Evidence map›Paper›PMID 32415379›Full record

ArticleClinical and experimental nephrology2020

A nationwide cross-sectional analysis of thrombotic microangiopathy in the Japan Renal Biopsy Registry (J-RBR).

Takayuki Katsuno, Yasuhiko Ito, Shoji Kagami, Hiroshi Kitamura, Shoichi Maruyama, Akira Shimizu, Hitoshi Sugiyama, Hiroshi Sato, Hitoshi Yokoyama, Naoki Kashihara

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In one paragraph

Article in Clinical and experimental 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
0.4field-weighted citation impact, top 41% 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, 6 citations in OpenAlex.

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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

10 authors at 9 institutions in 1 country.

Takayuki KatsunoDepartment of Nephrology and Rheumatology, Aichi Medical University, 1-1 Karimata, Yazaki, Nagakute, 480-1195, Japan. t-katsuno@aichi-med-u.ac.jp.
Yasuhiko ItoDepartment of Nephrology and Rheumatology, Aichi Medical University, 1-1 Karimata, Yazaki, Nagakute, 480-1195, Japan.
Shoji KagamiDepartment of Pediatrics, Tokushima University Graduate School of Medicine, Tokushima, Japan.
Hiroshi KitamuraDepartment of Pathology, National Hospital Organization Chibahigashi National Hospital, Chiba, Japan.
Shoichi MaruyamaDepartment of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Akira ShimizuDepartment of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan.
Hitoshi SugiyamaDepartment of Human Resource Development of Dialysis Therapy for Kidney Disease, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Hiroshi SatoDepartment of Internal Medicine, Sendai Hospital of East Japan Railway Company, Sendai, Japan.
Hitoshi YokoyamaDepartment of Nephrology, Kanazawa Medical University, Uchinada, Japan.
Naoki KashiharaDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Japan.
Yazaki (Japan) · JPEast Japan Railway (Japan) · JPKanazawa Medical University · JPKawasaki Medical School · JPNagoya University · JPNational Hospital Organization · JPNippon Medical School · JPOkayama University · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere have been only a few large-scale cohort studies that have reviewed accumulated cases of thrombotic microangiopathy (TMA). The aim of this study was to collect and analyze TMA cases based on the renal biopsy, as a nationwide survey in Japan.

methodsIn this cross-sectional study, large nationwide data from the Japan Renal Biopsy Registry (J-RBR) were used. Among the patients registered in the J-RBR online system from July 2007 to July 2017, TMA cases were extracted and epidemiological data and clinical findings were investigated.

resultsOut of the 38,495 patients enrolled in a period of 10 years, 152 (0.39%) cases had been diagnosed with TMA. The patient age was widely distributed, including 9.2%, 66.4%, and 24.3% for children, adults, and the elderly, respectively. There were various causes of TMA. Among them, hemolytic uremic syndrome (HUS)/thrombotic thrombocytopenic purpura (TTP) (16.4%), connective tissue disease (CTD)-related (17.1%), and drug-induced (16.4%) were frequently observed. The background factors of TMA were different in children and adults. In a comparison between groups consisting of HUS/TTP, CTD-related, and drug-induced, the HUS/TTP group was significantly younger (p = 0.01), and the drug-induced TMA group tended to have a high urinary protein positive rate (p = 0.05). A comparative analysis according to the age group showed significantly higher serum creatinine levels in the elderly (p < 0.01).

conclusionThis is the first report of epidemiological and clinical data of biopsy-proven TMA in Japan. The characteristics of TMA with diversity based on the underlying disease and age group were reported.

Indexed as

AdolescentAdultAgedAged, 80 and overAge FactorsBiopsyBlood PressureChildChild, PreschoolConnective Tissue DiseasesCreatinineCross-Sectional StudiesDiabetes MellitusDrug-Related Side Effects and Adverse ReactionsFemaleHemolytic-Uremic SyndromeCreatinineConnective tissue diseaseHemolytic uremic syndromeJapan renal biopsy registry (J-RBR)Renal biopsyThrombotic microangiopathyThrombotic thrombocytopenic purpura

Identifiers

PMID32415379
OpenAlexW3024137470

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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.