

Clinical laboratory testing is generally done by measurement of substances in serum or urine. In order to validate a method for use in the diagnosis of clinical disorders, the hormones or chemical substances must be measured in large normal populations of various ages and both genders. Once the reference intervals for normal subjects are determined, the test can then be used more accurately for the diagnosis of clinical disorders. The purpose of this protocol is to collect both blood and urine specimens from normal subjects for the purpose of determining pediatric reference intervals for a number of clinical laboratory assays.
Length of Study: Indefinite (2–3 years will probably be required)
Number of Subjects: 1,680 for entire study
Characteristics of Participants: Boys and girls between the ages of 6 months and 7 years who are willing and able to provide a blood sample
Subject Groups Excluded: Those with any chronic medical condition requiring prescription medications(s)
Location of Study: Primary Children's Medical Center, Salt Lake City, Utah
Analytes:
Serum (45):
Albumin
Aldolase
Amylase
Androstenedione
Calcium
Ceruloplasmin
Cobalt
Copper
C-reactive protein
Creatine
Creatine kinase
Creatinine
CTx
Dehydroepiandrosterone sulfate (DHEAS)
11-Deoxycortisol
Dihydrotestoterone
Essential fatty acids
Estradiol
Estrone
FSH
Growth hormone
Guanidinoacetate
17-Hydroxypregenolone
17-Hydroxyprogesterone
IgA
IgE
IgG
IgG subclasses
IgM
Insulin-like growth factor I
Insulin-like growth factor binding protein-3
LH
Manganese
Nickel
N-telopeptide
Osteocalcin
P1NP
Parathyroid hormone
Prealbumin
Pregnenolone
Prolactin
Sex hormone binding globulin (SHBG)
Testosterone
Uric acid
Zinc