Rapid maturation of the reproductive axis during perimenarche independent of body composition.

The development of the reproductive axis is thought to be a gradual process, but our understanding of the complex endocrine changes that accompany the transition from premenarche to reproductive life in women has been hampered by the paucity of longitudinal studies. We studied 112 premenarchal Caucasian females at 6-month intervals over 4 yr and obtained a detailed reproductive and dietary history. We quantified reproductive hormones in 24-h urine collections as a measure of daily output and measured body composition biometrically and with the use of dual energy x-ray absortiometry scans. The percent body fat did not change appreciably in the study period (range, 21-24%) and was unrelated to menarche. Sex steroid and gonadotropin levels changed exponentially in the year approaching menarche. FSH levels peaked at menarche and then progressively declined thereafter. Estradiol output increased rapidly in the year approaching menarche and then plateaued thereafter. The frequency of menstrual bleeding increased rapidly and plateaued at 1 yr postmenarche. At 1 yr, 65% of these adolescent women had established a pattern of 10 or more menstrual episodes/yr, and by 3 yr postmenarche this figure exceeded 90%. There were no significant changes in dietary intake of protein, carbohydrate, or fat in the same period. Menarche occurs as a result of rapid maturation of the reproductive axis and heralds the reestablishment of a negative sex steroid feedback loop that parallels the adult threshold. These events appear to develop independent of changes in body composition and diet, but may reflect the improved nutrition and socioeconomic status of the late 20th century.

[1]  S. Schlicker,et al.  The weight and fitness status of United States children. , 2009, Nutrition reviews.

[2]  F. de Zegher,et al.  Anovulation after precocious pubarche: early markers and time course in adolescence. , 1999, The Journal of clinical endocrinology and metabolism.

[3]  Ramzi W. Nahhas,et al.  Leptin is inversely related to age at menarche in human females. , 1997, The Journal of clinical endocrinology and metabolism.

[4]  G. Koch,et al.  Secondary sexual characteristics and menses in young girls seen in office practice: a study from the Pediatric Research in Office Settings network. , 1997, Pediatrics.

[5]  P. Illingworth,et al.  Changes in dimeric inhibin A and B during normal early puberty in boys and girls , 1997, Clinical endocrinology.

[6]  M Litaker,et al.  Body-composition measurement in 9-11-y-old children by dual-energy X-ray absorptiometry, skinfold-thickness measurements, and bioimpedance analysis. , 1996, The American journal of clinical nutrition.

[7]  D. Counts,et al.  Patterns of human growth. , 1995, Science.

[8]  C. Cowell,et al.  Body-composition assessment by dual-energy x-ray absorptiometry in subjects aged 4-26 y. , 1995, The American journal of clinical nutrition.

[9]  L. Dunkel,et al.  Age-related course of urinary gonadotropins in children. , 1995, The Journal of clinical endocrinology and metabolism.

[10]  M Lampl,et al.  Saltation and stasis: a model of human growth. , 1992, Science.

[11]  P. Bruning,et al.  Body fat mass, body fat distribution, and pubertal development: a longitudinal study of physical and hormonal sexual maturation of girls. , 1992, The Journal of clinical endocrinology and metabolism.

[12]  J. Landis,et al.  Determinants of bone density in young women. I. Relationships among pubertal development, total body bone mass, and total body bone density in premenarchal females. , 1992, The Journal of clinical endocrinology and metabolism.

[13]  T. Lloyd,et al.  Urinary hormonal concentrations and spinal bone densities of premenopausal vegetarian and nonvegetarian women. , 1991, The American journal of clinical nutrition.

[14]  D. Bates,et al.  CLINICAL USE OF BONE DENSITOMETRY , 1991 .

[15]  D. Miller,et al.  Age at menarche of European, Afro-Caribbean and Indo-Pakistani schoolgirls living in London. , 1991, Annals of human biology.

[16]  R. Schoemaker,et al.  LUTEINIZING HORMONE AND FOLLICLE STIMULATING HORMONE SECRETION PATTERNS IN BOYS THROUGHOUT PUBERTY MEASURED USING HIGHLY SENSITIVE IMMUNORADIOMETRIC ASSAYS , 1989, Clinical endocrinology.

[17]  G. Chrousos,et al.  Developmental processes in early adolescence. Relations among chronologic age, pubertal stage, height, weight, and serum levels of gonadotropins, sex steroids, and adrenal androgens. , 1987, Journal of adolescent health care : official publication of the Society for Adolescent Medicine.

[18]  M. Metcalf,et al.  Incidence of ovulation in the years after the menarche. , 1983, The Journal of endocrinology.

[19]  R. Santen,et al.  A model for validation of radioimmunoassay kit reagents: measurement of follitropin and lutropin in blood and urine. , 1981, Clinical chemistry.

[20]  D. Apter SERUM STEROIDS AND PITUITARY HORMONES IN FEMALE PUBERTY: A PARTLY LONGITUDINAL STUDY , 1980, Clinical endocrinology.

[21]  R. Osathanondh,et al.  The production of progesterone, androgens, and estrogens by granulosa cells, thecal tissue, and stromal tissue from human ovaries in vitro. , 1979, The Journal of clinical endocrinology and metabolism.

[22]  F. Katch,et al.  Estimation of body fat from skinfolds and surface area. , 1979, Human biology.

[23]  P. Leaverton,et al.  Secondary sex characteristics of girls 12 to 17 years of age: the U.S. Health Examination Survey. , 1979, The Journal of pediatrics.

[24]  W M Moore,et al.  Physical growth: National Center for Health Statistics percentiles. , 1979, The American journal of clinical nutrition.

[25]  James M. Tanner,et al.  Foetus into Man: Physical Growth from Conception to Maturity , 1978 .

[26]  R. Penny,et al.  Gonadotropin excretion and body composition. , 1978, Pediatrics.

[27]  P. A. Lee,et al.  Puberty in girls: correlation of serum levels of gonadotropins, prolactin, androgens, estrogens, and progestins with physical changes. , 1976, The Journal of clinical endocrinology and metabolism.

[28]  R. Frisch,et al.  Menstrual Cycles: Fatness as a Determinant of Minimum Weight for Height Necessary for Their Maintenance or Onset , 1974, Science.

[29]  A. Johanson Fluctuations of gonadotropin levels in children. , 1974, The Journal of clinical endocrinology and metabolism.

[30]  J. Winter,et al.  The development of cyclic pituitary-gonadal function in adolescent females. , 1973, The Journal of clinical endocrinology and metabolism.

[31]  R. Revelle,et al.  Components of weight at menarche and the initiation of the adolescent growth spurt in girls: estimated total water, llean body weight and fat. , 1973, Human biology.

[32]  R. Revelle,et al.  Height and Weight at Menarche and a Hypothesis of Critical Body Weights and Adolescent Events , 1970, Science.

[33]  V. Chinchilli,et al.  The Effect of Enhanced Bone Gain Achieved with Calcium Supplementation During Ages 12 to 16 Does Not Persist in Late Adolescence , 1998 .

[34]  M M Goodsitt,et al.  Evaluation of a new set of calibration standards for the measurement of fat content via DPA and DXA. , 1992, Medical physics.

[35]  M. Grumbach The neuroendocrinology of human puberty. An ontogenetic perspective , 1990 .