Study of Modified Atkins Diet in Kabuki Syndrome
Primary Purpose
Kabuki Syndrome
Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Modified Atkins diet
Sponsored by
About this trial
This is an interventional treatment trial for Kabuki Syndrome
Eligibility Criteria
Inclusion Criteria:We will recruit 15 total participants with clinically-definite and genetically-confirmed Kabuki syndrome type 1 age 18 years and older. . will also be required.
- Clinical diagnosis of KS will be made based on recently published consensus diagnosis criteria
- Genetic confirmation of a pathogenic mutation in KMT2D
Exclusion Criteria:
- presence of another known genetic syndrome
- a health problem that would make a modified Atkins diet harmful
- inability to travel to Baltimore for 2 visits separated by 12 weeks
Sites / Locations
- Kennedy Krieger InstituteRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MAD diet group
Arm Description
15 adult participants with confirmed KMT2D pathogenic mutations. Baseline labs and education about Modified Atkins Diet. Then 12 weeks on a Modified Atkins Diet. Weekly urine dips for ketones and diet logs. Blood draw every 3 weeks.
Outcomes
Primary Outcome Measures
Benton Judgement of Line Orientation
Established measure to determine visuospatial perception. There are 30 items and each item is worth 1 point. Will assess change in score from baseline to post-diet.
Brief Visuospatial memory test
Established measure to determine visuospatial memory. Scores range from 0 to 36 and a higher score indicates more correct responses. Will assess change in score from baseline to post-diet.
NIH Toolbox Picture Sequence Memory
Established measure to determine visuospatial memory. Scaled scores based on age have a mean of 100 and a standard deviation of 15 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Beery Developmental Test of Visual Motor Integration
Established measure to determine visuomotor integration. Scaled scores based on age have a mean of 100 and a standard deviation of 15 with a floor of 45 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Beery Developmental Test of Visual Perception
Established measure to determine visual perception. Scaled scores based on age have a mean of 100 and a standard deviation of 15 with a floor of 45 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Wechsler Intelligence Scale for Children -V Block Design
Established measure to determine visuospatial processing. Scaled scores which will be scaled to age 16:11 for all participants have a mean of 10 and a standard deviation of 1.5 with a range of 1-19 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Hopkins Verbal Learning Test
Established measure to determine verbal memory. Scores range from 0 to 36 and a higher score indicates more correct responses. Will assess change in score from baseline to post-diet.
Secondary Outcome Measures
DNA Methylation analysis
Measure genome-wide methylation signature in blood of participants. To obtain genome-scale methylation measurements, bisulfite treated DNA from patient blood samples will be processed on the Infinium HumanMethylation450 BeadChip at the Johns Hopkins SNP Center in accordance with the manufacturer's recommendation. The Infinium HumanMethylation450 BeadChip measures DNA methylation levels at 485,512 loci across the genome. The array data will then be analyzed to get the proportion of methylation at a given CpG site from 0 to 1. These will be logit transformed to create M-values. Kabuki syndrome is known to have a unique signature methylation profile (determined by M-values across loci) that can be detected in blood. This genome wide DNA methylation will be done every 3 weeks to determine whether this signature changes with dietary therapy.
Caregiver behavior rating scales: GAS-ID
Rating scale for anxiety consists of 27 items with scores ranging from 0-70 with higher scores indicating more anxiety. Performed at baseline and post-diet.
Full Information
NCT ID
NCT04722315
First Posted
November 24, 2020
Last Updated
November 17, 2022
Sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT04722315
Brief Title
Study of Modified Atkins Diet in Kabuki Syndrome
Official Title
Pilot Clinical Trial of Modified Atkins Diet for Kabuki Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Animal models of Kabuki syndrome have showed a reversal of the cognitive phenotype with ketogenic diet. Modified Atkins diet is safer and easier tolerated than full ketogenic diet and still has the histone deacetylase inhibition believed to be responsible for the cognitive improvement. This study aims to examine a small number of adults with Kabuki syndrome before and after 12 weeks on a modified Atkins diet to determine if there is any cognitive improvement and if the diet can be tolerated.
Detailed Description
Consented participants will participate in an initial 2 day study visit. These participants will undergo cognitive and neurobehavioral testing and also will have baseline labs drawn and will meet with a Johns Hopkins nutritionist trained in modified Atkins diet for education. The labs are standard of care for diet initiation to rule out contraindications to the diet. Participants and/or their caregivers will keep a daily diet log and will be asked to download the free Carb Manager application onto their smartphone. They will send the logs and data back weekly. Participants will be given urine ketone strips and asked to use and record in their diet log twice weekly. Participants will have blood and urine samples collected locally every 3 weeks and sent back to study team to measure Beta-hydroxybutyrate, metabolic studies and methylation. Participants will return to Baltimore at the end of 12 weeks for a one day visit to repeat the cognitive assessment protocol, neurobehavioral measures, and repeat the initial and follow up lab tests.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kabuki Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
15 participants with Kabuki syndrome will receive a 12 week dietary intervention.
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MAD diet group
Arm Type
Experimental
Arm Description
15 adult participants with confirmed KMT2D pathogenic mutations. Baseline labs and education about Modified Atkins Diet. Then 12 weeks on a Modified Atkins Diet. Weekly urine dips for ketones and diet logs. Blood draw every 3 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Modified Atkins diet
Intervention Description
12 weeks of modified Atkins diet
Primary Outcome Measure Information:
Title
Benton Judgement of Line Orientation
Description
Established measure to determine visuospatial perception. There are 30 items and each item is worth 1 point. Will assess change in score from baseline to post-diet.
Time Frame
12 weeks
Title
Brief Visuospatial memory test
Description
Established measure to determine visuospatial memory. Scores range from 0 to 36 and a higher score indicates more correct responses. Will assess change in score from baseline to post-diet.
Time Frame
12 weeks
Title
NIH Toolbox Picture Sequence Memory
Description
Established measure to determine visuospatial memory. Scaled scores based on age have a mean of 100 and a standard deviation of 15 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Time Frame
12 weeks
Title
Beery Developmental Test of Visual Motor Integration
Description
Established measure to determine visuomotor integration. Scaled scores based on age have a mean of 100 and a standard deviation of 15 with a floor of 45 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Time Frame
12 weeks
Title
Beery Developmental Test of Visual Perception
Description
Established measure to determine visual perception. Scaled scores based on age have a mean of 100 and a standard deviation of 15 with a floor of 45 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Time Frame
12 weeks
Title
Wechsler Intelligence Scale for Children -V Block Design
Description
Established measure to determine visuospatial processing. Scaled scores which will be scaled to age 16:11 for all participants have a mean of 10 and a standard deviation of 1.5 with a range of 1-19 and higher scores indicate more correct responses. Will assess change in this score from baseline to post-diet.
Time Frame
12 weeks
Title
Hopkins Verbal Learning Test
Description
Established measure to determine verbal memory. Scores range from 0 to 36 and a higher score indicates more correct responses. Will assess change in score from baseline to post-diet.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
DNA Methylation analysis
Description
Measure genome-wide methylation signature in blood of participants. To obtain genome-scale methylation measurements, bisulfite treated DNA from patient blood samples will be processed on the Infinium HumanMethylation450 BeadChip at the Johns Hopkins SNP Center in accordance with the manufacturer's recommendation. The Infinium HumanMethylation450 BeadChip measures DNA methylation levels at 485,512 loci across the genome. The array data will then be analyzed to get the proportion of methylation at a given CpG site from 0 to 1. These will be logit transformed to create M-values. Kabuki syndrome is known to have a unique signature methylation profile (determined by M-values across loci) that can be detected in blood. This genome wide DNA methylation will be done every 3 weeks to determine whether this signature changes with dietary therapy.
Time Frame
Every 3 weeks for 12 weeks
Title
Caregiver behavior rating scales: GAS-ID
Description
Rating scale for anxiety consists of 27 items with scores ranging from 0-70 with higher scores indicating more anxiety. Performed at baseline and post-diet.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:We will recruit 15 total participants with clinically-definite and genetically-confirmed Kabuki syndrome type 1 age 18 years and older. . will also be required.
Clinical diagnosis of KS will be made based on recently published consensus diagnosis criteria
Genetic confirmation of a pathogenic mutation in KMT2D
Exclusion Criteria:
presence of another known genetic syndrome
a health problem that would make a modified Atkins diet harmful
inability to travel to Baltimore for 2 visits separated by 12 weeks
Facility Information:
Facility Name
Kennedy Krieger Institute
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacqueline Harris, MD
Phone
667-205-4295
First Name & Middle Initial & Last Name & Degree
Jennifer Johnson
Phone
667-205-4295
Email
johnsonjen@kennedykrieger.org
12. IPD Sharing Statement
Plan to Share IPD
No
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Study of Modified Atkins Diet in Kabuki Syndrome
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