Evidence map›Paper›PMID 32967631›Full record

ReviewBMC nephrology2020

Concurrent minimal change nephrotic syndrome and type 1 diabetes mellitus in an adult Japanese woman: a case report.

Ryuzoh Nishizono, Hiroki Kogou, Yuri Ishizaki, Akihiro Minakawa, Masao Kikuchi, Hiroko Inagaki, Yuji Sato, Shouichi Fujimoto

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in BMC nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

8 authors at 2 institutions in 1 country.

Ryuzoh NishizonoDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan. ryuzou_nishizono@med.miyazaki-u.ac.jp.ORCID 0000-0002-8185-618X
Hiroki KogouDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Yuri IshizakiDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Akihiro MinakawaDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Masao KikuchiDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Hiroko InagakiDialysis Division, University of Miyazaki Hospital, Miyazaki, Japan.
Yuji SatoDepartment of Nephrology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Shouichi FujimotoDialysis Division, University of Miyazaki Hospital, Miyazaki, Japan.
University of Miyazaki · JPUniversity of Miyazaki Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConcurrent type 1 diabetes mellitus (T1DM) and idiopathic nephrotic syndrome is rare, and most previously reported cases were in children. We report the case of an adult woman who developed T1DM and minimal change nephrotic syndrome (MCNS) nearly simultaneously. CASE PRESENTATION: A 24-year-old woman had first presented to another hospital with nausea, vomiting, and fatigue. She was diagnosed with diabetic ketoacidosis and T1DM on the basis of her hyperglycemia, ketoacidosis, and positive anti-glutamic acid decarboxylase antibody test result. Rapid infusion of normal saline and insulin administration alleviated hyperglycemia and ketoacidosis. Two weeks after admission, however, she developed nephrotic syndrome (NS) with rapidly decreasing urine volume. She was referred to our hospital with a diagnosis of acute kidney injury. Although she temporarily required dialysis and high doses of insulin, within 1 month NS and acute kidney injury had been alleviated by oral prednisolone and low-density lipoprotein apheresis. Renal biopsy showed minor glomerular abnormalities without diabetic nephropathy, so we diagnosed her with MCNS. Seven weeks after the discharge, NS relapsed, and cyclosporine was added to prednisolone. However, NS relapsed twice within the next 4 months, so we started her on rituximab. At 6 months after initiating rituximab therapy, she remained in complete remission. Her mother also had T1DM but not MCNS. The patient had HLA-DRB1*09:01/09:01, DQB1*03:03/03:03, and her mother had HLA-DRB1*04:05/09:01, DQB1*03:03/04:01.

conclusionsConcurrent T1DM and MCNS is rare and their coexistence might be coincidental. Alternatively, they might have been caused by an underlying, unidentified genetic predisposition. Previous reports and our patient's findings suggest that specific HLA alleles and haplotypes or a Th1/Th2 imbalance might be associated with T1DM and MCNS that occurred nearly simultaneously.

Indexed as

AdultBiopsyBlood Chemical AnalysisBlood Component RemovalChildChild, PreschoolDiabetes Mellitus, Type 1FemaleGlucocorticoidsHumansHypoglycemic AgentsInfantInfant, NewbornInsulinJapanKidney GlomerulusGlucocorticoidsHypoglycemic AgentsInsulinPrednisoloneGenetic factorsMinimal change nephrotic syndromeSteroid-sensitive nephrotic syndromeType 1 diabetes mellitus

Identifiers

PMID32967631
PMCPMC7510261
OpenAlexW3088835519

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.