Serum Preadipocyte Factor 1 Levels Are Not Associated with Bone Mineral Density among Healthy Postmenopausal Korean Women

被引:1
作者
Choi, Hoon Sung [1 ]
Kim, Sang-Wook [1 ]
Cho, Eun-Hee [1 ]
机构
[1] Kangwon Natl Univ, Dept Internal Med, Sch Med, Chunchon, South Korea
关键词
Preadipocyte factor 1; Postmenopausal women; Bone density; Osteoporosis; FACTOR-I LEVELS; ANOREXIA-NERVOSA; OSTEOPOROSIS; ADIPOSITY; MECHANISM; STRENGTH; ESTROGEN; PREF-1; CELLS; FAT;
D O I
10.3803/EnM.2017.32.1.124
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Multipotent mesenchymal stem cells can differentiate into adipocytes or osteoblasts through closely regulated lineagecontrol processes. However, adipocyte precursor cells release preadipocyte factor 1 (Pref-1), which inhibits the differentiation of mesenchymal stem cells into mature adipocytes and osteoblasts. Previous studies have also reported an inverse association between Pref-1 levels and bone mineral density (BMD) among patients with anorexia nervosa. Methods: In this retrospective study, we examined the correlations between Pref-1 levels and BMD among 124 healthy postmenopausal women (>50 years old). The patients had provided information regarding their clinical characteristics, and underwent blood testing and serum Pref-1 testing. Results: The subjects' mean age was 59.9 +/- 7.1 years and the median time since menopause onset was 9.1 years. A history of osteoporotic fracture was identified in 23 subjects (19%). Serum Pref-1 levels were not significantly correlated with BMD values at the lumbar spine (R-2=0.038, P=0.109), femur neck (R-2=0.017, P=0.869), and total hip (R-2=0.041, P=0.09), and multivariate analyses with adjustment for age and body mass index also did not detect any significant correlations. Subgroup analyses according to a history of fracture also did not detect significant associations between Pref-1 levels and BMD values. Conclusion: In our study population, it does not appear that serum Pref-1 levels are significantly associated with BMD values and osteoporosis.
引用
收藏
页码:124 / 128
页数:5
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