Serum inhibin A and inhibin B in healthy prepubertal, pubertal, and adolescent girls and adult women: Relation to age, stage of puberty, menstrual cycle, follicle-stimulating hormone, luteinizing hormone, and estradiol levels
A. Sehested et al., Serum inhibin A and inhibin B in healthy prepubertal, pubertal, and adolescent girls and adult women: Relation to age, stage of puberty, menstrual cycle, follicle-stimulating hormone, luteinizing hormone, and estradiol levels, J CLIN END, 85(4), 2000, pp. 1634-1640
Biochemical assessment of gonadal function during maturation in girls and i
n adult women can be troublesome. With the recent advent of specific assays
for the gonadal peptides inhibin A and inhibin B, it might be possible to
achieve a clearer picture of events. We therefore determined serum levels o
f inhibin A, inhibin B, FSH, LH and estradiol in a cross-sectional study of
403 healthy schoolgirls (aged 6-20 yr) in relation to age and stage of pub
erty and in 181 healthy non-pregnant women (aged 20-32 yr) in relation to s
tage of the menstrual cycle. In addition, inhibin A and inhibin B were meas
ured daily throughout the menstrual cycle in 10 healthy adult women. Levels
of inhibin B are low or undetectable in prepubertal girls (median, 26.5 pg
/mL; 95% prediction interval, <20-100 pg/mL), increase sharply through pube
rtal stage II to peak in stage III (median, 84 pg/mL; 95% prediction interv
al, 28-227 pg/mL) and thereafter decline through pubertal stages IV and V.
These changes presumably reflect increasing ovarian stimulation through ear
ly puberty, resulting in an increased number of developing follicles, folli
cles reaching a later stage of development before undergoing atresia, or bo
th. Declining levels in late puberty and adulthood probably reflect the ons
et of the menstrual cycle and the subsequent appearance of the luteal phase
, where inhibin B levels are low. Inhibin A levels are undetectable or very
low in early puberty (median, <7 pg/mL; 95% prediction interval, <7-14) pg
/mL), increasing gradually through pubertal stages to reach their highest v
alues in adult women (median, 21.5 pg/mL; 95% prediction interval, <7-129 p
g/mL). Levels of inhibin A greater than 19 pg/mL, are only seen in postmena
rcheal girls in puberty and in adult women, again consistent with inhibin A
being primarily produced by the corpus luteum. Determining cut-off levels
of serum inhibin B regarding whether a girl had entered puberty resulted in
similar (low) sensitivities and specificities as those found for cut-off l
evels of LII or estradiol due to the large overlap between serum values in
Tanner stages I and II. Correlations between inhibin A and inhibin B and FS
H, LH, and estradiol within pubertal stages are presented. In early puberty
both inhibin A and inhibin B correlated positively with LH and FSH. In lat
e puberty inhibin A correlated negatively with FSH and did not correlate wi
th LH; inhibin B still correlated positively with both FSH and LH, now most
strongly with FSH. In adult women during the menstrual cycle, serum inhibi
n B levels increased during the follicular phase, indicating the greatest p
roduction by follicles in early stages of development. In contrast, serum i
nhibin A levels peaked during the luteal phase, indicating the greatest pro
duction by the corpus luteum.
In conclusion, serum inhibin A and inhibin B levels in normal puberty in gi
rls show consistency with our knowledge of the manner in which these hormon
es are secreted within the menstrual cycle in adult women. The presented re
ference values may be of use in the clinical evaluation of pubertal develop
ment in girls.