Ontology type: schema:ScholarlyArticle
2021-10-19
AUTHORST.G. Goetz, N. Nair, S. Shiau, R.R. Recker, J.M. Lappe, D.W. Dempster, H. Zhou, B. Zhao, X. Guo, W. Shen, T.L. Nickolas, M. Kamanda-Kosseh, M. Bucovsky, J. Stubby, E. Shane, A. Cohen
ABSTRACTSummaryWe examined serum IGF-1 in premenopausal IOP, finding relationships that were opposite to those expected: higher IGF-1 was associated with lower bone formation and higher body fat, and lower BMD response to teriparatide. These paradoxical relationships between serum IGF-1, bone, and fat may contribute to the mechanism of idiopathic osteoporosis in premenopausal women.Introduction Premenopausal women with idiopathic osteoporosis (IOP) have marked deficits in bone microarchitecture but variable bone remodeling. We previously reported that those with low tissue-level bone formation rate (BFR) are less responsive to teriparatide and have higher serum IGF-1, a hormone anabolic for osteoblasts and other tissues. The IGF-1 data were unexpected because IGF-1 is low in other forms of low turnover osteoporosis—leading us to hypothesize that IGF-1 relationships are paradoxical in IOP. This study aimed to determine whether IOP women with low BFR have higher IGF-1 and paradoxical IGF-1 relationships in skeletal and non-skeletal tissues, and whether IGF-1 and the related measures predict teriparatide response.MethodsThis research is an ancillary study to a 24 month clinical trial of teriparatide for IOP. Baseline assessments were related to trial outcomes: BMD, bone remodeling. Subjects: Premenopausal women with IOP(n = 34); bone remodeling status was defined by baseline cancellous BFR/BS on bone biopsy. Measures: Serum IGF-1 parameters, compartmental adiposity (DXA, CT, MRI), serum hormones, and cardiovascular-risk-markers related to fat distribution.ResultsAs seen in other populations, lower BFR was associated with higher body fat and poorer teriparatide response. However, in contrast to observations in other populations, low BFR, higher body fat, and poorer teriparatide response were all related to higher IGF-1: IGF-1 Z-score was inversely related to BFR at all bone surfaces (r = − 0.39 to − 0.46; p < 0.05), directly related to central fat (p = 0.05) and leptin (p = 0.03). IGF-1 inversely related to 24 month hip BMD %change (r = − 0.46; p = 0.01).ConclusionsParadoxical IGF-1 relationships suggest that abnormal or atypical regulation of bone and fat may contribute to osteoporosis mechanisms in premenopausal IOP. More... »
PAGES659-672
http://scigraph.springernature.com/pub.10.1007/s00198-021-06196-8
DOIhttp://dx.doi.org/10.1007/s00198-021-06196-8
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/34665288
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"description": "Abstract\nSummaryWe examined serum IGF-1 in premenopausal IOP, finding relationships that were opposite to those expected: higher IGF-1 was associated with lower bone formation and higher body fat, and lower BMD response to teriparatide. These paradoxical relationships between serum IGF-1, bone, and fat may contribute to the mechanism of idiopathic osteoporosis in premenopausal women.Introduction\nPremenopausal women with idiopathic osteoporosis (IOP) have marked deficits in bone microarchitecture but variable bone remodeling. We previously reported that those with low tissue-level bone formation rate (BFR) are less responsive to teriparatide and have higher serum IGF-1, a hormone anabolic for osteoblasts and other tissues. The IGF-1 data were unexpected because IGF-1 is low in other forms of low turnover osteoporosis\u2014leading us to hypothesize that IGF-1 relationships are paradoxical in IOP. This study aimed to determine whether IOP women\u00a0with low BFR have higher IGF-1 and paradoxical IGF-1 relationships in skeletal and non-skeletal tissues, and whether IGF-1 and the related measures predict teriparatide response.MethodsThis research is an ancillary study to a\u00a024\u00a0month clinical trial of teriparatide for IOP. Baseline assessments were related to trial outcomes: BMD, bone remodeling. Subjects:\u00a0Premenopausal women with IOP(n\u2009=\u200934); bone remodeling status was\u00a0defined by baseline cancellous BFR/BS on bone biopsy. Measures:\u00a0Serum IGF-1 parameters, compartmental adiposity (DXA, CT, MRI), serum hormones, and cardiovascular-risk-markers related to fat distribution.ResultsAs seen in other populations, lower BFR was associated with higher body fat and poorer teriparatide response. However, in contrast to observations in other populations, low BFR, higher body fat, and poorer teriparatide response were all related to higher IGF-1: IGF-1 Z-score was inversely related to BFR at all bone surfaces (r\u2009=\u2009\u2009\u2212\u20090.39 to\u2009\u2212\u20090.46; p\u2009<\u20090.05), directly related to central fat (p\u2009=\u20090.05) and leptin (p\u2009=\u20090.03). IGF-1 inversely related to 24\u00a0month hip BMD %change (r\u2009=\u2009\u2009\u2212\u20090.46; p\u2009=\u20090.01).ConclusionsParadoxical IGF-1 relationships suggest that abnormal or atypical regulation of bone and fat may contribute to osteoporosis mechanisms in premenopausal IOP.",
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