Evidence map›Paper›PMID 41458378›Full record

ArticleFrontiers in physiology2025

Combined effect of esaxerenone and dapagliflozin on aldosterone-mediated sodium reabsorption and potassium excretion.

Motonobu Nakamura, Nobuhiko Satoh, Tomohito Mizuno, Mayuko Takagi, Shoko Horita, Masaomi Nangaku

Abstract read
In one paragraph

Article in Frontiers in physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Motonobu NakamuraDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.
Nobuhiko SatohDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.
Tomohito MizunoDivision of Nephrology, Japan Community Healthcare Organization Tokyo Yamate Medical Center, Tokyo, Japan.
Mayuko TakagiDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.
Shoko HoritaDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.
Masaomi NangakuDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The efficacy of nonsteroidal mineralocorticoid receptor blockers (MRBs) in inhibiting the progression of diabetic kidney disease (DKD) is well-known. However, MRB therapy often leads to hyperkalemia and remains a major concern. Recent studies suggest that combining potassium-retaining diuretics, renin-angiotensin system inhibitors, and sodium-glucose cotransporter 2 inhibitors (SGLT2i) reduces the incidence of hyperkalemia. However, how SGLT2i, specifically affecting the proximal tubule (PT), suppresses hyperkalemia is unclear. This study aimed to elucidate the interaction between the aldosterone (Ald)/mineralocorticoid receptor (MR) signaling pathway and SGLT2i specifically in the PT, focusing on the synergistic effects on PT sodium (Na Methods: We investigated the effects of Ald and SGLT2i on PT Na Results: Ald increased not only the activity of NBCe1 and NHE3 but also the expression of TWIK-1/ Discussion: The findings indicate that Ald stimulates Na

Indexed as

dapagliflozindiabetic kidney diseaseesaxerenonehyperkalemiaproximal tubule

Identifiers

PMID41458378
PMCPMC12738813

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Registered trials

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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.