Autoimmune and Autoinflammatory Genetics Study

Autoimmune Disease Clinical Trial

Official title:

Natural History and Genetics of VEXAS Syndrome and Related Autoinflammatory Syndromes

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06004349
• Other study ID #: 22-00038
• Status: Recruiting
• Start date: April 15, 2022
• Est. completion date: April 5, 2032

Study information

• Verified date: September 2023
• Source: NYU Langone Health
• Contact: David Beck, MD, PhD
• Phone: 646-501-7400
• Email: BeckClinic[@]nyulangone.org
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is an exploratory natural history protocol that will enroll patients with known genetic diseases, such as VEXAS syndrome, or as yet undiagnosed disorders of inflammation with the goal of improving our understanding of disease processes. Blood, saliva, hair, nail, or buccal samples may be collected for genetic analysis, blood samples will be obtained for immunologic and other functional studies, and a small number of subjects may undergo skin biopsy.

Description:

This is a single-site protocol designed to test the hypothesis that genetic factors contribute to susceptibility to human disorders of inflammation, and the hypothesis that identifying such genetic susceptibility factors will contribute to our understanding of the immunologic mechanisms of these diseases. There are 3 main objectives: Primary Objective: To discover the genetic basis of human disorders of inflammation or autoinflammatory diseases. Secondary Objective: To enumerate immunologic features and genotype-phenotype associations in specific inflammatory diseases, such as VEXAS syndrome. Tertiary/Exploratory Objective: To describe the clinical features of poorly characterized or newly defined disorders of inflammation, such as VEXAS syndrome, through the retrospective chart review of standard medical practice follow up

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1500
• Est. completion date: April 5, 2032
• Est. primary completion date: April 5, 2032
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Month and older

Eligibility

Inclusion Criteria:

In order to be eligible to participate in this study as a subject with known or suspected

autoinflammatory disease, an individual must meet all of the following criteria:

• Stated willingness to participate in study procedures (which at the very least includes providing a mail-in blood or saliva sample for genetic analysis);
• Regardless of sex assigned at birth, at least one month of age;
• A medical history that, in the expert opinion of the PI and study team, is consistent with the possibility of autoinflammatory disease or known diagnosis of an autoinflammatory disease, such as VEXAS syndrome; and
• Ability of the subject, parents (in the case of children), or Legally Authorized Representative to understand and the willingness to sign a written informed consent document. In order to be eligible to participate in this study as a family member of a subject with known or suspected autoinflammatory disease, an individual must meet all of the following

criteria:

• Stated willingness to participate in study procedures (which at the very least includes providing a mail-in sample for genetic analysis);
• Regardless of sex assigned at birth, at least one month of age;
• Relationship, either by blood or marriage, to an individual enrolled or about to be enrolled in the study with known or suspected autoinflammatory disease;
• Likelihood, in the expert opinion of the PI and study team, that analysis of a sample from the individual would advance genetic or functional analysis of the affected relative's possible autoinflammatory condition; and
• Ability of the subject, parents (in the case of children), to understand and the willingness to sign a written informed consent document. In order to be eligible to participate in this study as a healthy volunteer, an individual

must meet all of the following criteria:

• Stated willingness to participate in study procedures for healthy volunteers;
• Regardless of sex assigned at birth, at least five years old, and not pregnant (by history of a missed menstrual period);
• Likelihood, in the expert opinion of the PI that a sample from the individual would advance the functional analysis of an autoinflammatory condition under study; and
• Ability of the subject to understand and the willingness to sign a written informed consent document by a capacity assessment provided by the PI and study team. Exclusion Criteria: For any of the three categories of subjects, an individual will be excluded from participation in this study for the following reasons: Probands: an individual will not be enrolled as a proband if the study team has a low suspicion of having an autoinflammatory disease or a genetic cause for an autoinflammatory disease. Family Members: an individual will not be enrolled as a family member if the study team believes they may have an autoinflammatory disease, in which case, they will be enrolled as a proband. Healthy controls: an individual will not be enrolled as a healthy control if they have an autoinflammatory disease, or any condition that may mimic an autoinflammatory disease, such as hematologic malignancy, rheumatologic disease.

Related Conditions & MeSH terms

• Autoimmune Disease
• Autoimmune Diseases
• Autoinflammatory Disease
• Collagen Diseases
• Rheumatic Disease
• Rheumatic Diseases

Locations

Country	Name	City	State
United States	NYC H+H/Bellevue	New York	New York
United States	NYU Langone Health	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

References & Publications (2)

Beck DB, Bodian DL, Shah V, Mirshahi UL, Kim J, Ding Y, Magaziner SJ, Strande NT, Cantor A, Haley JS, Cook A, Hill W, Schwartz AL, Grayson PC, Ferrada MA, Kastner DL, Carey DJ, Stewart DR. Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population. JAMA. 2023 Jan 24;329(4):318-324. doi: 10.1001/jama.2022.24836. — View Citation

Ferrada MA, Savic S, Cardona DO, Collins JC, Alessi H, Gutierrez-Rodrigues F, Kumar DBU, Wilson L, Goodspeed W, Topilow JS, Paik JJ, Poulter JA, Kermani TA, Koster MJ, Warrington KJ, Cargo C, Tattersall RS, Duncan CJA, Cantor A, Hoffmann P, Payne EM, Bonnekoh H, Krause K, Cowen EW, Calvo KR, Patel BA, Ombrello AK, Kastner DL, Young NS, Werner A, Grayson PC, Beck DB. Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood. 2022 Sep 29;140(13):1496-1506. doi: 10.1182/blood.2022016985. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of newly discovered rare, high penetrance germline variants that cause human inflammatory disease		Study End (Up to Year 5)
Primary	Number of newly discovered structural genomic variants that cause human inflammatory disease		Study End (Up to Year 5)
Primary	Number of newly discovered common, low penetrance germline variants that confer susceptibility to human inflammatory disease		Study End (Up to Year 5)
Primary	Number of newly discovered somatic mutations that give rise to human inflammatory disease		Study End (Up to Year 5)