脂质运载蛋白2和老年2型糖尿病患者骨密度和骨转换标志物的相关性研究
The association of serum lipocalin 2 with bone mineral density and bone turnover marker in elderly patients with type 2 diabetes mellitus
  
DOI:10.3969/j.issn.1006-7108.2018.06.004
中文关键词:  脂质运载蛋白2  2型糖尿病  骨密度  骨转换标志物  老年  骨质疏松
英文关键词:Lipocalin 2  Type 2 diabetes mellitus  Bone mineral density  Bone turnover marker  Elderly  Osteoporosis
基金项目:国家自然科学基金青年基金(81100558);国家重点研发计划(2016YFB1000905);安徽省中央引导地方科技发展专项资金(2017070802D147);安徽省公益性技术应用研究联动计划(1704f0804012)
作者单位
王炜1,2* 叶山东1,2 钱立庭3 任安1 陈超1 邢学农1 李素梅1 徐将1 刘茜1 周婉1 1.中国科学技术大学附属第一医院(安徽省立医院)内分泌科安徽 合肥 230001 2.中国科学技术大学附属第一医院(安徽省立医院)糖尿病研究室安徽 合肥 230001 3.中国科学技术大学附属第一医院(安徽省立医院)肿瘤放疗科安徽 合肥 230001 
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中文摘要:
      目的 探讨脂质运载蛋白2(lipocalin 2,LCN2)对老年2型糖尿病(type 2 diabetes mellitus,T2DM)患者骨代谢的影响。方法 研究对象共119例,其中84例为老年T2DM患者,35例为非T2DM对照。采取静脉血检测空腹血糖(serum fasting glucose,FPG)、糖化血红蛋白(glycosylated hemoglobin,HbAlc)、25-羟维生素D3[25(OH)D3]、I型胶原交联羧基末端肽(collagen type 1 cross-linked C-telopeptide,CTX)、Ⅰ型前胶原氨基端延长肽(type 1 N-terminal procollagen,P1NP)、全段甲状旁腺素以及肌酐、血钙(Ca)、血磷(P)等指标,用ELISA法检测血清LCN2。用双能X线骨密度仪检测股骨颈和腰椎1~4(L1~4)的骨密度(bone mineral density,BMD)。结果 老年T2DM患者血清LCN2水平高于非T2DM对照组(197.13±42.15 ng/mL vs 172.29±54.71,P=0.01)。按照血清LCN2水平三分位数将T2DM患者分为3组。其中腰椎BMD、股骨颈BMD、P1NP和CTX伴随LCN2水平增高而增高,而FPG和HbA1c伴随LCN2水平增高而降低(所有趋势P<0.05)。Pearson相关性分析显示,LCN2和T2DM患者BMD呈正相关(股骨颈:r=0.350,P=0.001;腰椎:r=0.355,P=0.001),和骨转换标志物呈正相关(P1NP:r=0.354,P=0.001;CTX:r=0.438,P<0.001),和糖代谢指标呈负相关(FPG:r=-0.321,P=0.003;HbA1c:r=-0.342,P=0.002)。进一步回归分析显示,LCN2是T2DM患者腰椎BMD的影响因素(P<0.05)。结论 血清LCN2水平和老年T2DM患者骨代谢相关,LCN2水平增高可能有助于BMD的增加。
英文摘要:
      Objective This study was aimed to explore the relationship between lipocalin 2 (LCN2) and bone mineral density (BMD) as well as bone turnover marker (BTM) in elderly patients with type 2 diabetes mellitus (T2DM). Methods A total of 119 subjects were included in this study, including 84 elderly patients with T2DM and 35 non-T2DM subjects as control. The BMDs of the lumbar spine 1-4 and femoral neck were measured using duaI energy X-ray absorptiometry. Venous blood samples were collected and serum 25-hydroxyvitamin D3 (25-OH-D3), fasting plasma glucose (FPG), type 1 N-terminal procollagen (P1NP), collagen type 1 cross-linked C-telopeptide (CTX) and other biochemical parameters were assayed. Results Serum LCN2 levels were significantly higher in T2DM subjects than those without T2DM (197.13±42.15 vs.172.29 ±54.71 ng/mL, P=0.01). The subjects were divided into three groups according to tertiles of serum LCN2 level. With the increase in LCN2 levels, both BMDs and BTMs increased significantly (all P<0.05). LCN2 positively correlated with BMDs (femoral neck: r=0.350, P=0.001; lumbar spine: r=0.355, P=0.001), and BTMs (P1NP, r=0.354, P=0.001; CTX, r=0.438, P<0.001), and negatively correlated with the indexes of glucose metabolism (FPG, r=-0.321; P=0.003; HbA1c, r=-0.342, P=0.002). Regression analysis showed that LCN2 was an independent predictor for lumbar spine BMD (P<0.05). Conclusion LCN2 was related to bone metabolism in elderly patients with T2DM and increased LCN2 was associated with higher BMD.
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