Long-Term Treatment of Central Precocious Puberty with a Long-Acting Analogue of Luteinizing Hormone-Releasing Hormone: Effects on Somatic Growth and Skeletal Maturation

The gonadotropin-releasing hormone–like agonist d-Trp 6 -Pro 9 -NEt-LHRH (LHRH a ) has been shown to induce a reversible short-term suppression of gonadotropins and gonadal steroids in patients with central precocious puberty. Since accelerated statural growth and bone maturation are clinical featur...

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Veröffentlicht in:The New England journal of medicine 1983-11, Vol.309 (21), p.1286-1290
Hauptverfasser: Mansfield, M.Joan, Beardsworth, Donna E, Loughlin, Jacquelyn S, Crawford, John D, Bode, Hans H, Rivier, Jean, Vale, Wylie, Kushner, David C, Crigler, John F, Crowley, William F
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container_end_page 1290
container_issue 21
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container_title The New England journal of medicine
container_volume 309
creator Mansfield, M.Joan
Beardsworth, Donna E
Loughlin, Jacquelyn S
Crawford, John D
Bode, Hans H
Rivier, Jean
Vale, Wylie
Kushner, David C
Crigler, John F
Crowley, William F
description The gonadotropin-releasing hormone–like agonist d-Trp 6 -Pro 9 -NEt-LHRH (LHRH a ) has been shown to induce a reversible short-term suppression of gonadotropins and gonadal steroids in patients with central precocious puberty. Since accelerated statural growth and bone maturation are clinical features of precocity not well controlled by conventional therapies, we examined the effects of prolonged LHRH a therapy for 18 consecutive months on growth and skeletal maturation in nine girls with neurogenic or idiopathic precocious puberty. Suppression of gonadotropin pulsations and gonadal steroids was maintained in all subjects. Growth velocity fell from a mean rate (±S.E.M.) of 9.35±0.64 cm per year during the 19 months before treatment to 4.58±0.60 cm per year during treatment (P
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Since accelerated statural growth and bone maturation are clinical features of precocity not well controlled by conventional therapies, we examined the effects of prolonged LHRH a therapy for 18 consecutive months on growth and skeletal maturation in nine girls with neurogenic or idiopathic precocious puberty. Suppression of gonadotropin pulsations and gonadal steroids was maintained in all subjects. Growth velocity fell from a mean rate (±S.E.M.) of 9.35±0.64 cm per year during the 19 months before treatment to 4.58±0.60 cm per year during treatment (P&lt;0.001). Bone age advanced a mean of 9.4 ±2.3 months during treatment. These changes resulted in a mean increase of 3.3 cm in predicted height (P&lt;0.01). Complete suppression of the pituitary-gonadal axis can be maintained by LHRH a therapy, resulting in slowing of excessively rapid growth and skeletal maturation and in increased predicted adult height in girls with precocious puberty. (N Engl J Med 1983; 309:1286–90.) 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Treatment with progestins and antiandrogens has controlled breast development and menstruation in the majority of female subjects but not in all of them 1 2 3 4 5 6 7 ; antiandrogens have met with similar limited success in male subjects. 2 3 4 , 6 , 7 However, . . .</description><identifier>ISSN: 0028-4793</identifier><identifier>EISSN: 1533-4406</identifier><identifier>DOI: 10.1056/NEJM198311243092104</identifier><identifier>PMID: 6415479</identifier><identifier>CODEN: NEJMAG</identifier><language>eng</language><publisher>Boston, MA: Massachusetts Medical Society</publisher><subject>Age ; Age Determination by Skeleton ; Biological and medical sciences ; Body Height - drug effects ; Bone Development - drug effects ; Child ; Child, Preschool ; Female ; Follicle Stimulating Hormone - blood ; Genital system. 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Since accelerated statural growth and bone maturation are clinical features of precocity not well controlled by conventional therapies, we examined the effects of prolonged LHRH a therapy for 18 consecutive months on growth and skeletal maturation in nine girls with neurogenic or idiopathic precocious puberty. Suppression of gonadotropin pulsations and gonadal steroids was maintained in all subjects. Growth velocity fell from a mean rate (±S.E.M.) of 9.35±0.64 cm per year during the 19 months before treatment to 4.58±0.60 cm per year during treatment (P&lt;0.001). Bone age advanced a mean of 9.4 ±2.3 months during treatment. These changes resulted in a mean increase of 3.3 cm in predicted height (P&lt;0.01). Complete suppression of the pituitary-gonadal axis can be maintained by LHRH a therapy, resulting in slowing of excessively rapid growth and skeletal maturation and in increased predicted adult height in girls with precocious puberty. (N Engl J Med 1983; 309:1286–90.) 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Treatment with progestins and antiandrogens has controlled breast development and menstruation in the majority of female subjects but not in all of them 1 2 3 4 5 6 7 ; antiandrogens have met with similar limited success in male subjects. 2 3 4 , 6 , 7 However, . . .</description><subject>Age</subject><subject>Age Determination by Skeleton</subject><subject>Biological and medical sciences</subject><subject>Body Height - drug effects</subject><subject>Bone Development - drug effects</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Follicle Stimulating Hormone - blood</subject><subject>Genital system. 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Reproduction</topic><topic>Gonadotropin-Releasing Hormone - adverse effects</topic><topic>Gonadotropin-Releasing Hormone - analogs &amp; derivatives</topic><topic>Gonadotropin-Releasing Hormone - pharmacology</topic><topic>Gonadotropin-Releasing Hormone - therapeutic use</topic><topic>Growth - drug effects</topic><topic>Growth rate</topic><topic>Humans</topic><topic>Long-Term Care</topic><topic>Luteinizing Hormone - blood</topic><topic>Medical sciences</topic><topic>Patients</topic><topic>Pharmacology. 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Since accelerated statural growth and bone maturation are clinical features of precocity not well controlled by conventional therapies, we examined the effects of prolonged LHRH a therapy for 18 consecutive months on growth and skeletal maturation in nine girls with neurogenic or idiopathic precocious puberty. Suppression of gonadotropin pulsations and gonadal steroids was maintained in all subjects. Growth velocity fell from a mean rate (±S.E.M.) of 9.35±0.64 cm per year during the 19 months before treatment to 4.58±0.60 cm per year during treatment (P&lt;0.001). Bone age advanced a mean of 9.4 ±2.3 months during treatment. These changes resulted in a mean increase of 3.3 cm in predicted height (P&lt;0.01). Complete suppression of the pituitary-gonadal axis can be maintained by LHRH a therapy, resulting in slowing of excessively rapid growth and skeletal maturation and in increased predicted adult height in girls with precocious puberty. (N Engl J Med 1983; 309:1286–90.) IN the child with precocious puberty in the absence of a correctable anatomic lesion, the goal of therapy is suppression of gonadal function in order to arrest or reverse secondary sexual development, decrease the linear growth rate to a normal prepubertal velocity, and slow skeletal maturation to prevent short stature caused by premature epiphyseal fusion. To date, no therapeutic approach has achieved all these objectives. Treatment with progestins and antiandrogens has controlled breast development and menstruation in the majority of female subjects but not in all of them 1 2 3 4 5 6 7 ; antiandrogens have met with similar limited success in male subjects. 2 3 4 , 6 , 7 However, . . .</abstract><cop>Boston, MA</cop><pub>Massachusetts Medical Society</pub><pmid>6415479</pmid><doi>10.1056/NEJM198311243092104</doi><tpages>5</tpages></addata></record>
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subjects Age
Age Determination by Skeleton
Biological and medical sciences
Body Height - drug effects
Bone Development - drug effects
Child
Child, Preschool
Female
Follicle Stimulating Hormone - blood
Genital system. Reproduction
Gonadotropin-Releasing Hormone - adverse effects
Gonadotropin-Releasing Hormone - analogs & derivatives
Gonadotropin-Releasing Hormone - pharmacology
Gonadotropin-Releasing Hormone - therapeutic use
Growth - drug effects
Growth rate
Humans
Long-Term Care
Luteinizing Hormone - blood
Medical sciences
Patients
Pharmacology. Drug treatments
Physical growth
Puberty, Precocious - drug therapy
Sexual Maturation - drug effects
Triptorelin Pamoate - analogs & derivatives
title Long-Term Treatment of Central Precocious Puberty with a Long-Acting Analogue of Luteinizing Hormone-Releasing Hormone: Effects on Somatic Growth and Skeletal Maturation
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