Urinary beta-luteinizing hormone and beta-follicle stimulating hormone immunoenzymometric assays for population research.

Abstract:

OBJECTIVE:We developed assays for measurement of urinary betaLH and betaFSH under collection and storage conditions typical of non-clinical research settings. DESIGN AND METHODS:IEMAs for free betaLH and total betaFSH were validated by standard methods. Stability of urinary betaLH and betaFSH was tested across freeze-thaws and stored long term at 4 degrees C or -20 degrees C, or short term at room temperature, and with heating to dissociate the subunits. RESULTS:The IEMAs exhibited acceptable parallelism, specificity, recovery (averaging 100% for betaLH, 97% for betaFSH), imprecision (maximum within-run and between run CVs, respectively, 4.8% and 25.7% for betaLH, 5.6% and 17.0% for betaFSH), and minimum detectable dose (2.5 pmol/L for betaLH, 6.8 pmol/L for betaFSH). Urine and serum measures were highly correlated (r=0.95 for LH, 0.86 for FSH). There was no consistent decline with any storage type. Dissociation of subunits by heating was needed for betaLH, but not betaFSH. CONCLUSION:These IEMAs measure free betaLH and total betaFSH, overcoming inter-individual variability in, and collection and storage effects on, subunit dissociation, without the need for urine preservatives.

journal_name

Clin Biochem

journal_title

Clinical biochemistry

authors

Brindle E,Miller RC,Shofer JB,Klein NA,Soules MR,O'Connor KA

doi

10.1016/j.clinbiochem.2006.08.009

subject

Has Abstract

pub_date

2006-11-01 00:00:00

pages

1071-9

issue

11

eissn

0009-9120

issn

1873-2933

pii

S0009-9120(06)00274-8

journal_volume

39

pub_type

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