Ignite Creation Date:
2024-05-05 @ 11:29 AM
Last Modification Date:
2024-10-26 @ 9:08 AM
Study NCT ID:
NCT00055055
Status:
COMPLETED
Last Update Posted:
2024-07-03
First Post:
2003-02-15
Brief Title:
Study of Families With Twins or Siblings Discordant for Rheumatic Disorders
Sponsor:
National Institute of Environmental Health Sciences NIEHS
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
Pathogenic Studies In Families With Twins Or Siblings Discordant For Systemic Rheumatic Disorders
Status:
COMPLETED
Status Verified Date:
2024-06-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will examine families in which one sibling of a sibling pair or twin pair has developed a systemic rheumatic disease and one has not to see if and how the two differ in the following
Blood cell metabolism
Types of cells in the blood
Environmental exposures or genetic factors that might explain why one developed disease and the other did not
Families in which one sibling has developed a systemic rheumatic disease rheumatoid arthritis systemic lupus erythematosus scleroderma dermatomyositis or myositis and the other has not are eligible for this study The siblings may or may not be twins but must be of the same gender and be within a 5-year age difference Biological parents or in some cases children will also be included in the study Normal healthy volunteers will serve as control subjects
Participants will undergo some or all of the following tests and procedures
Medical history and physical examination Participants will also be asked permission to obtain medical records for review
Questionnaires about environmental exposures at work at home and elsewhere Probands participants with rheumatic disease and their healthy siblings will also answer questions about infections vaccinations medications or dietary supplements sun exposure and stressful events during the year before disease diagnosis in the affected sibling
Blood and urine collection for the following tests
Routine blood chemistries and other studies to rule out certain diseases or medical problems
Evidence of past toxic exposures and certain infections
Presence of cells from the mother in the child s blood and vice versa Recent studies suggest that during pregnancy or delivery cells from the mother and baby may be exchanged and circulate in the body for many years possibly causing problems
In twin or sibling pairs presence of certain genes that may be more common in patients with systematic rheumatic diseases as compared with their unaffected siblings and normal volunteers
In identical twins comparison of their blood cell metabolism to see if and how the metabolism differs in people with rheumatic disease
Participants may be asked for permission to have some of their blood and urine samples stored and to obtain previously collected blood or tissue biopsy specimens that are no longer needed for clinical care for research purposes They may also be asked to give additional blood or urine samples
Participants will be followed every year for 5 years either in person or by questionnaire to evaluate any changes in their condition The final 5-year evaluation will repeat some of the questionnaires and procedures described above
Blood cell metabolism
Types of cells in the blood
Environmental exposures or genetic factors that might explain why one developed disease and the other did not
Families in which one sibling has developed a systemic rheumatic disease rheumatoid arthritis systemic lupus erythematosus scleroderma dermatomyositis or myositis and the other has not are eligible for this study The siblings may or may not be twins but must be of the same gender and be within a 5-year age difference Biological parents or in some cases children will also be included in the study Normal healthy volunteers will serve as control subjects
Participants will undergo some or all of the following tests and procedures
Medical history and physical examination Participants will also be asked permission to obtain medical records for review
Questionnaires about environmental exposures at work at home and elsewhere Probands participants with rheumatic disease and their healthy siblings will also answer questions about infections vaccinations medications or dietary supplements sun exposure and stressful events during the year before disease diagnosis in the affected sibling
Blood and urine collection for the following tests
Routine blood chemistries and other studies to rule out certain diseases or medical problems
Evidence of past toxic exposures and certain infections
Presence of cells from the mother in the child s blood and vice versa Recent studies suggest that during pregnancy or delivery cells from the mother and baby may be exchanged and circulate in the body for many years possibly causing problems
In twin or sibling pairs presence of certain genes that may be more common in patients with systematic rheumatic diseases as compared with their unaffected siblings and normal volunteers
In identical twins comparison of their blood cell metabolism to see if and how the metabolism differs in people with rheumatic disease
Participants may be asked for permission to have some of their blood and urine samples stored and to obtain previously collected blood or tissue biopsy specimens that are no longer needed for clinical care for research purposes They may also be asked to give additional blood or urine samples
Participants will be followed every year for 5 years either in person or by questionnaire to evaluate any changes in their condition The final 5-year evaluation will repeat some of the questionnaires and procedures described above
Detailed Description:
Most autoimmune diseases are thought to develop as a result of chronic immune activation and dysregulation after selected environmental exposures in genetically susceptible individuals Current evidence suggests that the adult and juvenile forms of systemic rheumatic disorders -- defined here as rheumatoid arthritis RA systemic lupus erythematosus SLE systemic sclerosis SSc and idiopathic inflammatory myopathies IIM -- share many common clinical manifestations immune responses genetic hormonal and environmental risk factors and possible pathogeneses Conversely other studies imply that each rheumatic disease as currently defined may be composed of more homogeneous subgroups known as elemental disorders with different pathogeneses This protocol will explore pathogenic mechanisms for systemic rheumatic disorders and possible elemental disorders through the evaluation of families with monozygotic or dizygotic twins or other siblings discordant for systemic rheumatic disorders twin-sib pairs Parents and healthy volunteers will also be evaluated as needed for the experimental designs of each portion of the protocol A clinical evaluation using standardized physician and patient clinical and environmental exposure questionnaires and specimen collections from 400 twin-sib pairs discordant for systemic rheumatic disorders will be performed to confirm diagnoses document medical histories and assess possible risk factors implicated in the development of autoimmunity This study will evaluate children who will make up 25-50 of the twin-sib pairs and adults in similar ways to attempt to understand possible similarities and differences in pathogeneses of systemic rheumatic disorders based upon age of onset Hypothesis-testing studies will assess differences in peripheral blood cell gene activationsuppression levels and types of microchimerism between affected and unaffected individuals selected genetic risk factors for these disorders and occupational and hormonal exposures hypothesized to be potential risk factors for these diseases Exploratory studies will be conducted to begin to assess other environmental risk factors for systemic rheumatic disorders and to better understand associations among phenotypes and genotypes Biologic specimens -- including blood urine and other clinical specimens or biopsies no longer necessary for clinical care -- will be collected for directed biomarker assays and the development of repositories for future research
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 03-E-0099 | None | None | None |