Evidence map›Paper›PMID 40454659›Full record

ArticleAddiction biology2025

Cerebrospinal Fluid Biomarkers in Opioid Dependence: Evidence of Neuroimmune Activation and Ion Composition Changes, Without Alteration in Orexin-A.

Tim Lyckenvik, Malin Woock, Kalle Johansson, Markus Axelsson, Henrik Zetterberg, Kaj Blennow, Eric Hanse, Pontus Wasling

Abstract read
In one paragraph

Article in Addiction biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Tim LyckenvikDepartment of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Malin WoockDepartment of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0000-0002-9291-3151
Kalle JohanssonDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-6028-0695
Markus AxelssonDepartment of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Kaj BlennowDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Eric HanseDepartment of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Pontus WaslingDepartment of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0000-0002-9106-9032

Funding

Alzheimer's Drug Discovery Foundation #201809-2016862European Union's Horizon Europe No 101053962Familjen Erling-Perssons StiftelseHjärnfonden (#FO2022-0270NEuroBioStand #22HLT07Olav Thon StiftelsenStiftelsen för Gamla TjänarinnorSwedish Research Council #2019-02397Swedish Research Council #2022-01018Swedish Research Council #2023-00356;Swedish Research Council VR 00986Swedish State Support for Clinical Research ALFGBG 427611Swedish State Support for Clinical Research (#ALFGBG-71320Swedish State Support for Clinical Research #ALFGBG-715986Swedish State Support for Clinical Research #ALFGBG-965240the AD Strategic Fund and the Alzheimer's Association #ADSF-21-831376-Cthe AD Strategic Fund and the Alzheimer's Association #ADSF-21-831377-Cthe AD Strategic Fund and the Alzheimer's Association #ADSF-21-831381-C,
6 · The paper itself

Abstract

Opioid abuse is a severe global health challenge, leading to rising morbidity, mortality, and increasing societal costs. The aim of this study was to investigate neuroinflammation, neuronal damage and potential changes in the orexin system or beta-amyloid metabolism in the cerebrospinal fluid (CSF) of individuals undergoing opioid substitution therapy (OST). This cross-sectional study investigates CSF biomarkers in individuals undergoing OST, compared to control subjects. Participants receiving OST were recruited from the outpatient clinic at the Department of Psychiatry, Sahlgrenska University Hospital, Gothenburg (Sweden). Each participant provided a complete medical history, including details of drug use over the past 6 months, followed by a lumbar puncture to obtain CSF samples. Molecules associated with neuroinflammation, neuronal and glial damage, beta-amyloid metabolism and orexinergic function were analysed in the participants' CSF, alongside electrolyte levels. Specifically, we analysed levels of sTREM-2, YKL-40, IL-1β, IL-6, IL-8, IL-10, TNF-α, AXL, MER, TYRO3, GAS6, NfL, GFAP, total tau (T-tau), phosphorylated tau (P-tau), neurogranin, Aβ40, Aβ42, the Aβ42/Aβ40 ratio, orexin-A, sPDGFR-β and electrolytes. The study included 15 control subjects and 17 in the opioid substitution group. Patients undergoing opioid substitution therapy exhibited elevated levels of sTREM-2, Aβ42/Aβ40 ratio and NfL in their CSF. Conversely, concentrations of Na

Indexed as

Opioid-Related DisordersOrexinsAdultAmyloid beta-PeptidesBiomarkersChitinase-3-Like Protein 1Cross-Sectional StudiesFemaleHumansMaleMiddle AgedOpiate Substitution TreatmentAmyloid beta-PeptidesBiomarkersCHI3L1 protein, humanChitinase-3-Like Protein 1Orexins

Identifiers

PMID40454659
PMCPMC12127996

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Registered trials

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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.