Skip to main content

Comparison of two bone markers with growth evolution in 74 girls with central precocious puberty

Abstract

Background

The bone markers bone alkaline phosphatase (BAP) and C-terminal telopeptide of type I collagen crosslinks (CTX) are correlated with growth rate during normal puberty. The objective of this study was to evaluate the relationship between the serum concentrations of BAP and CTX and growth evolution in girls with idiopathic central precocious puberty (CPP) to help predict adult height.

Methods

A retrospective single-center study was conducted in 74 girls with CPP for whom a serum sample at initial evaluation was available to retrospectively measure BAP and CTX concentrations; 66.2% of them were untreated.

Results

The serum BAP concentrations showed significant positive correlations with height in standard deviations (SDS) at the initial evaluation (n = 62; r = 0.31; p = 0.015) and with the difference between bone and chronological ages (n = 61; r = 0.39; p = 0.002). BAP was also positively correlated with adult height as measured in both cm and SDS in untreated patients (n = 19; r = 0.58; p = 0.009).

The serum CTX concentrations showed significant positive correlations with growth rate the year before the initial evaluation as measured in both cm and SDS (n = 65; r = 0.34; p = 0.006).

Conclusions

This study revealed significant correlations of serum BAP and CTX concentrations with growth evolution in girls with CPP. The high positive correlation between serum BAP and adult height in untreated girls suggests that BAP can possibly be used to optimize models of adult height prediction in girls with CPP.

Peer Review reports

Background

Biochemical markers of bone turnover are routinely used in clinical practice to monitor osteoporosis in post-menopausal women [1]. In addition, such markers are being documented and utilized in children more frequently than in the past. Among these biochemical markers, bone alkaline phosphatase (BAP) is a marker of bone formation present in the membrane of the osteoblasts and released into the circulation. BAP is a more sensitive diagnostic tool than total alkaline phosphatase activity [2]. In contrast, C-terminal telopeptide of type I collagen crosslinks (CTX) is a marker of bone resorption that is generated from translational modification of bone collagen and is released during matrix resorption [2].

Some previous studies have evaluated these markers in healthy girls during puberty [3,4,5,6,7]. For example, it was demonstrated that BAP and CTX concentrations vary with chronological age [5, 6] and pubertal Tanner stage [3,4,5,6], which has led to established reference values [6, 7]. The peak levels of these bone markers occurred at Tanner breast stage 3 and decrease to adult concentrations at the end of puberty [3,4,5,6]. It has also been shown that BAP is positively correlated with growth rate (cm/year) during normal puberty [5].

Central precocious puberty (CPP) in girls is defined as the development of sexual characteristics before the age of 8 years due to premature activation of the hypothalamic-pituitary-ovarian axis [8]. In girls, CPP is idiopathic in the majority of cases [9]. Genetic [10, 11] and/or environmental factors, particularly obesity, contribute to early onset of puberty. An analysis of the presentation of 493 consecutive girls with CPP in a single-center study showed that obesity accelerates adrenarche but not maturation of the hypothalamic-pituitary-ovarian axis, which mainly depends on genetic factors [12].

Premature secretion of estradiol increases the growth rate and accelerates bone maturation, which can shorten the growing period, resulting in short adult height (AH). Treatment with a gonadotropin-releasing hormone (GnRH) analog blocks the pituitary-ovarian axis and thus estradiol secretion, thereby slowing bone age (BA) progression and preserving growth potential [13]. However, the effect of this treatment on AH varies, primarily because idiopathic CPP progression differs between unsustained forms, also called slowly progressing forms [14], and rapidly progressing forms [15].

Despite the breadth of reported data concerning AH in girls with idiopathic CPP, major questions remain about the indications for GnRH analog treatment [16]. As the reported height gain (AH-predicted AH at onset of treatment) varies from 0.3 [17] to 9.8 cm [18], it is difficult to determine whether to treat a given girl who has idiopathic CPP with GnRH analogs. Tools have been developed to predict AH in girls with CPP [19], but bone markers have not been used to date.

In this study, serum concentrations of BAP and CTX in girls with CPP were examined in relation to patient characteristics at initial evaluation, to growth rates at 6 months and 1 year after this evaluation, and to AH after spontaneous growth. The objective was to evaluate the relationship between serum concentrations of BAP and CTX and the growth evolution in girls with idiopathic CPP to help predict AH.

Methods

Study design

We conducted a single-center study in girls who had been monitored for idiopathic CPP by a senior pediatric endocrinologist (R. Brauner) in a university pediatric unit from June 1981 to July 2012 and for whom a serum sample at initial evaluation preserved at − 22 °C was still available to retrospectively measure serum BAP and CTX concentrations.

Participants

All clinical investigations were conducted according to the principles outlined in the Declaration of Helsinki. Written informed consent for the evaluation was obtained from the children’s parents and included in their hospital medical record. With the exception of routine patient care, no other activities were performed for the study. The authors had no direct interaction with the patients enrolled in the study, except for their medical follow-up, which was performed by R. Brauner. Patients derived from a previous study [12] which was approved by the Ethical Review Committee (Comité de Protection des Personnes, Ile de France III) (Ref. CPP: AC 038), which states that “This study appears to be in accordance with scientific principles generally accepted and to ethical standards of research; this study was lead in the respect of the French law and regulation”.

The primary outcome was to evaluate the relationship between serum concentrations of BAP and CTX and the growth evolution, mainly the AH after spontaneous evolution. The secondary outcome was to compare these concentrations to the patient characteristics at initial evaluation.

The 74 girls included were selected from 493 girls with CPP [12]. At the initial evaluation, the characteristics of the 74 girls included in the study were similar to those of the 419 girls without available samples, except for basal FSH concentration and peak, which were significantly lower in the included patients (Table 1).

Table 1 Patients characteristics

In all patients, CPP was diagnosed based on the appearance of breast development before the age of 8 years, accompanied by the presence of pubic or axillary hair (n = 47/74; 63.5%), a growth rate greater than 2 standard deviations (SDS) the year before the initial evaluation (n = 32/70; 45.7%), and/or BA more than 2 years greater than their chronological age (n = 24/73; 32.9%). (Table 1). We also considered CPP, but not premature thelarche, for girls for whom breast development at initial evaluation was clinically isolated (n = 13/74; 17.6%) but associated with a uterus length greater than 35 mm on ultrasound (n = 4/9 evaluated), a luteinizing hormone (LH)/follicle stimulating hormone (FSH) peak ratio greater than 0.66 by a GnRH test (n = 7/13), and/or a serum estradiol concentration greater than 15 pg/mL (n = 6/13). According to these criteria, only 3 girls (4%) had isolated breast development at initial evaluation, but their clinical picture became complete before 8 years of age, with ages at first menstruation of 10 and 11.5 years in the 2 patients for whom this information is available.

Methods

Organic intracranial lesions were excluded by neuroradiological evaluation except in 12 cases (16.2%) with a familial history of early puberty, age greater than 6 years at onset of puberty, normal neurological evaluation, prepubertal serum estradiol concentrations and LH/FSH peak ratio < 0.66.

The patients were assigned to one of two groups: treated patients (n = 25/74, 33.8%) had been given a GnRH analog, whereas untreated patients (n = 49/74, 66.2%) were followed without treatment. The criteria for treatment were a predicted AH < 155 cm at initial evaluation (n = 4), an LH/FSH peak ratio > 0.66 (n = 17), and/or a serum estradiol concentration > 15 pg/mL (n = 8). Treatment (D-Trp-GnRH, 3.75 mg, i.m., every 24–26 days; half doses in patients weighing < 20 kg) was continued for at least 2 years. Among the untreated CPP patients, growth rate at 6 months and one year after initial evaluation were available for 57.1% (n = 28/49) and 32.6% (n = 16/49), respectively. AH was available for 42.8% (n = 21/49) of these patients.

The following data were collected at the initial evaluation: age at onset of puberty (corresponding to the age at breast development) and at initial evaluation; pubertal stage; height; body mass index (weight in kg/height in m2); growth rate the year before evaluation; BA; and evaluation of the hypothalamic-pituitary-ovarian axis by measuring basal and GnRH-stimulated LH and FSH peaks and the serum concentration of estradiol. A pelvic ultrasound was performed in 47 patients. The ensuing examinations included height and growth rate at 6 months and 1 year in the untreated girls.

Height (measured in all by R.Brauner with a Harpenden stadiometer), growth rate and body mass index are expressed as SDS for chronological age [20, 21]. The pubertal stage was rated according to Marshall and Tanner [22]. BA was assessed by R. Brauner for all patients according to the Greulich and Pyle method [23]. Target height was calculated based on parental heights reported by the parents [24].

LH and FSH concentrations were measured using a two-site monoclonal immunoradiometric assay (LH-Coatria and FSH-Coatria; bioMerieux, SA, Marcy-l’Etoile, France). Estradiol was extracted with ether and measured by radioimmunoassay (Estradiol-2; Sorin Biomedica, Antony, France). BAP and CTX concentrations were assessed by means of chemiluminescent immunoassays using the Cobas automated platform (Roche Diagnostic, Meylan, France).

For the GnRH stimulation test, we used Relefact (100 μg/m2) with serum samples collected at 0, 30, 60 and 90 min after the injection. Serum LH, FSH and estradiol concentrations were measured using various radioimmunoassays during the study period. Each new assay for a given hormone was cross-correlated with the previous method to ensure comparable results for a given parameter throughout the study period. The following values were considered to be pubertal: uterus length > 35 mm, LH/FSH peak ratio after GnRH test > 0.66, and serum estradiol concentration > 15 pg/mL (55 pmol/L).

Statistical analysis

The numeric data are expressed as the mean ± standard deviation. Differences in auxological and clinical data between groups were analyzed using the Mann Whitney U test. Correlations were assessed with Spearman’s using GraphPad Prism (GraphPad Software Inc., San Diego, CA, USA). The magnitudes of correlation are expressed as trivial (r < 0.1), small (0.1 < r < 0.3), moderate (0.3 < r < 0.5), large (0.5 < r < 0.7), very large (0.7 < r < 0.9), and nearly perfect (r > 0.9) [25]. A p value < 0.05 was considered significant.

Results

Characteristics at initial evaluation (Table 1)

According to Tanner breast stage development, 62% of patients were stage 2 (n = 46/74), 36.5% were stage 3 (n = 27/74) and 1.5% were stage 4 (n = 1/74). Breast development was associated with 1 additional pubertal sign (n = 20/74; 27%), 2 additional pubertal signs (n = 21/74; 28.4%), 3 additional pubertal signs (n = 16/74; 21.6%), 4 additional pubertal signs (n = 9/74; 12.2%) or 5 additional pubertal signs (n = 4/74; 5.4%) (See Participants). One patient (1.5%) exhibited all the pubertal signs evaluated, whereas 3 (4%) had isolated breast development.

Correlations (Table 2)

The serum BAP concentration showed moderate significant positive correlations with height in SDS at initial evaluation (n = 62; r = 0.31; p = 0.015) and with the difference between bone and chronological ages (n = 61; r = 0.39; p = 0.002) and a small positive correlation with the serum basal FSH concentration (n = 57; r = 0.27; p = 0.042) (Fig. 1).

Table 2 Correlations between BAP and CTX and characteristics of girls with CPP
Fig. 1
figure1

Correlation between serum BAP concentrations and height at initial evaluation (a), BAP and differences between bone and chronological ages in girls with CPP (b), and with adult height in girls with untreated CPP (c)

The serum CTX concentration showed a small significant positive correlation with growth rate in cm (n = 65; r = 0.26; p = 0.035) and a moderate correlation with growth rate in SDS (n = 65; r = 0.34; p = 0.006) the year before the initial evaluation (Fig. 2).

Fig. 2
figure2

Correlation between CTX and growth rate the year before initial evaluation in girls with CPP. An extreme value of CTX (54,627 pmol/L) was removed for better visibility

There was no correlation between BAP and CTX concentrations. Furthermore, there were no correlations of serum BAP or CTX concentrations with age at onset of puberty, age at initial evaluation, body mass index, BA, basal LH concentration, FSH or LH peak, LH/FSH ratio, or estradiol concentration.

Among the untreated patients, there was no correlation of BAP or CTX concentrations with growth rate at 6 months or 1 year (in cm and SDS) after diagnosis.

The mean AH in untreated patients was 163.7 ± 6.4 cm. Height at the initial evaluation and AH were largely positively correlated (n = 21; r = 0.58; p = 0.005). The BAP concentration was largely positively correlated with AH in cm and in SDS (n = 19; r = 0.58; p = 0.009 for both) in untreated patients (Fig. 1).

Discussion

The objective of the present study was to evaluate the relationship between the serum concentrations of BAP and CTX and the growth rate and AH in girls with CPP. BAP displayed significant positive correlations with the following parameters at initial evaluation: height in SDS, difference between bone and chronological ages, and serum basal FSH concentration. Moreover, serum BAP was positively correlated with AH in untreated patients who had spontaneous growth. The CTX concentration displayed a significant positive correlation with growth rate the year before the initial evaluation.

Serum BAP concentration in girls with CPP

Based on the results of this study, serum BAP can serve as a marker of growth and bone maturation. A positive correlation between BAP and height was described in some previous studies [6, 26] but was not confirmed by other studies [4, 7, 27]. However, these former studies differ from the present study by several criteria, including different technical assessments of BAP and CTX concentrations (use a wheat germ agglutinin assay) [4], different studied populations (obese patients and post-pubertal patients) [4, 7], and different comparisons of bone markers to height (in cm but not in SDS) [4].

CPP can reduce growth potential because premature secretion of estradiol accelerates BA progression, followed by a reduction in growing period and subsequently in growth potential. In the present study, 32.9% of patients encountered a significant BA advance (a difference of greater than 2 years between bone and chronological ages). The positive correlation between the BAP level and BA advance suggests that BAP concentrations give an approach of epiphyseal maturation and may be useful in predicting the AH.

We found the BAP concentration to be positively correlated with AH in untreated patients with CPP. No study to date has evaluated such a correlation. The fact that BAP was correlated with height at initial evaluation, BA advance and AH is consistent with the tables proposed by Bayley and Pinneau for predicting AH, which were based on height at evaluation associated with BA at the time of assessment [28]. Specific tables were established in patients with advanced BA, and although this method is currently controversial because it is considered to overestimate AH, it has been used for decades.

Moreover, the fact that BAP was correlated with both height at initial evaluation and AH is consistent with previous studies showing that height at treatment initiation in girls with CPP is the most important positive factor influencing AH [29, 30]. This finding is reinforced by the fact that we found a large correlation between height at initial evaluation and AH. Recently designed mathematical models predict AH in patients with CPP [19] by using mother and father heights and the following data at initial evaluation: chronological age, height, and LH/FSH peak ratio. The correlation between BAP and AH suggests that it can be used as an additional tool to predict AH, potentially assisting with the decision of whether to introduce treatment with a GnRH analog. This has to be evaluated.

BAP was positively correlated with basal FSH concentrations but not with the LH/FSH peak ratio. A link between serum BAP and FSH concentrations has not yet been reported.

Serum CTX concentration in girls with CPP

The serum CTX concentration was positively correlated with growth rate the year before the initial evaluation. This result is consistent with several studies demonstrating the link between growth rate and bone markers more specifically during puberty, in children with a normal age of puberty onset [2, 4, 6]. Growth rates and serum bone markers concentrations (BAP, alkaline phosphatase, osteocalcin, procollagen type I propeptide, type I carboxyterminal telopeptide) increase significantly in puberty compared to the prepubertal period, reaching a peak at Tanner breast stage 3, after which they decrease to reach the adult concentration just as the growth rate slows. No study thus far has evaluated the correlation between bone markers and growth rate in children with CPP.

Strengths and limitations

A strength of our study is that we performed a homogeneous and comparable evaluation of all patients. Except for the classification of the pubertal stage, the evaluation criteria were all objective (quantitative). However, the evaluation of all patients by the same hospital practitioner allows for homogenization of this partially subjective result. In addition, as bone remodeling markers are correlated with the acquisition of bone mass in girls during puberty [4], the evaluation of these markers may allow for optimal treatment of patients whose bone mass is insufficient.

This study has limitations. It is a retrospective study, but the large number of patients and the use of a single investigator limited this bias. Although AH after spontaneous growth was available for only 21 (42.8% of the untreated) of the patients, the correlation is large. The exclusion of girls due to the absence of an available blood sample may have introduced bias. We postulate that the similarity among the data from these girls to the patients who were included, with regard to the variables analyzed (except for FSH basal and peak concentrations), limits this bias. This study did not have a control population of the same pubertal stage. The AH of the parents weren’t measured but reported which may have introduce bias [31].

Conclusions

In conclusion, this study showed a significant correlation between serum BAP concentrations and AH in untreated girls with idiopathic CPP. The results also revealed several correlations with precocious pubertal features. Therefore, these bone markers could be possibly used to optimize models of AH prediction in girls with CPP.

Abbreviations

AH:

adult height

BA:

bone age

BAP:

bone alkaline phosphatase

CPP:

central precocious puberty

CTX:

C-terminal telopeptide of type I collagen crosslinks

FSH:

follicle stimulating hormone

GnRH:

gonadotropin-releasing hormone

LH:

luteinizing hormone

SDS:

standard deviation score

References

  1. 1.

    Delmas PD, Eastell R, Garnero P, Seibel MJ, Stepan J, Committee of Scientific Advisors of the International Osteoporosis Foundation]. The use of biochemical markers of bone turnover in osteoporosis. Committee of Scientific Advisors of the International Osteoporosis Foundation. Osteoporos Int J Establ Result Coop Eur Found Osteoporos Natl Osteoporos Found USA. 2000;11(Suppl 6):S2–17.

    Article  Google Scholar 

  2. 2.

    Szulc P, Seeman E, Delmas PD. Biochemical measurements of bone turnover in children and adolescents. Osteoporos Int J Establ Result Coop Eur Found Osteoporos Natl Osteoporos Found USA. 2000;11(4):281–94.

    Article  CAS  Google Scholar 

  3. 3.

    Blumsohn A, Hannon RA, Wrate R, Barton J, al-Dehaimi AW, Colwell A, et al. Biochemical markers of bone turnover in girls during puberty. Clin Endocrinol. 1994;40(5):663–70.

    Article  CAS  Google Scholar 

  4. 4.

    van Coeverden SCCM, Netelenbos JC, de Ridder CM, Roos JC, Popp-Snijders C, Delemarre-van de Waal HA. Bone metabolism markers and bone mass in healthy pubertal boys and girls. Clin Endocrinol. 2002;57(1):107–16.

    Article  CAS  Google Scholar 

  5. 5.

    Chailurkit L, Suthutvoravut U, Mahachoklertwattana P, Charoenkiatkul S, Rajatanavin R. Biochemical markers of bone formation in Thai children and adolescents. Endocr Res. 2005;31(3):159–69.

    Article  PubMed  CAS  Google Scholar 

  6. 6.

    Rauchenzauner M, Schmid A, Heinz-Erian P, Kapelari K, Falkensammer G, Griesmacher A, et al. Sex- and age-specific reference curves for serum markers of bone turnover in healthy children from 2 months to 18 years. J Clin Endocrinol Metab. 2007;92(2):443–9.

    Article  PubMed  CAS  Google Scholar 

  7. 7.

    Alberti C, Chevenne D, Mercat I, Josserand E, Armoogum-Boizeau P, Tichet J, et al. Serum concentrations of insulin-like growth factor (IGF)-1 and IGF binding Protein-3 (IGFBP-3), IGF-1/IGFBP-3 ratio, and markers of bone turnover: reference values for French children and adolescents and z-score comparability with other references. Clin Chem. 2011;57(10):1424–35.

    Article  PubMed  CAS  Google Scholar 

  8. 8.

    Carel J-C, Eugster EA, Rogol A, Ghizzoni L, Palmert MR. ESPE-LWPES GnRH analogs consensus conference group, et al. consensus statement on the use of gonadotropin-releasing hormone analogs in children. Pediatrics. 2009;123(4):e752–62.

    Article  PubMed  Google Scholar 

  9. 9.

    Chemaitilly W, Trivin C, Adan L, Gall V, Sainte-Rose C, Brauner R. Central precocious puberty: clinical and laboratory features. Clin Endocrinol. 2001;54(3):289–94.

    Article  CAS  Google Scholar 

  10. 10.

    de Vries L, Kauschansky A, Shohat M, Phillip M. Familial central precocious puberty suggests autosomal dominant inheritance. J Clin Endocrinol Metab. 2004;89(4):1794–800.

    Article  PubMed  CAS  Google Scholar 

  11. 11.

    Durand A, Bashamboo A, McElreavey K, Brauner R. Familial early puberty: presentation and inheritance pattern in 139 families. BMC Endocr Disord [Internet]. 2016 [cited 2018 Apr 23];16(1). Available from: http://bmcendocrdisord.biomedcentral.com/articles/10.1186/s12902-016-0130-x

  12. 12.

    Giabicani E, Allali S, Durand A, Sommet J, Couto-Silva A-C, Brauner R. Presentation of 493 consecutive girls with idiopathic central precocious puberty: a single-center study. PLoS One. 2013;8(7):e70931.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  13. 13.

    Brauner R, Adan L, Malandry F, Zantleifer D. Adult height in girls with idiopathic true precocious puberty. J Clin Endocrinol Metab. 1994;79(2):415–20.

    PubMed  CAS  Google Scholar 

  14. 14.

    Palmert MR, Malin HV, Boepple PA. Unsustained or slowly progressive puberty in young girls: initial presentation and long-term follow-up of 20 untreated patients. J Clin Endocrinol Metab. 1999;84(2):415–23.

    PubMed  CAS  Google Scholar 

  15. 15.

    Fontoura M, Brauner R, Prevot C, Rappaport R. Precocious puberty in girls: early diagnosis of a slowly progressing variant. Arch Dis Child. 1989;64(8):1170–6.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. 16.

    Willemsen RH, Elleri D, Williams RM, Ong KK, Dunger DB. Pros and cons of GnRHa treatment for early puberty in girls. Nat Rev Endocrinol. 2014;10(6):352–63.

    Article  PubMed  CAS  Google Scholar 

  17. 17.

    Cassio A, Cacciari E, Balsamo A, Bal M, Tassinari D. Randomised trial of LHRH analogue treatment on final height in girls with onset of puberty aged 7.5-8.5 years. Arch Dis Child. 1999;81(4):329–32.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  18. 18.

    Klein KO, Barnes KM, Jones JV, Feuillan PP, Cutler GB. Increased final height in precocious puberty after long-term treatment with LHRH agonists: the National Institutes of Health experience. J Clin Endocrinol Metab. 2001;86(10):4711–6.

    Article  PubMed  CAS  Google Scholar 

  19. 19.

    Giabicani E, Lemaire P, Brauner R. Models for predicting the adult height and age at first menstruation of girls with idiopathic central precocious puberty. Wolfe A, editor PLOS ONE. 2015;10(4):e0120588.

    Article  CAS  Google Scholar 

  20. 20.

    Rolland-Cachera MF, Cole TJ, Sempé M, Tichet J, Rossignol C, Charraud A. Body mass index variations: centiles from birth to 87 years. Eur J Clin Nutr. 1991;45(1):13–21.

    PubMed  CAS  Google Scholar 

  21. 21.

    Sempé A, Pedron G, Roy-Pernot M-P. Auxologie, méthode et séquences, Paris. Laboratoire Théraplix; 1979.

  22. 22.

    Marshall WA, Tanner JM. Variations in pattern of pubertal changes in girls. Arch Dis Child. 1969;44(235):291–303.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. 23.

    Greulich WW, Pyle SI. Radiographic atlas of skeletal development of the hand and wrist. 2nd edition. I volume-atlante di 256 pagine. Stanford University press, Stanford, California, 1959. Acta Genet Med Gemellol. 1959;8(04):513.

    Article  Google Scholar 

  24. 24.

    Tanner JM, Goldstein H, Whitehouse RH. Standards for Children’s height at age 2 to 9 years allowing for height of parents. Arch Dis Child. 1970;45(244):819.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. 25.

    Hopkins WG, Marshall SW, Batterham AM, Hanin J. Progressive statistics for studies in sports medicine and exercise science. Med Sci Sports Exerc. 2009;41(1):3–13.

    Article  PubMed  Google Scholar 

  26. 26.

    Mora S, Cafarelli L, Erba P, Puzzovio M, Zamproni I, Giacomet V, et al. Differential effect of age, gender and puberty on bone formation rate assessed by measurement of bone-specific alkaline phosphatase in healthy Italian children and adolescents. J Bone Miner Metab. 2009;27(6):721–6.

    Article  PubMed  CAS  Google Scholar 

  27. 27.

    Gajewska J, Klemarczyk W, Ambroszkiewicz J, Szamotulska K, Chełchowska M, Weker H. Associations between IGF-I, IGF-binding proteins and bone turnover markers in prepubertal obese children. J Pediatr Endocrinol Metab [Internet]. 2015 [cited 2018 Apr 23];28(5–6). Available from: https://www.degruyter.com/view/j/jpem.2015.28.issue-5-6/jpem-2014-0326/jpem-2014-0326.xml

  28. 28.

    Bayley N, Pinneau SR. Tables for predicting adult height from skeletal age: revised for use with the Greulich-Pyle hand standards. J Pediatr. 1952;40(4):423–41.

    Article  PubMed  CAS  Google Scholar 

  29. 29.

    Pasquino AM, Pucarelli I, Accardo F, Demiraj V, Segni M, Di Nardo R. Long-term observation of 87 girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone analogs: impact on adult height, body mass index, bone mineral content, and reproductive function. J Clin Endocrinol Metab. 2008;93(1):190–5.

    Article  PubMed  CAS  Google Scholar 

  30. 30.

    Oostdijk W, Rikken B, Schreuder S, Otten B, Odink R, Rouwé C, et al. Final height in central precocious puberty after long term treatment with a slow release GnRH agonist. Arch Dis Child. 1996;75(4):292–7.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  31. 31.

    Cizmecioglu F, Doherty A, Paterson WF, Young D, Donaldson MDC. Measured versus reported parental height. Arch Dis Child. 2005;90(9):941–2.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

Download references

Funding

The study was self-funded.

Availability of data and materials

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Author information

Affiliations

Authors

Contributions

AV drafted the manuscript, collected and analyzed the data; JCS participated in the design of the study and drafted the manuscript; RB conceived the study and participated in its design and coordination and drafted the manuscript. All the authors read and approved the final manuscript.

Corresponding author

Correspondence to Raja Brauner.

Ethics declarations

Ethics approval and consent to participate

All clinical investigations were conducted according to the principles outlined in the Declaration of Helsinki. Written informed consent for the evaluation was obtained from the children’s parents and included in their hospital medical record. With the exception of routine patient care, no other activities were performed for the study. The authors had no direct interaction with the patients enrolled in the study, except for their medical follow-up, which was performed by R. Brauner. Patients derived from a previous study [12] which was approved by the Ethical Review Committee (Comité de Protection des Personnes, Ile de France III) (Ref. CPP: AC 038), which states that “This study appears to be in accordance with scientific principles generally accepted and to ethical standards of research; this study was lead in the respect of the French law and regulation”.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no financial and non-financial competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Vincent, A., Souberbielle, JC. & Brauner, R. Comparison of two bone markers with growth evolution in 74 girls with central precocious puberty. BMC Pediatr 18, 224 (2018). https://doi.org/10.1186/s12887-018-1194-8

Download citation

Keywords

  • Bone markers
  • Growth evolution
  • Central precocious puberty
  • Adult height
  • Bone alkaline phosphatase
  • CTX