Evidence map›Paper›PMID 41051412›Full record

ArticleDiabetologia2025

Beyond pain relief: the effects of chronic opioid use on brain structure and function in diabetic neuropathy-a multimodal neuroimaging study.

Gordon Sloan, Kevin Teh, Marni Greig, Pallai Shillo, Sharon Caunt, Iain D Wilkinson, Solomon Tesfaye, Dinesh Selvarajah

Abstract read
In one paragraph

Article in Diabetologia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Gordon SloanDiabetes Research Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Glossop Road, Sheffield, UK.ORCID http://orcid.org/0000-0001-6164-2662
Kevin TehDivision of Clinical Medicine, University of Sheffield, Sheffield, UK.
Marni GreigDiabetes Research Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Glossop Road, Sheffield, UK.
Pallai ShilloDiabetes Research Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Glossop Road, Sheffield, UK.
Sharon CauntDiabetes Research Unit, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Glossop Road, Sheffield, UK.
Iain D WilkinsonDivision of Clinical Medicine, University of Sheffield, Sheffield, UK.
Solomon TesfayeDivision of Clinical Medicine, University of Sheffield, Sheffield, UK.
Dinesh SelvarajahDivision of Clinical Medicine, University of Sheffield, Sheffield, UK. d.selvarajah@sheffield.ac.uk.

Funding

Knowledge Exchange Support Fund, University of Sheffield X/162218the Efficacy and Mechanism Evaluation Programme NIHR129921
6 · The paper itself

Abstract

aims/hypothesisDespite being commonly prescribed to treat painful diabetic peripheral neuropathy (DPN), the impact on the brain of long-term opioid use as analgesia is unknown. The aim of this study was to determine the structural and functional brain alterations associated with prescription opioid use in a large cohort of people with painful DPN.

methodsA total of 82 patients with diabetes were enrolled: 57 with painful DPN (18 with long-term opioid prescription [O+ individuals] and 39 who were not prescribed opioids [O- individuals]) and a control group of 25 patients with diabetes but without DPN (no DPN) matched for age (± 2 years), sex and type of diabetes. All participants underwent detailed clinical/neurophysiological assessment and brain MRI at 3 T, and a subset (14 in each group, n=42) also underwent resting-state functional MRI.

resultsO+ individuals had greater caudate volume (ANOVA, p=0.03) compared with O- individuals (p=0.03) and those with no DPN (p=0.01). Functional connectivity was lower between the caudate and thalamus (r β = -0.24, seed-level correction -3.9, p CONCLUSIONS/

interpretationWe demonstrate that disruption of dopaminergic pathways occurs within the brain when opioids are used for analgesic purposes for painful DPN, which may reflect alterations in reward systems. This study has important clinical implications, as the measures of dopaminergic pathways found in this study may represent neuroimaging biomarkers that could be used to diagnose and monitor the negative consequences of prescription opioid use.

Indexed as

Analgesics, OpioidBrainDiabetic NeuropathiesAdultAgedFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeuroimagingPain ManagementAnalgesics, OpioidDiabetic neuropathyOpioidsPainful diabetic neuropathyResting-state functional MRI

Identifiers

PMID41051412
PMCPMC12594651

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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.