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Clinical and biobehavioral phenotypic assessments and data harmonization for the RE-JOIN research consortium: Recommendations for common data element selection.
Cruz-Almeida, Yenisel; Mehta, Bella; Haelterman, Nele A; Johnson, Alisa J; Heiting, Chloe; Ernberg, Malin; Orange, Dana; Lotz, Martin; Boccanfuso, Jacqueline; Smith, Shad B; Pela, Marlena; Boline, Jyl; Otero, Miguel; Allen, Kyle; Perez, Daniel; Donnelly, Christopher; Almarza, Alejandro; Olmer, Merissa; Balkhi, Henah; Wagenaar, Joost; Martone, Maryann.
Afiliação
  • Cruz-Almeida Y; Pain Research & Intervention Center of Excellence, University of Florida, FL, USA.
  • Mehta B; Hospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
  • Haelterman NA; Department of Human and Molecular Genetics, Baylor College of Medicine, TX, USA.
  • Johnson AJ; Pain Research & Intervention Center of Excellence, University of Florida, FL, USA.
  • Heiting C; Hospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
  • Ernberg M; Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Orange D; The Rockefeller University, New York, USA.
  • Lotz M; Department of Molecular and Cellular Biology & Department of Molecular Medicine, Scripps Research, CA, USA.
  • Boccanfuso J; Department of Biostatistics, Epidemiology & Informatics, University of Pennsylvania, PA, USA.
  • Smith SB; Department of Anesthesiology, Duke University Medical Center, NC, USA.
  • Pela M; Department of Neurosciences, University of California San Diego, CA, USA.
  • Boline J; Department of Neurosciences, University of California San Diego, CA, USA.
  • Otero M; Hospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
  • Allen K; Department of Biomedical Engineering, University of Florida, FL, USA.
  • Perez D; University of Texas Health San Antonio, TX, USA.
  • Donnelly C; Department of Anesthesiology, Duke University Medical Center, NC, USA.
  • Almarza A; Department of Oral and Craniofacial Sciences, University of Pittsburgh, PA, USA.
  • Olmer M; Department of Molecular and Cellular Biology & Department of Molecular Medicine, Scripps Research, CA, USA.
  • Balkhi H; The Rockefeller University, New York, USA.
  • Wagenaar J; Department of Biostatistics, Epidemiology & Informatics, University of Pennsylvania, PA, USA.
  • Martone M; Department of Neurosciences, University of California, CA, USA.
Neurobiol Pain ; 16: 100163, 2024.
Article em En | MEDLINE | ID: mdl-39281853
ABSTRACT

Background:

The Restoring Joint Health and Function to Reduce Pain (RE-JOIN) Consortium is part of the Helping to End Addiction Long-term® (HEAL) Initiative. HEAL is an ambitious, NIH-wide initiative to speed scientific solutions to stem the national opioid public health crisis. The RE-JOIN consortium's over-arching goal is to define how chronic joint pain-mediating neurons innervate different articular and peri-articular tissues, with a focus on the knee and temporomandibular joints (TMJ) across species employing the latest neuroscience approaches. The aim of this manuscript is to elucidate the human data gathered by the RE-JOIN consortium, as well as to expound upon its underlying rationale and the methodologies and protocols for harmonization and standardization that have been instituted by the RE-JOIN Consortium.

Methods:

The consortium-wide human models working subgroup established the RE-JOIN minimal harmonized data elements that will be collected across all human studies and set the stage to develop parallel pre-clinical data collection standards. Data harmonization considerations included requirements from the HEAL program and recommendations from the consortium's researchers and experts on informatics, knowledge management, and data curation.

Results:

Multidisciplinary experts - including preclinical and clinical researchers, with both clinician-scientists- developed the RE-JOIN's Minimal Human Data Standard with required domains and outcome measures to be collected across projects and institutions. The RE-JOIN minimal data standard will include HEAL Common Data Elements (CDEs) (e.g., standardized demographics, general pain, psychosocial and functional measures), and RE-JOIN common data elements (R-CDE) (i.e., both general and joint-specific standardized and clinically important self-reported pain and function measures, as well as pressure pain thresholds part of quantitative sensory testing). In addition, discretionary, site-specific measures will be collected by individual institutions (e.g., expanded quantitative sensory testing and gait biomechanical assessments), specific to the knee or TMJ. Research teams will submit datasets of standardized metadata to the RE-JOIN Data Coordinating Center (DCG) via a secure cloud-based central data repository and computing infrastructure for researchers to share and conduct analyses on data collected by or acquired for RE-JOIN. RE-JOIN datasets will have protected health information (PHI) removed and be publicly available on the SPARC portal and accessible through the HEAL Data Ecosystem.

Conclusion:

Data Harmonization efforts provide the multidisciplinary consortium with an opportunity to effectively collaborate across decentralized research teams, and data standardization sets the framework for efficient future analyses of RE-JOIN data collected by the consortium. The harmonized phenotypic information obtained will significantly enhance our understanding of the neurobiology of the pain-pathology relationships in humans, providing valuable insights for comparison with pre-clinical models.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurobiol Pain Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurobiol Pain Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos