Steroid and Behaviour Changes Under Metformin

Autistic Disorder Clinical Trial

Official title:

A Multi-center, Prospective, Cohort Study to Elucidate the Effects of Metformin Treatment on Steroid Hormones and Social Behavior. Linking Autistic Behaviorial Symptoms to Changes in Steroid Hormone Availability

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04930471
• Other study ID #: Steroid Changes Metformin
• Status: Not yet recruiting
• Start date: June 2021
• Est. completion date: December 2023

Study information

• Verified date: June 2021
• Source: University Hospital Inselspital, Berne
• Contact: Benedikt Gasser, MD
• Phone: +41788170711
• Email: benedikt.gasser[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Background

Based on various suggestions, social behavior is mediated by a change in steroid hormones. These have diverse effects on the (neuro-)development during critical stages, whereby especially androgen and insulin metabolism seem to play a key role. Various lines of evidence indicate that metformin could influence and improve the symptoms of social withdrawal. Therefore, the investigators will analyze urinary samples of patients before and after treatment with metformin to elucidate the changes in steroid hormone profiles and measure changes in social behavior to examine a potential correlation.

Material & Methods

Steroid hormone analysis including the most prominent androgen, estrogen, progesterone, aldosterone, corticosterone, cortisone and cortisol metabolites analyzed with gas chromatography mass spectrometry and a questionnaire (Autism-Spectrum Quotient) will be performed prior to and after 12-weeks metformin treatment.

Discussion

It is likely, that due to different pathophysiological mechanisms such as an effect on respiratory chain in mitochondria or via AMP activated protein kinase a general reduction of total androgens will be detected prior versus post metformin treatment. The encompassing measurement of steroid hormones will allow to detect influences on different metabolites and in consequence enzyme activities. The potential changes prior versus post shall give hints concerning the involvement of specific cascades involved, with potential pharmacological targets for future research.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 45
• Est. completion date: December 2023
• Est. primary completion date: August 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with type 2 diabetes mellitus and an indication for metformin according to the American Diabetes Association (American Diabetes Association, 2021a) starting a new metformin treatment. The main marker will be fasting plasma glucose levels of 7.0mmol/L and/or HbA1c 6.5% (American Diabetes Association, 2021a).

• Written informed consent.

Exclusion Criteria:

• Patients under 18 years of age.

• Clinically significant concomitant disease (e.g. advanced renal failure, hepatic dysfunction, neoplasia).

• Significant musculoskeletal disease.

• Active infection during sample collection.

• Immunosuppressive medical therapy.

• Hormonal/steroid treatment.

• Pregnancy.

• Psychiatric disease and known social behavior altering medication (e.g. antipsychotic medication).

• Known or suspected malcompliance, drug or alcohol abuse.

• Inability to follow the procedures of the study, e.g. due to insufficient language skills, severe dementia.

• Life-expectancy < 6 months.

• Poor tolerability to metformin treatment with following treatment discontinuation within duration of follow up.

Related Conditions & MeSH terms

• Autistic Disorder

Intervention

Drug:
• Metformin
Treatment with Metformin as prescribed by the treating physician.

Locations

Country	Name	City	State
Switzerland	Lindenhofgruppe	Berne

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital Inselspital, Berne	Lindenhofstiftung

Country where clinical trial is conducted

Switzerland, 

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Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in GC-MS measured urinary androgen metabolite levels.	Changes in urinary androgen metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Androgen-Metabolites (Androsterone, Androstenediol, 11-Oxoetiocholanolone, 11ß-Hydroxyandrosterone, 11ß-Hydroxyetiocholanolone, Dehydroepiandrosterone, 5-Androstene-3ß,17ß-diol, 16a-Hydroxydehydroepiandrosterone, 5-Androstene-3ß,16a,17ß-triol, 5-Pregnene-3ß, 16a,17ß-triol, Testosterone, 5a-Dihydrotestosterone). All will be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary oestrogen metabolite levels.	Changes in urinary oestrogen metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Oestrogen-Metabolites (Estriol, 17b-Estradiol), Progesterone-Metabolites (17-Hydroxypregnanolone, Pregnanediol, Pregnanetriol, 11-Oxo-Pregnanetriol). All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary progesterone metabolite levels.	Changes in urinary progesterone metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Progesterone-Metabolites (17-Hydroxypregnanolone, Pregnanediol, Pregnanetriol, 11-Oxo-Pregnanetriol).; All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary aldosterone metabolite levels.	Changes in urinary aldosterone metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Aldosterone-Metabolites (Tetrahydroaldosterone). All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary corticosterone metabolite levels.	Changes in urinary corticosterone metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Corticosterone-Metabolites (TetrahydroDOC, Tetrahydrodehydrocorticosterone, Tetrahydrocorticosterone, 5a-Tetrahydrocorticosterone, 18-Hydroxy-tetrahydrocompound A, Cortisone).; All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary cortisone metabolite levels.	Changes in urinary cortisone metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Cortisone-Metabolites (Tetrahydrocortisone, a-Cortolone, b-Cortolone, 20a-Dihydrocortisone, 20b-Dihydrocortisone).; All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Changes in GC-MS measured urinary cortisol metabolite levels.	Changes in urinary cortisol metabolite levels of interest (see below) prior to metformin treatment start and after 12-weeks of treatment.; Hormones of interest include Cortisol-Metabolites (Cortisol, Tetrahydrocortisol, 5a-Tetrahydrocortisol, a-Cortol, b-Cortol, 20a-Dihydrocortisol, 6b-Hydroxycortisol, 18-Hydroxycortisol).; All wil be measured in urinary samples using GC-MS (gas-chromatography mass-spectrometry).	After 12 weeks follow-up
Primary	Behavioral Changes	Changes in social behavior measured by the Autism-Spectrum Quotient AQ prior to metformin treatment start and after 12-weeks of treatment.	After 12 weeks follow-up
Secondary	Correlation between urinary steroid hormone level changes (metabolites of androgen, oestrogen, progesterone, aldosterone, corticosterone, cortisone and cortisol) and behavioral changes measured with pearson correlation coefficient.	A potential correlation and/or dosage effect between the primary outcomes will be evaluated using the pearson correlation coefficient.	After 12 weeks follow-up

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