Evidence map›Paper›PMID 42352308›Full record

ArticleBiomolecules2026

Physiological Adaptations and Serum-Based Biomarker Dynamics During Multimodal Rehabilitation in Chronic Pain: Analysis of a Prospective Cohort Study.

Meike Meinzer, Markus Bassler, Franziska Kessemeier, Corinna Webering, Detlef Neumann, Heike Bähre, Ralf Lichtinghagen, Mathias Rhein, Johannes Achenbach, Christoph Gutenbrunner and 1 more

Abstract read
In one paragraph

Article in Biomolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Meike MeinzerDepartment of Pharmacology, Hannover Medical School, 30625 Hannover, Germany.
Markus BasslerInstitute for Social Medicine, Rehabilitation Sciencesand Health Services Research (ISRV), Nordhausen University of Applied Sciences, 99734 Nordhausen, Germany.ORCID 0000-0003-3279-3386
Franziska KessemeierInstitute for Quality Assurance in Prevention and Rehabilitation (IQPR), German Sport University Cologne, 50933 Cologne, Germany.
Corinna WeberingRehabilitation Center Bad Pyrmont, 31812 Bad Pyrmont, Germany.
Detlef NeumannDepartment of Pharmacology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-0145-7507
Heike BähreResearch Core Unit Metabolomics, Hannover Medical School, 30625 Hannover, Germany.
Ralf LichtinghagenInstitute of Clinical Chemistry and Central Laboratory of Hannover Medical School, 30625 Hannover, Germany.
Mathias RheinLaboratory for Molecular Neuroscience, Department of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-1685-9843
Johannes AchenbachDepartment of Anaesthesia and Intensive Care Medicine, Royal Devon University Healthcare NHS-Foundation Trust, Barnstaple EX31 4JB, UK.
Christoph GutenbrunnerDepartment of Rehabilitation and Sports Medicine, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-6522-1942
Matthias KarstDepartment of Anesthesiology and Intensive Care Medicine, Pain Clinic, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-3502-0023

Funding

Rentenversicherung Braunschweig/ Hannover 68,073 EURVayamed GmbH 10,000 EUR
6 · The paper itself

Abstract

backgroundChronic pain is a multifactorial condition for which interdisciplinary multimodal rehabilitation is guideline-recommended, yet the biological mechanisms underlying treatment response remain incompletely understood and validated predictive biomarkers have not been established.

objectiveThis exploratory prospective cohort study examined clinical outcomes and circulating biomarker changes, encompassing the endocannabinoid system (ECS), inflammatory mediators, stress-regulatory markers, and metabolic parameters, in 410 patients with chronic pain of predominantly musculoskeletal etiology undergoing a standardized five-week rehabilitation program. MATERIALS AND

methodsPain intensity and affective pain were assessed at baseline and end of rehabilitation; global performance of treatment (GPT) was additionally recorded. Serum analyses included anandamide (AEA), 2-arachidonoylglycerol (2-AG), IL-6, cortisol, IGF-1, BDNF, and leptin. Biomarker-outcome associations were examined via multiple regression analyses adjusted for demographics and biological and clinical confounders.

resultsStatistically significant reductions were observed in pain intensity (-0.785 points, NRS;

conclusionsBaseline 2-AG emerges as a candidate predictor of treatment response, with lower pre-treatment levels potentially reflecting reduced stress-adaptive capacity, supporting inclusion of ECS markers in future controlled biomarker studies.

Indexed as

Adaptation, PhysiologicalBiomarkersChronic PainAdultArachidonic AcidsEndocannabinoidsFemaleGlyceridesHumansInterleukin-6MaleMiddle AgedPolyunsaturated AlkamidesProspective StudiesanandamideArachidonic AcidsBiomarkersEndocannabinoidsGlyceridesglyceryl 2-arachidonateInterleukin-6Polyunsaturated Alkamides2-arachidonoylglycerolbiomarkerschronic painendocannabinoid systemmultimodal pain rehabilitationtreatment response

Identifiers

PMID42352308
PMCPMC13297331

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.