Evaluation of red blood cell parameters provided by the UF-5000 urine auto-analyzer in patients with glomerulonephritis
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Genki Mizuno
, Kentaro Nakamoto
Abstract
Objectives
The microscopic examination of hematuria, a cardinal symptom of glomerulonephritis (GN), is time-consuming and labor-intensive. As an alternative, the fully automated urine particle analyzer UF-5000 can interpret the morphological information of the glomerular red blood cells (RBCs) using parameters such as UF-5000 small RBCs (UF-%sRBCs) and Lysed-RBCs.
Methods
Hematuria samples from 203 patients were analyzed using the UF-5000 and blood and urine chemistries to determine the cut-off values of RBC parameters for GN and non-glomerulonephritis (NGN) classification and confirm their sensitivity to the IgA nephropathy and non-IgA nephropathy groups.
Results
The UF-%sRBCs and Lysed-RBCs values differed significantly between the GN and NGN groups. The cut-off value of UF-%sRBCs was >56.8% (area under the curve, 0.649; sensitivity, 94.1%; specificity, 38.1%; positive predictive value, 68.3%; and negative predictive value, 82.1%), while that for Lysed-RBC was >4.6/μL (area under the curve, 0.708; sensitivity, 82.4%; specificity, 56.0%; positive predictive value, 72.6%; and negative predictive value, 69.1%). Moreover, there was no significant difference in the sensitivity between the IgA nephropathy and non-IgA nephropathy groups (87.1 and 89.8% for UF-%sRBCs and 83.9 and 78.4% for Lysed-RBCs, respectively). In the NGN group, the cut-off values showed low sensitivity (56.0% for UF-%sRBCs and 44.0% for Lysed-RBCs).
Conclusions
The RBC parameters of the UF-5000, specifically UF-%sRBCs and Lysed-RBCs, showed good cut-off values for the diagnosis of GN.
Funding source: Fujita Health University Grant
Acknowledgments
We would like to thank Editage (www.editage.jp) for English language editing.
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Research funding: This study was supported by a Fujita Health University Grant (M. H.).
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Author contributions: Mizuno G and Hoshi M planned the study. Mizuno G, Hoshi M, Nakamoto K, Sakurai M, Nagashima K, and Fujita T performed the experiments. Mizuno G, Hoshi M, and Nakamoto K were responsible for the data integrity and analysis. Mizuno G, Hoshi M, Nakamoto K, Sakurai M, Nagashima K, Fujita T, Ito H, and Hata T discussed the results. Mizuno G, Hoshi M, and Nakamoto K wrote the manuscript. Hoshi M, Ito H, and Hata T conducted the study. Hata T assumes the primary responsibility for the final content. All authors reviewed the manuscript.
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Competing interests: The authors declare no potential conflicts of interest.
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Informed consent: Informed consent was obtained from patients through an opt-out form posted on the hospital wall.
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Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the authors’ Institutional Review Board Ethics Review Committee of Fujita Health University or equivalent committee (approval no. HM19-182).
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Supplementary Material
The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2021-0287).
© 2021 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorial
- High-sensitivity assay for cardiac troponins with POCT methods. The future is soon
- Review
- The assessment of circulating cell-free DNA as a diagnostic tool for breast cancer: an updated systematic review and meta-analysis of quantitative and qualitative ssays
- Mini Review
- Which laboratory technique is used for the blood sodium analysis in clinical research? A systematic review
- Guidelines and Recommendations
- IFCC interim guidelines on rapid point-of-care antigen testing for SARS-CoV-2 detection in asymptomatic and symptomatic individuals
- General Clinical Chemistry and Laboratory Medicine
- Multicenter evaluation of use of dried blood spot compared to conventional plasma in measurements of globotriaosylsphingosine (LysoGb3) concentration in 104 Fabry patients
- S100B protein, cerebral ultrasound and magnetic resonance imaging patterns in brain injured preterm infants
- Urinary exosomal CD26 is associated with recovery from acute kidney injury in intensive care units: a prospective cohort study
- Evaluation of red blood cell parameters provided by the UF-5000 urine auto-analyzer in patients with glomerulonephritis
- Reference Values and Biological Variations
- Pediatric reference interval verification for common biochemical assays on the Abbott Alinity system
- Paediatric reference range for overnight urinary cortisol corrected for creatinine
- Cancer Diagnostics
- Circulating pro-gastrin releasing peptide (ProGRP) in patients with medullary thyroid carcinoma
- Cardiovascular Diseases
- Determination of sex-specific 99th percentile upper reference limits for a point of care high sensitivity cardiac troponin I assay
- Comparison of the analytical performance of the PATHFAST high sensitivity cardiac troponin I using fresh whole blood vs. fresh plasma samples
- Infectious Diseases
- Comprehensive assessment of humoral response after Pfizer BNT162b2 mRNA Covid-19 vaccination: a three-case series
- Analytical validation of an automated assay for the measurement of adenosine deaminase (ADA) and its isoenzymes in saliva and a pilot evaluation of their changes in patients with SARS-CoV-2 infection
- A new tool for sepsis screening in the Emergency Department
- Letters to the Editor
- Caveat emptor – hidden pitfalls in defining the 99th percentile of cardiac troponin assays
- Assay requirements for COVID-19 testing: serology vs. rapid antigen tests
- Stability of SARS-CoV-2 RNA in FTA card spot-prep samples derived from nasopharyngeal swabs
- Homocysteine (Hcy) assessment to predict outcomes of hospitalized Covid-19 patients: a multicenter study on 313 Covid-19 patients
- Concomitant immune thrombocytopenia and bone marrow hemophagocytosis in a patient with SARS-CoV-2
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- Congress Abstracts
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