THE IMPACT OF GENDER AND PUBERTY ON REFERENCE VALUES FOR URINARY GROWTH-HORMONE EXCRETION - A STUDY OF 3 MORNING URINE SAMPLES IN 517 HEALTHY-CHILDREN AND ADULTS
Km. Main et al., THE IMPACT OF GENDER AND PUBERTY ON REFERENCE VALUES FOR URINARY GROWTH-HORMONE EXCRETION - A STUDY OF 3 MORNING URINE SAMPLES IN 517 HEALTHY-CHILDREN AND ADULTS, The Journal of clinical endocrinology and metabolism, 79(3), 1994, pp. 865-871
Some recent studies have indicated that measurement of urinary GH (U-G
H) excretion may be a useful tool for the evaluation of GH insufficien
cy in children with growth disorders, although some investigators are
skeptical about the diagnostic value of U-GH. Most current assays are
only available for specific laboratories or require time-intensive pre
treatments of the specimens. This limits the possibility for many cent
ers to compare their patients' data with others or to establish their
own reference ranges for U-GH excretion. Therefore, we investigated th
e performance of a commercially available kit, which allows direct mea
surement of U-GH in untreated urine specimens. We established a refere
nce range for the geometric mean of 3 morning urine samples in 446 hea
lthy children and 71 adults. U-GH could be determined in all but 9 of
1526 samples (99.4%). U-GH excretion was significantly dependent on pu
bertal maturation (P < 0.0001) and sex (P < 0.001), whereas age had no
significant influence in the prepubertal group (P > 0.3). Peak values
occurred in Tanner stages 3 and 4 (369 and 391 pg/h in females; 503 a
nd 882 pg/h in males), corresponding to an age interval of 11-18 yr in
boys and 9-15 yr in girls. Short collection periods (<6 h) were relat
ed to low values for U-GH excretion (nanograms per night; P < 0.02). T
his time effect disappeared if U-GH excretion was expressed as picogra
ms per h. If U-GH was related to creatinine output, there was a decrea
se in U-GH excretion during prepuberty, a blunting of the pubertal pea
k, and lower values in adults than in prepubertal children (P < 0.0002
). The intraindividual variation in U-GH excretion (picograms per h) r
anged from 40-61%, constituting approximately two thirds of the interi
ndividual variation. This variation was not lowered by relating U-GH t
o creatinine. We conclude that the assay was suitable for measurement
of U-GH excretion in virtually all healthy volunteers. Sex and puberta
l stage as well as urinary volume and clock times for collection perio
ds should be registered when establishing a reference range for U-GH e
xcretion and applying it for clinical purposes. Our reference values m
ay be useful for further studies of patients with GH disorders.