Evidence map›Paper›PMID 30631161›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2019

Mineralocorticoid receptor blockade suppresses dietary salt-induced ACEI/ARB-resistant albuminuria in non-diabetic hypertension: a sub-analysis of evaluate study.

Mitsuhiro Nishimoto, Hiroshi Ohtsu, Takeshi Marumo, Wakako Kawarazaki, Nobuhiro Ayuzawa, Kohei Ueda, Daigoro Hirohama, Fumiko Kawakami-Mori, Shigeru Shibata, Miki Nagase and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Salt and chronic kidney disease.Nature reviews. Nephrology · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Lysine-specific demethylase 1 as a corepressor of mineralocorticoid receptor.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article
  11. Mineralocorticoid receptor blockers for moderate kidney dysfunction: more merit than ever?Hypertension research : official journal of the Japanese Society of Hypertension · 2021
    Article
  12. Review
  13. Impact of mineralocorticoid receptor blockade with direct renin inhibition in angiotensin II-dependent hypertensive mice.Hypertension research : official journal of the Japanese Society of Hypertension · 2020
    Article
  14. PGIInternational journal of molecular sciences · 2020
    Article
  15. Serum-soluble (pro)renin receptor concentration as a biomarker for organ damage in primary aldosteronism.Hypertension research : official journal of the Japanese Society of Hypertension · 2019
    Article
  16. Review
  17. Evaluation of the pathophysiological mechanisms of salt-sensitive hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2019
    Review
  18. Escaping residual albuminuria in hypertension: should we start eplerenone or reduce salt intake?Hypertension research : official journal of the Japanese Society of Hypertension · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 1 country.

Mitsuhiro NishimotoDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan. nishimoto-tky@umin.ac.jp.
Hiroshi OhtsuClinical Epidemiology Section, Department of Clinical Study and Informatics, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, Japan.
Takeshi MarumoDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Wakako KawarazakiDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Nobuhiro AyuzawaDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Kohei UedaDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Daigoro HirohamaDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Fumiko Kawakami-MoriDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Shigeru ShibataDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
Miki NagaseDepartment of Anatomy, Kyorin University Faculty of Medicine, Tokyo, Japan.
Masashi IsshikiDepartment of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
Shigeyoshi ObaDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Tatsuo ShimosawaDepartment of Clinical Laboratory, School of Medicine, International University of Health and Welfare, Otawara, Japan.
Toshiro FujitaDivision of Clinical Epigenetics, Research Center of Advanced Science and Technology, The University of Tokyo, Tokyo, Japan. Toshiro.FUJITA@rcast.u-tokyo.ac.jp.
The University of Tokyo · JPInternational University of Health and Welfare · JPJapan Science and Technology Agency · JPKyorin University · JPNational Center for Global Health and Medicine · JPSaitama Medical University · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excessive dietary salt intake can counteract the renoprotective effects of renin-angiotensin system (RAS) blockade in hypertensive patients with chronic kidney disease (CKD). In rodents, salt loading induces hypertension and renal damage by activating the mineralocorticoid receptor (MR) independently of plasma aldosterone levels. Thus, high salt-induced resistance to RAS blockade may be mediated by MR activation. To test this, a post hoc analysis of the Eplerenone Combination Versus Conventional Agents to Lower Blood Pressure on Urinary Antialbuminuric Treatment Effect (EVALUATE) trial was conducted. Thus, 304 non-diabetic hypertensive patients on RAS-blocking therapy were divided into tertiles according to salt intake (estimated 24-h urinary sodium excretion at baseline) and compared in terms of percent reduction in urinary albumin-to-creatinine ratio (UACR) at 52 weeks relative to baseline. The eplerenone-treated patients in the highest sodium excretion tertile exhibited significantly greater reduction in UACR than the placebo subjects in the same tertile (-22.5% vs. +21.8%, p = 0.02). This disparity was not observed in the lowest (-10.2% vs. -0.84%, p = 0.65) or middle (-19.5% vs. +9.5%, p = 0.22) tertiles. Similar systolic blood pressure changes were observed. In the whole cohort, reduction in UACR correlated positively with reduction in systolic blood pressure (r

Indexed as

AdultAgedAlbuminuriaBlood PressureEplerenoneFemaleHumansHypertensionMaleMiddle AgedMineralocorticoid Receptor AntagonistsRenin-Angiotensin SystemSodium Chloride, DietaryYoung AdultEplerenoneMineralocorticoid Receptor AntagonistsSodium Chloride, DietaryAlbuminuriaAngiotensinBlood pressureMineralocorticoid receptorSodium chloride

Identifiers

PMID30631161
OpenAlexW2910448349

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.