Evidence map›Paper›PMID 36123398›Full record

Trial reportHypertension research : official journal of the Japanese Society of Hypertension2022

The FimAsartaN proTeinuriA SusTaIned reduCtion in comparison with losartan in diabetic chronic kidney disease (FANTASTIC) trial.

Tae-Hyun Yoo, Soon Jun Hong, Sunggyun Kim, Seokjoon Shin, Dong Ki Kim, Jung Pyo Lee, Sang Youb Han, Sangho Lee, Jong Chul Won, Young Sun Kang and 6 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Hypertension research : official journal of the Japanese Society of Hypertension, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02620306 (A Randomized, Double-blind, Active Control, Parallel Group, Titration, Multicenter Study to Evaluate the Efficacy and Safety of Fimasartan), which is not on this map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% 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.

NCT02620306 phase3completednot on this map

A Randomized, Double-blind, Active Control, Parallel Group, Titration, Multicenter Study to Evaluate the Efficacy and Safety of Fimasartan

TypeinterventionalSponsorBoryung Pharmaceutical Co., LtdRan2016 to 2022Enrolled351ConditionsChronic Kidney DiseaseArmsFimsartan 60mg~120mg, Losartan 50mg~100mg
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Review
  7. Article
  8. 2023 update and perspectives.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Review
  9. Review
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

16 authors at 14 institutions in 1 country.

Tae-Hyun YooDivision of Nephrology, Severance Hospital, Seoul, Korea.
Soon Jun HongDepartment of Cardiology, Korea University Anam Hospital, Seoul, Korea.
Sunggyun KimDivision of Nephrology, Hallym University Sacred Heart Hospital, Ansan, Korea.
Seokjoon ShinDivision of Nephrology, Incheon St. Mary's Hospital, The Catholic University, Incheon, Korea.
Dong Ki KimDivision of Nephrology, Seoul National University Hospital, Seoul, Korea.
Jung Pyo LeeDepartment of Internal Medicine, Seoul National University Boramae Medical Center, Seoul, Korea.
Sang Youb HanDivision of Nephrology, Inje University Ilsan-Paik Hospital, Goyang, Korea.
Sangho LeeDepartment of Nephrology, College of Medicine, Kyung Hee University, Seoul, Korea.
Jong Chul WonDivision of Endocrinology and Metabolism, Inje University Sanggye-Paik Hospital, Inje University School of Medicine, Seoul, Korea.
Young Sun KangDivision of Nephrology, Korea University Ansan Hospital, Ansan, Korea.
Jongha ParkDivision of Nephrology, Ulsan University Hospital, Ulsan, Korea.
Byoung-Geun HanDepartment of Nephrology, Yonsei University Wonju College of Medicine, Wonju, Korea.
Ki-Ryang NaDivision of Nephrology, Chungnam National University Hospital, Daejeon, Korea.
Kyu Yeon HurDivision of Endocrinology and Metabolism, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Yong-Jin KimDivision of Cardiology, Seoul National University Hospital, Seoul, Korea.
Sungha ParkDivision of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea. shpark0530@yuhs.ac.
Seoul National University Hospital · KRYonsei University · KRChungnam National University Hospital · KRHallym University Sacred Heart Hospital · KRInje University Ilsan Paik Hospital · KRInje University Sanggye Paik Hospital · KRKorea University · KRKorea University Medical Center · KRKyung Hee University · KRSeoul National University · KRSeverance Hospital · KRSungkyunkwan University · KRThe Catholic University of Korea Incheon St. Mary's Hospital · KRUlsan University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As angiotensin II type 1 receptor blockers (ARBs) may have different antiproteinuric effects in diabetic kidney disease (DKD), we ascertained the albuminuria-reducing effect of fimasartan and losartan in patients with DKD. This was a randomized, multicenter, double-blind, 4-parallel-group, dose-titration, phase III study designed to compare the efficacy of fimasartan and losartan in reducing albuminuria in patients with DKD (NCT02620306). The primary endpoint was the rate of change in albuminuria from baseline to week 24. A total of 341 patients were randomized to different groups. The urinary albumin-to-creatinine ratio (ACR), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were not different between the fimasartan and losartan groups at baseline (ACR: 1376.84 vs. 1521.07 mg/gCr, SBP: 154.69 vs. 154.47 mmHg, DBP: 83.96 vs. 83.83 mmHg). However, ACR reduction was significantly larger in the fimasartan group than in the losartan group during the entire study period (% changes in the ACR at 4, 8, 12, and 24 weeks were -23.58, -33.06, -35.00, and -38.13 in the fimasartan group vs. -8.74, -10.17, -14.91, and -19.71 in the losartan group, p < 0.01, respectively). The superior antiproteinuric effect of fimasartan compared to losartan was still significant after adjustment for SBP levels. There were no significant differences in adverse events, including the incidences of estimated glomerular filtration decline and hyperkalemia. This study demonstrates that compared to losartan, fimasartan significantly reduces albuminuria in patients with DKD, even after adjustment for SBP and DBP.

Indexed as

Diabetes MellitusDiabetic NephropathiesHypertensionRenal Insufficiency, ChronicAlbuminuriaAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsBiphenyl CompoundsBlood PressureDouble-Blind MethodHumansLosartanProteinuriaPyrimidinesTetrazolesAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsBiphenyl CompoundsfimasartanLosartanPyrimidinesTetrazolesBlood pressureDiabetic nephropathyMortalityProteinuriaRenal endpoint

Identifiers

PMID36123398
OpenAlexW4296336362

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.