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Familial Hypercholesterolemia Biomarker Distribution in Dried Blood Spots - 22/08/23

Doi : 10.1016/j.jpeds.2023.113469 
Patrice K. Held, PhD 1, 2, Michael Lasarev, MS 3, Xiao Zhang, PhD 4, Amy E. Wiberley-Bradford, PhD 5, Kristin Campbell, BS 5, Vanessa Horner, PhD 5, 6, Xiangqiang Shao, PhD 4, 5, Megan Benoy, MGCS, CGC 7, Ann M. Dodge, MS, RN, CPNP 4, Amy L. Peterson, MD, MS 4,
1 Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR 
2 Oregon State Public Health Laboratory, Oregon Health Authority, Hillsboro, OR 
3 Department of Biostatistics and Medical Informatics, University of Wisconsin School of Medicine and Public Health, Madison, WI 
4 Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI 
5 Wisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, WI 
6 Department of Pathology, University of Wisconsin School of Medicine and Public Health, Madison, WI 
7 Pediatric Specialty Clinics, University of Wisconsin Hospital and Clinics, Madison, WI 

Reprint requests: Amy L. Peterson, MD, MS, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, H6/534 CSC MC 4108, 600 Highland Ave, Madison, WI 53792.Department of PediatricsUniversity of Wisconsin School of Medicine and Public HealthH6/534 CSC MC 4108600 Highland AveMadisonWI53792

Abstract

Objective

To evaluate distribution profiles of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and apolipoprotein B (apoB) as candidate markers of familial hypercholesterolemia in newborns, taking into consideration potential confounding factors, such as gestational age, birth weight, sex, and race.

Study design

TC, LDL-C, and apoB were measured from 10 000 residual deidentified newborn dried blood spot cards. Concentrations for each biomarker were reported as multiples of the median, with emphasis on describing the 99th percentile values based on birth weight, gestational age, sex, and race. Seasonal variation of biomarkers was also explored.

Results

LDL-C and apoB had distribution curves with tails showing extreme elevation, whereas the distribution of TC was less elevated and had the smallest range. Neonates born at early gestational age and low birth weight had significantly greater 99th percentile of multiples of the median values for apoB but not TC or LDL-C. Differences in biomarker concentration based on sex and race were minimal. All biomarkers showed greatest concentrations in the winter as compared with summer months.

Conclusions

LDL-C and apoB had distribution curves supporting candidacy for neonatal familial hypercholesterolemia screening. Future studies are needed to correlate newborn screening results with molecular testing to validate these 2 biomarkers, along with measured cholesterol levels later in childhood.

Le texte complet de cet article est disponible en PDF.

Keywords : newborn screening, dried blood spots, pediatric cholesterol screening

Abbreviations : apoB, ASCVD, DBS, E/V preterm, FH, HBW, LBW, LDL-C, MoM, NBW, TC


Plan


 These data were presented as an abstract at the 2022 American Heart Association Scientific Sessions, November 5-7, 2022, Chicago, Illinois.


© 2023  Elsevier Inc. Tous droits réservés.
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Vol 259

Article 113469- août 2023 Retour au numéro
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