Evidence map›Paper›PMID 40311069›Full record

ArticleBlood advances2025

Use of the microfluidic impedance red cell assay in sickle cell disease.

Akshay A Patwardhan, Ashwin Patel, Abhinav Pasupuleti, Solomon Oshabaheebwa, Christopher A Delianides, Zoe Sekyonda, Justin J Yoo, Jonathan Wade, Erica Evans, Michael A Suster and 3 more

Abstract read
In one paragraph

Article in Blood advances, 2025. 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
–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

3 citing papers in PubMed.

  1. Article
  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

13 authors.

Akshay A PatwardhanAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0009-0000-4088-6107
Ashwin PatelAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-0075-3304
Abhinav PasupuletiAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Solomon OshabaheebwaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH.
Christopher A DelianidesDepartment of Electrical, Computer, and Systems Engineering, Case Western Reserve University, Cleveland, OH.ORCID 0000-0001-5823-860X
Zoe SekyondaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH.
Justin J YooAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0001-9357-2742
Jonathan WadeAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Erica EvansAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Michael A SusterDepartment of Electrical, Computer, and Systems Engineering, Case Western Reserve University, Cleveland, OH.
Pedram MohseniDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH.ORCID 0000-0002-2849-4677
Umut A GurkanDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH.
Vivien A SheehanAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-2837-2255

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIn sickle cell disease (SCD), red blood cells (RBCs) are poorly deformable, even under normoxia (NOI). With deoxygenation, deformability of sickle RBCs is further reduced due to polymerization of hemoglobin S (HbS). Rigid, poorly deformable sickle RBCs block microvasculature, causing ischemia, pain, and organ damage. The microfluidic impedance red cell assay (MIRCA) can mechanically measure RBC deformability, providing occlusion index under NOI or hypoxia (HOI) as readouts. We analyzed RBCs from 68 adult and 34 pediatric patients with SCD using the MIRCA. Higher HOI and NOI values were positively associated with markers of inflammation, hemolysis, RBC density, older age, and severe SCD genotypes (homozygous HbSS or HbS β0-thalassemia. Each 1% higher NOI across individuals was associated with a 6.3% higher incidence of acute complications per year. Individuals with chronic complications in the past year had a 3.1% higher median NOI than those without chronic complications. Individuals on chronic transfusion therapy exhibit a subpopulation of poorly deformable RBCs captured by the MIRCA but not by a commercially available device that also measures RBC deformability, the laser assisted optical rotational cell analyzer (LoRRca). In vitro addition of voxelotor or osivelotor to samples from individuals on chronic transfusion therapy improved the deformability of these endogenous RBCs. Longitudinally collected NOI and HOI values in individuals with HbSS were stable, with a median percent point change of 13.3% and 15.7%, respectively. MIRCA can be used in combination with clinical laboratory tests to monitor RBC deformability as a biomarker of clinical status at routine clinic visits and included in clinical trials of disease-modifying agents.

Indexed as

Anemia, Sickle CellErythrocyte DeformabilityErythrocytesMicrofluidicsAdolescentAdultChildChild, PreschoolElectric ImpedanceFemaleHumansMaleYoung Adult

Identifiers

PMID40311069
PMCPMC12345286

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Registered trials

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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.