LH, Pediatric




Test Mnemonic

LHPED

CPT Codes

  • 83002 - QTY (1)

LOINC ®

10501-5

Aliases

  • Luteinizing Hormone, Pediatric

Includes

  • LH, Pediatrics, S

Performing Laboratory

Mayo Clinic Dpt of Lab Med & Pathology


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.25 mLSerumNo additive (Red) RefrigeratedSeparate serum from cells ASAP or within 2 hours of collection. Transfer serum to standard aliquot tube.

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.25 mLSerumSST (Gold) RefrigeratedSeparate serum from cells ASAP or within 2 hours of collection.

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.15 mL     

Stability

Environmental Condition Description
AmbientAfter separation from cells: Unacceptable
RefrigeratedAfter separation from cells: 14 days
FrozenAfter separation from cells: 90 days

Days Performed

Tue, Thu

Turnaround Time

3 - 7 days

Methodology

Name Description
Chemiluminescence Immunoassay (CLIA) 

Reference Range

LH, Pediatric
Sex Age From Age To Type Range Range Unit
Female  Days364 DaysNormal<0.02-18.3IU/L
Female1 Years8 YearsNormal<0.02-0.3IU/L
Female9 Years10 YearsNormal<0.02-4.8IU/L
Female11 Years13 YearsNormal<0.02-11.7IU/L
Female14 Years17 YearsNormal<0.02-16.7IU/L
Female      NormalTanner Stage I (1-8 years): <0.02-0.3IU/L
Female      NormalTanner Stage II: <0.02-4.1IU/L
Female      NormalTanner Stage IIl: 0.6-7.2IU/L
Female      NormalTanner Stage IV-V: 0.9-13.3IU/L
Male  Days364 DaysNormal<0.02-5.0IU/L
Male1 Years8 YearsNormal<0.02-0.5IU/L
Male9 Years10 YearsNormal<0.02-3.6IU/L
Male11 Years13 YearsNormal0.1-5.7IU/L
Male14 Years17 YearsNormal0.8-8.7IU/L
Male      NormalTanner Stage I (1-8 years): <0.02-0.5IU/L
Male      NormalTanner Stage II: 0.03-3.7IU/L
Male      NormalTanner Stage IIl: 0.09-4.2IU/L
Male      NormalTanner Stage IV-V: 1.3-9.8IU/L

Special Info

Grossly hemolyzed, lipemic or icteric specimens will be rejected. This test is New York DOH approved.

Clinical Info

This test is useful for diagnosis of precocious puberty and delayed puberty in children. Luteinizing hormone (LH) is a glycoprotein hormone consisting of 2 noncovalently bound subunits (alpha and beta). LH is produced by the anterior pituitary gland under regulation of the hypothalamic gonadotropin releasing hormone (GnRH) and feedback from gonadal steroid hormones. In children, LH, along with follicle-stimulating hormone (FSH), is used to diagnose precocious (early) and delayed puberty. Precocious puberty refers to the appearance of physical and hormonal signs of pubertal development at an earlier age than is considered normal (before 8 years of age in girls and 9 years of age in boys). Evaluation of precocious puberty includes measurement of LH and FSH to determine whether gonadotropins are increased in relation to chronologic age (gonadotropin-dependent) or whether sex steroid secretion is occurring independent of LH and FSH (gonadotropin-independent). In gonadotropin-dependent precocious puberty, basal LH levels are often elevated into the pubertal range and show a pubertal (heightened) response to GnRH stimulation. In gonadotropin-independent precocious puberty, the LH level is low at baseline and fails to respond to GnRH stimulation. Delayed puberty is defined clinically by the absence or incomplete development of secondary sexual characteristics by age 14 years in boys and by age 12 years in girls. Delayed puberty usually results from inadequate gonadal steroid secretion that, in turn, is most often caused by a defective gonadotropin secretion from the anterior pituitary, due to defective production of GnRH from the hypothalamus. Random measurements of LH and FSH, together with estradiol (females) or testosterone (males), are useful to distinguish between primary and secondary causes of delayed puberty. This assay is sensitive to 0.02 IU/L and is more appropriate for use in children.

Clinical Limitation

Cross-reactivity with thyroid-stimulating hormone (TSH) (<5%) might be observed at TSH concentrations of 500 mIU/L. Some patients who have been exposed to animal antigens, either in the environment or as part of treatment or imaging procedures, may have circulating anti-animal antibodies present. These antibodies may interfere with the assay reagents to produce unreliable results.