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Familial Hypercholesterolemia Biomarker Distribution in Dried Blood Spots.
Held, Patrice K; Lasarev, Michael; Zhang, Xiao; Wiberley-Bradford, Amy E; Campbell, Kristin; Horner, Vanessa; Shao, Xiangqiang; Benoy, Megan; Dodge, Ann M; Peterson, Amy L.
Afiliação
  • Held PK; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR; Oregon State Public Health Laboratory, Oregon Health Authority, Hillsboro, OR.
  • Lasarev M; Department of Biostatistics and Medical Informatics, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Zhang X; Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Wiberley-Bradford AE; Wisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Campbell K; Wisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Horner V; Wisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, WI; Department of Pathology, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Shao X; Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI; Wisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Benoy M; Pediatric Specialty Clinics, University of Wisconsin Hospital and Clinics, Madison, WI.
  • Dodge AM; Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI.
  • Peterson AL; Division of Pediatric Cardiology, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI. Electronic address: apeterson@pediatrics.wisc.edu.
J Pediatr ; 259: 113469, 2023 08.
Article em En | MEDLINE | ID: mdl-37182660
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperlipoproteinemia Tipo II Tipo de estudo: Diagnostic_studies Limite: Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperlipoproteinemia Tipo II Tipo de estudo: Diagnostic_studies Limite: Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article