Delayed puberty medical therapy: Difference between revisions
/* All medical therapy options for delayed puberty at a glance{{cite journal |vauthors=Wei C, Crowne EC |title=Recent advances in the understanding and management of delayed puberty |journal=Arch. Dis. Child. |volume=101 |issue=5 |pages=481–8 |year=2... |
|||
Line 308: | Line 308: | ||
* [[hCG]] plus [[recombinant]] [[FSH]] | * [[hCG]] plus [[recombinant]] [[FSH]] | ||
| | | | ||
* [[ | * [[Subcutaneous]] or [[intramuscular]] [[hCG]] | ||
* [[ | * [[Subcutaneous]] [[FSH|FSH]] | ||
| | | | ||
* Not recommended routinely | * Not recommended routinely |
Revision as of 15:55, 3 October 2017
Delayed puberty Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Delayed puberty medical therapy On the Web |
American Roentgen Ray Society Images of Delayed puberty medical therapy |
Risk calculators and risk factors for Delayed puberty medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Eiman Ghaffarpasand, M.D. [2]
Overview
Generally, the main pharmacological medical therapy for delayed puberty is sex hormone replacement therapy. The aim of treatment is to initiate the progress of puberty and to merge the secondary sexual characteristics in patients. Regarding that the delayed puberty involve only adolescents, all of the therapy options are for them. The various formulations of estrogen, progesterone, and testosterone are used in both genders for medical therapy of delayed puberty. Other types of treatments are include low-dose oxandrolone, dihydrotestosterone (DHT), and kisspeptin agonist.
Medical Therapy
General approach to pharmacological medical therapy for delayed puberty[1]
Delayed Puberty | |||||||||||||||||||||||||||||||||||
Initial assessment | |||||||||||||||||||||||||||||||||||
• Clinical history • Physical examinations • Pubertal phenotype • Left wrist radiograph for bone age | |||||||||||||||||||||||||||||||||||
Unremarkable | Abnormal | Chronic disease | |||||||||||||||||||||||||||||||||
• Delayed puberty • Lack of growth spurt • Bone age delayed upon chronological age | • Possibility of chromosomal disorder • Bone age may delayed | • Chronic disease • Decreased growth rate or short stature • Bone age delayed upon chronological age | |||||||||||||||||||||||||||||||||
Diagnosis: • Constitutional delay of growth and puberty (CDGP) • Gonadotropin deficiency • Primary gonadal failure • Extreme athletic exercise | Diagnosis: Girls: • Turner syndrome Boys: • Klinefelter syndrome | Diagnosis: • Hypopituitarism • Chronic systemic diseases • Anorexia nervosa • Malnutrition • Kallman syndrome • Iatrogenic | |||||||||||||||||||||||||||||||||
Actions: • Evaluation hypothalamus-pituitary-gonadal axis • Consider an MRI to exclude the CNS lesions | Actions: • Chromosome analysis (Karyotyping) | Actions: • Upon the underlying disease | |||||||||||||||||||||||||||||||||
Treatment: 1. Psychologic support 2. Observation 3. Sex hormone replacement therapy | Treatment: 1. Psychologic support 2. Sex hormone replacement 3. Excision of ovaries in Turner syndrome because of risk of malignancy | ||||||||||||||||||||||||||||||||||
- Generally, the main pharmacological medical therapy for delayed puberty is sex hormone replacement therapy.
- The aim of treatment is to initiate the progress of puberty and to merge the secondary sexual characteristics in patients.
- Regarding that the delayed puberty involve only adolescents, all of the therapy options are for them.
Delayed puberty[2]
- 1 Stage 1 - Constitutional delay of growth and puberty
- 1.1 Boys
- Preferred regimen (1): Testosterone, not indicated before 14 years of age
- Initial dose: 50-100 mg IM every 4 weeks for 3-6 months
- Repeated treatment: To add 25-50 mg in dose (maximum, 100 mg per dose)
- Preferred regimen (2): Letrozole 2.5 mg PO per day
- Preferred regimen (3): Anastozole 1mg PO per day
- Preferred regimen (1): Testosterone, not indicated before 14 years of age
- 1.2 Girls
- Preferred regimen (1): Ethinyl estradiol (EE)
- Initial dose: 2 μg PO per day for 6-12 months
- Repeated treatment: Increase to 5 μg PO per day after 6-12 months
- Preferred regimen (2): 17β-estradiol (pill)
- Initial dose: 5 μg/kg PO per day for 6-12 months
- Repeated treatment: Increase to 10 μg/kg PO per day after 6-12 months
- Preferred regimen (3): 17β-estradiol (transdermal patch)
- Initial dose: 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day for 6 months
- Repeated treatment: Increase 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day every 6 months
- Preferred regimen (4): Conjugated equine estrogens (CEE)
- Initial dose: 0.1625 mg PO per day for 6-12 months
- Repeated treatment: Titrating to 0.325 mg PO per day after 6-12 months
- Alternative regimen (1): Progestogens/Progestins in various formulations, only if treatment last more than 12 months
- Preferred regimen (1): Ethinyl estradiol (EE)
- 1.1 Boys
- 2 Stage 2 - Hypogonadism
- 2.1 Pediatric
- 2.1.1 Boys
- Preferred regimen (1): Testosterone, can be started after 12 years of age
- Initial dose of 50 mg IM per month
- Increase with 50 mg in dose IM every 6-12 months
- After reaching 100-150 mg IM monthly, decrease interval to every 2 weeks
- Preferred regimen (2): Pulsatile GnRH
- Initial dose: 5-25 ng/kg/pulse SC every 90-120 min
- Continued treatment: Increase to 25-600 ng/kg/pulse SC every 90-120 min
- Alternative regimen (1): Testosterone undecanoate 1000 mg IM every 10-14 weeks
- Alternative regimen (2): Testosterone gel, apply at bed time
- Started when approximately 50% adult dose has been achieved with intramuscular testosterone
- Alternative regimen (3): hCG plus recombinant FSH
- hCG: 500 to 3000 IU SC or IM twice weekly, increased to every 2 days
- rhFSH: 75 to 225 IU SC 2-3 times weekly
- Preferred regimen (1): Testosterone, can be started after 12 years of age
- 2.1.2 Girls
- Preferred regimen (1): Ethinyl estradiol (EE)
- Initial dose: 2 μg PO per day for 6-12 months
- Repeated treatment: Increase every 6-12 months to 5 μg, 10 μg, and 20 μg PO per day
- Preferred regimen (2): 17β-estradiol (pill)
- Initial dose: 5 μg/kg PO per day for 6-12 months
- Repeated treatment: Increase to 10 μg/kg PO per day after 6-12 months, then to 15 μg/kg, and to 20μg/kg per day
- Preferred regimen (3): 17β-estradiol (transdermal patch)
- Initial dose: 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day for 6 months
- Repeated treatment: Increase 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day every 6 months
- Preferred regimen (4): Conjugated equine estrogens (CEE)
- Initial dose: 0.1625 mg PO per day for 6-12 months
- Repeated treatment: Increase every 6-12 months to 0.325, 0.45, and 0.625 mg PO per day
- Alternative regimen (1): Progestogens/Progestins in various formulations, only if treatment last more than 12 months
- Preferred regimen (1): Ethinyl estradiol (EE)
- 2.1.1 Boys
- 2.1 Adults
- 2.1.1 Male
- Preferred regimen (1): Testosterone 200 mg IM every 2 weeks
- Preferred regimen (2): Testosterone undecanoate 1000 mg IM every 10-14 weeks
- Preferred regimen (3): Testosterone gel 50-80 mg transdermal per day
- Alternative regimen (1): Pulsatile GnRH
- Initial dose: 5-25 ng/kg/pulse SC every 90-120 min
- Continued treatment: Increase to 25-600 ng/kg/pulse SC every 90-120 min
- Alternative regimen (2): hCG plus recombinant FSH
- hCG: 500 to 3000 IU SC or IM twice weekly, increased to every 2 days
- rhFSH: 75 to 225 IU SC 2-3 times weekly
- 2.1.2 Female
- Preferred regimen (1): Ethinyl estradiol (EE) 20 μg PO per day
- Preferred regimen (2): 17β-estradiol (pill) 1-2 mg PO per day
- Preferred regimen (3): 17β-estradiol (transdermal patch) 50-100 μg transdermal per day
- Preferred regimen (4): Conjugated equine estrogens (CEE) 0.625 mg PO per day
- Alternative regimen (1): Progestogens/Progestins 5-10 mg of medroxyprogesterone acetate (MPA) PO per day during the last 7 days of menstrual cycle
- Alternative regimen (2): Micronized progesterone 100-200 μg PO per day
- 2.1.1 Male
- 2.1 Pediatric
All medical therapy options for delayed puberty at a glance[2][3][4]
Group | Medicine | Route | Constitutional Delay of Growth and Puberty
(CDGP) |
Hypogonadism | Side effects | Notes | |
---|---|---|---|---|---|---|---|
Girls | Estrogen | Ethinyl estradiol (EE) | PO |
|
|
|
|
17β-estradiol | PO |
|
|
|
|||
Transdermal patch or gel
(Evorel 25 patches= 25 μg/24 h) |
|
- |
| ||||
Conjugated equine estrogens (CEE) | PO |
|
|
|
|||
Progestogens | Progestogens/Progestins | PO |
|
|
Progesterone added to induce endometrial cycling after 12-18 months of estrogen therapy:
| ||
Pulsatile GnRH |
|
SC |
|
|
- |
| |
Boys | Testosterone | IM |
|
|
|
| |
|
PO |
|
| ||||
|
Transdermal |
|
|
| |||
Aromatase inhibitors | PO |
|
|
|
| ||
PO |
|
|
- | ||||
Pulsatile GnRH |
|
SC |
|
|
- |
| |
Combination therapy |
|
|
|
|
| ||
Synthetic anabolic steroid | PO |
|
|
|
| ||
Androgen sex steroid |
|
IM |
|
|
|
Other types of treatments
Low-dose oxandrolone
- It is used in constitutional delay of growth and puberty (CDGP). The main purpose of the oxandrolone is to speed up the height growth.[3]
- The increase in the height growth velocity continues even after treatment has done.[7]
- The possibility to use earlier in the disease progress is an advantage. However, other treatment options are available if puberty is delayed later.[8]
Dihydrotestosterone (DHT)
- This drug can help patients with CDGP to develop secondary sex characteristics (Tanner II), increase lean body mass, and decreased body fat percentage; with no change in IGF-I, mean nocturnal GH, and estradiol concentrations.[9]
- Theoretically, lack of estradiol can affect the final adult height, that a child with CDGP could have in the future; like the influence of adding aromatase inhibitor.[3]
Testosterone (other therapeutic regimen)
- Recently, researchers suggested that twice monthly low doses of testosterone with gradual and periodic increase would be better for CDGP management, especially in early to middle stages of puberty.
- The protocol consists of:
- Testosterone enanthate IM 15 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 20 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 25 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 30 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 35 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 40 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 45 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 50 mg Q 2 weeks for 2 months
- Testosterone enanthate IM 60 mg Q 2 weeks for 2 months.[3]
Kisspeptin-10 agonist
- It is stimulate the hypothalamus-pituitary-gonadal (HPG) axis and play role in idiopathic hypogonadotropic hypogonadism.
- In male patients the kisspeptin agonist infusion can increase the testosterone level.[10]
Reference
- ↑ Blondell RD, Foster MB, Dave KC (1999). "Disorders of puberty". Am Fam Physician. 60 (1): 209–18, 223–4. PMID 10414639.
- ↑ 2.0 2.1 Palmert, Mark R.; Dunkel, Leo (2012). "Delayed Puberty". New England Journal of Medicine. 366 (5): 443–453. doi:10.1056/NEJMcp1109290. ISSN 0028-4793.
- ↑ 3.0 3.1 3.2 3.3 Soliman AT, De Sanctis V (2012). "An approach to constitutional delay of growth and puberty". Indian J Endocrinol Metab. 16 (5): 698–705. doi:10.4103/2230-8210.100650. PMC 3475892. PMID 23087852.
- ↑ Wei C, Crowne EC (2016). "Recent advances in the understanding and management of delayed puberty". Arch. Dis. Child. 101 (5): 481–8. doi:10.1136/archdischild-2014-307963. PMID 26353794.
- ↑ Hero M, Toiviainen-Salo S, Wickman S, Mäkitie O, Dunkel L (2010). "Vertebral morphology in aromatase inhibitor-treated males with idiopathic short stature or constitutional delay of puberty". J. Bone Miner. Res. 25 (7): 1536–43. doi:10.1002/jbmr.56. PMID 20200972.
- ↑ Wickman S, Dunkel L (2001). "Inhibition of P450 aromatase enhances gonadotropin secretion in early and midpubertal boys: evidence for a pituitary site of action of endogenous E". J. Clin. Endocrinol. Metab. 86 (10): 4887–94. doi:10.1210/jcem.86.10.7927. PMID 11600558.
- ↑ Crowne EC, Wallace WH, Moore C, Mitchell R, Robertson WH, Holly JM, Shalet SM (1997). "Effect of low dose oxandrolone and testosterone treatment on the pituitary-testicular and GH axes in boys with constitutional delay of growth and puberty". Clin. Endocrinol. (Oxf). 46 (2): 209–16. PMID 9135704.
- ↑ Joss EE, Schmidt HA, Zuppinger KA (1989). "Oxandrolone in constitutionally delayed growth, a longitudinal study up to final height". J. Clin. Endocrinol. Metab. 69 (6): 1109–15. doi:10.1210/jcem-69-6-1109. PMID 2584350.
- ↑ Saad RJ, Keenan BS, Danadian K, Lewy VD, Arslanian SA (2001). "Dihydrotestosterone treatment in adolescents with delayed puberty: does it explain insulin resistance of puberty?". J. Clin. Endocrinol. Metab. 86 (10): 4881–6. doi:10.1210/jcem.86.10.7913. PMID 11600557.
- ↑ George JT, Veldhuis JD, Tena-Sempere M, Millar RP, Anderson RA (2013). "Exploring the pathophysiology of hypogonadism in men with type 2 diabetes: kisspeptin-10 stimulates serum testosterone and LH secretion in men with type 2 diabetes and mild biochemical hypogonadism". Clin. Endocrinol. (Oxf). 79 (1): 100–4. doi:10.1111/cen.12103. PMID 23153270.