Abstract:ObjectiveTo identify correlates and longitudinal changes in circulating antimüllerian hormone (AMH) levels as a marker of ovarian primordial follicle recruitment in normal peripubertal girls.DesignObservational study using mixed longitudinal and cross-sectional analyses.SettingNot applicable.Patient(s)Unselected girls assessed at ages 7–11 years.Intervention(s)None.Main Outcome Measure(s)AMH, inhibin B, and FSH levels were analyzed in blood samples collected at ages 7, 9, and 11 years for longitudinal analyses… Show more
“…Our findings of stable AMH levels in females during childhood and early adolescence, their inverse association with FSH before puberty, and loss of the inverse correlation between AMH and both LH and FSH at the onset of puberty are consistent with those of other studies (20,23,24,29). Collectively, these data, combined with known early follicular recruitment dynamics and its association with AMH across the life-course (31), suggest that the pituitary-gonadal axis may be partially active during childhood.…”
Section: Figure 5 Models By Age At Lh and Fshsupporting
confidence: 93%
“…Second, we do not have testosterone measurements, and although AMH is known to be negatively associated with testosterone from the time of puberty and in adulthood, whether this is causal remains unknown (22,23). Third, we also lacked inhibin B measurements in the girls, which would have allowed us to examine the recently reported divergence with AMH (24). In girls, analysis of AMH levels in relation to oestradiol and inhibin B levels would provide a fuller understanding of changes in the rate of ovarian follicle recruitment and follicle activity.…”
Section: Figure 5 Models By Age At Lh and Fshmentioning
confidence: 99%
“…They described stable AMH levels and weak inverse correlations with FSH. Lashen et al (24) reported a pilot longitudinal study of 32 girls measured thrice from 7 years onwards, who appeared to show a small prepubertal peak in AMH and similar inverse correlations with FSH.…”
Our longitudinal data clarified the development of individual AMH levels over a 10-year period. We described modest late prepubertal peaks in both boys and girls, and confirmed the pubertal decline in boys. The inverse association of AMH with gonadotrophins in young females supports its role as a marker of ovarian function, while the precise role for AMH in relation to testicular function in young males remains unclear.
“…Our findings of stable AMH levels in females during childhood and early adolescence, their inverse association with FSH before puberty, and loss of the inverse correlation between AMH and both LH and FSH at the onset of puberty are consistent with those of other studies (20,23,24,29). Collectively, these data, combined with known early follicular recruitment dynamics and its association with AMH across the life-course (31), suggest that the pituitary-gonadal axis may be partially active during childhood.…”
Section: Figure 5 Models By Age At Lh and Fshsupporting
confidence: 93%
“…Second, we do not have testosterone measurements, and although AMH is known to be negatively associated with testosterone from the time of puberty and in adulthood, whether this is causal remains unknown (22,23). Third, we also lacked inhibin B measurements in the girls, which would have allowed us to examine the recently reported divergence with AMH (24). In girls, analysis of AMH levels in relation to oestradiol and inhibin B levels would provide a fuller understanding of changes in the rate of ovarian follicle recruitment and follicle activity.…”
Section: Figure 5 Models By Age At Lh and Fshmentioning
confidence: 99%
“…They described stable AMH levels and weak inverse correlations with FSH. Lashen et al (24) reported a pilot longitudinal study of 32 girls measured thrice from 7 years onwards, who appeared to show a small prepubertal peak in AMH and similar inverse correlations with FSH.…”
Our longitudinal data clarified the development of individual AMH levels over a 10-year period. We described modest late prepubertal peaks in both boys and girls, and confirmed the pubertal decline in boys. The inverse association of AMH with gonadotrophins in young females supports its role as a marker of ovarian function, while the precise role for AMH in relation to testicular function in young males remains unclear.
“…Six cross‐sectional studies used cross‐sectional data to report the mean/median serum AMH with the reference ranges (SD/10th‐90th/5‐95th/2.5‐97.5th centile) from birth into adult life . Six studies reported this data in a longitudinal study design . All studies show a consistent pattern of an increase in AMH in childhood, a slight decrease at puberty followed by constant levels throughout adolescence.…”
Section: Resultsmentioning
confidence: 99%
“…Mean, Childhood: Lee, Cui, Savas‐Erdeve, Sahin and Korkmaz . Median, Adolescence: Lee, Lashen, Anderson, Pinola, Elchuri, Cui, Hart, Hernandez and Yetim . Mean, Adolescence: Lee, Elchuri, Cui, Akin, Kim, Reinehr and Sophor…”
Introduction
Certain medical disorders as well as their management may affect gonadal function. Recent advances in the management of these conditions accompanied by the availability and success of methods of fertility preservation has highlighted the need for assessment of ovarian reserve in childhood and adolescence. Serum anti‐Mullerian hormone (AMH) and antral follicle count are well established markers of ovarian reserve and serum inhibin has also been used. However, literature on reference ranges for ovarian reserve markers in this age‐group is relatively scarce. Thus, our aim was to evaluate published data to estimate reference values of ovarian reserve makers in childhood and adolescence.
Material and methods
We performed a systematic review of the literature reporting ovarian reserve markers in childhood and adolescence. We included only those studies examining markers of ovarian reserve in the normal healthy population between the ages of 0 and 19 years. PROSPERO registration: CRD42018119064.
Results
Serum AMH emerged as the most common biomarker assessed. Serum AMH was detectable at birth and, after a transient increase in infancy, increased steadily in childhood. Following a slight decrease at puberty, levels were constant throughout adolescence with a peak in adolescence or early adulthood. The mean serum AMH values during infancy, childhood and adolescence were 10.55, 22.32 and 31.84 pmol/L, respectively. The corresponding median values were 9.85, 24.49 and 26.32 pmol/L. It was not possible to construct age‐specific reference intervals because of methodological heterogeneity, variations in the assay used to measure AMH and differing interval width for age used in included studies. Serum inhibin showed an increase from childhood to adolescence, with median serum inhibin values of 53.86 pg/mL in adolescence. Antral follicle count showed a significant positive correlation with serum AMH and a median value of 30.52 in adolescence.
Conclusions
We summarize the trends and levels of biomarkers of ovarian reserve from birth until young adulthood. Peak levels of serum AMH are reported in adolescence or early adulthood. We have reported median/mean values for serum AMH in different age‐groups based on data pooled from several studies, which may be used as a reference when evaluating ovarian reserve in childhood and adolescence especially when considering fertility preservation.
This chapter discusses ovarian processes starting in uterine life and subsequently across the following phases: from birth until puberty, the pubertal period itself, then from post puberty until menopause, and finally during menopause and the postmenopausal phase. The ovary has three important functions: first, oocyte and follicle formation and storage; second, oocyte and follicle development resulting in ovulation; and third, reproductive hormone production. The hormone production is inseparable from follicular development. The various processes are described in each of the different phases of life.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.