Evidence map›Paper›PMID 33689292›Full record

ArticleAnalytical chemistry2021

Allele-Specific Recombinase Polymerase Amplification to Detect Sickle Cell Disease in Low-Resource Settings.

Mary E Natoli, Megan M Chang, Kathryn A Kundrod, Jackson B Coole, Gladstone E Airewele, Venée N Tubman, Rebecca R Richards-Kortum

Abstract read
In one paragraph

Article in Analytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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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

7 authors.

Mary E NatoliDepartment of Bioengineering, Rice University, Houston, Texas 77005, United States.ORCID 0000-0001-8115-4746
Megan M ChangDepartment of Bioengineering, Rice University, Houston, Texas 77005, United States.
Kathryn A KundrodDepartment of Bioengineering, Rice University, Houston, Texas 77005, United States.
Jackson B CooleDepartment of Bioengineering, Rice University, Houston, Texas 77005, United States.
Gladstone E AireweleTexas Children's Cancer and Hematology Centers, Houston, Texas 77030, United States.
Venée N TubmanTexas Children's Cancer and Hematology Centers, Houston, Texas 77030, United States.
Rebecca R Richards-KortumDepartment of Bioengineering, Rice University, Houston, Texas 77005, United States.ORCID 0000-0003-2347-9467

Funding

Characterization of B Lymphocyte Deficiency in Pediatric Sickle Cell DiseaseK23HL148548 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI TUBMAN, VENEE N · 2020 to 2024
$816k
NHLBI NIH HHS K23 HL148548
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a group of common, life-threatening disorders caused by a point mutation in the β globin gene. Early diagnosis through newborn and early childhood screening, parental education, and preventive treatments are known to reduce mortality. However, the cost and complexity of conventional diagnostic methods limit the feasibility of early diagnosis for SCD in resource-limited areas worldwide. Although several point-of-care tests are commercially available, most are antibody-based tests, which cannot be used in patients who have recently received a blood transfusion. Here, we describe the development of a rapid, low-cost nucleic acid test that uses real-time fluorescence to detect the point mutation encoding hemoglobin S (HbS) in one round of isothermal recombinase polymerase amplification (RPA). When tested with a set of clinical samples from SCD patients and healthy volunteers, our assay demonstrated 100% sensitivity for both the β

Indexed as

Anemia, Sickle CellRecombinasesAllelesChild, PreschoolHemoglobin, SickleHumansInfant, NewbornNucleic Acid Amplification TechniquesPoint-of-Care SystemsSensitivity and SpecificityHemoglobin, SickleRecombinases

Identifiers

PMID33689292
PMCPMC7992048

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.