The Fibromyalgia Family Study identifies and collects blood samples from families with two or more members affected with Fibromyalgia Syndrome (FMS). The primary goal of the study is to identify genes that predispose people to FMS and/or symptoms related to FMS; identifying these genes may lead to a better understanding of the disease and more effective treatments.

Official Title

Fibromyalgia Family Study Registry

Conditions

– Fibromyalgia- Irritable Bowel Syndrome- Chronic Fatigue Syndrome- Depression

Study Type

Observational

Study Design

Natural History, Cross-Sectional, Convenience Sample, Retrospective Study

Further Details

FMS predominantly affects women and is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbance, and multiple tender points on physical examination. The pathophysiological mechanisms underlying FMS are not clearly understood, but neuroendocrine factors seem to be of major importance. Studies of familial association suggest that genetic factors play a role in FMS. This study will establish patterns of genetic linkage in families with FMS. Participating family members will undergo a brief physical exam (including tender point exam), donate a blood sample, and complete a detailed questionnaire that includes experience with pain, fatigue, depression, bowel symptoms, headache, anxiety, and physical limitations. Measurements of serum serotonin and related compounds will also be obtained. To detect genetic factors, a genome-wide linkage scan using 405 microsatellite markers will be performed.

Study Start

Eligibility & Criteria

Ages Eligible for Study: 12 Years and above, Genders Eligible for Study: Both Criteria Inclusion CriteriaDiagnosed with fibromyalgia according to the criteria of the American College of Rheumatology Have at least one living family member who has also been diagnosed with fibromyalgia No other major rheumatological disease

Total Enrolment

560

Contact Details

[1] Jane M. Olson, PhD, Study Chair, Case Western Reserve University

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