Dried Blood Spot Reference Intervals for Steroids and Amino Acids in a Neonatal Cohort of the National Children's Study

Author:

Dietzen Dennis J1,Bennett Michael J2,Lo Stanley F3,Grey Vijay L4,Jones Patti M5

Affiliation:

1. Department of Pediatrics, Washington University School of Medicine and St. Louis Children's Hospital, St. Louis, MO

2. Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia and University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA

3. Department of Pathology, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI

4. Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada

5. Department of Pathology, University of Texas Southwestern Medical Center and Children's Medical Center, Dallas, TX

Abstract

Abstract BACKGROUND Reference intervals from children are limited by access to healthy children and their limited blood volumes. In this study we set out to fill gaps in pediatric reference intervals for amino acids and steroid hormones using dried blood spots (DBS) from a cohort of the National Children's Study. METHODS Deidentified DBS annotated with age, birthweight, sex, and geographic location were obtained from 310 newborns aged 0–4 days and analyzed for 25 amino acids and 4 steroid hormones using LC-MS/MS. Nonparametric statistical approaches were used to generate the 2.5th–97.5th percentile distributions for newborns. Paired plasma/DBS specimens were used to mathematically transform DBS reference intervals to corresponding plasma intervals. RESULTS 10 of 25 DBS amino acid distributions were dependent on sex. There was little correlation with age, birthweight, or geographic location over the first 4 days of life. In most cases, transformation of DBS distributions to plasma distributions faithfully reflected independent studies of newborn plasma amino acid distributions. In general newborn steroid distributions were negatively correlated with age and birthweight over the first 4 days of life. Data distributions for the 4 steroids were not found related to geographic location, but testosterone concentrations displayed sex dependence. Transformation of DBS distributions to plasma intervals did not faithfully replicate other neonate steroid reference intervals determined directly with plasma. CONCLUSIONS These data demonstrate the feasibility and utility of deriving newborn reference intervals from large numbers of archived DBS samples such as those obtained from the National Children's Study biobank.

Funder

AACC International

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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