Evidence map›Paper›PMID 39281853›Full record

ArticleNeurobiology of pain (Cambridge, Mass.)

Clinical and biobehavioral phenotypic assessments and data harmonization for the RE-JOIN research consortium: Recommendations for common data element selection.

Yenisel Cruz-Almeida, Bella Mehta, Nele A Haelterman, Alisa J Johnson, Chloe Heiting, Malin Ernberg, Dana Orange, Martin Lotz, Jacqueline Boccanfuso, Shad B Smith and 12 more

Abstract read
In one paragraph

Article in Neurobiology of pain (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Osteoarthritis as a systemic disease.Nature reviews. Rheumatology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Yenisel Cruz-AlmeidaPain Research & Intervention Center of Excellence, University of Florida, FL, USA.
Bella MehtaHospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
Nele A HaeltermanDepartment of Human and Molecular Genetics, Baylor College of Medicine, TX, USA.
Alisa J JohnsonPain Research & Intervention Center of Excellence, University of Florida, FL, USA.
Chloe HeitingHospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
Malin ErnbergDepartment of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
Dana OrangeThe Rockefeller University, New York, USA.
Martin LotzDepartment of Molecular and Cellular Biology & Department of Molecular Medicine, Scripps Research, CA, USA.
Jacqueline BoccanfusoDepartment of Biostatistics, Epidemiology & Informatics, University of Pennsylvania, PA, USA.
Shad B SmithDepartment of Anesthesiology, Duke University Medical Center, NC, USA.
Marlena PelaDepartment of Neurosciences, University of California San Diego, CA, USA.
Jyl BolineDepartment of Neurosciences, University of California San Diego, CA, USA.
Miguel OteroHospital for Special Surgery, New York, USA and Weill Cornell Medical College, New York, USA.
Kyle AllenDepartment of Biomedical Engineering, University of Florida, FL, USA.
Daniel PerezUniversity of Texas Health San Antonio, TX, USA.
Christopher DonnellyDepartment of Anesthesiology, Duke University Medical Center, NC, USA.
Alejandro AlmarzaDepartment of Oral and Craniofacial Sciences, University of Pittsburgh, PA, USA.
Merissa OlmerDepartment of Molecular and Cellular Biology & Department of Molecular Medicine, Scripps Research, CA, USA.
Henah BalkhiThe Rockefeller University, New York, USA.
Joost WagenaarDepartment of Biostatistics, Epidemiology & Informatics, University of Pennsylvania, PA, USA.
Maryann MartoneDepartment of Neurosciences, University of California, CA, USA.
RE-JOIN Consortium Investigators

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
RE-JOIN NEURONAL ANATOMY, CONNECTIVITY, AND PHENOTYPIC INNERVATION OF THE KNEE JOINTUC2AR082200 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI Benjamin R Arenkiel, Brendan Lee · 2022 to 2026
$14.4M
Innervation of the knee and TMJUC2AR082196 · NIAMS · UNIVERSITY OF FLORIDA · PI Kyle D Allen, Alejandro Jose Almarza · 2022 to 2026
$11.2M
NCATS NIH HHS UL1 TR001873NCATS NIH HHS UL1 TR002384NIAMS NIH HHS UC2 AR082196NIAMS NIH HHS UC2 AR082200
6 · The paper itself

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 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.

Indexed as

InnervationJoint painNeurobiologyNeuronal types

Identifiers

PMID39281853
PMCPMC11399706

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.