Evidence map›Paper›PMID 29356944›Full record

ArticleCEN case reports2018

A case of lipoprotein glomerulopathy with a rare apolipoprotein E isoform combined with neurofibromatosis type I.

Satoshi Takasaki, Akira Matsunaga, Kensuke Joh, Takao Saito

Open access · bronzeAbstract read
In one paragraph

Article in CEN case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

4 authors at 4 institutions in 1 country.

Satoshi TakasakiDepartment of Internal Medicine, Saiseikai Yamagata Saisei Hospital, 79-1 Oki-machi, Yamagata, 990-8545, Japan. stakasak@yahoo.co.jp.ORCID http://orcid.org/0000-0001-8485-2929
Akira MatsunagaDepartment of Laboratory Medicine, Fukuoka University School of Medicine, Fukuoka, Japan.
Kensuke JohDepartment of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Takao SaitoSanko Clinic, Fukuoka, Japan.
Fukuoka University · JPOno Clinic · JPTohoku University · JPYamagata City Hospital Saiseikan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipoprotein glomerulopathy (LPG) is a rare inherited disease characterized by histopathological features of lipoprotein thrombi in dilated glomerular capillaries and type III like hyperlipoproteinemia with heterozygous mutation of the apolipoprotein (apo) E gene. We herein present the case of a 50-year-old woman with LPG complicated by neurofibromatosis type 1 (NF1). To the best of our knowledge, this is the first report of a case of LPG complicated by NF1. On the other hand, she had not only a heterozygous apoE-Sendai mutation, which is one of the most frequent apoE variants in LPG patients, but also a rare isoform of ApoE5 (Glu3Lys). Although apoE mutation has been recognized as having a principal role in the pathogenesis of LPG, some other factors are assumed to be present in the pathogenesis of LPG, because many asymptomatic carriers of apoE variants are recognized. The coexistence of NF1 or apoE5 (Glu3Lys) allele might play a role as an additional factor in the development of LPG.

Indexed as

ApoE5ApoE-SendaiLipoprotein glomerulopathyNeurofibromatosis type I

Identifiers

PMID29356944
PMCPMC5886940
OpenAlexW2784694135

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.