Evidence map›Paper›PMID 38481514›Full record

ArticleKidney international reports2024

Development of a Kidney Prognostic Score in a Japanese Cohort of Patients With Antineutrophil Cytoplasmic Autoantibody Vasculitis.

Rei Takeda, Kazuya Takahashi, Andreas Kronbichler, Daiichiro Akiyama, Shunichiro Hanai, Yoshiaki Kobayashi, Ayako Matsuki, Takeshi Umibe, Chisaki Ito, Toyohiko Sugimoto and 10 more

Open access · goldAbstract read
In one paragraph

Article in Kidney international reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

20 authors at 8 institutions in 2 countries.

Rei TakedaDepartment of Rheumatology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Kazuya TakahashiDepartment of Nephrology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Andreas KronbichlerDepartment of Internal Medicine IV, Nephrology and Hypertension, Medical University Innsbruck, Innsbruck, Austria.
Daiichiro AkiyamaDepartment of Nephrology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Shunichiro HanaiDepartment of Rheumatology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Yoshiaki KobayashiDepartment of Rheumatology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Ayako MatsukiDepartment of Rheumatology, Matsudo City General Hospital, Matsudo, Chiba, Japan.
Takeshi UmibeDepartment of Rheumatology, Matsudo City General Hospital, Matsudo, Chiba, Japan.
Chisaki ItoDepartment of Rheumatology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Toyohiko SugimotoDepartment of Rheumatology, National Hospital Organization, Shimoshizu Hospital, Yotsukaido, Chiba, Japan.
Takao SugiyamaDepartment of Rheumatology, National Hospital Organization, Shimoshizu Hospital, Yotsukaido, Chiba, Japan.
Shun YoshidaDepartment of Nephrology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Yasuhide NishioDepartment of Nephrology, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.
Ikuo NukuiDepartment of Nephrology, Yamanashi Prefectural Central Hospital, Kofu, Yamanashi, Japan.
Ayumu NakashimaDepartment of Nephrology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
Hanae WakabayashiDepartment of Nephrology, Chiba University Graduate School of Medicine, Chuo, Chiba, Japan.
Katsuhiko AsanumaDepartment of Nephrology, Chiba University Graduate School of Medicine, Chuo, Chiba, Japan.
Shunsuke FurutaDepartment of Allergy and Clinical Immunology, Chiba University Hospital, Chuo, Chiba, Japan.
Hiroshi NakajimaDepartment of Allergy and Clinical Immunology, Chiba University Hospital, Chuo, Chiba, Japan.
Daiki NakagomiDepartment of Rheumatology, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.
University of Yamanashi Hospital · JPNational Hospital Organization · JPChiba University · JPChiba University Hospital · JPMatsudo City Hospital · JPYamanashi Prefectural Central Hospital · JPInnsbruck Medical University · ATTokyo Metropolitan Tama Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Glomerulonephritis is frequent in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and crucial to disease outcomes. We conducted a detailed assessment of renal pathology in Japanese patients with AAV, and developed a new score that would predict renal outcome. Methods: Two hundred twenty-one patients who were diagnosed with AAV and underwent a kidney biopsy were enrolled. Data on glomerular, tubular, interstitial, and vascular lesions from kidney biopsies were analyzed; the 3 established classification and prognostic scoring systems (Berden Classification, Mayo Clinic/RPS Chronicity Score [MCCS], and ANCA Renal Risk Score [ARRS]) were validated. Further, we developed a new prognostic score by including variables relevant for Japanese patients with ANCA-glomerulonephritis. Results: Median follow-up was 60 months (interquartile range: 6-60). End-stage kidney disease (ESKD) risk prediction by the MCCS and the ARRS was confirmed. Moreover, our analysis identified 4 items with significant ESKD risk prediction capacity, namely percentage of cellular, fibrocellular, and fibrous crescents; and sclerotic glomeruli. Based on our findings, we created a score evaluating the percentage of these lesions to total glomeruli, the Percentage of ANCA Crescentic Score (PACS). The area under the receiver operating characteristic (ROC) curve evaluating PACS was 0.783. The PACS had a comparable performance as the ARRS in predicting ESKD. The optimal PACS cut-off for ESKD risk over 60 months was 43%. In addition, the percentage of cellular crescents and presence of interstitial inflammation were independent predictors of kidney function recovery. Conclusion: We developed a new score predicting renal prognosis using histopathological data of Japanese patients with ANCA-glomerulonephritis. Studies are needed to validate our results in international cohorts.

Indexed as

ANCA-associated vasculitiscrescentglomerulonephritisoutcome measurerenal pathology

Identifiers

PMID38481514
PMCPMC10927481
OpenAlexW4390675595

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.