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- Publisher Website: 10.1210/jcem-66-3-611
- Scopus: eid_2-s2.0-0023857984
- PMID: 3127420
- WOS: WOS:A1988M305400024
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Article: Long term pulsatile growth hormone (GH)-releasing hormone therapy in children with GH deficiency
Title | Long term pulsatile growth hormone (GH)-releasing hormone therapy in children with GH deficiency |
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Authors | |
Issue Date | 1988 |
Publisher | The Endocrine Society. The Journal's web site is located at http://jcem.endojournals.org |
Citation | Journal Of Clinical Endocrinology And Metabolism, 1988, v. 66 n. 3, p. 611-617 How to Cite? |
Abstract | We treated seven GH-deficient children with 3-hourly 1 μg/kg sc pulses of GHRH-(1-44) for 6 months and 2 μg/kg·pulse for another 6 months. Four patients had a serum GH response to iv GHRH before treatment, and an additional patient responded to iv GHRH after 1 month of pulsatile sc GHRH administration. The mean cumulative growth velocity increased from a pretreatment mean of 2.7 ± 0.2 (± SE) to 8.4 ± 2.5 and 5.4 ± 0.7 cm/yr after 2 months and 1 yr of treatment, respectively. Low dose pulsatile GHRH therapy was effective in promoting growth in five of seven children, with height gain ranging from 4.4-7.5 cm at the end of 1 yr's therapy. Only one of the two patients who did not respond to GHRH had an improvement in linear growth when they were subsequently treated with synthetic GH. The other patient, a 16.5-yr-old pubertal girl who had both satisfactory GH and somatomedin-C responses during GHRH therapy, did not respond to either GHRH or, later, synthetic GH. The pretreatment serum GH response to iv GHRH, the serum somatomedin-C concentrations, and the peak serum GH response during sc GHRH therapy were not reliable predictors of clinical response. |
Persistent Identifier | http://hdl.handle.net/10722/170232 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 1.899 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Low, LCK | en_US |
dc.contributor.author | Wang, C | en_US |
dc.contributor.author | Cheung, PT | en_US |
dc.contributor.author | Ho, P | en_US |
dc.contributor.author | Lam, KSL | en_US |
dc.contributor.author | Young, RTT | en_US |
dc.contributor.author | Yeung, CY | en_US |
dc.contributor.author | Ling, N | en_US |
dc.date.accessioned | 2012-10-30T06:06:52Z | - |
dc.date.available | 2012-10-30T06:06:52Z | - |
dc.date.issued | 1988 | en_US |
dc.identifier.citation | Journal Of Clinical Endocrinology And Metabolism, 1988, v. 66 n. 3, p. 611-617 | en_US |
dc.identifier.issn | 0021-972X | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/170232 | - |
dc.description.abstract | We treated seven GH-deficient children with 3-hourly 1 μg/kg sc pulses of GHRH-(1-44) for 6 months and 2 μg/kg·pulse for another 6 months. Four patients had a serum GH response to iv GHRH before treatment, and an additional patient responded to iv GHRH after 1 month of pulsatile sc GHRH administration. The mean cumulative growth velocity increased from a pretreatment mean of 2.7 ± 0.2 (± SE) to 8.4 ± 2.5 and 5.4 ± 0.7 cm/yr after 2 months and 1 yr of treatment, respectively. Low dose pulsatile GHRH therapy was effective in promoting growth in five of seven children, with height gain ranging from 4.4-7.5 cm at the end of 1 yr's therapy. Only one of the two patients who did not respond to GHRH had an improvement in linear growth when they were subsequently treated with synthetic GH. The other patient, a 16.5-yr-old pubertal girl who had both satisfactory GH and somatomedin-C responses during GHRH therapy, did not respond to either GHRH or, later, synthetic GH. The pretreatment serum GH response to iv GHRH, the serum somatomedin-C concentrations, and the peak serum GH response during sc GHRH therapy were not reliable predictors of clinical response. | en_US |
dc.language | eng | en_US |
dc.publisher | The Endocrine Society. The Journal's web site is located at http://jcem.endojournals.org | en_US |
dc.relation.ispartof | Journal of Clinical Endocrinology and Metabolism | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Child, Preschool | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Growth Disorders - Blood - Drug Therapy | en_US |
dc.subject.mesh | Growth Hormone - Blood - Deficiency | en_US |
dc.subject.mesh | Growth Hormone-Releasing Hormone - Administration & Dosage - Therapeutic Use | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Insulin-Like Growth Factor I - Blood | en_US |
dc.subject.mesh | Male | en_US |
dc.title | Long term pulsatile growth hormone (GH)-releasing hormone therapy in children with GH deficiency | en_US |
dc.type | Article | en_US |
dc.identifier.email | Low, LCK:lcklow@hkucc.hku.hk | en_US |
dc.identifier.email | Cheung, PT:ptcheung@hkucc.hku.hk | en_US |
dc.identifier.email | Lam, KSL:ksllam@hku.hk | en_US |
dc.identifier.authority | Low, LCK=rp00337 | en_US |
dc.identifier.authority | Cheung, PT=rp00351 | en_US |
dc.identifier.authority | Lam, KSL=rp00343 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1210/jcem-66-3-611 | - |
dc.identifier.pmid | 3127420 | en_US |
dc.identifier.scopus | eid_2-s2.0-0023857984 | en_US |
dc.identifier.volume | 66 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.spage | 611 | en_US |
dc.identifier.epage | 617 | en_US |
dc.identifier.isi | WOS:A1988M305400024 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Low, LCK=7007049461 | en_US |
dc.identifier.scopusauthorid | Wang, C=7501631357 | en_US |
dc.identifier.scopusauthorid | Cheung, PT=7202595465 | en_US |
dc.identifier.scopusauthorid | Ho, P=7402211336 | en_US |
dc.identifier.scopusauthorid | Lam, KSL=8082870600 | en_US |
dc.identifier.scopusauthorid | Young, RTT=8959321900 | en_US |
dc.identifier.scopusauthorid | Yeung, CY=7201354144 | en_US |
dc.identifier.scopusauthorid | Ling, N=35500564400 | en_US |
dc.identifier.issnl | 0021-972X | - |