Genetic Determinants of Ankylosing Spondylitis Severity
NCT00056849 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 134
Last updated 2020-01-07
Summary
This study will explore how genes-units of heredity-may influence the severity of ankylosing spondylitis. It will examine whether some genes may cause people with ankylosing spondylitis to have more rapid fusion of the bones of the spine, more difficulty performing daily activities, or be more likely to need joint surgery.
Patients who developed ankylosing spondylitis after age 16 and have had the disease for 20 years or more may be eligible for this study. The onset of disease is dated to the first appearance of symptoms of inflammatory low back pain or restricted spinal motion. Patients with a spondyloarthropathy other than AS may not enroll.
Participants will complete a brief medical history and physical exam. They will fill out a 30-minute questionnaire that includes questions on demographics (such as age, ethnicity, marital status, etc.), medication history, work history, hip surgeries, and assessment of functional disability. Fifty milliliters (about 3-1/3 tablespoons) of blood will be drawn for gene testing, and X-rays will be taken of the pelvis, lower back, and neck, if recent X-rays (within 1 year) are not available. Women of childbearing age will have a urine pregnancy test before having X-rays.
Conditions
Sponsors & Collaborators
-
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
lead NIH
Principal Investigators
-
Michael M Ward, M.D. · National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Eligibility
- Min Age
- 18 Years
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-03-24
- Primary Completion
- 2020-01-03
- Completion
- 2020-01-03
Countries
- United States
Study Locations
More Related Trials
-
Genetic Analysis of Psoriasis and Psoriatic Arthritis
NCT00341809 ·Status: COMPLETED
-
Identification of Mutations Responsible for Rare Familial Skin Diseases by Next Generation Sequencing
NCT02509650 ·Status: UNKNOWN
-
Deciphering the Genetic Architecture of Autoimmune Diseases
NCT06948110 ·Status: RECRUITING
-
The Role of Genetic Polymorphisms in Innate Immune Response Genes in Susceptibility to Infections
NCT00597090 ·Status: COMPLETED
-
Study of Genotype and Phenotype in Patients With Alpha 1-Antitrypsin Deficiency
NCT00005098 ·Status: TERMINATED
-
Genes and Phenotype (GAP) A National Resource for Genotype-Phenotype Studies of Immunological and Inflammatory Pathways
NCT01161056 ·Status: COMPLETED
-
Genetics of Rheumatoid Arthritis
NCT00001678 ·Status: COMPLETED
-
Study of Genetic Risk Factors for Spina Bifida and Anencephaly
NCT00031122 ·Status: UNKNOWN
-
Implications of Maternal 45,X Mosaicism as a Secondary Genomic Finding Following Cell-Free DNA Sequencing During Pregnancy: A Deep Phenotype Study
NCT05548881 ·Status: WITHDRAWN
-
Study of Heritable Connective Tissue Disorders
NCT00001641 ·Status: COMPLETED
-
Studies of Heritable Disorders of Connective Tissue
NCT00270686 ·Status: COMPLETED
-
Hidradenitis - an Analysis of Genetic Traits and Linkages in Families
NCT05710393 ·Status: TERMINATED
-
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
NCT02886611 ·Status: RECRUITING
-
Web-based Genetic Research on Lupus
NCT02530944 ·Status: COMPLETED
-
Genetic Study of Patients and Families With Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma of the Bone
NCT00007046 ·Status: COMPLETED
-
Prevalence of Pituitary Incidentaloma in Relatives of Patients With Pituitary Adenoma
NCT00598949 ·Status: UNKNOWN
-
Study of Disease Severity in Adults With Neurofibromatosis Type 1 (NF1)
NCT00111384 ·Status: COMPLETED
-
The Role of Genetic Factors in the Development of Idiopathic Scoliosis in the Kazakh Population
NCT05095129 ·Status: COMPLETED
-
Genetic Studies of X-linked Lymphoproliferative Disease
NCT00359411 ·Status: COMPLETED
-
Evaluating Genetic Modifiers of Cutaneous Neurofibromas in Adults With Neurofibromatosis Type 1
NCT04941027 ·Status: COMPLETED
-
Genetic Susceptibility to Severe Infections
NCT06102070 ·Status: RECRUITING
-
Study of Gene Associations and Infertility
NCT01223092 ·Status: ENROLLING_BY_INVITATION
-
Genetic Clues to Chordoma Etiology: A Protocol to Identify Sporadic Chordoma Patients for Studies of Cancer-Susceptibility Genes
NCT01200680 ·Status: ACTIVE_NOT_RECRUITING
-
Genetic Analysis of Craniofrontonasal Syndrome
NCT00339846 ·Status: COMPLETED
-
Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
NCT06325878 ·Status: RECRUITING ·Phase: NA