Evidence map›Paper›PMID 35524473›Full record

ArticleJournal of diabetes investigation2022

Concomitant treatment with insulin and sodium-glucose cotransporter 2 inhibitors was associated with the renal composite outcome in Japanese patients with type 2 diabetes and chronic kidney disease: A propensity score-matched analysis.

Masao Toyoda, Nobumichi Saito, Moritsugu Kimura, Nobuo Hatori, Kouichi Tamura, Masaaki Miyakawa, Kazuyoshi Sato, Akira Kanamori, Kazuo Kobayashi

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Masao ToyodaCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.ORCID https://orcid.org/0000-0003-4142-1218
Nobumichi SaitoDivision of Nephrology, Endocrinology and Metabolism, Department of internal Medicine, Tokai University School of Medicine, lsehara, Japan.
Moritsugu KimuraDivision of Nephrology, Endocrinology and Metabolism, Department of internal Medicine, Tokai University School of Medicine, lsehara, Japan.
Nobuo HatoriCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.
Kouichi TamuraDepartment of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Masaaki MiyakawaCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.
Kazuyoshi SatoCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.
Akira KanamoriCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.
Kazuo KobayashiCommittee of Hypertension and Kidney Disease, Kanagawa Physicians Association, Yokohama, Japan.ORCID https://orcid.org/0000-0002-1284-9728
Kanagawa Prefecture Medical Association · JPTokai University · JPYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionWe previously reported that sodium-glucose cotransporter 2 inhibitor (SGLT2i) treatment was associated with an improvement of the albumin-to-creatinine ratio in Japanese patients with type 2 diabetes mellitus and chronic kidney disease. The present study clarified how concomitant insulin treatment (IT) with SGLT2i therapy influences the renal composite outcome (RCO). MATERIALS AND

methodsWe retrospectively evaluated 624 Japanese patients with type 2 diabetes mellitus and chronic kidney disease who underwent SGLT2i treatment. The renal composite outcome was set as progression of the stage of albuminuria or a ≥15% decrease in the estimated glomerular filtration rate per year. We developed a cohort model of patients managed with and without IT (Ins [+], Ins [-]) using propensity score matching methods. Furthermore, all patients in our study population were stratified into quintiles according to their propensity score.

resultsThe incidence of the RCO was in Ins (+) patients significantly higher than that in Ins (-) (P = 0.033). The estimated hazard ratio for the RCO was 1.55 (P = 0.035) in Ins (+) patients. The change in the estimated glomerular filtration rate and albumin-to-creatinine ratio in the groups was not statistically significant. The analysis, which was based on the quintiles, showed a statistically significant difference between the Ins (+) and Ins (-) groups (P = 0.01); the odds ratio for the RCO in patients managed with IT was 2.20 (P = 0.01).

conclusionsConcomitant administration of IT with SGLT2is influenced the RCO in Japanese patients with type 2 diabetes mellitus and chronic kidney disease. We might need to consider the influence of concomitant agents on the renoprotective effects of SGLT2i therapy.

Indexed as

Diabetes Mellitus, Type 2InsulinRenal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsAlbuminsCreatinineGlucoseHumansJapanPropensity ScoreRetrospective StudiesSodiumTreatment OutcomeAlbuminsCreatinineGlucoseInsulinSodiumSodium-Glucose Transporter 2 InhibitorsInsulin treatmentRenal composite outcomeSodium-glucose cotransporter 2 inhibitors

Identifiers

PMID35524473
PMCPMC9434580
OpenAlexW4229333671

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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.