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Completed

NCT Number: NCT02708901

Gut to Brain Interaction in Autism. Role of Probiotics on Clinical, Biochemical and Neurophysiological Parameters

The purpose of this study is to assess the effects of a 6-months supplementation with probiotic Vivomixx® on inflammatory and gastrointestinal (GI) biomarkers, gastrointestinal disturbances, behavioral and developmental profiles, and neurophysiological features in preschoolers with Autism Spectrum Disorders (ASD) with or without GI symptoms.

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Key information

Age range

18 month–72 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IRCCS Stella Maris Foundation

Calambrone, Pisa, 56128, Italy

About this study

Autism Spectrum Disorders (ASD) are most likely multifactorial diseases in which the combination of genetic and environmental factors might have a role in the expression of the phenotype. A high incidence of gastrointestinal (GI) symptoms is reported in ASD. GI disturbances and altered gut microflora could make a child with a genetic predisposition for ASD more prone to express the ASD phenotype or increase the severity of his behavioral symptoms. The exploitation of strategies which can reduce the gut production and absorption of toxins or restore normal gut microbiota, such as probiotics may represent a non-pharmacological option in the treatment of GI disturbances in ASD. The aim of this study is to determine effects of probiotics supplementation with Vivomixx® in ASD children on specific GI symptoms, ASD core deficits, cognitive and language development, on inflammatory and gastrointestinal (GI) biomarkers and on Quantitative Electroencephalographic measures (QEEG). Vivomixx® is a probiotic mixture of 8 probiotic strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus and Streptococcus thermophilus). An additional aim of the study is to determine the environmental exposure to phthalates (chemical pollutant) in ASD children, and the possible effects of probiotic supplementation on their urinary concentrations. A group of 100 unselected preschoolers with ASD will be classified as belonging to the Gastro Intestinal (GI) group or to the Not Gastro Intestinal (NGI) group on the basis of the presence of significant GI symptoms at GI severity Index. Subjects belonging to the two groups (GI and NGI) will be blind randomized 1:1 to regular diet with probiotic Vivomixx® or with placebo for 6 months. All the participants will be assessed at the baseline, after three months and after six months from the baseline in order to evaluate the possible changes in GI symptoms, in ASD symptomatology, in other affective and behavioral comorbid symptoms, in plasmatic, urinary and fecal biomarkers related to abnormal intestinal function and in the electrophysiological patterns. The effects of treatments with probiotics on children with ASD need to be confirmed by rigorous controlled trials. Aiming to examine the impact of this treatment not only on clinical but also on neurophysiological patterns this trial sets out to provide new insights into the gut-brain connection in autism. Moreover, this study's results could add new data on the relationship between the presence of phthalates, clinical features and neurophysiological patterns in ASD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age-range: 18-72 months
  • ASD diagnosis according to Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) criteria

Exclusion criteria

  • brain anomalies detected by Magnetic Resonance Imaging (MRI)
  • neurological syndromes or focal neurological signs
  • anamnesis of birth asphyxia, severe premature birth (≤ 28 gestational weeks) or perinatal injuries
  • epilepsy
  • significant sensory impairment
  • diagnosis of organic GI Disorder (i.e. gastroesophageal reflux, food allergies, Inflammatory Bowel Disease)
  • diagnosis of Coeliac Disease
  • special diet (i.e. gluten-free diet, casein-free diet, high-protein diet, ketogenic diet)

Treatment and study plan

Vivomixx®

Dietary Supplement

Two packets (900 billions bacteria) per os (P.O.) daily x 1 month and one packet (450 billions bacteria) P.O. daily x 5 months

Placebo

Dietary Supplement

Two packets (4,4 grams of maltose and silicon dioxide x 2) P.O. daily x 1 month and one packet (4,4 grams of maltose and silicon dioxide) P.O. daily x 5 months

Primary outcomes

  1. Changes in severity level of ASD symptomatology

    Time frame: 6 months

    Delta of scores at Autism Diagnostic Observation Schedule-2

Secondary outcomes

  1. Changes in GI symptomatology

    Time frame: 3 months and 6 months

    Delta of scores at GI Severity Index

  2. Changes in Electroencephalogram (EEG) power

    Time frame: 6 months

    Registration with a 128-channels digital EEG: power will be assessed within each frequency band

  3. Changes in EEG coherence

    Time frame: 6 months

    Registration with a 128-channels digital EEG: coherence will be assessed within each frequency band

  4. Changes in EEG asymmetry

    Time frame: 6 months

    Registration with a 128-channels digital EEG: asymmetry will be assessed within each frequency band

  5. Changes in levels of serum Lipopolysaccharide

    Time frame: 6 months

    Delta of values of serum Lipopolysaccharide

  6. Changes in levels of serum Leptin

    Time frame: 6 months

    Delta of values of serum Leptin

  7. Changes in levels of serum Resistin

    Time frame: 6 months

    Delta of values of serum Resistin

  8. Changes in levels of serum Tumor Necrosis Factor - alfa

    Time frame: 6 months

    Delta of values of serum Tumor Necrosis Factor - alfa

  9. Changes in levels of serum Interleukin-6 (IL-6)

    Time frame: 6 months

    Delta of values of serum Interleukin-6 (IL-6)

  10. Changes in levels of serum Plasminogen Activator Inhibitor-1 (PAI-1)

    Time frame: 6 months

    Delta of values of serum Plasminogen Activator Inhibitor-1 (PAI-1)

  11. Changes in levels of fecal calprotectin

    Time frame: 3 months and 6 months

    Delta of values of fecal calprotectin

  12. Changes in global ASD symptomatology assessed by Childhood Autism Rating Scale

    Time frame: 6 months

    Delta of scores at Childhood Autism Rating Scale

  13. Changes in ASD symptomatology: repetitive behaviors

    Time frame: 3 months and 6 months

    Delta of scores at Repetitive Behavior Scale

  14. Changes in ASD symptomatology: sensory profiles

    Time frame: 3 months and 6 months

    Delta of scores at Sensory Profile

  15. Changes in global ASD symptomatology assessed by Social Communication Questionnaire

    Time frame: 3 months and 6 months

    Delta of scores at Social Communication Questionnaire

  16. Changes in Developmental Quotient

    Time frame: 6 months

    Delta of score at Griffiths Mental Developmental Scale

  17. Changes in Adaptive Functioning

    Time frame: 6 months

    Delta of scores at Vineland Adaptive Behavior Scale-II

  18. Changes in Behavioral Profiles

    Time frame: 3 months and 6 months

    Delta of scores at Child Behavior Checklist 1.5-5

  19. Changes in Parental Stress

    Time frame: 3 months and 6 months

    Delta of scores at Parenting Stress Index

Sponsors and collaborators

Lead sponsor

IRCCS Fondazione Stella Maris

Other

Collaborators

  • Istituto di Fisiologia Clinica CNR
  • Ministry of Health, Italy

Registry information

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Mar 15, 2016
Registry last updated
Feb 18, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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