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Open AccessJournal ArticleDOI

Vertebral bone marrow fat is positively associated with visceral fat and inversely associated with IGF-1 in obese women.

TLDR
The study showed that vertebral bone marrow fat is positively associated with visceral fat and inversely associated with IGF‐1 and BMD, which suggests that the detrimental effect of visceral fat on bone health may be mediated in part by IGF-1 as an important regulator of the fat and bone lineage.
Abstract
Recent studies have demonstrated an important physiologic link between bone and fat. Bone and fat cells arise from the same mesenchymal precursor cell within bone marrow, capable of differentiation into adipocytes or osteoblasts. Increased BMI appears to protect against osteoporosis. However, recent studies have suggested detrimental effects of visceral fat on bone health. Increased visceral fat may also be associated with decreased growth hormone (GH) and insulin-like growth factor 1 (IGF-1) levels which are important for maintenance of bone homeostasis. The purpose of our study was to assess the relationship between vertebral bone marrow fat and trabecular bone mineral density (BMD), abdominal fat depots, GH and IGF-1 in premenopausal women with obesity. We studied 47 premenopausal women of various BMI (range: 18–41 kg/m2, mean 30 ± 7 kg/m2) who underwent vertebral bone marrow fat measurement with proton magnetic resonance spectroscopy (1H-MRS), body composition, and trabecular BMD measurement with computed tomography (CT), and GH and IGF-1 levels. Women with high visceral fat had higher bone marrow fat than women with low visceral fat. There was a positive correlation between bone marrow fat and visceral fat, independent of BMD. There was an inverse association between vertebral bone marrow fat and trabecular BMD. Vertebral bone marrow fat was also inversely associated with IGF-1, independent of visceral fat. Our study showed that vertebral bone marrow fat is positively associated with visceral fat and inversely associated with IGF-1 and BMD. This suggests that the detrimental effect of visceral fat on bone health may be mediated in part by IGF-1 as an important regulator of the fat and bone lineage.

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Citations
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Journal ArticleDOI

Fate decision of mesenchymal stem cells: adipocytes or osteoblasts?

TL;DR: External factors and their signaling processes dictating the reciprocal regulation between adipocytes and osteoblasts during MSC differentiation and the ultimate control of the adipo-osteogenic balance are reviewed.
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Marrow fat and bone--new perspectives.

TL;DR: It is concluded that whereas most animal and human data demonstrate an inverse association between marrow adipose tissue and measures of bone density and strength, understanding the functional significance of marrow adiposes tissue and its hormonal determinants will be critical to better understanding its role in skeletal integrity.
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Dynamic niches in the origination and differentiation of haematopoietic stem cells

TL;DR: New insights are found that significantly improve the understanding of haematopoiesis and raise fundamental questions about what truly constitutes a stem cell niche.
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Bone marrow fat composition as a novel imaging biomarker in postmenopausal women with prevalent fragility fractures.

TL;DR: It is suggested that altered bone marrow fat composition is linked with fragility fractures and diabetes and MRS of spinal bone marrowfat may serve as a novel tool for BMD‐independent fracture risk assessment.
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New Insights into Osteoporosis: The Bone-Fat Connection

TL;DR: New insights into osteoporosis: the bone–fat connection are found in Osaka, Japan and São Paulo, Brazil.
References
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Abdominal adiposity and coronary heart disease in women

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Journal ArticleDOI

Mechanisms of disease: is osteoporosis the obesity of bone?

TL;DR: In this review, a provocative question is asked: does fat infiltration in the bone marrow cause low bone mass or is it a result of bone loss?
Journal ArticleDOI

Growth hormone and bone.

TL;DR: The biphasic model of GH action in bone remodeling is proposed, based on findings in GHD adults, and it appears that the "transition point" occurs after approximately 6 months and that a net increase of bone mass will be seen after 12-18 months of GH treatment.
Journal ArticleDOI

Growth Hormone, Insulin-Like Growth Factors, and the Skeleton

TL;DR: GH and IGF-I secretion are decreased in aging individuals, and abnormalities in the GH/IGF-I axis play a role in the pathogenesis of the osteoporosis of anorexia nervosa and after glucocorticoid exposure.
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