纤瘦青春期女孩炎症标志物与骨密度之间的关系

J. Jürimäe, A. Tamm, Liina Remmel, V. Tillmann
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摘要

我们调查了常见的炎症标志物是否与瘦弱青春期女孩的骨积累有关。对34名10 ~ 12岁青春期2 ~ 4期瘦弱女孩进行了研究。测定血浆样品中的12项炎症参数[白细胞介素(IL)-2、IL-4、IL-6、IL-8、IL-10、血管内皮生长因子、干扰素-γ (IFN-γ)、肿瘤坏死因子α、IL-1α、IL-1β、单核细胞趋化蛋白-1 (MCP-1)和表皮生长因子]。采用DXA法测定全身(WB)、腰椎(LS)和股骨颈(FN)骨矿物质密度(BMD)和股骨颈(WB)骨矿物质含量(BMC)。血浆IFN-γ浓度与WB BMC (r= -0.45)、WB BMD (r= -0.46)、FN BMD (r= -0.43)呈负相关(p<0.05)。血浆IL-6 (r= -0.37;p<0.05), IL-1α (r= -0.40;p<0.05)和MCP-1 (r= -0.38;p<0.05),浓度与骨密度值呈负相关。逐步回归分析显示,IFN-γ单独和联合IL-1α分别解释了WB骨密度变异的18.6%和27.6%,IL-1α和MCP-1共同解释了LS骨密度变异的25.5%,IL-1α联合IFN-γ解释了FN骨密度变异的34.1%。综上所述,血浆中IFN-γ、IL-6、IL-1α和MCP-1浓度与骨密度相关,提示这些细胞因子可能参与了瘦型青春期女孩的骨蓄积。
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Associations between inflammatory markers and bone mineral density in lean pubertal girls
We investigated whether common inflammatory markers are associated with bone accumulation in lean pubertal girls. Thirty-four 10–12-yearold lean girls at pubertal stages 2–4 were studied. Twelve inflammatory parameters [interleukin (IL)-2, IL-4, IL-6, IL-8, IL-10, vascular endothelial growth factor, interferon-gamma (IFN-γ), tumour necrosis factoralpha, IL-1α, IL-1β, monocyte chemotactic protein-1 (MCP-1) and epidermal growth factor] were measured from plasma samples. Whole body (WB), lumbar spine (LS) and femoral neck (FN) bone mineral density (BMD), and WB bone mineral content (BMC) were assessed by DXA. Plasma IFN-γ concentration was negatively correlated (p<0.05) with WB BMC (r=–0.45), WB BMD (r=–0.46) and FN BMD (r=–0.43). In addition, plasma IL–6 (r= –0.37; p<0.05), IL-1α (r=–0.40; p<0.05) and MCP-1 (r=–0.38; p<0.05) concentrations were also negatively correlated to measured BMD values. The stepwise regression analysis showed that IFN-γ alone and together with IL-1α explained 18.6% and 27.6%, respectively, of the variability in WB BMD, while IL-1α and MCP-1 together explained 25.5% of the variability in LS BMD, and IL-1α together with IFN-γ explained 34.1% of the variability in FN BMD. In conclusion, plasma IFN-γ, IL-6, IL-1α and MCP-1 concentrations were associated with BMD variables, suggesting that these cytokines may participate in bone accumu lation in lean pubertal girls.
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