Evidence map›Paper›PMID 25350944›Full record

ArticleDiagnostic pathology2014

Pathological similarities between low birth weight-related nephropathy and nephropathy associated with mitochondrial cytopathy.

Toshiyuki Imasawa, Masashi Tanaka, Naoki Maruyama, Takehiko Kawaguchi, Yutaka Yamaguchi, Rodrigue Rossignol, Hiroshi Kitamura, Motonobu Nishimura

Open access · goldAbstract read
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Article in Diagnostic pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

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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

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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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Focal segmental glomerulosclerosis with a mutation in theMolecular genetics and metabolism reports · 2023
    Article
  4. Proteomic Study of Low-Birth-Weight Nephropathy in Rats.International journal of molecular sciences · 2021
    Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Toshiyuki Imasawa
Masashi Tanaka
Naoki Maruyama
Takehiko Kawaguchi
Yutaka Yamaguchi
Rodrigue Rossignol
Hiroshi Kitamura
Motonobu Nishimura
Chiba East Hospital · JPTokyo Metropolitan Geriatric Hospital · JPTokyo Metropolitan Institute of Gerontology · JPUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividuals born with a low birth weight (LBW) have a higher risk of developing kidney dysfunction during their lifetime and sometimes exhibit focal segmental glomerulosclerosis (FSGS) lesions in their glomeruli. We herein try to obtain other pathological characteristics of LBW-related nephropathy.

methodsWe retrospectively evaluated the renal pathology of four patients demonstrating FSGS with a history of LBW. Two mitochondrial cytopathy patients were also analyzed. DNA mutations were surveyed using a PCR-Luminex assay.

resultsIn all four FSGS patients with a history of LBW, focal segmental glomerulosclerosis were detected. Interestingly, granular swollen epithelial cells (GSECs), which have previously been reported exclusively in patients with mitochondrial cytopathy, were also observed in the distal tubules and/or collecting ducts of all four patients with a history of low birth weight in this study. Electron microscopy revealed that these granular swollen epithelial cells included an increased number of enlarged mitochondria. Furthermore, cytochrome c oxidase subunit IV staining of patients with a history of low birth weight and patients with mitochondrial DNA mutations showed unbalanced expression patterns in glomeruli and a part of tubular cells. However, no mitochondrial gene mutations were detected in any of our four patients with low birth weight-related nephropathy.

conclusionsThis is the first report to show the pathological similarities not only in glomeruli but also tubuli between nephropathy with a LBW history and nephropathy with mitochondrial cytopathy. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_181.

Indexed as

AdultDNA, MitochondrialFemaleGlomerulosclerosis, Focal SegmentalHumansInfant, Low Birth WeightInfant, NewbornKearns-Sayre SyndromeKidney GlomerulusMaleMiddle AgedMitochondrial MyopathiesMutationProteinuriaRetrospective StudiesSequence Analysis, DNADNA, Mitochondrial

Identifiers

PMID25350944
PMCPMC4189739
OpenAlexW2160906524

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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.