Evidence map›Paper›PMID 40599821›Full record

ReviewClinical kidney journal2025

Clinical management of peripheral arterial disease in chronic kidney disease-a comprehensive review from the European Renal Association CKD-MBD Working Group.

Sharon Huish, Saira Nawaz, Antonio Bellasi, Juan Miguel Diaz-Tocados, Mathias Haarhaus, Smeeta Sinha

Abstract readReview
In one paragraph

Review in Clinical kidney journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. Implications of inflammation and sex in lower extremity arterial disease.European journal of clinical investigation · 2026
    Review
  13. 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

6 authors.

Sharon HuishDepartment of Renal Dietetics, Royal Devon University Healthcare NHS Foundation Trust, and University of Exeter, Exeter, UK.
Saira NawazDepartment of Renal Medicine, Northern Care Alliance NHS Foundation Trust, Salford, UK.
Antonio BellasiService of Nephrology, Ospedale Regionale di Lugano, Ospedale Civico, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Juan Miguel Diaz-TocadosVascular and Renal Translational Research Group, Institut de Recerca Biomèdica de Lleida, Lleida, Spain.
Mathias HaarhausDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden.ORCID https://orcid.org/0000-0001-8274-6356
Smeeta SinhaDepartment of Renal Medicine, Northern Care Alliance NHS Foundation Trust, Salford, UK.ORCID https://orcid.org/0000-0003-4117-4085

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral artery disease (PAD) is a common and serious complication in people with chronic kidney disease (CKD) and end-stage kidney disease, occurring four to six times more frequently than in the general population. PAD is characterized by atherosclerotic narrowing or occlusion of peripheral arteries, leads to lower limb ischaemia, and is associated with increased morbidity and mortality. People with CKD and PAD are at higher risk for cardiovascular events and presence of chronic limb-threatening ischaemia further doubles mortality risk in this population. The pathophysiology of PAD in CKD is multifactorial, involving endothelial dysfunction, inflammation, oxidative stress and disordered mineral metabolism; these are key CKD features that exacerbate vascular disease. Traditional risk factors, such as diabetes, hypertension, dyslipidaemia and smoking, also contribute to the development of PAD. Mineral imbalances and metabolic disturbances, seen in CKD-related mineral bone disorders (MBD), including vitamin D deficiency, are an emerging interest area in the development of PAD. Diagnosing PAD in CKD is challenging due to symptom overlap; non-invasive and inexpensive diagnostic tools such as ankle brachial index and toe brachial index offer potential for routine screening. Management of PAD is largely based on guidelines for the general population overlooking the unique differences in CKD patients. A multifaceted approach is fundamental (including lifestyle modifications, pharmacotherapy and, in some cases, revascularization procedures). This comprehensive review (i) outlines the epidemiology, aetiology and pathophysiology of PAD in CKD, (ii) discusses the role of CKD-MBD in PAD and (iii) highlights ongoing studies and the future therapeutic landscape.

Indexed as

chronic kidney diseasedialysisperipheral artery diseasevascular calcification

Identifiers

PMID40599821
PMCPMC12209849

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.