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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.

調査の概要

詳細な説明

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.

研究の種類

観察的

入学 (推定)

750

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Maryland
      • Bethesda、Maryland、アメリカ、20892
        • 募集
        • National Institutes of Health Clinical Center
        • コンタクト:
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

Outside provider referral, current NIH study patients

説明

  • 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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing.
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Characterization of laboratory, radiologic examinations, biopsies, and physical exam findings.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠:Length of study
Identify effective treatments for inflammatory symptoms among those with trisomy 8 mosaicism and related disorders.
Length of study

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Kalpana Manthiram, M.D.、National Institute of Allergy and Infectious Diseases (NIAID)

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月23日

一次修了 (推定)

2056年5月1日

研究の完了 (推定)

2056年6月1日

試験登録日

最初に提出

2026年7月2日

QC基準を満たした最初の提出物

2026年7月2日

最初の投稿 (実際)

2026年7月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月17日

最終確認日

2026年9月9日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

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.

IPD 共有時間枠

Upon publication

IPD 共有アクセス基準

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

IPD 共有サポート情報タイプ

  • SAP
  • ANALYTIC_CODE
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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