Evidence map›Paper›PMID 38339083›Full record

ArticleInternational journal of molecular sciences2024

Keratin Expression in Podocytopathies, ANCA-Associated Vasculitis and IgA Nephropathy.

Paraskevi Pavlakou, Harikleia Gakiopoulou, Sonja Djudjaj, Kostas Palamaris, Maria Stella Trivyza, Kostas Stylianou, Dimitrios S Goumenos, Evangelos Papachristou, Marios Papasotiriou

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Article in International journal of molecular sciences, 2024. 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, top 99% of its field
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, 0 citations in OpenAlex.

  1. Review
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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

9 authors at 4 institutions in 2 countries.

Paraskevi PavlakouDepartment of Nephrology and Kidney Transplantation, University Hospital of Patras, 26504 Patras, Greece.ORCID 0000-0001-9958-7590
Harikleia Gakiopoulou1st Department of Pathology, National and Kapodistrian University of Athens Medical School, 34400 Athens, Greece.
Sonja DjudjajInstitute of Pathology, RWTH University of Aachen, 52074 Aachen, Germany.
Kostas Palamaris1st Department of Pathology, National and Kapodistrian University of Athens Medical School, 34400 Athens, Greece.
Maria Stella TrivyzaDepartment of Nephrology and Kidney Transplantation, University Hospital of Patras, 26504 Patras, Greece.
Kostas StylianouDepartment of Nephrology, University Hospital of Heraklion, 71500 Heraklion, Greece.ORCID 0000-0003-3678-9421
Dimitrios S GoumenosDepartment of Nephrology and Kidney Transplantation, University Hospital of Patras, 26504 Patras, Greece.
Evangelos PapachristouDepartment of Nephrology and Kidney Transplantation, University Hospital of Patras, 26504 Patras, Greece.
Marios PapasotiriouDepartment of Nephrology and Kidney Transplantation, University Hospital of Patras, 26504 Patras, Greece.ORCID 0000-0001-9375-989X
General University Hospital of Patras · GRNational and Kapodistrian University of Athens · GRRWTH Aachen University · DEUniversity Hospital of Heraklion · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Keratins are the main components of the cell cytoskeleton of epithelial cells. Epithelial cells under stressful stimuli react by modifying their keratin expression pattern. Glomerular diseases are pathological conditions that may lead to loss of kidney function if not timely diagnosed and treated properly. This study aims to examine glomerular and tubular keratin expression in podocytopathies, ANCA-associated vasculitis, and IgA nephropathy and how this expression correlates to clinical outcomes. We included 45 patients with podocytopathies (minimal change disease and focal segmental glomerulosclerosis), ANCA-associated vasculitis, and IgA nephropathy, with or without crescentic lesions, and healthy controls. All tissues were assessed by photon microscopy and immunohistochemistry. Biopsy sections were examined for keratins 7, 8, 18, and 19 expression in the glomerular and tubulointerstitial areas separately. Moreover, we examined how keratin expression was correlated with long-term kidney function outcomes. All four studied keratins had significantly increased glomerular expression in patients with ANCA vasculitis compared to controls and MCD patients. Tubular expression of keratins 7, 8, and 19 was related to kidney outcome in all groups. Patients with crescents had higher expression of all keratins in both glomeruli and tubulointerstitium. The presence of tubular atrophy, interstitial fibrosis, mesangial hyperplasia, and interstitial inflammation did not affect keratin expression. Keratins, an abundant component of renal epithelial cells, have the potential to be featured as a biomarker for kidney function prognosis in patients with glomerular diseases.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisGlomerulonephritis, IGACytoskeletonHumansKeratinsKidneyKeratinsbiomarkerend-stage kidney diseaseglomerulonephritiskeratins

Identifiers

PMID38339083
PMCPMC10855225
OpenAlexW4391485736

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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.