Volume 10 - 2019 | https://doi.org/10.3389/fendo.2019.00681
Metabolic Perspectives for Non-classical Congenital Adrenal Hyperplasia With Relation to the Classical Form of the Disease
- 1Clinic of Endocrinology, Diabetes and Metabolic Diseases, Clinical Center of Serbia, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
- 2Division of Endocrinology, University Children's Hospital, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
- 3Department of Endocrinology, UMC Bežanijska kosa, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
- 4Unit of Endocrine Diseases, Aretaieion Hospital, National and Kapodistrian University of Athens, Athens, Greece
- 5Faculty of Medicine, Instituto de Patologia e Imunologia Molecular da Universidade do Porto/I3S Research Institute, Hospital S João, University of Porto, Porto, Portugal
Non-classical congenital adrenal hyperplasia (NC-CAH) represents mild form of CAH with the prevalence of 0. 6 to 9% in women with androgen excess. Clinical and hormonal findings in females with NC-CAH are overlapping with other hyperandrogenic entities such as polycystic ovary syndrome hence causing difficulties in diagnostic approach. Metabolic consequences in subjects with NC-CAH are relatively unknown. We are lacking longitudinal follow of these patients regarding natural course of the disease or the therapeutic effects of the different drug regiments. Patients with NC-CAH similarly to those with classical form are characterized with deteriorated cardiovascular risk factors that are probably translated into cardiometabolic diseases and events. An increased preponderance of obesity and insulin resistance in patients with NC-CAH begin at young age could result in increased rates of metabolic sequelae and cardiovascular disease later during adulthood in both sexes. On the other hand, growth disorder was not proven in patients with NC-CAH in comparison to CAH patients of both gender characterized with reduced final adult height. Similarly, decreased bone mineral density and osteoporosis are not constant findings in patients with NC-CAH and could depend on the sex, and type or dose of corticosteroids applied. It could be concluded that NC-CAH represent a particular form of CAH that is characterized with specificities in clinical presentation, diagnosis, therapeutic approach and metabolic outcomes.
The non-classical form of congenital adrenal hyperplasia (NC-CAH) was initially called late-onset as clinical presentation was observed in adolescents and adults. Presentation of NC-CAH is subtle and diagnosis requires implementation of different tests to exclude other problems. Moreover, clinical expression of NC-CAH is variable in patients carrying the same mutation. This suggests that additional factors may modify the clinical expression of the disease including age, steroid metabolic pathways, variation in androgen production, individual sensitivity to androgens, differences in skin sensitivity to androgens and possibly the existence of other genes modifying 21-hydroxylase activity (1, 2). In patients with NC-CAH predominant signs are those of androgen excess including premature pubarche, acne, hirsutism, polycystic ovary syndrome (PCOS) and subfertility (3).
NC-CAH is more frequently observed in females. The preponderance of NC-CAH in women with androgen excess, and according to ethnicity and genotype, is ranging from 0.6 to 9% (2). Males with NC-CAH are diagnosed significantly less often than females due to less frequently presented and recognizedsigns of androgen excess (4). One of the scarce and small studies showed in men with NC-CAH premature pubarche in 29% before 9 years of age (5). Gynecomastia has been reported as the presenting symptom in two male adolescents with non-classical congenital adrenal hyperplasia. Considering diagnosing NC-CAH, basal values of 17-OHP below 6 nmol/L were found in 2.1% of subjects with disease while concentrations of over 30 nmol/L after ACTH test is confirmatory for diagnosis (5).
As CAH is considered as disease spectrum, disease phenotype is ascertained by the less severe mutation with the highest residual enzymatic activity of CYP21A2 (6). The prevalence of classical CAH is from 1:10,000 to 1:20,000 births (7, 8) while in the non-classical CAH it is 1:1,000 births (9) and occurs in about 6% of hirsute women (10) (Supplementary Table 1).
Metabolic consequences in subjects with NC-CAH are relatively unknown and we are missing longitudinal follow up data of these patients regarding either the natural course of the disease or the outcomes of therapeutic regiments mainly based on glucocorticoids. Therefore, metabolic consequences in NC-CAH subjects could be analyzed from scarce clinical studies (11) or extrapolated from as well scarce clinical follow-up of patients with classical CAH.
Clinical Characteristics in Different Age Periods
Patients With Non-classical CAH
Both boys and girls with NC-CAH could be characterized with fast linear growth, advanced bone age with consequent tall stature (4, 12). On the other hand, short stature was reported in subjects with NC-CAH as well particularly in patients on glucocorticoid therapy that commenced before the start of puberty. However, risk for short stature is relatively small with majority of children having almost normal final height (13).
Patients With Classical CAH
Birth length of salt wasting (SW) boys and girls at neonatal screening is above the average at birth while during infancy their height velocity declines by the age of 1.5 years in boys, and by the age of 3 years in girls (14). Patients with simple virilizing (SV) form of CAH have relative androgen insensitivity during the first year of life with consequent absence of increased height velocity (15). Before puberty, patients with SW are growing close to the reference values. True pubertal growth spurt is not noticeable in both forms and genders (16).
The first meta-analysis on the height outcome in classical CAH showed similar mean final height SD score (SDS) of −1.37 (~10 cm) in both genders compared to their target height (17). Studies on the outcomes in adults with classical CAH showed those on smaller glucocorticoid doses had slightly better SDS outcome of −1 below the target height. Patients with both CAH forms had reduced final adult height. However, women with simple virilizing form of CAH had shorter stature in comparison to those with salt wasting phenotype (18) (Supplementary Table 1).
Sexual Maturation Characteristics
Howig et al. reported that the mean age for the onset of puberty was 9.8 years for girls with simple virilizing form, and 10.3 years for girls with SW CAH, and similar age at menarche of 13.3 and 13.7 years, respectively. In boys with SV form the onset of puberty was at 9.8, and 10.6 years for those with SW (19). Moreover, dissociation of pubarche and adrenarche was shown in classical CAH. Namely, in both boys and girls an earlier pubarche, gonadarche, and thelarche was confirmed with the absence of typical signs of adrenarche. Children having advanced skeletal maturation are at risk for early pubertal development (20). Elevated androgens may induce secondary central precocious puberty. High adrenal androgens resulting from non-suppression of HPA axis cause early puberty in both forms, more prevalent in SV than SW forms (21).
In those with NC-CAH pubertal delay, pubertal development progressed well after the initiation of glucocorticoid therapy with attainment of menarche and subsequently regular menstrual cycles (22) (Supplementary Table 1).
Importance of Differential Diagnosis
NC-CAH and Early Adrenarche/Pubarche
Adrenarche is characterized with elevated secretion of adrenal androgen precursors (AAPs), namely, dehydroepiandrosterone (DHEA) and DHEA-sulfate (DHEAS) that occurs at 5–8 years of age (23). Premature adrenarche (PA) and premature pubarche (PP) are defined as early appearance (before 9 years in boys and 8 years in girls) of axillary and pubic hair, adult type body odor or acne, with the absence of true central puberty. AAPs concentrations are above the prepubertal level with DHEAS > 1 μmol/l (termed as biochemical adrenarche) (24). The mechanisms of PA are not fully elucidated but the obesity and genetic factors seems to contribute in apparently multifactorial etiology (24).
Premature adrenarche is a benign condition but before the diagnosis can be accepted, differential diagnosis should consider defects of cortisol synthesis, androgen-producing tumors originated from adrenals or gonads, central precocious puberty, primary hypothyroidism, Cushing's syndrome, exposure to exogenous androgens, and most importantly NC-CAH (25).
The reported prevalence of CAH in PP patients differs from study populations (0–43% for all types of CAH) (26). Differential diagnosis between PA and NC-CAH, as well as other genetic reasons for adrenal hyperandrogenism, is not always obvious based on clinical examination. However, rapidly accelerating growth, remarkable androgenic signs and bone age advancement, and a positive family history are clues toward a genetic disorder (27).
NC-CAH and PCOS
Clinical and hormonal findings that are overlapping with other hyperandrogenic entities such as PCOS may cause some difficulties in diagnostic approach in patient with suspected NC-CAH. Therefore, one should question what endocrine tests are appropriate to confirm or exclude NC-CAH, and if genetic analyses are indicated (5, 28, 29).
PCOS is considered frequent endocrine disease of women during reproductive period that is characterized with hyperandrogenism (30). As PCOS is a disease of exclusion, clinicians are obliged to perform necessary basal and functional endocrine testing to exclude other causes of androgen excess. Serum total testosterone determination is the main androgen determinant of PCOS (30). Approach to the hormonal analyses depends on the severity of hyperandrogenism. Determination of total testosterone is requested in patients with regular menstrual cycles and mild hirsutism (30). Determination of total testosterone together with FSH and LH is requested in patients with moderate hirsutism. In subjects with sudden development of hirsutism in adolescents and adults, and high concentrations of testosterone and androstenedione, an additional ACTH stimulation test with determination of 17-OHP together with CYP21A2 genotyping is requested (31).
Gonads could contribute to increase in 17-OHP as they also secrete this hormone. A hyperresponsiveness of 17-OHP to gonadotropin-releasing hormone agonist (GnRHa) is confirming ovarian hyperandrogenism. Hence, PCOS is considered as a result of ovarian thecal cell overactivity associated with 17,20-lyase activity down-regulation (32). As a consequence, hyperandrogenemia in PCOS could lead toward estrogen oversecretion. However, LH to estradiol ratio is kept normal in functional ovarian hyperandrogenism in the presence of elevated 17-OHP (33).
Therapy for NC-CAH
Concerning therapy for NC-CAH patients in contrast to classical CAH patients, adrenal replacement is not required. Therefore, pharmacological treatment is focused on the management of the signs of androgen excess. Use of glucocorticosteroid (GCS) therapy should be reserved for special outcomes such as restauration of fertility. When talking on the long-term outcomes of androgen excess including menstrual cycle derangement, first line options are antiandrogens and oral contraceptives (34) (Supplementary Table 1).
Therapy for Classical CAH
Glucocorticoids and All Forms of CAH
Longitudinal growth and bone age development are the most important clinical parameters for monitoring adequate glucocorticoid replacement in children with CAH (35). Serum levels of 17-OHP, androstenedione and testosterone need to be monitored frequently and the hydrocortisone dose adjusted to maintain treatment efficacy. The levels of androstenedione and testosterone are more important in monitoring the glucocorticoid dosage than 17-OHP that should be kept a little above the normal range.
Analysis of growth in CAH patients reveal that the two most rapid phases of growth (first year of life and pubertal growth spurt) are vulnerable ones, during which glucocorticoid overtreatment should be avoided (14, 19). During infancy hydrocortisone dose should be decreased in patients with slower growth velocity, but strict hydrocortisone dose adjustments are necessary during childhood to avoid accelerated growth and advanced skeletal maturation (16). Pharmacokinetics of free cortisol showed shorter half-life in pubertal girls than in pubertal boys (36). Consequently, female patients at puberty need more frequent hydrocortisone replacement regimen. Besides decreased compliance of adolescents with CAH, use of oral contraceptive pills, aromatase inhibitors, thyroxine, or ingestion of hydrocortisone with food could influence cortisol dynamics and altering hydrocortisone dosing (37).
Hydrocortisone three times per day is the mostly prescribed regimen by pediatricians (38). Prednisolone or dexamethasone could be used in children with late puberty and in adults, but are avoided in childhood due to the potent effect on growth. It was observed several rises in cortisol concentrations during the day in children on hydrocortisone therapy. These phased are interchanged with periods of hypocortisolemia between the doses, especially during the night. Reduction of glucocorticoid dose during puberty is of clinical importance as pubertal height gain represent a predictor of final height. On the other hand, low glucocorticoid dose with concomitant hyperandrogenism can lead to premature epiphyseal closure and short stature (17). Other treatment options to improve final height and metabolic outcome might include subcutaneous hydrocortisone infusion through a pump, as well as plenadren (modified-release hydrocortisone) and chronocort (modified-release hydrocortisone formula, under development) that have a delayed and sustained absorption profile (38) (Supplementary Table 1).
Endocrine Society (USA) recommended fludrocortisone (0.05–0.2 mg once or twice per day) to be used in all patients with classical CAH (13). Fludrocortisone is used more frequently and in higher doses in patients with more severe genotypes. Overtreatment, defined by renin concentrations either in the lower reference range or suppressed, was only rarely observed throughout the different mutation groups (22) (Supplementary Table 1).
Metabolic Outcomes of NC-CAH
Obesity and Cardiometabolic Risk During Life
One third of untreated NC-CAH women have insulin resistance (11, 39). In children with both classical CAH and NC-CAH prevalence of obesity is approximately 35% and exceeds obesity rates in children and adolescent in the general population (18). Obese children with either forms of CAH are hyperinsulinemic and hyperleptinemic but predominantly in those with classical form of CAH (18, 40). However, Saygili et al. did not show difference in leptin concentrations in hyperinsulinemic and hyperandrogenemic adult women with NC-CAH in comparison to controls (39). Moreover, an association of leptin levels with hyperinsulinemia and hyperandrogenism in women with NC-CAH was not established with conclusion that potential relation of leptin with hyperinsulinemia and reproduction in NC-CAH patients need further investigation (39).
We are lacking clinical studies in NC-CAH children regarding obesity, metabolic syndrome and their consequences (41). Concerning adult NC-CAH patients, it was recently shown an increased risk of metabolic and cardiovascular morbidities in both males and females (42).
Adrenal androgen secretion is increased in NC-CAH in the presence of normal levels of ACTH in the majority of subjects (43). Moreover, NC-CAH patients have normal levels of DHEAS while androstenedione and testosterone are similarly elevated to the levels in PCOS women (43, 44). As mentioned previously, altered enzyme kinetics due to CYP21A2 missense mutations is associated with adrenal androgen oversecretion in NC-CAH (2). Another mechanisms contributing to hyperandrogenism in NC-CAH includes ovarian dysfunction and peripheral synthesis of androgens from steroid precursors (41). As a consequence, use of glucocorticoids around puberty in hyperandrogenic state could favor abdominal visceral adiposity, insulin resistance with concomitant metabolic derangement and further exacerbation of androgen production (45). It was recently proposed a backdoor pathway for hyperandrogenism of NC-CAH with transformation of 17-OHP and progesterone into more potent androgens such as dihydrotestosterone (46) (Supplementary Table 1).
It was observed an existence of higher rates of obesity and insulin resistance in adult patients with CAH (22). Hyperandrogenism was suggested as an intrinsic hormonal imbalance in classical CAH. Life-long glucocorticoid treatments are conferring to the increased risk for obesity and cardiovascular disease (CVD). Moreover, higher doses of glucocorticoids were associated with obesity in adults irrespectively on their family predisposition to obesity (18).
Leptin and other adipokines are elevated in almost all ages of patients with classical CAH, and characterized with abdominal obesity, consequent changes in food consumption, insulin sensitivity, and energy homeostasis. Therefore, it seems that adipokines are involved in the pathogenesis of obesity in patients with CAH (47). The increase in amount of fat commenced during childhood, it is existing even in children adequately treated, and was found in young adults with CAH as well (48). However, we are lacking information on the metabolic activity of abdominal adipose tissue in CAH patients. Recently, Kim et al. (47) showed that CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of pro inflammatory visceral adipose tissue (VAT) than subcutaneous adipose tissue. This places CAH patients at even greater risk for harmful metabolic sequelae from obesity linked to CVD risk. Moreover, strong correlation was obtained between VAT and adipokines or inflammatory markers (i.e., leptin, PAI-1, and hs-CRP). These findings implicated on the association of insulin resistance and metabolic syndrome in young patients with CAH (49). Consequently, adolescents and young adults with CAH express similar low-grade inflammation as obese individuals without CAH (49).
Clinical studies based on dual x-ray absorptiometry (DXA) showed that either males or females with classic CAH exhibit higher total fat mass and reduced lean body mass than controls. In respect to therapy used, a week correlation was found for cumulative glucocorticoid dose and total fat mass in females only (50). However, there was no observed differences between males and females for body composition or obesity in either classical CAH or NC-CAH (18, 40, 47, 51) (Supplementary Table 1).
Impact of Therapies on the Disease Prevalence
In respect to the therapy used, different studies analyzing patients with classical CAH showed variation in prevalence of obesity from 16.8 to 35% on hydrocortisone doses ranging from 13.3 to 15 mg/m2/day while only one study reported prevalence of obesity of 60.7% on the dose of 19.5 mg/m2/day (50). As meta-analyses was not performed yet, it could not be suggested a linear correlation between the prevalence of obesity and increasing doses of hydrocortisone as a frequently used therapeutic modality.
Many studies analyzing patients with CAH indicate an increased prevalence of insulin resistance but very few indicated an increased prevalence of diabetes including gestational diabetes. This could be partly explained with CAH studies analyzing patients younger than 50 as age group that is not typical for development of diabetes (4). In respect to glucocorticosteroids used, a few reports on classical CAH patients are giving opposite results with elevated insulin resistance index (HOMA-IR) in 18 and 44.4% on hydrocortisone doses of 19.5 and 11.2 mg/m2/day, respectively (50).
Androgen Excess and Cardiovascular Risk
Classical CAH as hyperandrogenic state is characterized in women with increased cardiovascular risk (52). Either low or high testosterone levels have an increased risk for CVD independently of age, adiposity, ovarian function, and smoking (53). Traditional and non-traditional cardiovascular risk markers as well as their functional and morphological effects recognized throughout the surrogate indices, imply on the existence of increased cardiovascular risk and subclinical CVD in various types of women with androgen excess (52). Study by Falhammar et al. (54) on small number of patients analyzed cardiovascular and metabolic risk profiles in adult CAH males on lifelong glucocorticoid treatment. The authors showed that younger CAH males did not differ from age-matched controls while risk increased in subjects older than 30 years (54). However, we are lacking data on the frequency of established cardiovascular disease and mortality. It was shown that stroke is common in women with NC-CAH (odds ratio 5.8) while acute coronary syndrome is characteristic for males with classical CAH (odds ratio 9.9) (42). Hazard ratio of death was higher for females, and with 32% caused by cardiovascular diseases (55).
Higher concentrations of testosterone and DHEA in post-menopausal women are associated with the progression of atherosclerosis and development of hypertension (56). It was recently suggested an association of hyperandrogenism with the occurrence of inflammation and oxidative stress at the level of vascular endothelium, and concomitant renal reabsorption of sodium and water (56). Androgens have an adverse effects on insulin sensitivity, visceral adiposity and lipolysis, low-density-lipoprotein cholesterol (LDL-C) clearance, and high-density-lipoprotein cholesterol (HDL-C) concentrations (57). Moreover, androgen excess is deteriorating lipid profile making it more atherogenic through lower HDL-C, increased LDL-C level as a consequence of blunted LDL-receptor activity, or by enhanced lipoprotein lipase activity (57).
CAH is characterized by an existence of cardiovascular risk factors including dyslipidemia, obesity and insulin resistance, as well as cardiovascular outcomes as hypertension (58). There is a similarity in respect to the presence of cardiovascular risk factors in CAH patients and PCOS patients. Glucocorticoid used in high doses for the androgen suppression could induce Cushing syndrome characteristics with further aggravation of existing cardiovascular risk factors (59). Some data in children's populations showed decreased HDL-C in ~10% of both classic CAH and NC-CAH subjects (18). In another study, an association of androgen concentrations with dyslipidemia, obesity, and IR was shown in CAH patients (58) as well as elevated triglyceride concentrations confirmed in children with classical CAH on prednisone therapy (60). Moreover, prepubertal children with classical CAH could have elevated leptin and insulin levels constituting a group with increased life-long cardiovascular risk (61).
Hypertension is frequent finding in patients with classical CAH. It could be a consequence of the disease or the effect of therapy. Moreover, hypertension is considered the main cause of cardiovascular morbidity in young patients with CAH (62). In respect to the activity of the disease, elevated blood pressure was more likely diagnosed all patients with classical CAH than in NC-CAH ones, and associated with children of younger age and adult male gender, respectively (18). Moreover, deranged systolic blood pressure in children with classical CAH was characterized with higher daytime values and the absence of the nocturnal descent (63). Monitoring of blood pressure in children is of importance. Namely, it was observed an increased hypertension rate in young patients with classical CAH on fludrocortisone therapy (64). Available studies on CAH patients of different age showed similar prevalence of hypertension between males and females with CAH (18, 40, 63) with few exceptions showing more deteriorated BP in younger females likely to be related to androgen excess (50).
Carotid intima-media thickness (CIMT) is used as surrogate marker of arterial damage. It was shown that CIMT was increased in CAH patients including different age groups and independently of androgen levels, insulin levels or glucocorticoid treatment (65). Moreover, when comparing adolescents with classical CAH and NC-CAH, even those with NC-CAH may be at higher risk of having increased CIMT, possibly related to intermittent iatrogenic hypercortisolism and secondary insulin resistance (66). In respect to gender differences, there was no association between CIMT and androstenedione and 17OH progesterone in exposed females with classical CAH (51) (Supplementary Table 1).
Bone Mineral Density and Risk for Osteoporosis
Adult patients with classical CAH are shorter than average individuals in the general population by ~10 cm (17). This is caused by the parallel effects of earlier exposure to androgens causing accelerated growth rate in childhood and premature epiphyseal closure in the long bones, and suppressive effects of excessive GCS doses on the secretion of growth hormone on the other.
The age and duration-related data on the assessment of bone mineral density (BMD) in patients with CAH are varying. While some authors showed lower BMD in adults with classical CAH and NC-CAH (18) others showed differences in BMD in relation only to glucocorticoid use (67). Curiously, while GCS therapy in children did not show a decrease in BMD, significantly lower BMD was demonstrated in adult patients with CAH on GCS treatment, and specially in those having salt-wasting CAH managed with highest doses of GCS (68, 69). In respect to the drug used, lower BMD values are found in patients managed with longer-acting GCS compared to those managed with hydrocortisone (70). An additional factor influencing decrease in BMD could be the reduced levels of DHEA and DHEAS that was shown in post-menopausal women treated with long-acting GCS (68).
Apart from the assessment of height and BMD using dual energy X-ray absorptiometry, there is not an established role for the bone turnover biochemical markers in patients with CAH (69).
Use of glucocorticoids could result in long-term complications including osteoporosis and fractures (4). In respect to the CAH variant, while some authors reported normal or even better BMD in different age-groups of patients with NC-CAH in comparison to classical CAH (71, 72), other authors found similar frequency of osteoporosis in NCAH in comparison to classical CAH (18).
Osteoporosis could be expected in adults with classical CAH on chronic glucocorticoid therapy. GCS therapy is influencing the activity of osteoblasts with consequent decreased in BMD (67). In line with this is low activity of the markers of bone formation such as osteocalcin, in adults with CAH (73). Apart from the more pronounced decrease in BMD after the age of 30, an increased rate of osteoporotic fractures was shown in women with classic CAH treated with GCS (71). Moreover, males older than 30 years had lower BMD in all measured sites similarly to women of the same age (67, 71). However, in spite of lower BMD and osteocalcin concentrations in males on prednisolone therapy in comparison to the ones hydrocortisone treatment, they did not have higher frequency of fractures (67). Taking into consideration all the aspects of GCS treatment on BMD, and in spite of decreased bone turnover markers, most patients with CAH have normal BMD. Preservation of bone integrity over GCS treatment could be explained with the commonly increased body mass index, which is protective to bones, as well as with the anabolic effects of androgens in both males and females (73). However, the most likely explanation for the preserved BMD could rely in the positive net effect of the GCS type and dose adjustment during patient's follow-up (Supplementary Table 1).
Patients with NC-CAH are prone to develop metabolic consequences. Those patients are with higher rates of obesity and insulin resistance, as well as with increased rates of metabolic sequelae and cardiovascular disease during an adult period in both males and females. These patients could be at higher risk of having increased arterial intima-media thickness, possibly related to intermittent iatrogenic hypercortisolism and secondary insulin resistance. Decreased BMD and osteoporosis is not a constant finding in these patients and could depend on the sex, and type or dose of glucocorticosteroids applied.
The present work was designed by DM, VZ, JB-M, GM, and DP. The initial manuscript draft was prepared by DM and subsequently revised by VZ, J-BM, GM, and DP. All the authors approved the final submitted version.
This study was funded by the Serbian Ministry of Education, Science and Technological Development (grant numbers 175032 and 41009).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fendo.2019.00681/full#supplementary-material
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Keywords: non-classical congenital adrenal hyperplasia, metabolism, obesity, cardiovascular risk, stature, osteoporosis, glucocorticoids, antiandrogens
Citation: Macut D, Zdravković V, Bjekić-Macut J, Mastorakos G and Pignatelli D (2019) Metabolic Perspectives for Non-classical Congenital Adrenal Hyperplasia With Relation to the Classical Form of the Disease. Front. Endocrinol. 10:681. doi: 10.3389/fendo.2019.00681
Received: 31 October 2018; Accepted: 19 September 2019;
Published: 02 October 2019.
Edited by:Richard Ivell, University of Nottingham, United Kingdom
Reviewed by:Dana Manuela Savulescu, National Institute of Communicable Diseases (NICD), South Africa
Ariadni Spyroglou, University Hospital Zürich, Switzerland
Copyright © 2019 Macut, Zdravković, Bjekić-Macut, Mastorakos and Pignatelli. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Djuro Macut, email@example.com