Purpose

Study Description: This is a natural history protocol designed to characterize the clinical spectrum of trisomy 8 mosaicism and trisomy 8-associated autoinflammatory disease (TRIAD) and related autoinflammatory disorders and further evaluate approaches to screening, diagnosis, and management. We will enroll affected patients and their unaffected relatives and collect a variety of clinical data and biological specimens for research analyses to better understand disease mechanisms. Biological samples from affected participants may include biopsies from the oral mucosa, skin, and bone marrow; swabs of the mouth, skin, and vagina; urine, stool, and saliva collections; and hair and fingernail clippings. Other clinical data may include imaging studies (such as magnetic resonance imaging [MRI], x-rays, and echocardiogram), questionnaires, and results from medical consults and clinically indicated procedures. Biological samples from unaffected relatives of participants may include blood, mouth swabs, stool, urine, and saliva. Participants may be seen in person or remotely via telehealth and provide send-in samples. After the initial baseline assessment, optional follow-up visits will occur approximately every 1 to 2 years, depending on the scientific needs of the study team and the participant s clinical status and interest. Objectives: Primary Objectives: 1. Characterize the clinical spectrum and natural history of trisomy 8 mosaicism and related disorders. 2. Characterize the immunologic profile in blood, tissue, and bone marrow of participants with trisomy 8 mosaicism and related disorders. Secondary Objectives: 1. Determine appropriate screening and diagnostic workup of individuals with trisomy 8 mosaicism and related disorders. 2. Identify the long-term risk of and association with neoplasm among individuals with trisomy 8 mosaicism. 3. Characterize the distribution of trisomy 8 cells in different tissues and cell types and describe how this contributes to disease manifestations and variability. 4. Evaluate or characterize immune responses to targeted therapeutics to better understand the pathophysiology of trisomy 8 mosaicism and related disorders. Exploratory Objectives: 1. Identify the specific genes and immunologic pathways that lead to disease manifestations seen in patients with trisomy 8. 2. Identify new genetic diseases that lead to mucosal ulcers and understand the immunologic mechanisms that contribute to mucosal ulcerations. Endpoints: Primary Endpoints: 1. Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing. 2. Characterization of immunologic profile of participants with trisomy 8 mosaicism and related disorders over time in comparison to healthy controls using cellular and molecular techniques including, but not limited to immune cell phenotyping, transcriptomics, proteomics, and ex vivo functional studies. Secondary Endpoints: 1. Characterization of laboratory, radiologic, biopsy, and physical exam findings. 2. Identification of individuals with trisomy 8 who develop malignancy and assessment of risk factors including but not limited to history, findings on bone marrow biopsies and complete blood counts (CBCs), next-generation sequencing (NGS) for risk variants, and flow cytometry. 3. Determination of the percentage of trisomy 8 cells in various tissue types including bone marrow, blood, fibroblasts cultured from skin, and biopsy samples, and the association with clinical phenotype. 4. Assessment of immune response to therapeutics based on inflammatory markers, clinical history, and physical exam findings. Exploratory Endpoint: 1. Identification of genes that may lead to mucosal ulcerative disease when mutated or over/underexpressed.

Conditions

Eligibility

Eligible Ages
Between 1 Day and 99 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

To be eligible to participate in this study, an individual must meet the following criteria: 1. Stated willingness to comply with study requirements. 2. Aged <= 99 (ability to be seen at NIH vs. remote visit may be determined by age and location). 3. Willingness to allow storage of data and specimens for future research. Additional Inclusion Criteria for Affected Participants 1. Must have one of the following: 1. Trisomy 8 mosaicism verified by genetic testing (including but not limited to karyotype, fluorescence in situ hybridization [FISH], whole genome sequencing [WGS], whole exome sequencing [WES], or microarray), or 2. Inflammatory mucosal ulcerative disease clinically similar to TRIAD at the discretion of the principal investigator. 2. Ability of participant or LAR to provide informed consent. Additional Inclusion Criteria for Biological Relatives 1. Be an unaffected biological relative of an affected participant. 2. Ability to provide informed consent. 3. Willingness to provide at least one biospecimen.

Exclusion Criteria

Individuals with any condition or who are taking any medications that, in the opinion of the investigator, contraindicates participation in the study will be excluded. Co-enrollment guidelines: Enrollment in this protocol does not preclude individuals from enrolling or participating in any other NIH protocols, including studies of investigational agents. Participants will be asked about their participation in other studies to ensure that blood draws do not exceed NIH limits for research protocols.

Study Design

Phase
Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Affected Participants Individuals ages <= 99 with known or suspected trisomy 8 mosaicism, or with clinical phenotype consisting of mucosal ulcerations similar to TRIAD.
Non-affected biological family member participants Non-affected biological family members of enrolled participants.

Recruiting Locations

National Institutes of Health Clinical Center
Bethesda, Maryland 20892
Contact:
Laura Failla, M.S.
240-669-5323
laura.failla@nih.gov

More Details

Status
Recruiting
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

Study Contact

Laura E Failla, C.R.N.P.
(240) 669-5323
laura.failla@nih.gov

Detailed Description

Study Description: This is a natural history protocol designed to characterize the clinical spectrum of trisomy 8 mosaicism and trisomy 8-associated autoinflammatory disease (TRIAD) and related autoinflammatory disorders and further evaluate approaches to screening, diagnosis, and management. We will enroll affected patients and their unaffected relatives and collect a variety of clinical data and biological specimens for research analyses to better understand disease mechanisms. Biological samples from affected participants may include biopsies from the oral mucosa, skin, and bone marrow; swabs of the mouth, skin, and vagina; urine, stool, and saliva collections; and hair and fingernail clippings. Other clinical data may include imaging studies (such as magnetic resonance imaging [MRI], x-rays, and echocardiogram), questionnaires, and results from medical consults and clinically indicated procedures. Biological samples from unaffected relatives of participants may include blood, mouth swabs, stool, urine, and saliva. Participants may be seen in person or remotely via telehealth and provide send-in samples. After the initial baseline assessment, optional follow-up visits will occur approximately every 1 to 2 years, depending on the scientific needs of the study team and the participant s clinical status and interest. Objectives: Primary Objectives: 1. Characterize the clinical spectrum and natural history of trisomy 8 mosaicism and related disorders. 2. Characterize the immunologic profile in blood, tissue, and bone marrow of participants with trisomy 8 mosaicism and related disorders. Secondary Objectives: 1. Determine appropriate screening and diagnostic workup of individuals with trisomy 8 mosaicism and related disorders. 2. Identify the long-term risk of and association with neoplasm among individuals with trisomy 8 mosaicism. 3. Characterize the distribution of trisomy 8 cells in different tissues and cell types and describe how this contributes to disease manifestations and variability. 4. Evaluate or characterize immune responses to targeted therapeutics to better understand the pathophysiology of trisomy 8 mosaicism and related disorders. Exploratory Objectives: 1. Identify the specific genes and immunologic pathways that lead to disease manifestations seen in patients with trisomy 8. 2. Identify new genetic diseases that lead to mucosal ulcers and understand the immunologic mechanisms that contribute to mucosal ulcerations. Endpoints: Primary Endpoints: 1. Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing. 2. Characterization of immunologic profile of participants with trisomy 8 mosaicism and related disorders over time in comparison to healthy controls using cellular and molecular techniques including, but not limited to immune cell phenotyping, transcriptomics, proteomics, and ex vivo functional studies. Secondary Endpoints: 1. Characterization of laboratory, radiologic, biopsy, and physical exam findings. 2. Identification of individuals with trisomy 8 who develop malignancy and assessment of risk factors including but not limited to history, findings on bone marrow biopsies and complete blood counts (CBCs), next-generation sequencing (NGS) for risk variants, and flow cytometry. 3. Determination of the percentage of trisomy 8 cells in various tissue types including bone marrow, blood, fibroblasts cultured from skin, and biopsy samples, and the association with clinical phenotype. 4. Assessment of immune response to therapeutics based on inflammatory markers, clinical history, and physical exam findings. Exploratory Endpoint: 1. Identification of genes that may lead to mucosal ulcerative disease when mutated or over/underexpressed.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.