises instruments for assessing behavioral, emotional, social, and thought problems and adaptive functioning. It includes the Child Behavior Checklist (CBCL) which acts as a diagnostic screener for children with abnormal behaviors.  

 

Autism - PS128 vs. Other Probiotics
(Italy, 2021)

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Study Summary

  • Type: open-label, double-arm, baseline-controlled study
  • Location: San Matteo Foundation (Pavia), Italy
  • Participants: 131 autistic individuals, average age of 7, male and female
Participants received a daily dose of either PS128 or other probiotics for 6 months. Clinical Global Impression (CGI) scores based on a clinician’s overall assessment of each patient were collected before and after the treatment period.

Results

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Patients improved by taking PS128
  • 87% of the PS128 group showed improvement, while 40% of those taking other probiotics did.
  • Of the improved PS128 group, 34% were “very much improved” or “much improved.”
  • The most common benefits were
    • increased shared attention
    • reduced stereotyped (repetitive) movements, and
    • improved communication skills.
Reduced severity
after PS128
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  • Average CGI-Severity score of the PS128 group improved from "markedly ill" to "moderately ill."
  • The PS128 group's average improvement was more than twice of those taking other probiotics.
  • Very few side effects and no serious adverse events were reported.
ASD Italy 2021
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Study Summary

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Condition improvement after treatment
  • ​Significantly improved CGI-Improvement scores (measuring a clinician’s assessment of each patient’s improvement during the trial) were seen in those given both PS128 and oxytocin.
  • Participants taking only PS128 or oxytocin also improved much more than the placebo group.
  • SRS and ABC scores improved in subjects given PS128 and even more in the combination therapy, with p values that were not statistically significant.
  • These benefits, as well as substantial increases in beneficial species of gut microbiota, suggest synergy between PS128 and oxytocin.
  • All treatment was well-tolerated, without serious adverse events.

Autism - PS128 + Oxytocin vs. Placebo
(USA, 2021)

  • Type: randomized, placebo-controlled, double-blinded, two-stage pilot trial
  • Location: Massachusetts General Hospital, USA
  • Participants: 35 individuals with ASD, ages 3-20, male and female
Participants received a daily dose of either PS128 or a placebo for 28 weeks. Once 16 weeks had passed, daily nasal oxytocin therapy was added to the regimen of both groups.
 
They were evaluated at the beginning of the trial, at 16 weeks before oxytocin was added, and again at 28 weeks after the study finished. Social behaviors were measured by the Social Responsiveness Scale (SRS) and Aberrant Behavior Checklist (ABC). Assessments also included the Clinical Global Impression (CGI) scale, biomarkers, and fecal microbiome evaluations.

Results

ASD USA 2021

Autism - PS128 vs. Placebo
(Taiwan, 2019)

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Study Summary

  • Type: randomized, placebo-controlled, double-blinded
  • Location: YuNing Psychiatry Clinic, Taiwan
  • Participants: 71 individuals with ASD, ages 7-15, male
Participants received a daily dose of either PS128 or a placebo for 4 weeks. They were evaluated at baseline and again after the study finished. Assessments included the Social Responsiveness Scale (SRS); the Autism Behavior Checklist-Taiwan version (ABC-T); the Child Behavior Checklist (CBCL); the Taiwan version of Swanson, Nolan, and Pelham-IV (SNAP-IV); and the Clinical Global Impression (CGI) scale.

Results

Opposition, defiance, and other autism-related behaviors were improved.

The SNAP-IV scale measures core signs of attention-deficit/hyperactivity disorder and oppositional defiant disorder. Changes in the scores of younger children (ages 7-12) taking PS128 daily for four weeks were compared with their placebo counterparts. Significantly lower (improved) scores were found in the PS128 group, suggesting it helped alleviate select behaviors.

 

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Anxiety levels were reduced.

A wide range of behaviors are evaluated using the Child Behavior Checklist.
 
  • Significantly decreased levels of anxiousness were shown by those who took PS128 during the trial.

 

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  • No adverse events were reported during the study

 

The SRS gauges social communication, awareness, and emotions, as well as limited interests and repetitious actions typical to autism.
  • Assessments at baseline and again after four weeks of treatment showed significant improvement for those children given PS128.

 

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Improvements in social communication and interaction, restricted interests, and repetitive behaviors were seen.

ASD Taiwan 2019

Tourette Syndrome - PS128 vs. Placebo
(Taiwan, 2021)

TS Taiwan 2021
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Study Summary

  • Type: randomized, placebo-controlled, double-blinded
  • Location: National Taiwan University Children's Hospital
  • Participants: 57 individuals with Tourette syndrome, ages 5-18, male and female
Participants took a daily dose of two capsules, each containing either 30 billion CFUs of PS128 or placebo for two months. They were evaluated at baseline, after one month, and again at two months. The primary outcome assessed improvement in tic symptoms, evaluated by Yale Global Tic Severity Scale (YGTSS). The secondary outcome involved changes in comorbidities in these children, including attention deficit hyperactivity disorder (ADHD) measured by the Swanson, Nolan, and Pelham IV Scale (SNAP-IV) and Conners’ Continuous Performance Test II (CPT-2), obsessive-compulsive disorder (OCD), migraines, and depression.

Results

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  • Both groups, PS128 and the placebo, showed tic symptom improvements, with no significant difference between the two.​
  • As observed by parents of the children, ADHD symptoms (including ​inattention and hyperactivity/impulsivity) significantly improved in the group taking PS128.
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  • A computer-administered test for ADHD symptoms found significantly improvement after treatment with PS128 compared to the placebo group.
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  • All treatment was well-tolerated, with no adverse effects reported.

Probiotics
and
Neurodevelopment

Gut-

Brain

Connection

Our gut, which contains around 100 million neurons, is often called our “second brain,” and these enteric nerve cells can function independently of our central nervous system (CNS).

 

These two neural networks frequently communicate with and influence each other, and when neurological development is impaired, GI health can suffer.

 

For example, children with autism have higher rates of gastrointestinal (GI) symptoms such as diarrhea, constipation, or abdominal pain, than do children of typical neurological development.

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Multiple

Pathways

This interaction between our two “brains” has been found to not only take place directly via neural transmission but also through endocrine, immune, and metabolic pathways.

Martha Herbert, a leading autism researcher at Harvard Medical School, used MRI scans to examine the neural anatomy of children with autism. She found their brains were full of activated immune cells and inflammatory molecules, contributing to the chronic neuroinflammation often seen in those with autism.

 

In a paper reporting her findings, she proposed that autism disorders are not primarily caused by brain abnormalities but actually influenced by multiple body systems, including the digestive and immune systems [2].

Gut Microbiota and Autism

Gut-brain axis research has led to understanding of a direct, reciprocal influence that exists between GI tract microbiota and the CNS, including nervous system disorders such as autism, Parkinson’s, depression, and anxiety.

 

Regarding autism specifically, the gut microflora of individuals with autism is unique when compared to those without. Autism patients have a higher proportion of Firmicutes bacteria and relatively fewer Bacteroides. This has led to scientists asking whether gut microbe modification could lead to CNS improvements and neurological disorder treatments [3].

Treating Autism Via the Microbiome

Researcher Elaine Hsiao showed how this microbiome-gut-brain connection can influence autism-like behaviors in mice [4]. Knowing that immune cells and inflammatory cytokines in the brain contribute to autism symptoms [5], Hsiao’s team mimicked an infection to activate the immune systems of pregnant mice. Soon after, the newborn pups exhibited both autism-like behaviors (anxiety, repetitive behaviors, and impaired social interaction) and GI tract symptoms (atypical, imbalanced gut microbes and intestinal permeability.)

 

Notably, after the pups were treated with Bacteroides from a human gut, their intestinal walls became more stable. Post-treatment, not only were the pups’ gut microbiomes more like those of a healthy mouse, but their symptoms of anxiety, repetitive behavior, and social impairment were also attenuated.

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[1] https://www.cdc.gov/ncbddd/autism/data.html

[2] Liu, Y.-W.; Liong, M.T.; Chung, Y.-C.E.; Huang, H.-Y.; Peng, W.-S.; Cheng, Y.-F.; Lin, Y.-S.; Wu, Y.-Y.; Tsai, Y.-C. (2019.) Effects of Lactobacillus plantarum PS128 on Children with Autism Spectrum Disorder in Taiwan: A Randomized, Double-Blind, Placebo-Controlled Trial. Nutrients, 11, 820.

[3] Fattorusso, A., Di Genova, L., Dell'Isola, G. B., Mencaroni, E., & Esposito, S. (2019). Autism Spectrum Disorders and the Gut Microbiota. Nutrients, 11(3), 521.  

[4] Hsiao, E. Y., McBride, S. W., Hsien, S., Sharon, G., Hyde, E. R., McCue, T., … Mazmanian, S. K. (2013). Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders. Cell, 155(7), 1451–1463.

[5] Herbert M. R. (2005). Autism: A brain disorder or a disorder that affects the brain? Clinical Neuropsychiatry, 2(6) ,354-79.

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