Ignite Creation Date:
2024-05-06 @ 11:54 AM
Last Modification Date:
2024-10-26 @ 12:52 PM
Study NCT ID:
NCT03638791
Status:
COMPLETED
Last Update Posted:
2022-09-21
First Post:
2018-08-16
Brief Title:
Microbiome in Obsessive-compulsive Disorder
Sponsor:
Karolinska Institutet
Organization:
Karolinska Institutet
Study Overview
Official Title:
Longitudinal Study of Gut Microbiome in Obsessive-Compulsive Disorder
Status:
COMPLETED
Status Verified Date:
2022-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MIO
Brief Summary:
Background Humans live in symbiosis with microbes and their implication for health and disease is evident The importance of microbiome-gut-brain axis in psychiatric disorders is an area of increasing research interest OCD is a promising target for microbiome research as Pediatric Acute-onset Neuropsychiatric Syndrome PANS Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections PANDAS are reactions to infectious agents precipitating acute onset of severe OCD symptoms Furthermore preliminary evidence has associated probiotic treatment with alleviation of OCD symptoms We propose the first clinical study on the microbiome and its effects on OCD patients
Aim To analyze the gut microbiota in patients with OCD compared with healthy matched controls and assess changes in microbial composition following treatment
Outcome measures Differences in alpha diversity beta diversity and taxa abundance of bacterial groups at the phylum class order family genus and species levels and severity of OCD symptoms Moreover functional profiling will be conducted
Methods Our aim is to enroll 32 OCD patients and 32 matched controls Shotgun metagenomic sequencing will be used Sequenced data will be processed followed by non-parametric statistical testing
Significance gut microbiome in patients with OCD beofre and after ERP treatment has never been done before The microbial composition may impact on OCD symptoms severity and chronicity and could inform future therapeutic possibilities
Aim To analyze the gut microbiota in patients with OCD compared with healthy matched controls and assess changes in microbial composition following treatment
Outcome measures Differences in alpha diversity beta diversity and taxa abundance of bacterial groups at the phylum class order family genus and species levels and severity of OCD symptoms Moreover functional profiling will be conducted
Methods Our aim is to enroll 32 OCD patients and 32 matched controls Shotgun metagenomic sequencing will be used Sequenced data will be processed followed by non-parametric statistical testing
Significance gut microbiome in patients with OCD beofre and after ERP treatment has never been done before The microbial composition may impact on OCD symptoms severity and chronicity and could inform future therapeutic possibilities
Detailed Description:
Background
Obsessive-compulsive disorder OCD is a highly debilitating disorder with a lifetime prevalence of approximately 2 is equally distributed among men and women OCD generally starts at an early age and usually develops a chronic course if left untreated Many patients with OCD receive treatment after years of delay due to both patient and health care factors therefore OCD affects educational achievement ability to work and interpersonal relationships Moreover it poses a considerable burden and distress to family caregivers 1 and accounts for one of the ten most disabling mental health conditions worldwide 2
The role of the microbial community in health and disease has been a neglected subject in human research until recently despite the fact that human microbes comprise about 1-3 of our body mass 3 Gut microbes play important roles in nutrient metabolism production of vitamins and prevention of pathogens from colonizing our intestine 4 Recently microbiota in the gut has gained increasing interest due the extensive connection between the gut and the brain 5 The bidirectional communication through neural hormonal and immunological signaling involving the central autonomic and enteric nervous systems forms the microbiome-gut-brain axis 6 In psychiatry dysbioses have been reported in anorexia nervosa major depression autism and other major psychiatric disorders 9 10
Association between OCD onset and infection has long been known PANSPANDAS are acute-onset forms of OCD associated with autoimmune reactions from pathogens such as streptococcus infection 11 12 The connection between bacterial pathogen and immunological response which generates OCD symptoms is further evidence for the importance of the microbiome-gut-brain axis in OCD Lately there have been numerous hypotheses regarding the importance of gut microbiome and OCD symptoms 13 14
Aims Characterize composition and diversity of the gut microbiome in individuals with OCD compared with healthy controls
We hypothesize that patients with OCD will show evidence of gut dysbiosis imbalance marked by lower microbial diversity and specific taxonomic and gene content differences compared to healthy controls Primary outcome is α-diversity which refers to the number of species richness at one site β-diversity which refers to the differences in species composition between participants and taxonomic abundance of bacterial groups at the phylum class order family genus and species levels These measures yield information about individual microbial composition at each site and homogeneity in a group of people
We hypothesize that reduced α and β diversity in gut microbiome correlate with severity of obsessive-compulsive symptoms measured by Yale-Brown Obsessive-Compulsive Scale Y-BOCS and Obsessive-Compulsive Inventory Revised OCI-R We predict that greater symptom severity is associated with lower diversity A significant negative correlation will be supportive evidence for the microbiome-gut-brain axis
We hypothesize that there will be significant richer α diversity in gut microbiome composition after successful psychotherapy change in Y-BOCS score
Method
Recruitment Healthy controls will be recruited through advertisement or included from previous studies with their consent Male and female patients between 18-45 years of age from the OCD-clinic at Huddinge Hospital with a DSM-5 diagnosis of OCD and fear of contamination will be invited to participate Age matched controls will be recruited who have no personal or family history of OCD Exclusion criteria for all groups include history of GI tract surgery other than appendectomy or cholecystectomy history of inflammatory bowel disease irritable bowel syndrome celiac disease or any other diagnosis that could explain chronic or recurring bowel symptoms antibiotic use in the past 3 months pro-biotic use in the past 4 weeks pregnantcy Intellectual disability autism spectrum disorder and psychosis
Assessment All participants will meet an experienced psychiatrist for diagnostic assessments including MINI interview Participants will be asked to complete self-assessment forms on the Internet and answer questions about their dietary habits for the last three months Weight and height for body mass index BMI calculation will be measured All assessment forms information from interviews and medical examination will be documented in their medical record Further information eg antibiotics and previous therapies will be collected from their medical records with the participants consent
The investigators chose the following questionnaire battery to capture all relevant outcome variables OCD-symptoms nutrition and stool characteristics and frequency
Yale-Brown Obsessive Compulsive Scale Y-BOCS A commonly used clinical semi-structured interview assessing severity of OCD symptoms
Obsessive-Compulsive Inventory Revised OCI-R - An18 item self-report questionnaire estimating OCD symptom dimensionsThe OCI-R yields a total score and 5 subscales checking hoarding neutralizing obsessing ordering and washing
EDE-Q to capture eating behavior
Meal Q questionnaire A web-based food frequency questionnaire normed in Sweden will validate energy and macronutrient intake which affects the microbial composition
Bristol Stool Scale A medical diagnostic scale designed to classify the form of human faeces into seven categories
Furthermore the investigators will collect demographic information of all patients age sex age at onset occupation status somatic health and psychiatric comorbidities
Stool sampling procedure Patients and controls will be provided with clear instructions for home fecal sample collection Patients will collect one stool sample at the beginning of treatment and one at the end of treatment Controls will collect one sample at one time point only Participants will collect stool at home using OMNIgene kits that will be sent to the KI biobank
Exposure and Respons Prevention therapy ERP an evidence-based psychotherapy administered by experienced psychologists either individually in groups face-to-face or through internet A minimum of five exposure and respons prevention sessions is required in order for it to be considered an ERP treatment
Sample storage in biobank All samples will be stored at Karolinska Institutets KI biobank Application for biobank storage of samples is established according to rules and regulations
Metagenomic sequencing The investigators will use shotgun metagenomics sequencing methods Whole-genome shotgun sequencing can provide functional information on which genes are present in the gut microbiome of patients This method can also provide a more detailed taxonomical resolution that 16S rRNA sequencing
Metagenomic shotgun sequencing will be prepared and sequenced To efficiently utilize the flow cells about ten samples will be multiplexed with dual indices per lane of the flow cell Prior to downstream bioinformatics analysis raw sequence data will be quality filtered and trimmed to remove bases with Phred quality scores less than 20 Data generated will be processed by metagenome species concept Sequences are clustered into metagenomic species MGS based on their sequence similarity
Determination of sample size two previous studies with fewer or similar number of participants have shown that this study will be adequately powered Furthermore this is a pilot study based on new sequencing technology
Timeline Ethical application has been approved and all samples have been collected
Obsessive-compulsive disorder OCD is a highly debilitating disorder with a lifetime prevalence of approximately 2 is equally distributed among men and women OCD generally starts at an early age and usually develops a chronic course if left untreated Many patients with OCD receive treatment after years of delay due to both patient and health care factors therefore OCD affects educational achievement ability to work and interpersonal relationships Moreover it poses a considerable burden and distress to family caregivers 1 and accounts for one of the ten most disabling mental health conditions worldwide 2
The role of the microbial community in health and disease has been a neglected subject in human research until recently despite the fact that human microbes comprise about 1-3 of our body mass 3 Gut microbes play important roles in nutrient metabolism production of vitamins and prevention of pathogens from colonizing our intestine 4 Recently microbiota in the gut has gained increasing interest due the extensive connection between the gut and the brain 5 The bidirectional communication through neural hormonal and immunological signaling involving the central autonomic and enteric nervous systems forms the microbiome-gut-brain axis 6 In psychiatry dysbioses have been reported in anorexia nervosa major depression autism and other major psychiatric disorders 9 10
Association between OCD onset and infection has long been known PANSPANDAS are acute-onset forms of OCD associated with autoimmune reactions from pathogens such as streptococcus infection 11 12 The connection between bacterial pathogen and immunological response which generates OCD symptoms is further evidence for the importance of the microbiome-gut-brain axis in OCD Lately there have been numerous hypotheses regarding the importance of gut microbiome and OCD symptoms 13 14
Aims Characterize composition and diversity of the gut microbiome in individuals with OCD compared with healthy controls
We hypothesize that patients with OCD will show evidence of gut dysbiosis imbalance marked by lower microbial diversity and specific taxonomic and gene content differences compared to healthy controls Primary outcome is α-diversity which refers to the number of species richness at one site β-diversity which refers to the differences in species composition between participants and taxonomic abundance of bacterial groups at the phylum class order family genus and species levels These measures yield information about individual microbial composition at each site and homogeneity in a group of people
We hypothesize that reduced α and β diversity in gut microbiome correlate with severity of obsessive-compulsive symptoms measured by Yale-Brown Obsessive-Compulsive Scale Y-BOCS and Obsessive-Compulsive Inventory Revised OCI-R We predict that greater symptom severity is associated with lower diversity A significant negative correlation will be supportive evidence for the microbiome-gut-brain axis
We hypothesize that there will be significant richer α diversity in gut microbiome composition after successful psychotherapy change in Y-BOCS score
Method
Recruitment Healthy controls will be recruited through advertisement or included from previous studies with their consent Male and female patients between 18-45 years of age from the OCD-clinic at Huddinge Hospital with a DSM-5 diagnosis of OCD and fear of contamination will be invited to participate Age matched controls will be recruited who have no personal or family history of OCD Exclusion criteria for all groups include history of GI tract surgery other than appendectomy or cholecystectomy history of inflammatory bowel disease irritable bowel syndrome celiac disease or any other diagnosis that could explain chronic or recurring bowel symptoms antibiotic use in the past 3 months pro-biotic use in the past 4 weeks pregnantcy Intellectual disability autism spectrum disorder and psychosis
Assessment All participants will meet an experienced psychiatrist for diagnostic assessments including MINI interview Participants will be asked to complete self-assessment forms on the Internet and answer questions about their dietary habits for the last three months Weight and height for body mass index BMI calculation will be measured All assessment forms information from interviews and medical examination will be documented in their medical record Further information eg antibiotics and previous therapies will be collected from their medical records with the participants consent
The investigators chose the following questionnaire battery to capture all relevant outcome variables OCD-symptoms nutrition and stool characteristics and frequency
Yale-Brown Obsessive Compulsive Scale Y-BOCS A commonly used clinical semi-structured interview assessing severity of OCD symptoms
Obsessive-Compulsive Inventory Revised OCI-R - An18 item self-report questionnaire estimating OCD symptom dimensionsThe OCI-R yields a total score and 5 subscales checking hoarding neutralizing obsessing ordering and washing
EDE-Q to capture eating behavior
Meal Q questionnaire A web-based food frequency questionnaire normed in Sweden will validate energy and macronutrient intake which affects the microbial composition
Bristol Stool Scale A medical diagnostic scale designed to classify the form of human faeces into seven categories
Furthermore the investigators will collect demographic information of all patients age sex age at onset occupation status somatic health and psychiatric comorbidities
Stool sampling procedure Patients and controls will be provided with clear instructions for home fecal sample collection Patients will collect one stool sample at the beginning of treatment and one at the end of treatment Controls will collect one sample at one time point only Participants will collect stool at home using OMNIgene kits that will be sent to the KI biobank
Exposure and Respons Prevention therapy ERP an evidence-based psychotherapy administered by experienced psychologists either individually in groups face-to-face or through internet A minimum of five exposure and respons prevention sessions is required in order for it to be considered an ERP treatment
Sample storage in biobank All samples will be stored at Karolinska Institutets KI biobank Application for biobank storage of samples is established according to rules and regulations
Metagenomic sequencing The investigators will use shotgun metagenomics sequencing methods Whole-genome shotgun sequencing can provide functional information on which genes are present in the gut microbiome of patients This method can also provide a more detailed taxonomical resolution that 16S rRNA sequencing
Metagenomic shotgun sequencing will be prepared and sequenced To efficiently utilize the flow cells about ten samples will be multiplexed with dual indices per lane of the flow cell Prior to downstream bioinformatics analysis raw sequence data will be quality filtered and trimmed to remove bases with Phred quality scores less than 20 Data generated will be processed by metagenome species concept Sequences are clustered into metagenomic species MGS based on their sequence similarity
Determination of sample size two previous studies with fewer or similar number of participants have shown that this study will be adequately powered Furthermore this is a pilot study based on new sequencing technology
Timeline Ethical application has been approved and all samples have been collected
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None