Evidence map›Paper›PMID 34751116›Full record

ArticleCurrent neurovascular research2021

Point of Care Test Technology Suitable for Early Detection and Monitoring of Ischemic Stroke.

Young Mi Lee, Mi Jung Bae, Ye Seul Choi, Eunmi Lee, Junghwan Cho, Myung-Gwan Kim, Minh Tan Le, Thi Hong Duc Nguyen, Hyung Soo Han, Nora Jee-Young Park and 1 more

Open access · greenAbstract read
In one paragraph

Article in Current neurovascular research, 2021. 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
–field-weighted citation impact, top 83% 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, 3 citations in OpenAlex.

  1. Article
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 1 institution in 1 country.

Young Mi LeeDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Mi Jung BaeDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Ye Seul ChoiDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Eunmi LeeDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Junghwan ChoClinical Omics Institute, Kyungpook National University, Daegu 41405,Korea.
Myung-Gwan KimClinical Omics Institute, Kyungpook National University, Daegu 41405, Korea.
Minh Tan LeDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Thi Hong Duc NguyenDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Hyung Soo HanDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu 41405,Korea.
Nora Jee-Young ParkClinical Omics Institute, Kyungpook National University, Daegu 41405,Korea.
Gun Oh ChongClinical Omics Institute, Kyungpook National University, Daegu 41405,Korea.
Kyungpook National University · KR

Funding

Ministry of Health & Welfare, Republic of Korea HI15C0001
6 · The paper itself

Abstract

backgroundStroke is one of the leading causes of death and disability in adulthood worldwide. A simple and convenient diagnostic method is needed for monitoring high-risk patients for stroke. Few POCTs are available for stroke diagnosis. Soluble blood P-selectin is known as a biomarker for platelet aggregation. Increased expression of P-selectin is observed in coronary artery disease, acute myocardial infarction, stroke and peripheral arterial disease.

objectiveA simple method that can measure the increased expression of P-selectin in stroke patients is intended to be used for diagnosis or early detection and hospital monitoring of ischemic stroke.

methodsPlasma proteins in blood were separated using a three-layered filter system. Quantum dot and antibody were conjugated to detect biomarkers present in plasma and then measured with a fluorescence spectrophotometer.

resultsThe detection limit of soluble P-selectin confirmed by immunoassay was 1 ng/ul. In order to increase the sensitivity and simplify the reaction, the detection limit was measured to evaluate the sensitivity of the quantum dot labeled anti P-selectin antibody. As a result, P-selectin of 5 ng/ul or more showed saturation signal intensity, indicating the upper limit of detection, and 10 pg/ul was the lower limit of detection.

conclusionIn this study, we proposed a three-layer filter membrane system that can separate biomarker- rich fractions from whole blood, simplifying the analysis process and improving sensitivity by using quantum dot-labeled antibodies to detect biomarkers. We hope that our system complements the advantages of POCT and can be applied to real clinical applications.

Indexed as

Ischemic StrokeMyocardial InfarctionStrokeAdultHumansPoint-of-Care TestingP-SelectinTechnologyP-Selectinblood biomarkerdiagnosisIschemic strokemonitoringpoint of care testquantum dot.

Identifiers

PMID34751116
PMCPMC9175083
OpenAlexW3211897533

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.