Evidence map›Paper›PMID 42077594›Full record

ArticlePain reports2026

Higher disease burden and greater small fibre impairment in women with painful diabetic neuropathy.

Gordon Sloan, Dinesh Selvarajah, Jessica Smith, Shillo Pallai, Marni Greig, M Shaan Goonoo, Thomas Cash, Merhawit A Abera, Sharon Caunt, Iain D Wilkinson and 1 more

Abstract read
In one paragraph

Article in Pain reports, 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.

Gordon SloanDivision of Clinical Medicine, University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0000-0001-6164-2662
Dinesh SelvarajahDivision of Clinical Medicine, University of Sheffield, Sheffield, United Kingdom.
Jessica SmithDivision of Clinical Medicine, University of Sheffield, Sheffield, United Kingdom.
Shillo PallaiDiabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Marni GreigDiabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
M Shaan GoonooDiabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Thomas CashLeighton Hospital, Mid Cheshire Hospitals NHS Foundation Trust, Crewe, England, United Kingdom.
Merhawit A AberaMekelle University, Mek'ele, Tigray, Ethiopia.
Sharon CauntDiabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Iain D WilkinsonDivision of Clinical Medicine, University of Sheffield, Sheffield, United Kingdom.
Solomon TesfayeDiabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Although the incidence of Painful-Diabetic Peripheral Neuropathy (Painful-DPN) is higher in women, the underlying reasons for this are not known. This study investigated sex differences in pain and neurological phenotypes in 2 cohorts of patients with Painful-DPN. Methods: Two cohort analyses were performed in this retrospective analysis of participants with Painful-DPN recruited to cross-sectional studies: (1) Patient-Reported Outcomes Measures Cohort analysis (n = 184), which assessed neuropathic pain intensity (Numeric Rating Score), neuropathic symptoms (Neuropathic Pain Scale), mood (Hospital Anxiety and Depression Scale), quality of life (Norfolk QoL-DN), and sleep (Medical Outcomes Sleep Study); (2) Neurological Phenotyping Cohort analysis (n = 100), which assessed large- (Neuropathy Impairment Score of the Lower Limb plus Seven Neurophysiological Tests) and small-nerve fibre function. Participants were also divided into irritable (IR) and nonirritable nociceptor phenotypes. Results: In the first cohort analysis, women reported greater neuropathic pain symptom burden, poorer sleep, and higher anxiety prevalence than men. In the second cohort analysis, men had greater large-nerve fibre impairment, whereas women exhibited more severe small-fibre dysfunction. In addition, IR nociceptor phenotypes were more prevalent in women. Conclusion: Women with Painful-DPN experience a greater disease burden, increased small-fibre impairment, and are more likely to have the IR nociceptor phenotype, suggesting potential sex-specific disease mechanisms.

Indexed as

DiabetesNeuropathic painNeuropathyPainful diabetic neuropathy

Identifiers

PMID42077594
PMCPMC13132318

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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.