Test Code LAB3268 Luteinizing Hormone (LH), Pediatrics, Serum
Additional Codes
LH US
Useful For
Diagnosis of precocious puberty and delayed puberty in children
Method Name
Chemiluminescent Immunoassay (CIA)
Reporting Name
LH, Pediatrics, SSCH Clinical System Name: Luteinizing Hormone Ultra Sensitive
Specimen Type
SerumOrdering Guidance
This test is only available for pediatric patients. If testing request is for a patient 18 years of age or older, order LH / Luteinizing Hormone (LH), Serum.
Specimen Required
Supplies: Sarstedt 5 mL Aliquot Tube (T914)
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.25 mL
Collection Instructions:
1. Red-top tubes should be centrifuged, and the serum transferred to a plastic vial within 2 hours of collection.
2. Serum gel tubes should be centrifuged within 2 hours of collection.
Collect 1.0 mL whole blood (Min. 0.5 mL) in Red Top-Plain, Gold, or Gold Microtainer.
Specimen Minimum Volume
0.13 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum | Refrigerated (preferred) | 14 days |
Frozen | 90 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Reference Values
Females
<1 year: <0.02-18.3 IU/L
1-8 years: <0.02-0.3 IU/L
9-10 years: <0.02-4.8 IU/L
11-13 years: <0.02-11.7 IU/L
14-17 years: <0.02-16.7 IU/L
Tanner Stages*
Stage I (1-8 years): <0.02-0.3 IU/L
Stage II: <0.02-4.1 IU/L
Stage IIl: 0.6-7.2 IU/L
Stage IV-V: 0.9-13.3 IU/L
*Puberty onset (transition from Tanner stage I to Tanner stage II) occurs for girls at a median age of 10.5 (± 2) years. There is evidence that it may occur up to 1 year earlier in obese girls and in African-American girls. Progression through Tanner stages is variable. Tanner stage V (adult) should be reached by age 18.
Males
<1 year: <0.02-5.0 IU/L
1-8 years: <0.02-0.5 IU/L
9-10 years: <0.02-3.6 IU/L
11-13 years: 0.1-5.7 IU/L
14-17 years: 0.8-8.7 IU/L
Tanner Stages*
Stage I (1-8 years): <0.02-0.5 IU/L
Stage II: 0.03-3.7 IU/L
Stage IIl: 0.09-4.2 IU/L
Stage IV-V: 1.3-9.8 IU/L
*Puberty onset (transition from Tanner stage I to Tanner stage II) occurs for boys at a median age of 11.5 (± 2) years. For boys there is no proven relationship between puberty onset and body weight or ethnic origin. Progression through Tanner stages is variable. Tanner stage V (adult) should be reached by age 18.
Method Description
The AnshLite LH CLIA is a quantitative three-step sandwich type immunoassay. In the first step calibrators, controls, and unknown samples are added to luteinizing hormone (LH) antibody-coated microtiter wells and incubated. After washing, the wells are incubated with biotinylated LH antibody solution. After the second incubation and washing, the wells are incubated with streptavidin horseradish peroxidase conjugate solution. Finally, the antibody-antigen and conjugate complex bound to the well is detected by addition of a luminogenic substrate (AnshLite chemiluminescence substrate solution). The relative light output units are directly proportional to the concentration of LH in the samples.(Unpublished Mayo method)
Day(s) Performed
Monday, Wednesday, Friday
Report Available
2 to 6 daysEstimated TAT: 4 - 8 d
Performing Laboratory

Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
83002
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LHPED | LH, Pediatrics, S | 83103-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
62999 | LH, Pediatrics, S | 83103-2 |
Aliases: Third Generation LH assay; Ultrasensitive LH assay; Lutropin