Evidence map›Paper›PMID 35352885›Full record

ArticleYonsei medical journal2022

Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery.

Chan Joo Lee, Bogeum Choi, Hayeon Pak, Jung Mi Park, Ji Hyun Lee, Sang-Hak Lee

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Observational
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Chan Joo Lee *Division of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8756-409X
Bogeum Choi *Kyung Hee University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7256-6922
Hayeon PakDepartment of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul, Korea.ORCID https://orcid.org/0000-0001-8110-2225
Jung Mi ParkDepartment of Biostatistics and Computing, Graduate School, Yonsei University, Seoul, Korea.ORCID https://orcid.org/0000-0003-1572-5832
Ji Hyun LeeDepartment of Clinical Pharmacology and Therapeutics, Kyung Hee University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3640-2928
Sang-Hak LeeDivision of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea. shl1106@yuhs.ac.ORCID https://orcid.org/0000-0002-4535-3745
Kyung Hee University · KRYonsei University · KR

Funding

Ministry of Food and Drug Safety 18182MFDS410
6 · The paper itself

Abstract

purposeAngiotensin-converting enzyme inhibitors (ACEIs) are medications generally prescribed for patients with high cardiovascular risk; however, they are suboptimally used due to frequent adverse events (AEs). The present study aimed to identify and replicate the genetic variants associated with ACEI-related AEs in the Korean population. MATERIALS AND

methodsA two-stage approach employing genome-wide association study (GWAS)-based discovery and replication through target sequencing was used. In total, 1300 individuals received ACEIs from 2001 to 2007; among these, 228 were selected for GWAS. An additional 336 patients were selected for replication after screening 1186 subjects treated from 2008 to 2018. Candidate genes for target sequencing were selected based on the present GWAS, previous GWASs, and data from the PharmGKB database. Furthermore, association analyses were performed between no AE and AE or cough groups after target sequencing.

resultsFive genes, namely

conclusionSeveral variants, including novel and known variants, were successfully replicated and found to have associations with ACEI-related AEs. These results provide rare and clinically relevant information for safer use of ACEIs.

Indexed as

Angiotensin-Converting Enzyme InhibitorsGenome-Wide Association StudyAsian PeopleCoughHumansPolymorphism, Single NucleotideTranscription FactorsAngiotensin-Converting Enzyme InhibitorsTranscription FactorsVOPP1 protein, humanantihypertensive agentsdrug therapyheart failurePharmacogenomicssafety

Identifiers

PMID35352885
PMCPMC8965428
OpenAlexW4220689920

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.