Abstract
Background
Biological variation studies have shown that the complete blood count (CBC) has narrow within-individual variation and wide group variation, indicating that the use of reference intervals (RIs) is challenging. The aim of this study was to examine differences in CBC RIs according to race/ethnicity in a multiethnic population at a hospital in San Francisco in hopes of improving the medical utility of CBC testing.
Methods
Subject data were obtained by screening CBC results from the medical records of outpatients meeting certain criteria who visited Zuckerberg San Francisco General Hospital from April 2017 to January 2018. From these records, sex- and race/ethnicity-specific CBC RIs were calculated as the 2.5th to 97.5th percentiles.
Results
From a total of 552 subjects, 47.9% were male (65 White, 50 Black, 71 Hispanic and 54 Asian) and 52.1% were female (51 White, 39 Black, 122 Hispanic and 72 Asian). The RIs of neutrophil, lymphocyte and eosinophil counts; and hemoglobin, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) showed significant differences (p<0.05) among the four racial/ethnic groups: neutrophil, lymphocyte and eosinophil counts; and MCHC in males, and hemoglobin, MCV, MCH and MCHC in females.
Conclusions
Race/ethnicity-specific CBC RIs should be taken into consideration in a multiethnic population to better interpret patient status and make progress toward precision medicine.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
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©2019 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorial
- Sepsis biomarkers: past, present and future
- Reviews
- Making new biomarkers a reality: the case of serum human epididymis protein 4
- Faecal calprotectin in inflammatory bowel diseases: a review focused on meta-analyses and routine usage limitations
- Opinion Paper
- Procalcitonin (PCT)-guided antibiotic stewardship: an international experts consensus on optimized clinical use
- EFLM Paper
- Practice in financial support of third party organised conferences and courses at a national level for health care professionals in Europe
- General Clinical Chemistry and Laboratory Medicine
- Design and implementation of quality control plans that integrate moving average and internal quality control: incorporating the best of both worlds
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- Automated measurement of the erythrocyte sedimentation rate: method validation and comparison
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- Cancer Diagnostics
- Prognostic value of involved/uninvolved free light chain ratio determined by Freelite and N Latex FLC assays for identification of high-risk smoldering myeloma patients
- Cardiovascular Diseases
- Design of a study to investigate the mechanisms of obstructive sleep apnoea by means of drug-induced sleep endoscopy
- Infectious Diseases
- Evaluation of procalcitonin immunoassay concordance near clinical decision points
- Biomarker-assisted identification of sepsis-related acute liver impairment: a frequent and deadly condition in critically ill patients
- Letters to the Editor
- Differences in procalcitonin measurements between three BRAHMS-partnered immunoassays (Liaison, Elecsys and Architect)
- The short story of the long-term Sigma metric: shift cannot be treated as a linear parameter
- Analytical and diagnostic performance evaluation of five creatinine POCT devices in the identification of patients at risk for post-contrast acute kidney injury (PCAKI)
- Lesson from inappropriate TSH-receptor antibody measurement in hypothyroidism: case series and literature review
- Instrument dependent erroneous sodium measurements in hypoproteinemic critically ill patients are causing significant misclassification of dysnatremias
- Inherited bisalbuminemia with growth hormone deficiency
- The first report showing de novo partial 21q monosomy in an adult woman with occult primary ovarian insufficiency (POI)
- Reverse-hybridization resolves a rare HFE genotype untypable by real-time PCR and melting curve analysis in a patient with hyperferritinemia and alcoholic liver disease
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