The Association of Omentin Levels in Non-Diabetic Postmenopausal Women with Bone Mineral Density and Total Body Composition

Objectives: Positive relation between body mass and bone mineral density (BMD) is thought to be due to weight bearing effect. However, adipose tissue derived adipokines may have important effects on bone. Obese women have decreased levels of omentin in circulation which is related with adverse metabolic events. The hypothesis was that performed in this study, we aimed to study the association of omentin levels with body composition and BMD in non-diabetic postmenopausal women. Methods: Postmenopausal women aged 40 to 70 years, scheduled for BMD testing were prospectively evaluated. Patients with known diabetes, chronic renal failure, chronic liver disease, malabsorption, inflammatory bowel disease, 70 years of age were excluded. BMD and body composition were measured by DXA (GE-Lunar DPX pro). Fasting blood samples were obtained for analysis of complete blood count, glucose, creatinine, lipid profile and omentin. Statistical analyses were performed by using SPSS version 18 for windows. P<0.05 was considered statistically significant. Results: Mean age of the patients in the osteoporosis group was higher than that of the control group (59.1±7.6 vs 53.3±5.7, p<0.05). Mean omentin level was higher in osteoporosis group than in osteopenia and control groups (479.7±141.6 vs 342.3±173.6 and 346.8±127.2, p<0.05). Total body fat mass, muscle mass and the T score of lumbar spine had a negative correlation with omentin levels (r=-0.252, -0.276, -0.344, p<0.05). Conclusions: Body composition does not seem to effect omentin levels. Women with a lower BMI have increased omentin levels. Higher omentin levels are associated with lower T scores at the lumbar spine.

[1]  J. Nilsson,et al.  Low BMD is an independent predictor of fracture and early menopause of mortality in post-menopausal women--a 34-year prospective study. , 2013, Maturitas.

[2]  Tie-Jian Jiang,et al.  Relationship between serum omentin-1 level and bone mineral density in girls with anorexia nervosa , 2013, Journal of Endocrinological Investigation.

[3]  B. Larijani,et al.  Omentin-1, visfatin and adiponectin levels in relation to bone mineral density in Iranian postmenopausal women. , 2012, Bone.

[4]  G. Shao,et al.  Study on Bone Density at Various Skeletal Sites for the Diagnosis of Primary Osteoporosis , 2012, Cell Biochemistry and Biophysics.

[5]  E. Liao,et al.  Omentin-1 exerts bone-sparing effect in ovariectomized mice , 2012, Osteoporosis International.

[6]  S. Tang,et al.  Omentin inhibits osteoblastic differentiation of calcifying vascular smooth muscle cells through the PI3K/Akt pathway , 2011, Amino Acids.

[7]  I. Nabipour,et al.  Correlation of Circulating Omentin-1 with Bone Mineral Density in Multiple Sclerosis: The Crosstalk between Bone and Adipose Tissue , 2011, PloS one.

[8]  Jay J Cao Effects of obesity on bone metabolism , 2011, Journal of orthopaedic surgery and research.

[9]  C. Richart,et al.  New adipokines vaspin and omentin. Circulating levels and gene expression in adipose tissue from morbidly obese women , 2011, BMC Medical Genetics.

[10]  A. Shuldiner,et al.  Omentin Plasma Levels and Gene Expression Are Decreased in Obesity , 2007, Diabetes.

[11]  D. Balzi,et al.  Is insulin an anabolic agent in bone? Dissecting the diabetic bone for clues. , 2005, American journal of physiology. Endocrinology and metabolism.

[12]  J J Anderson,et al.  Effects of weight and body mass index on bone mineral density in men and women: The framingham study , 1993, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[13]  Jiyin Zhou,et al.  Omentin: linking metabolic syndrome and cardiovascular disease. , 2014, Current vascular pharmacology.

[14]  M. Tosun Sample Dilution in Omentin Measurement , 2012 .

[15]  H. Xie,et al.  Relationships between serum adiponectin, leptin, resistin, visfatin levels and bone mineral density, and bone biochemical markers in Chinese men. , 2008, Clinica chimica acta; international journal of clinical chemistry.