46
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Relation between Obesity and Bone Mineral Density and Vertebral Fractures in Korean Postmenopausal Women

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Purpose

          The traditional belief that obesity is protective against osteoporosis has been questioned. Recent epidemiologic studies show that body fat itself may be a risk factor for osteoporosis and bone fractures. Accumulating evidence suggests that metabolic syndrome and the individual components of metabolic syndrome such as hypertension, increased triglycerides, and reduced high-density lipoprotein cholesterol are also risk factors for low bone mineral density. Using a cross sectional study design, we evaluated the associations between obesity or metabolic syndrome and bone mineral density (BMD) or vertebral fracture.

          Materials and Methods

          A total of 907 postmenopausal healthy female subjects, aged 60-79 years, were recruited from woman hospitals in Seoul, South Korea. BMD, vetebral fracture, bone markers, and body composition including body weight, body mass index (BMI), percentage body fat, and waist circumference were measured.

          Results

          After adjusting for age, smoking status, alcohol consumption, total calcium intake, and total energy intake, waist circumference was negatively related to BMD of all sites (lumbar BMD p = 0.037, all sites of femur BMD p < 0.001) whereas body weight was still positively related to BMD of all sites ( p < 0.001). Percentage body fat and waist circumference were much higher in the fracture group than the non-fracture group ( p = 0.0383, 0.082 respectively). Serum glucose levels were postively correlated to lumbar BMD ( p = 0.016), femoral neck BMD ( p = 0.0335), and femoral trochanter BMD ( p = 0.0082). Serum high density lipoprotein cholesterol (HDLC) was positively related to femoral trochanter BMD ( p = 0.0366) and was lower in the control group than the fracture group ( p = 0.011).

          Conclusion

          In contrast to the effect favorable body weight on bone mineral density, high percentage body fat and waist circumference are related to low BMD and a vertebral fracture. Some components of metabolic syndrome were related to BMD and a vertebral fracture.

          Related collections

          Most cited references38

          • Record: found
          • Abstract: found
          • Article: not found

          Mechanisms of disease: is osteoporosis the obesity of bone?

          Osteoporosis and obesity, two disorders of body composition, are growing in prevalence. Interestingly, these diseases share several features including a genetic predisposition and a common progenitor cell. With aging, the composition of bone marrow shifts to favor the presence of adipocytes, osteoclast activity increases, and osteoblast function declines, resulting in osteoporosis. Secondary causes of osteoporosis, including diabetes mellitus, glucocorticoids and immobility, are associated with bone-marrow adiposity. In this review, we ask a provocative question: does fat infiltration in the bone marrow cause low bone mass or is it a result of bone loss? Unraveling the interface between bone and fat at a molecular and cellular level is likely to lead to a better understanding of several diseases, and to the development of drugs for both osteoporosis and obesity.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Relationship of obesity with osteoporosis.

            The relationship between obesity and osteoporosis has been widely studied, and epidemiological evidence shows that obesity is correlated with increased bone mass. Previous analyses, however, did not control for the mechanical loading effects of total body weight on bone mass and may have generated a confounded or even biased relationship between obesity and osteoporosis. The objective of this study was to reevaluate the relationship between obesity and osteoporosis by accounting for the mechanical loading effects of total body weight on bone mass. We measured whole body fat mass, lean mass, percentage fat mass, body mass index, and bone mass in two large samples of different ethnicity: 1988 unrelated Chinese subjects and 4489 Caucasian subjects from 512 pedigrees. We first evaluated the Pearson correlations among different phenotypes. We then dissected the phenotypic correlations into genetic and environmental components with bone mass unadjusted or adjusted for body weight. This allowed us to compare the results with and without controlling for mechanical loading effects of body weight on bone mass. In both Chinese and Caucasian subjects, when the mechanical loading effect of body weight on bone mass was adjusted for, the phenotypic correlation (including its genetic and environmental components) between fat mass (or percentage fat mass) and bone mass was negative. Further multivariate analyses in subjects stratified by body weight confirmed the inverse relationship between bone mass and fat mass, after mechanical loading effects due to total body weight were controlled. Increasing fat mass may not have a beneficial effect on bone mass.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              PPARgamma insufficiency enhances osteogenesis through osteoblast formation from bone marrow progenitors.

              Based on the fact that aging is associated with a reciprocal decrease of osteogenesis and an increase of adipogenesis in bone marrow and that osteoblasts and adipocytes share a common progenitor, this study investigated the role of PPARgamma, a key regulator of adipocyte differentiation, in bone metabolism. Homozygous PPARgamma-deficient ES cells failed to differentiate into adipocytes, but spontaneously differentiated into osteoblasts, and these were restored by reintroduction of the PPARgamma gene. Heterozygous PPARgamma-deficient mice exhibited high bone mass with increased osteoblastogenesis, but normal osteoblast and osteoclast functions, and this effect was not mediated by insulin or leptin. The osteogenic effect of PPARgamma haploinsufficiency became prominent with aging but was not changed upon ovariectomy. The PPARgamma haploinsufficiency was confirmed to enhance osteoblastogenesis in the bone marrow cell culture but did not affect the cultures of differentiated osteoblasts or osteoclast-lineage cells. This study demonstrates a PPARgamma-dependent regulation of bone metabolism in vivo, in that PPARgamma insufficiency increases bone mass by stimulating osteoblastogenesis from bone marrow progenitors.
                Bookmark

                Author and article information

                Journal
                Yonsei Med J
                YMJ
                Yonsei Medical Journal
                Yonsei University College of Medicine
                0513-5796
                1976-2437
                01 November 2010
                30 September 2010
                : 51
                : 6
                : 857-863
                Affiliations
                [1 ]Department of Family Medicine, Mizmedi Hospital, Seoul, Korea.
                [2 ]Graduate Program in Science for Aging, The Graduate School, Yonsei University College of Medicine, Seoul, Korea.
                [3 ]Sports and Medicine Research Center, INTOTO Inc., Seoul, Korea.
                [4 ]Department of Family Medicine, Yonsei University College of Medicine, Seoul, Korea.
                Author notes
                Corresponding author: Dr. Duk-Chul Lee, Department of Family Medicine, Yonsei University College of Medicine, 250 Seongsan-ro, Seodaemun-gu, Seoul 120-753, Korea. Tel: +82-2-2228-2330, Fax: +82-2-362-6835, faith@ 123456yuhs.ac
                Article
                10.3349/ymj.2010.51.6.857
                2995981
                20879051
                d533dcb0-106c-49cf-a0c5-212dfd434a17
                © Copyright: Yonsei University College of Medicine 2010

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 April 2010
                : 27 May 2010
                : 27 May 2010
                Categories
                Original Article
                Endocrinology & Metabolism

                Medicine
                metabolic syndrome,obesity,vertebral fracture,bone mineral density
                Medicine
                metabolic syndrome, obesity, vertebral fracture, bone mineral density

                Comments

                Comment on this article