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Natural History of Trisomy 8-Associated Autoinflammatory Disease (TRIAD) and Related Disorders

Background:

Trisomy 8 mosaicism is a genetic disorder that can increase inflammation in the body. Symptoms include fevers; sores or ulcers in the mouth, digestive tract, or genital area; skin rashes; problems in organs or tissues; and changes in bone marrow cells. Researchers want to conduct a natural history study to learn more about these symptoms and what causes them.

Objective:

To gather data and samples from people with and without the trisomy 8 mosaicism.

Eligibility:

People of any age with the trisomy 8 gene mosaicism. Their healthy relatives are also needed.

Design:

Affected participants will have visits every 1 to 2 years for 30 years at NIH. Each visit will take 1 to 5 days and may be in-person or remote. With remote visits, participants may have a video call with the study team and samples may be sent to researchers by mail.

Participants may have these procedures:

Physical exam, with blood tests.

Tests of brain function and motor skills.

Sensory tests. Researchers will see how participants respond to sensations such as pinpricks, heat, cold, and pressure.

Magnetic resonance imaging (MRI) scan of the brain and/or spine.

X-ray of the spine.

Ultrasound test of heart function (echocardiogram).

Tissues samples (biopsies) collected from the skin, inside of the mouth, and bone marrow.

Swabs to collect cells from the mouth, skin, and vagina.

Collection of blood, stool, urine, saliva, hair, and fingernail samples.

X-rays, MRI, and heart tests will be done only once. Other procedures may be repeated at each visit. All tests and procedures are voluntary.

Healthy relatives who enroll will have a baseline visit and then follow-up visits as needed. They will have a physical exam. The inside of their mouth may be swabbed. Samples of blood, stool, urine, and saliva may be taken.

Przegląd badań

Szczegółowy opis

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.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

750

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

    • Maryland
      • Bethesda, Maryland, Stany Zjednoczone, 20892
        • Rekrutacyjny
        • National Institutes of Health Clinical Center
        • Kontakt:
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

Outside provider referral, current NIH study patients

Opis

  • 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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
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.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing.
Ramy czasowe: Length of the study
Characterize the clinical spectrum and natural history of trisomy 8 mosaicism and related disorders.
Length of the study
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
Ramy czasowe: Length of the study
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.
Length of the study

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Characterization of laboratory, radiologic examinations, biopsies, and physical exam findings.
Ramy czasowe: Length of study
Determine appropriate screening and diagnostic workup of individuals with trisomy 8 mosaicism and related disorders.
Length of study
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 CBCs, NGS for risk variants, and flow cytometry.
Ramy czasowe: Length of study
Identify the long-term risk of and association with neoplasm among individuals with trisomy 8 mosaicism.
Length of study
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.
Ramy czasowe: Length of study
Characterize the distribution of trisomy 8 cells in different tissues and cell types and describe how this contributes to disease manifestations and variability.
Length of study
Assessment of treatment response based on inflammatory markers, clinical history, and physical exam findings.
Ramy czasowe: Length of study
Identify effective treatments for inflammatory symptoms among those with trisomy 8 mosaicism and related disorders.
Length of study

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Kalpana Manthiram, M.D., National Institute of Allergy and Infectious Diseases (NIAID)

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

23 września 2026

Zakończenie podstawowe (Szacowany)

1 maja 2056

Ukończenie studiów (Szacowany)

1 czerwca 2056

Daty rejestracji na studia

Pierwszy przesłany

2 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

2 lipca 2026

Pierwszy wysłany (Rzeczywisty)

6 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

18 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

17 września 2026

Ostatnia weryfikacja

9 września 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

TAK

Opis planu IPD

This study will comply with the NIH Data Management and Sharing (DMS) Policy, which applies to all new and ongoing NIH-funded research in the IRP, as of January 25, 2023, that is associated with a ZIA, with a clinical protocol that undergoes scientific review and/or will involve genomic data sharing. This study will comply with the NIH Genomic Data Sharing (GDS) Policy, which applies to all new and ongoing NIH IRP-funded research, as of August 31, 2015, that generates large-scale human or non-human genomic data, as well as the use of these data for subsequent research. Large-scale data include GWAS, SNP arrays, and genome sequence, transcriptomic, epigenomic, and gene expression data.

Ramy czasowe udostępniania IPD

Upon publication

Kryteria dostępu do udostępniania IPD

Requests will be assessed by the PI. Next generation sequencing data will be deposited into public repositories.

Typ informacji pomocniczych dotyczących udostępniania IPD

  • SOK ROŚLINNY
  • ANALITYCZNY_KOD
  • CSR

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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