Evidence map›Paper›PMID 35491532›Full record

ArticleDiabetes, obesity & metabolism2022

Rationale, design and baseline characteristics of the effect of canagliflozin in patients with type 2 diabetes and microalbuminuria in the Japanese population: The CANPIONE study.

Satoshi Miyamoto, Hiddo J L Heerspink, Dick de Zeeuw, Masao Toyoda, Daisuke Suzuki, Takashi Hatanaka, Tohru Nakamura, Shinji Kamei, Satoshi Murao, Kazuyuki Hida and 17 more

Open access · greenAbstract readClinical Trial Protocol
In one paragraph

Article in Diabetes, obesity & metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 5 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

27 authors at 20 institutions in 3 countries.

Satoshi MiyamotoCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.ORCID 0000-0002-9056-6395
Hiddo J L HeerspinkDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-3126-3730
Dick de ZeeuwDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Masao ToyodaDivision of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.
Daisuke SuzukiSuzuki Diadetes Clinic, Atsugi, Japan.
Takashi HatanakaDepartment of Diabetes and Endocrinology, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan.
Tohru NakamuraDiabetes Internal Medicine, Sumitomo Besshi Hospital, Nihama, Japan.
Shinji KameiDepartment of Diabetic Medicine, Kurashiki Central Hospital, Kurashiki, Japan.
Satoshi MuraoDepartment of Diabetes and Endocrinology, Takamatsu Hospital, Takamatsu, Japan.
Kazuyuki HidaDepartment of Diabetology and Metabolism, National Hospital Organization Okayama Medical Center, Okayama, Japan.
Shinichiro AndoDepartment of Internal Medicine Diabetic Center, Okayama City Hospital, Okayama, Japan.
Hiroaki AkaiDivision of Diabetes and Metabolism, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Yasushi TakahashiDepartment of Diabetes, Ochiai General Hospital, Maniwa, Japan.
Daisuke KoyaDepartment of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Japan.
Munehiro KitadaDepartment of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Japan.ORCID 0000-0002-3854-1385
Hisashi SuganoDepartment of Diabetes and Endocrinology, Kochi Health Sciences Center, Kochi, Japan.
Tomokazu NunoueNunoue Clinic, Tsuyama, Japan.
Akihiko NakamuraInternal Medicine, Osafune Clinic, Setouchi, Japan.
Motofumi SasakiDepartment of Diabetes and Endocrinology, Matsue City Hospital, Matsue, Japan.
Tatsuaki NakatouDiabetes Center, Okayama Saiseikai General Hospital, Okayama, Japan.
Kei FujimotoDivision of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, The Jikei University Kashiwa Hospital, Kashiwa, Japan.
Daiji KawanamiDepartment of Endocrinology and Diabetes Mellitus, Fukuoka University School of Medicine, Fukuoka, Japan.
Takashi WadaDepartment of Nephrology and Laboratory Medicine, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.
Nobuyuki MiyatakeDepartment of Hygiene, Faculty of Medicine, Kagawa University, Miki, Kagawa, Japan.
Michihiro YoshidaCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
Kenichi ShikataCenter for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.
CANPIONE study Investigators
Okayama University Hospital · JPInoue Hospital · JPKanazawa Medical University · JPUniversity Medical Center Groningen · NLFukuoka University · JPFukuyama Cardiovascular Hospital · JPJikei University Kashiwa hospital · JPKagawa University · JPKamiichi General Hospital · JPKanazawa University · JPKurashiki Central Hospital · JPMatsudo City Hospital · JPNational Hospital Organization · JPNational Hospital Organization Takamatsu Medical Center · JPOkayama Saiseikai General Hospital · JPSumitomo Besshi Hospital · JPSuzuki (Japan) · JPTohoku Medical and Pharmaceutical University · JPTokai University · JPUniversity of Kochi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the effect of canagliflozin, a sodium-glucose co-transporter-2 (SGLT2) inhibitor, on albuminuria and the decline of estimated glomerular filtration rate (eGFR) in participants with type 2 diabetes and microalbuminuria.

methodsThe CANPIONE study is a multicentre, randomized, parallel-group and open-labelled study consisting of a unique 24-week preintervention period, during which the rate of eGFR decline before intervention is estimated, followed by a 52-week intervention and a 4-week washout period. Participants with a geometric mean urinary albumin-to-creatinine ratio (UACR) of 50 and higher and less than 300 mg/g in two consecutive first-morning voids at two different time points, and an eGFR of 45 ml/min/1.73m

resultsA total of 258 participants were screened and 98 were randomized at 21 sites in Japan from August 2018 to May 2021. The mean baseline age was 61.4 years and 25.8% were female. The mean HbA1c was 7.9%, mean eGFR was 74.1 ml/min/1.73m

conclusionsThe CANPIONE study will determine whether the SGLT2 inhibitor canagliflozin can reduce albuminuria and slow eGFR decline in participants with type 2 diabetes and microalbuminuria.

Indexed as

Diabetes Mellitus, Type 2Sodium-Glucose Transporter 2 InhibitorsAlbuminuriaCanagliflozinFemaleGlomerular Filtration RateHumansJapanMaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicCanagliflozinSodium-Glucose Transporter 2 InhibitorscanagliflozinCANPIONE studydiabetic kidney diseaseeGFR slopeSGLT2 inhibitorurinary albumin-to-creatinine ratio

Identifiers

PMID35491532
PMCPMC9545385
OpenAlexW4225262821

What OpenQuestion holds

Texttitle and abstract
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.