Evidence map›Paper›PMID 37939667›Full record

ArticleThe Korean journal of internal medicine2023

Identification of novel variants for complicating cardiac disease in the scrub typhus infection using whole genome sequencing.

Ki-Woon Kang, Kyung-Won Hong, Seong-Kyu Lee

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in The Korean journal of internal medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03274869 (Prediction and Early Diagnosis for Cardiovascular Disease Complicated by Scrub Typhus Infection), which is not on this map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

NCT03274869 active not recruitingnot on this map

Prediction and Early Diagnosis for Cardiovascular Disease Complicated by Scrub Typhus Infection

TypeobservationalSponsorEulji University HospitalRan2022 to 2027Enrolled100ConditionsScrub Typhus, Cardiovascular Complication
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Ki-Woon KangDivision of Cardiology, Chung-Ang University Hospital, Chung-Ang University School of Medicine, Seoul, Korea.
Kyung-Won HongR&D Division, Theragen Health Co. Ltd., Seongnam, Korea.
Seong-Kyu LeeDivision of Endocrinology, Department of Internal Medicine, Eulji University Hospital, Daejeon, Korea.
Chung-Ang University Hospital · KREulji University · KRTheragen · KR

Funding

Chung-Ang UniversityMinistry of EducationNational Research Foundation of Korea 2020R1I1A3A04037859
6 · The paper itself

Abstract

BACKGROUND/

aimsScrub typhus infection has been known to complicate cardiovascular diseases mainly attributing to high mortality. Genetic susceptibility loci for complicating cardiac diseases such as atrial fibrillation, heart failure, and ischemic heart disease identified by genomic study have been limited in scrub typhus infection. Therefore, we investigated the genetic novel variants predicting complicating cardiac diseases in patients with confirmed scrub typhus infection using whole genome sequencing.

methodsWe performed a prospective study for eight consecutive patients with scrub typhus infection. During follow-up, six cases were clinically diagnosed with complicating cardiac diseases and two controls without complicating cardiac diseases. The whole genomes of the all patients were sequenced, and the individual sequence variants were compared between accordcase and control patients. Variant genotypes were compared and identified as a single nucleotide polymorphism (SNP) of the different genotype distributions between six cases and two controls.

resultsThe GG genotype in SNP (rs4977397) of solute carrier 24 family member 2 (SLC24A2) gene and non-TT genotype in SNP (rs2676750) of adenosine deaminase, RNA specific, B2 (ADARB2) gene were distinctively found in the case patients with complicated cardiac disease, compared with control patents in the scrub typhus infection.

conclusionWe suggest that the SNPs of SLC24A2 and ADARB2 might be genetic surrogate markers for complicating cardiac diseases in the scrub typhus infection. Our study show that early detection based on individual sequence variants might be feasible to predict complicating cardiac diseases in patients with scrub typhus infection, if further studies with more participants confirm these findings.

Indexed as

Heart FailureOrientia tsutsugamushiScrub TyphusGenotypeHumansProspective StudiesWhole Genome SequencingAdenosine deaminase RNA specific B2Cardiac diseasesScrub typhusSingle nucleotide polymorphismSolute carrier 24 family member 2

Identifiers

PMID37939667
PMCPMC10636548
OpenAlexW4388133077

What OpenQuestion holds

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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.