Evidence map›Paper›PMID 41530463›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2026

Renin-angiotensin system inhibitor use and cardio-renal outcomes in non-proteinuric chronic kidney disease: a post-hoc analysis of the Frontier of Renal Outcome Modification-Japan study.

Hirohito Sugawara, Kiryu Yoshida, Chie Saito, Yoshinori Saito, Masanori Kato, Akihiko Kato, Ichiei Narita, Shoichi Maruyama, Jun Wada, Takashi Wada and 4 more

Abstract read
In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Hirohito SugawaraDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan. a04m0532002@gmail.com.ORCID 0009-0009-0733-5843
Kiryu YoshidaDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.
Chie SaitoDepartment of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yoshinori SaitoDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.
Masanori KatoDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.
Akihiko KatoDepartment of Nephrology, Kosai Municipal Hospital, Kosai, Shizuoka, Japan.
Ichiei NaritaNiigata Institute for Health and Sports Medicine, Niigata, Japan.
Shoichi MaruyamaDepartment of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Jun WadaDepartment of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Takashi WadaDepartment of Nephrology and Rheumatology, Kanazawa University, Kanazawa, Japan.
Masahiro YamamotoDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.
Hidetoshi ItoDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.
Kunihiro YamagataDepartment of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Hiroaki OgataDivision of Nephrology, Department of Internal Medicine, Showa Medical University, Northern Yokohama Hospital, Yokohama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with chronic kidney disease (CKD) frequently experience cardiovascular events, and as per current therapeutic guidelines, renin-angiotensin system inhibitors (RASi) can protect the cardiovascular system in those with proteinuric CKD. Effectiveness of RASi in treating non-proteinuric CKD is still unknown, yet. In order to evaluate the impact of RASi on cardiovascular morbidity and mortality in patients with non-proteinuric CKD, we performed a post-hoc analysis of the Frontier of Renal Outcome Modification-Japan study. A urine protein-to-creatinine ratio less than 0.15 g/g or negative/trace protein on urinalysis was considered as non-proteinuric CKD. Those who have undergone dialysis, kidney transplant recipients, and patients who refused to give their consent were excluded. A composite of cardiovascular events, initiation of renal replacement therapy, and all-cause mortality was studied as the primary outcome. Of 2379 patients with CKD, 630 met the criteria for non-proteinuric CKD. Among them, 490 used RASi, and 140 did not. Although the RASi group was considerably younger and had a higher prevalence of hypertension and calcium channel blocker use, baseline characteristics were comparable. 12.1% of the control group and 16.7% of the RASi group experienced the primary outcome during follow-up, with no significant difference (adjusted HR: 1.37; 95% CI: 0.81-2.31). Secondary outcomes and analyses of RASi use for the whole observation period did not show any significant differences (adjusted HR: 0.81; 95% CI: 0.43-1.56). These results imply that RASi was not linked to a decreased risk of mortality or long-term events in those with nonproteinuric CKD.

Indexed as

Angiotensin-Converting Enzyme InhibitorsCardiovascular DiseasesRenal Insufficiency, ChronicRenin-Angiotensin SystemAgedFemaleHumansJapanMaleMiddle AgedProteinuriaTreatment OutcomeAngiotensin-Converting Enzyme InhibitorsCardiovascular eventsChronic kidney diseaseImplemental hypertensionNon-proteinuriaRenin–angiotensin system

Identifiers

PMID41530463
PMCPMC13050643

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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.