Evidence map›Paper›PMID 27217724›Full record

ArticleDrug design, development and therapy2016

Fimasartan for independent reduction of blood pressure variability in mild-to-moderate hypertension.

Mi-Seung Shin, Dae Ryong Kang, Changsoo Kim, Eun Joo Cho, Ki-Chul Sung, Seok-Min Kang, Dong-Soo Kim, Seung Jae Joo, Seung Hwan Lee, Kyung-Kuk Hwang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2016. 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
0.9field-weighted citation impact, top 22% 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, 4 citations in OpenAlex.

  1. Fimasartan: A new armament to fight hypertension.Journal of family medicine and primary care · 2019
    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

11 authors at 7 institutions in 1 country.

Mi-Seung ShinDivision of Cardiology, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, South Korea.
Dae Ryong KangOffice of Biostatistics, Ajou University School of Medicine, Suwon, South Korea.
Changsoo KimDepartment of Preventive Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Eun Joo ChoDivision of Cardiology, Department of Internal Medicine, St Paul's Hospital, Catholic University of Korea, Seoul, South Korea.
Ki-Chul SungDivision of Cardiology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Seok-Min KangCardiology Division, Severance Cardiovascular Hospital and Cardiovascular Research Institute, Yonsei University College of Medicine, Seoul, South Korea.
Dong-Soo KimDivision of Cardiology, Paik Hospital, Inje University College of Medicine, Busan, South Korea.
Seung Jae JooDivision of Cardiology, Jeju National University Hospital, Jeju, South Korea.
Seung Hwan LeeDivision of Cardiology, Wonju Severance Christian Hospital, Wonju Medical College, Yonsei University, Wonju, South Korea.
Kyung-Kuk HwangDepartment of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, South Korea.
Jeong Bae ParkDivision of Medicine/Cardiology, Department of Internal Medicine, Cheil General Hospital, Dankook University College of Medicine, Seoul, South Korea.
Chungbuk National University · KRGachon University Gil Medical Center · KRAjou University · KRGangnam Severance Hospital · KRKangbuk Samsung Hospital · KRSungkyunkwan University · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe angiotensin receptor antagonist fimasartan lowered blood pressure (BP) in a previous large population study. The purpose of this study was to evaluate whether fimasartan treatment for 3 months affects clinical and home BP variability in addition to reducing BP.

methodsThe study enrolled 1,396 patients (mean age 56.2±10.0 years; males 53.6%) with mild-to-moderate hypertension who had a complete set of home BP measurements (morning and evening) and metabolic risk evaluation. During the 3 months of study, fimasartan alone was used to control BP at a daily dose of 30-120 mg. Clinical and home BP measurements were performed before and after the 3-month treatment. BP variability included beat-to-beat variability (clinical) and day-to-day variability (home).

resultsFimasartan reduced BP after 3 months of treatment. The average reduction of clinical systolic BP (c-SBP) was 15.08±18.36 mmHg (P<0.0001), and the average reduction of morning home SBP (m-SBP) was 11.49±19.33 mmHg (P<0.0001). Beat-to-beat variability as standard deviation (SD) of c-SBP was reduced from 4.56±3.22 to 4.24±3.11 mmHg (P=0.0026). Day-to-day variability as SD of m-SBP was reduced from 7.92±6.74 to 6.95±4.97 mmHg (P<0.0001). Multiple regression analysis revealed an independent association between the change in the SD of c-SBP and the change in c-SBP (P=0.0268) and, similarly, between the change in the SD of m-SBP and the change in m-SBP (P=0.0258), after adjusting for age, sex, body mass index, and change in mean BP.

conclusionThis study indicated that 3 months of fimasartan treatment reduced day-to-day BP variability independent of BP reduction in patients with hypertension.

Indexed as

Angiotensin Receptor AntagonistsAntihypertensive AgentsBiphenyl CompoundsBlood PressureHumansHypertensionPyrimidinesTetrazolesAngiotensin Receptor AntagonistsAntihypertensive AgentsBiphenyl CompoundsfimasartanPyrimidinesTetrazolesangiotensin receptor blockersblood pressure variabilityhypertension

Identifiers

PMID27217724
PMCPMC4862351
OpenAlexW2346388546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.