Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy

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Standard

Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy. / Haugaard, Steen B; Andersen, Ove; Flyvbjerg, Allan; Ørskov, Hans; Madsbad, Sten; Iversen, Johan.

I: Journal of Infection, Bind 52, Nr. 6, 2006, s. 389-398.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Haugaard, SB, Andersen, O, Flyvbjerg, A, Ørskov, H, Madsbad, S & Iversen, J 2006, 'Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy', Journal of Infection, bind 52, nr. 6, s. 389-398. https://doi.org/10.1016/j.jinf.2005.08.025

APA

Haugaard, S. B., Andersen, O., Flyvbjerg, A., Ørskov, H., Madsbad, S., & Iversen, J. (2006). Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy. Journal of Infection, 52(6), 389-398. https://doi.org/10.1016/j.jinf.2005.08.025

Vancouver

Haugaard SB, Andersen O, Flyvbjerg A, Ørskov H, Madsbad S, Iversen J. Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy. Journal of Infection. 2006;52(6):389-398. https://doi.org/10.1016/j.jinf.2005.08.025

Author

Haugaard, Steen B ; Andersen, Ove ; Flyvbjerg, Allan ; Ørskov, Hans ; Madsbad, Sten ; Iversen, Johan. / Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy. I: Journal of Infection. 2006 ; Bind 52, Nr. 6. s. 389-398.

Bibtex

@article{464d71ac4d0541d3b2f951ec0ddecee6,
title = "Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy",
abstract = "OBJECTIVES: Low-dose growth hormone (GH) administration has been suggested as a treatment for HIV-lipodystrophy. METHODS: Postglucose GH-secretion, kinetics of insulin-like growth factors (IGFs), insulin, and glucose metabolism were examined in six male HIV-infected lipodystrophic patients (two normal-weight patients with normal glucose-tolerance (NGT), two normal-weight with impaired glucose-tolerance (IGT), and two obese patients with diabetes (DM)) during a 16 weeks open-labelled pilot-study of low-dose GH, 0.7 mg/day. RESULTS: DM, compared to NGT and IGT, displayed an impaired rebound of GH during a 5h oral glucose-tolerance test. Near lower normal limits in all patients before GH-therapy, total and free IGF-I increased between 87 and 152% during the GH-therapy (P<0.001), approaching upper normal limits in all patients with the highest incremental percentages shown in DM. A slight and temporary reduction in insulin sensitivity was caused by a reduction in non-oxidative glucose metabolism (n=5). GH-administration reduced hepatic extraction of insulin alleviating the demand for insulin secretion (n=5). No adverse effects of GH were detected. CONCLUSIONS: As judged from effects on circulating IGF-I, glucose metabolism, and insulin kinetics, 0.7 mg/day of GH may be expedient for treatment of HIV-infected males with lipodystrophy. Whether the patients' glucose metabolic status matters for the IGF-response to low-dose GH-therapy awaits further investigation.",
author = "Haugaard, {Steen B} and Ove Andersen and Allan Flyvbjerg and Hans {\O}rskov and Sten Madsbad and Johan Iversen",
year = "2006",
doi = "http://dx.doi.org/10.1016/j.jinf.2005.08.025",
language = "English",
volume = "52",
pages = "389--398",
journal = "Journal of Infection",
issn = "0163-4453",
publisher = "W.B.Saunders Co. Ltd.",
number = "6",

}

RIS

TY - JOUR

T1 - Growth factors, glucose and insulin kinetics after low dose growth hormone in HIV - lipodystrophy

AU - Haugaard, Steen B

AU - Andersen, Ove

AU - Flyvbjerg, Allan

AU - Ørskov, Hans

AU - Madsbad, Sten

AU - Iversen, Johan

PY - 2006

Y1 - 2006

N2 - OBJECTIVES: Low-dose growth hormone (GH) administration has been suggested as a treatment for HIV-lipodystrophy. METHODS: Postglucose GH-secretion, kinetics of insulin-like growth factors (IGFs), insulin, and glucose metabolism were examined in six male HIV-infected lipodystrophic patients (two normal-weight patients with normal glucose-tolerance (NGT), two normal-weight with impaired glucose-tolerance (IGT), and two obese patients with diabetes (DM)) during a 16 weeks open-labelled pilot-study of low-dose GH, 0.7 mg/day. RESULTS: DM, compared to NGT and IGT, displayed an impaired rebound of GH during a 5h oral glucose-tolerance test. Near lower normal limits in all patients before GH-therapy, total and free IGF-I increased between 87 and 152% during the GH-therapy (P<0.001), approaching upper normal limits in all patients with the highest incremental percentages shown in DM. A slight and temporary reduction in insulin sensitivity was caused by a reduction in non-oxidative glucose metabolism (n=5). GH-administration reduced hepatic extraction of insulin alleviating the demand for insulin secretion (n=5). No adverse effects of GH were detected. CONCLUSIONS: As judged from effects on circulating IGF-I, glucose metabolism, and insulin kinetics, 0.7 mg/day of GH may be expedient for treatment of HIV-infected males with lipodystrophy. Whether the patients' glucose metabolic status matters for the IGF-response to low-dose GH-therapy awaits further investigation.

AB - OBJECTIVES: Low-dose growth hormone (GH) administration has been suggested as a treatment for HIV-lipodystrophy. METHODS: Postglucose GH-secretion, kinetics of insulin-like growth factors (IGFs), insulin, and glucose metabolism were examined in six male HIV-infected lipodystrophic patients (two normal-weight patients with normal glucose-tolerance (NGT), two normal-weight with impaired glucose-tolerance (IGT), and two obese patients with diabetes (DM)) during a 16 weeks open-labelled pilot-study of low-dose GH, 0.7 mg/day. RESULTS: DM, compared to NGT and IGT, displayed an impaired rebound of GH during a 5h oral glucose-tolerance test. Near lower normal limits in all patients before GH-therapy, total and free IGF-I increased between 87 and 152% during the GH-therapy (P<0.001), approaching upper normal limits in all patients with the highest incremental percentages shown in DM. A slight and temporary reduction in insulin sensitivity was caused by a reduction in non-oxidative glucose metabolism (n=5). GH-administration reduced hepatic extraction of insulin alleviating the demand for insulin secretion (n=5). No adverse effects of GH were detected. CONCLUSIONS: As judged from effects on circulating IGF-I, glucose metabolism, and insulin kinetics, 0.7 mg/day of GH may be expedient for treatment of HIV-infected males with lipodystrophy. Whether the patients' glucose metabolic status matters for the IGF-response to low-dose GH-therapy awaits further investigation.

U2 - http://dx.doi.org/10.1016/j.jinf.2005.08.025

DO - http://dx.doi.org/10.1016/j.jinf.2005.08.025

M3 - Journal article

VL - 52

SP - 389

EP - 398

JO - Journal of Infection

JF - Journal of Infection

SN - 0163-4453

IS - 6

ER -

ID: 34067749