Neonatal Reference Intervals for the Complete Blood Count Parameters MicroR and HYPO-He: Sensitivity Beyond the Red Cell Indices for Identifying Microcytic and Hypochromic Disorders.


Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
12 2021
Historique:
received: 08 01 2021
revised: 26 04 2021
accepted: 04 08 2021
pubmed: 15 8 2021
medline: 4 1 2022
entrez: 14 8 2021
Statut: ppublish

Résumé

To create neonatal reference intervals for the MicroR and HYPO-He complete blood count (CBC) parameters and to test whether these parameters are sensitive early markers of disease at early stages of microcytic/hypochromic disorders while the CBC indices are still normal. We retrospectively collected the CBC parameters MicroR and HYPO-He, along with the standard CBC parameters, from infants aged 0-90 days at Intermountain Healthcare hospitals using Sysmex hematology analyzers. We created reference intervals for these parameters by excluding values from neonates with proven microcytic disorders (ie, iron deficiency or alpha thalassemia) from the dataset. From >11 000 CBCs analyzed, we created reference intervals for MicroR and HYPO-He in neonates aged 0-90 days. The upper intervals are considerably higher in neonates than in adults, validating increased anisocytosis and polychromasia among neonates. Overall, 52% of neonates with iron deficiency (defined by reticulocyte hemoglobin equivalent <25 pg) had a MicroR >90% upper interval (relative risk, 4.14; 95% CI, 3.80-4.53; P < .001), and 68% had an HYPO-He >90% upper interval (relative risk, 6.64; 95% CI, 6.03-7.32; P < .001). These 2 new parameters were more sensitive than the red blood cell (RBC) indices (P < .001) in identifying 24 neonates with iron deficiency at birth. We created neonatal reference intervals for MicroR and HYPO-He. Although Sysmex currently designates these as research use only in the US, they can be measured as part of a neonate's CBC with no additional phlebotomy volume or run time and can identify microcytic and hypochromic disorders even when the RBC indices are normal.

Identifiants

pubmed: 34389321
pii: S0022-3476(21)00757-5
doi: 10.1016/j.jpeds.2021.08.002
pmc: PMC9123644
mid: NIHMS1801390
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

95-100.e2

Subventions

Organisme : NIDDK NIH HHS
ID : U54 DK110858
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Références

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Auteurs

Timothy M Bahr (TM)

Division of Neonatology, University of Utah Health, Salt Lake City, UT; Center for Iron and Heme Disorders, University of Utah Health, Salt Lake City, UT. Electronic address: tim.bahr@hsc.utah.edu.

Thomas R Christensen (TR)

Student, University of Utah, Salt Lake City, UT.

Erick Henry (E)

Women and Newborns Clinical Program, Intermountain Healthcare, Salt Lake City, UT.

Jacob Wilkes (J)

Women and Newborns Clinical Program, Intermountain Healthcare, Salt Lake City, UT.

Robin K Ohls (RK)

Division of Neonatology, University of Utah Health, Salt Lake City, UT.

Sterling T Bennett (ST)

Department of Pathology, Intermountain Medical Center, Murray, UT.

Diane M Ward (DM)

Department of Pathology, University of Utah Health, Salt Lake City, UT.

Theodore J Pysher (TJ)

Department of Pathology, University of Utah Health, Salt Lake City, UT; Pediatric Pathology, Primary Children's Hospital, Salt Lake City, UT.

Robert D Christensen (RD)

Division of Neonatology, University of Utah Health, Salt Lake City, UT; Division of Hematology/Oncology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT; Center for Iron and Heme Disorders, University of Utah Health, Salt Lake City, UT; Women and Newborns Clinical Program, Intermountain Healthcare, Salt Lake City, UT.

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