Evidence map›Paper›PMID 32205326›Full record

ArticleBMJ open diabetes research & care2020

Conditions, pathogenesis, and progression of diabetic kidney disease and early decliner in Japan.

Yui Yoshida, Kosuke Kashiwabara, Yosuke Hirakawa, Tetsuhiro Tanaka, Shinsuke Noso, Hiroshi Ikegami, Mitsuru Ohsugi, Kohjiro Ueki, Tomoya Mita, Hirotaka Watada and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

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  12. Irbesartan ameliorates diabetic kidney injury inJournal of translational internal medicine · 2024
    Article
  13. Review
  14. Trajectories of kidney function and risk of mortality.International journal of epidemiology · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 11 institutions in 1 country.

Yui YoshidaDepartment of Biostatistics, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.ORCID 0000-0003-2764-073X
Kosuke KashiwabaraDepartment of Biostatistics, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Yosuke HirakawaDivision of Nephrology and Endocrinology, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Tetsuhiro TanakaDivision of Nephrology and Endocrinology, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Shinsuke NosoDepartment of Endocrinology, Metabolism and Diabetes, Faculty of Medicine, Kindai University, Osakasayama, Osaka, Japan.ORCID 0000-0002-0943-8450
Hiroshi IkegamiDepartment of Endocrinology, Metabolism and Diabetes, Faculty of Medicine, Kindai University, Osakasayama, Osaka, Japan.ORCID 0000-0001-8808-4605
Mitsuru OhsugiDiabetes and Metabolism Information Center, Research Institute, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo, Japan.
Kohjiro UekiDiabetes Research Center, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo, Japan.
Tomoya MitaDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.ORCID 0000-0002-4401-2965
Hirotaka WatadaDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Daisuke KoyaDepartment of Diabetology & Endocrinology, Kanazawa Medical University, Kahoku-gun, Ishikawa, Japan.
Koki MiseDepartment of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Jun WadaDepartment of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama, Japan.ORCID 0000-0003-1468-5170
Miho ShimizuDivision of Nephrology, Kanazawa University Hospital, Ishikawa, Japan.
Takashi WadaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Ishikawa, Japan.
Yumi ItoDivision of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Science Institute of Nephrology, Niigata, Japan.
Ichiei NaritaDivision of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Science Institute of Nephrology, Niigata, Japan.
Naoki KashiharaDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Okayama, Japan.
Masaomi NangakuDivision of Nephrology and Endocrinology, The University of Tokyo, Bunkyo-ku, Tokyo, Japan mnangaku-tky@umin.ac.jp.
Yutaka MatsuyamaDepartment of Biostatistics, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
The University of Tokyo · JPJuntendo University · JPKindai University · JPNational Center for Global Health and Medicine · JPNiigata University · JPOkayama University · JPKanazawa Medical University · JPKanazawa University · JPKanazawa University Hospital · JPKawasaki Medical School · JPUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGlomerular filtration rate (GFR) decreases without or prior to the development of albuminuria in many patients with diabetes. Therefore, albuminuria and/or a low GFR in patients with diabetes is referred to as diabetic kidney disease (DKD). A certain proportion of patients with diabetes show a rapid progressive decline in renal function in a unidirectional manner and are termed early decliners. This study aimed to elucidate the prevalence of DKD and early decliners and clarify their risk factors. RESEARCH DESIGN AND

methodsThis combination cross-sectional and cohort study included 2385 patients with diabetes from 15 hospitals. We defined DKD as a urinary albumin to creatinine ratio (ACR) ≥30 mg/gCr and/or estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m². We classified patients into four groups based on the presence or absence of albuminuria and a decrease in eGFR to reveal the risk factors for DKD. We also performed a trajectory analysis and specified the prevalence and risk factors of early decliners with sequential eGFR data of 1955 patients in five facilities.

resultsOf our cohort, 52% had DKD. Above all, 12% with a low eGFR but no albuminuria had no traditional risk factors, such as elevated glycated hemoglobin, elevated blood pressure, or diabetic retinopathy in contrast to patients with albuminuria but normal eGFR. Additionally, 14% of our patients were early decliners. Older age, higher basal eGFR, higher ACR, and higher systolic blood pressure were significantly associated with early decliners.

conclusionsThe prevalence of DKD in this cohort was larger than ever reported. By testing eGFR yearly and identifying risk factors in the early phase of diabetes, we can identify patients at high risk of developing end-stage renal disease.

Indexed as

Diabetes MellitusDiabetic NephropathiesAgedCohort StudiesCross-Sectional StudiesDisease ProgressionHumansJapanchronic diabetic complicationschronic kidney diseaseGFR

Identifiers

PMID32205326
PMCPMC7206926
OpenAlexW3012803100

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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.