- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07683104
Natural History of Trisomy 8-Associated Autoinflammatory Disease (TRIAD) and Related Disorders
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:
- Characterize the clinical spectrum and natural history of trisomy 8 mosaicism and related disorders.
- Characterize the immunologic profile in blood, tissue, and bone marrow of participants with trisomy 8 mosaicism and related disorders.
Secondary Objectives:
- Determine appropriate screening and diagnostic workup of individuals with trisomy 8 mosaicism and related disorders.
- Identify the long-term risk of and association with neoplasm among individuals with trisomy 8 mosaicism.
- Characterize the distribution of trisomy 8 cells in different tissues and cell types and describe how this contributes to disease manifestations and variability.
- Evaluate or characterize immune responses to targeted therapeutics to better understand the pathophysiology of trisomy 8 mosaicism and related disorders.
Exploratory Objectives:
- Identify the specific genes and immunologic pathways that lead to disease manifestations seen in patients with trisomy 8.
- Identify new genetic diseases that lead to mucosal ulcers and understand the immunologic mechanisms that contribute to mucosal ulcerations.
Endpoints:
Primary Endpoints:
- Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing.
- 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:
- Characterization of laboratory, radiologic, biopsy, and physical exam findings.
- 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.
- 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.
- 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.
Panoramica dello studio
Stato
Descrizione dettagliata
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:
- Characterize the clinical spectrum and natural history of trisomy 8 mosaicism and related disorders.
- Characterize the immunologic profile in blood, tissue, and bone marrow of participants with trisomy 8 mosaicism and related disorders.
Secondary Objectives:
- Determine appropriate screening and diagnostic workup of individuals with trisomy 8 mosaicism and related disorders.
- Identify the long-term risk of and association with neoplasm among individuals with trisomy 8 mosaicism.
- Characterize the distribution of trisomy 8 cells in different tissues and cell types and describe how this contributes to disease manifestations and variability.
- Evaluate or characterize immune responses to targeted therapeutics to better understand the pathophysiology of trisomy 8 mosaicism and related disorders.
Exploratory Objectives:
- Identify the specific genes and immunologic pathways that lead to disease manifestations seen in patients with trisomy 8.
- Identify new genetic diseases that lead to mucosal ulcers and understand the immunologic mechanisms that contribute to mucosal ulcerations.
Endpoints:
Primary Endpoints:
- Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing.
- 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:
- Characterization of laboratory, radiologic, biopsy, and physical exam findings.
- 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.
- 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.
- 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.
Tipo di studio
Iscrizione (Stimato)
Contatti e Sedi
Contatto studio
- Nome: Kalpana Manthiram, M.D.
- Numero di telefono: (301) 529-4787
- Email: kalpana.manthiram@nih.gov
Backup dei contatti dello studio
- Nome: Laura E Failla, C.R.N.P.
- Numero di telefono: (240) 669-5323
- Email: laura.failla@nih.gov
Luoghi di studio
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Maryland
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Bethesda, Maryland, Stati Uniti, 20892
- Reclutamento
- National Institutes of Health Clinical Center
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Contatto:
- Kalpana Manthiram, M.D.
- Numero di telefono: (301) 529-4787
- Email: kalpana.manthiram@nih.gov
-
Contatto:
- Laura Failla, M.S.
- Numero di telefono: 240-669-5323
- Email: laura.failla@nih.gov
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-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
- INCLUSION CRITERIA:
To be eligible to participate in this study, an individual must meet the following criteria:
- Stated willingness to comply with study requirements.
- Aged <= 99 (ability to be seen at NIH vs. remote visit may be determined by age and location).
- Willingness to allow storage of data and specimens for future research.
Additional Inclusion Criteria for Affected Participants
Must have one of the following:
- 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
- Inflammatory mucosal ulcerative disease clinically similar to TRIAD at the discretion of the principal investigator.
- Ability of participant or LAR to provide informed consent.
Additional Inclusion Criteria for Biological Relatives
- Be an unaffected biological relative of an affected participant.
- Ability to provide informed consent.
- 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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
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Affected Participants
Individuals ages <= 99 with known or suspected trisomy 8 mosaicism, or with clinical phenotype consisting of mucosal ulcerations similar to TRIAD.
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Non-affected biological family member participants
Non-affected biological family members of enrolled participants.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Clinical characterization of participants with trisomy 8 mosaicism and related disorders based on history, physical examination, radiologic imaging, and laboratory testing.
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Characterization of laboratory, radiologic examinations, biopsies, and physical exam findings.
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: Length of study
|
Identify effective treatments for inflammatory symptoms among those with trisomy 8 mosaicism and related disorders.
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Length of study
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Kalpana Manthiram, M.D., National Institute of Allergy and Infectious Diseases (NIAID)
Pubblicazioni e link utili
Pubblicazioni generali
- Manthiram K, Preite S, Dedeoglu F, Demir S, Ozen S, Edwards KM, Lapidus S, Katz AE; Genomic Ascertainment Cohort; Feder HM Jr, Lawton M, Licameli GR, Wright PF, Le J, Barron KS, Ombrello AK, Barham B, Romeo T, Jones A, Srinivasalu H, Mudd PA, DeBiasi RL, Gul A, Marshall GS, Jones OY, Chandrasekharappa SC, Stepanovskiy Y, Ferguson PJ, Schwartzberg PL, Remmers EF, Kastner DL. Common genetic susceptibility loci link PFAPA syndrome, Behcet's disease, and recurrent aphthous stomatitis. Proc Natl Acad Sci U S A. 2020 Jun 23;117(25):14405-14411. doi: 10.1073/pnas.2002051117. Epub 2020 Jun 9.
- Ades L, Itzykson R, Fenaux P. Myelodysplastic syndromes. Lancet. 2014 Jun 28;383(9936):2239-52. doi: 10.1016/S0140-6736(13)61901-7. Epub 2014 Mar 21.
- Ando S, Maemori M, Sakai H, Ando S, Shiraishi H, Sakai K, Ruhnke GW. Constitutional trisomy 8 mosaicism with myelodysplastic syndrome complicated by intestinal Behcet disease and antithrombin III deficiency. Cancer Genet Cytogenet. 2005 Oct 15;162(2):172-5. doi: 10.1016/j.cancergencyto.2005.01.010.
- Becker K, Fitzgerald O, Green AJ, Keogan M, Newbury-Ecob R, Greenhalgh L, Withers S, Hollox EJ, Aldred PM, Armour JA. Constitutional trisomy 8 and Behcet syndrome. Am J Med Genet A. 2009 May;149A(5):982-6. doi: 10.1002/ajmg.a.32756.
- Hasle H, Clausen N, Pedersen B, Bendix-Hansen K. Myelodysplastic syndrome in a child with constitutional trisomy 8 mosaicism and normal phenotype. Cancer Genet Cytogenet. 1995 Jan;79(1):79-81. doi: 10.1016/0165-4608(94)00099-w.
- Altiner S, Kutlay NY, Ilhan O. Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis. Cytogenet Genome Res. 2016;150(1):35-39. doi: 10.1159/000452358. Epub 2016 Nov 12.
- Nielsen J, Wohlert M. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet. 1991 May;87(1):81-3. doi: 10.1007/BF01213097.
- Saumell S, Sole F, Arenillas L, Montoro J, Valcarcel D, Pedro C, Sanzo C, Luno E, Gimenez T, Arnan M, Pomares H, De Paz R, Arrizabalaga B, Jerez A, Martinez AB, Sanchez-Castro J, Rodriguez-Gambarte JD, Raya JM, Rios E, Rodriguez-Rivera M, Espinet B, Florensa L. Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not? PLoS One. 2015 Jun 12;10(6):e0129375. doi: 10.1371/journal.pone.0129375. eCollection 2015.
- Maserati E, Aprili F, Vinante F, Locatelli F, Amendola G, Zatterale A, Milone G, Minelli A, Bernardi F, Lo Curto F, Pasquali F. Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. Genes Chromosomes Cancer. 2002 Jan;33(1):93-7. doi: 10.1002/gcc.1214.
- Baidas S, Chen TJ, Kolev V, Wong LJ, Imholte J, Qin N, Meck J. Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities. Am J Med Genet A. 2004 Feb 1;124A(4):383-7. doi: 10.1002/ajmg.a.20390.
- Seghezzi L, Maserati E, Minelli A, Dellavecchia C, Addis P, Locatelli F, Angioni A, Balloni P, Miano C, Cavalli P, Danesino C, Pasquali F. Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases. Genes Chromosomes Cancer. 1996 Oct;17(2):94-101. doi: 10.1002/(SICI)1098-2264(199610)17:23.0.CO;2-W.
- Wesner N, Drevon L, Guedon A, Fraison JB, Trad S, Kahn JE, Aouba A, Gillard J, Ponsoye M, Hanslik T, Gourguechon C, Liozon E, Laribi K, Rossignol J, Hermine O, Ades L, Carrat F, Fenaux P, Mekinian A, Fain O; GFM, MINHEMON (French Network of Dysimmune Disorders Associated to Hemopathies). Inflammatory disorders associated with trisomy 8-myelodysplastic syndromes: French retrospective case-control study. Eur J Haematol. 2019 Jan;102(1):63-69. doi: 10.1111/ejh.13174. Epub 2018 Nov 14.
- Wesner N, Drevon L, Guedon A, Fraison JB, Terrier B, Trad S, Kahn JE, Aouba A, Gillard J, Ponsoye M, Hanslik T, Gourguechon C, Liozon E, Laribi K, Rossignol J, Hermine O, Seksik P, Ades L, Carrat F, Fenaux P, Mekinian A, Fain O; On behalf GFM and MINHEMON (French Network of dysimmune disorders associated with hemopathies). Gastrointestinal Behcet's-like disease with myelodysplastic neoplasms with trisomy 8: a French case series and literature review. Leuk Lymphoma. 2019 Jul;60(7):1782-1788. doi: 10.1080/10428194.2018.1542152. Epub 2018 Nov 20.
- Garcia-Manero G, Chien KS, Montalban-Bravo G. Myelodysplastic syndromes: 2021 update on diagnosis, risk stratification and management. Am J Hematol. 2020 Nov;95(11):1399-1420. doi: 10.1002/ajh.25950.
Collegamenti utili
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Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie trasmesse da vettori
- Infezioni
- Infezioni da virus a RNA
- Malattie virali
- Malattie ematologiche
- Infezioni da Picornaviridae
- Malattie del midollo osseo
- Infezioni batteriche
- Infezioni batteriche e micosi
- Infezioni batteriche Gram-negative
- Infezioni da borrelia
- Infezioni da Spirochaetales
- Malattie trasmesse dalle zecche
- Malattie emiche e linfatiche
- Malattie degli animali
- Sindromi mielodisplastiche
- Afta epizootica
- Febbre ricorrente
- Chromosome 8, mosaic trisomy
Altri numeri di identificazione dello studio
- 10002326
- 002326-I
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Periodo di condivisione IPD
Criteri di accesso alla condivisione IPD
Tipo di informazioni di supporto alla condivisione IPD
- LINFA
- CODICE_ANALITICO
- RSI
Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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