| Jump to: | Authorized Access | | | Attribution | | | Authorized Requests |
- Substudies
-
phs000762.v1.p1 : OPPERA baseline case-control study of chronic TMJD phs000850.v1.p1 : OPPERA Prospective Cohort Study of First-Onset TMJD - Study Description
-
Important Links and Information
-
Request access via Authorized Access
- Instructions for requestors
- Data Use Certification (DUC) Agreement
- Talking Glossary of Genetic Terms
The OPPERA project has two sub-studies investigating effects of genetic, physiological, psychological and clinical factors on the risk of developing painful temporomandibular disorder (TMD).
- OPPERA I baseline case-control study of chronic TMJD (dbGaP study accession phs000762). This sub-study uses a case-control study design to investigate characteristics associated with chronic TMD. The parent OPPERA phenotype file contains an indicator variable (PHASE1CASECONTROL) identifying participants in this sub-study. Data users should use the relevant case-classification variable (CHRNONICTMDCASE) and apply statistical methods appropriate for case-control studies when analyzing TMJD in this sub-study.
- OPPERA I prospective cohort for first onset of TMJD (dbGaP study accession phs000850). This sub-study uses a prospective cohort study design to investigate characteristics that predict risk of developing first-onset TMD. The parent OPPERA phenotype file contains an indicator variable (PROSPECTIVECOHORT) identifying participants in this sub-study. Data users should use the relevant case-classification variable (INCIDENTCASE) and the relevant time-in-study variable (FOLLOWUPYEARS) when analyzing TMJD in this sub-study. It is recommended that data users apply statistical methods appropriate for cohort studies of a dynamic population (for example, Cox regression models, where INCIDENTCASE is the censoring variable and FOLLOWUPYEARS is time in study).
- Study Weblinks:
- Study Design:
- Case-Control
- Study Type:
- Case-Control
- Cohort
- Total number of consented subjects: 3446
- Subject Sample Telemetry Report (SSTR)
-
Request access via Authorized Access
- Authorized Access
- Publicly Available Data
- Link to other NCBI resources related to this study
- Study Inclusion/Exclusion Criteria
Inclusion criteria were all three of:
- Age 18-44 years
- Planning on living in the area for the next two years
- Fluent in written and spoken English.
Exclusion criteria were any one of 13 conditions:
- Traumatic facial injury or surgery on the face or jaw within the six months preceding enrollment
- Currently receiving orthodontic treatment
- Pregnant or nursing
- Kidney failure or renal dialysis
- Heart disease or heart failure
- Chronic respiratory disease that is not controlled with medication
- Hypertension that is not controlled with medication
- Epilepsy or medication to control grand mal seizures
- Hyperthyroidism
- Diabetes that is not controlled with medication or diet
- Drug or alcohol abuse
- Psychiatric disorders or conditions that have required hospitalization
- Chemotherapy or radiation therapy.
- Molecular Data
-
Type Source Platform Number of Oligos/SNPs SNP Batch Id Comment Targeted Genotyping Algynomics Algynomics Pain Research Panel N/A N/A - Study History
The OPPERA project began in 2006 with enrollment of participants into two studies at four U.S. study sites: Baltimore, MD; Buffalo, NY; Chapel Hill, NC; and Gainesville, FL. In 2012, the National Institute of Dental and Craniofacial Research (NIDCR) awarded funding to support the study for an additional five year period.
- Selected Publications
- Diseases/Traits Related to Study (MeSH terms)
-
- Primary Phenotype: Temporomandibular Joint Disorders
- Chronic Pain
- Authorized Data Access Requests
-
See articles in PMC citing this study accession
- Study Attribution
-
-
Co-Program Directors
- William Maixner, DDS, PhD. Center for Pain Research and Innovation, Department of Endodontics, Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
- Gary D. Slade, PhD. Center for Pain Research and Innovation, Department of Dental Ecology, Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
-
Principal Investigators
- Roger B. Fillingim, PhD. Department of Community Dentistry and Behavioral Science, University of Florida, College of Dentistry, Gainesville, FL, USA.
- Richard Ohrbach, DDS, PhD. Department of Oral Diagnostic Sciences, University at Buffalo, Buffalo, NY, USA.
- Joel D. Greenspan, PhD. Department of Neural and Pain Sciences and Brotman Facial Pain Center, University of Maryland Dental School, Baltimore, MD, USA.
- Charles Knott, PhD, Data Coordinating Center Director. Battelle Memorial Institute, Durham, NC, USA.
-
Neurogenomics Core Co-Directors
- Luda Diatchenko, MD, PhD. Alan Edwards Centre for Research on Pain, McGill University, Montreal, Canada.
- Bruce S. Weir, PhD. Department of Biostatistics, University of Washington, Seattle, WA, USA.
-
Co-Investigators
- Shad B. Smith, PhD. Center for Pain Research and Innovation, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
- Eric Bair, PhD. Center for Pain Research and Innovation, Department of Biostatistics, Department of Endodontics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
- Ronald Dubner, DDS, PhD. Department of Neural and Pain Sciences and Brotman Facial Pain Center, University of Maryland Dental School, Baltimore, MD, USA.
-
Funding Source
- U01DE017018. National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
-
Co-Program Directors