1992
DOI: 10.1016/0140-6736(92)91594-x
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Effects of insulin-like growth factor on linear growth, head circumference, and body fat in patients with Laron-type dwarfism

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Cited by 203 publications
(100 citation statements)
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“…A modest, but significant dose dependency was observed during that first year of therapy. These findings differ somewhat from an earlier report from Ecuador, which showed no difference in 1-and 2-year growth responses to 80 vs 120 mg/kg twice a day (9). Since the Ecuador study was confined to patients homozygous for a severe mutation of GHR, characterized by markedly reduced serum concentrations of not only IGF-I but also IGF-binding protein-3 (IGFBP-3) and ALS, it is not entirely clear whether the lack of differential response to IGF-I dosage reflects limitations induced by the low serum levels of IGFBPs.…”
Section: Igf-i Therapycontrasting
confidence: 57%
See 1 more Smart Citation
“…A modest, but significant dose dependency was observed during that first year of therapy. These findings differ somewhat from an earlier report from Ecuador, which showed no difference in 1-and 2-year growth responses to 80 vs 120 mg/kg twice a day (9). Since the Ecuador study was confined to patients homozygous for a severe mutation of GHR, characterized by markedly reduced serum concentrations of not only IGF-I but also IGF-binding protein-3 (IGFBP-3) and ALS, it is not entirely clear whether the lack of differential response to IGF-I dosage reflects limitations induced by the low serum levels of IGFBPs.…”
Section: Igf-i Therapycontrasting
confidence: 57%
“…Whether expressed as mean height velocity, dheight velocity over baseline, or dheight SDS, IGF-I Rx fails to parallel results with GH therapy of GHD (9). A variety of explanations have been proposed: 1) failure to identify optimal IGF-I dosage; 2) failure of IGF-I treatment (unlike GH treatment of GHD) to normalize the typically low serum concentrations of IGFBP-3 and ALS, resulting in rapid clearance of administered IGF-I; 3) failure of injected IGF-I to fully reach the epiphyseal growth plate, compounded by the potential ability of GH to stimulate local production of IGF-I in epiphyseal chondrocytes; and 4) possible IGF-independent actions of GH on skeletal growth.…”
Section: Igf-i Therapymentioning
confidence: 99%
“…28 A growing body of data suggests that the role of the insulin growth factor family in the regulation of the early stages of hemopoiesis might be over-stated. Accordingly, mice with deletional mutations of genes encoding IGF-I, IGF-2, IGF-R and IRS-1, [39][40][41][42][43] Laron dwarf patients with drastically reduced IGF-I levels 44 or acromegalic patients with elevated IGF-I levels, all show normal erythropoiesis. 45 Moreover, the individuals with an inherited absence of INS-R, 46,47 and IGF-I 48 were found to also be hematologically normal.…”
Section: Discussionmentioning
confidence: 99%
“…Recombinant human IGF-I has been used to exert a growth-promoting effect in patients with Laron-type dwarfism [13]. It has also been used as a glucose-lowering agent in patients with extreme insulin resistance syndromes including Rabson-Mendenhall syndrome [7], type A insulin resistance [6,8], congenital generalized lipodystrophy and leprechaunism [6].…”
Section: Resultsmentioning
confidence: 99%