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2型糖尿病患者血清铁蛋白水平与体脂分布的相关性分析OA北大核心CSTPCD

Association between serum ferritin levels and body fat distribution in patients with type 2 diabetes mellitus

中文摘要英文摘要

目的 探讨2型糖尿病(T2DM)患者血清铁蛋白水平与体脂分布的关系.方法 收集2020年6-11月在兰州大学第一医院内分泌科住院的151例T2DM患者进行回顾性分析.所有患者根据血清铁蛋白水平分为高血清铁蛋白组(n=50)与正常血清铁蛋白组(n=101).测量两组患者的血糖、血脂,以及内脏脂肪面积(VFA)、皮下脂肪面积(SFA)、肝脂肪、身高、体重和腰围(WC),计算体重指数(BMI)和内脏肥胖指数(VAI),并进行组间比较;采用Pearson或Spearman相关性分析及多元线性回归分析血清铁蛋白水平与体脂分布的相关性.结果 高血清铁蛋白组VAI和WC均明显高于正常血清铁蛋白组[分别为3.13(2.16,4.58)vs.2.66(1.66,3.81),(96.66±7.78)cm vs.(91.96±9.75)cm,P<0.05].高血清铁蛋白组中心性肥胖和血脂异常的患病率明显高于正常血清铁蛋白组(分别为88.0%vs.68.3%,90.0%vs.75.2%,P<0.05),且血糖控制差、胰岛素抵抗的构成比也高于正常血清铁蛋白组(分别为96.0%vs.78.2%、62.0%vs.40.6%,P<0.05),而两组间BMI、VFA、SFA水平,以及降糖药物使用情况和糖尿病慢性并发症差异无统计学意义(P>0.05).T2DM患者血清铁蛋白水平与VAI、WC、三酰甘油(TG)、空腹血糖(FPG)、糖化血红蛋白(HbA1c)、血脂异常、血清肌酐(SCr)呈正相关(r=0.171、0.207、0.187、0.243、0.270、0.162、0.162,P<0.05),与年龄、性别和糖尿病病程呈负相关(r=-0.191、-0.434、-0.352,P<0.05).多元线性回归显示,在男性T2DM患者中,糖尿病病程和FPG是血清铁蛋白水平增高的危险因素,但WC及VAI对血清铁蛋白的影响不明显;而在女性T2DM患者中,糖尿病病程、TG和VAI是血清铁蛋白水平增高的危险因素(P<0.05).结论 女性T2DM患者的血脂紊乱和内脏脂肪增加是血清铁蛋白水平增高的危险因素.

Objective To explore the relationship between serum ferritin levels and body fat distribution in patients with type 2 diabetes mellitus(T2DM).Methods A retrospective analysis was conducted on 151 patients with T2DM who were hospitalized in the Department of Endocrinology of the First Hospital of Lanzhou University from June to November 2020,and all the patients were divided into high serum ferritin(n=50)and normal serum ferritin(n=101)groups according to their serum ferritin levels.The visceral fat area(VFA),subcutaneous fat area(SFA),liver fat,height,weight and waist circumference(WC)were measured,as well as blood glucose,lipid indexes,body mass index(BMI)and visceral adiposity index(VAI)were also calculated.t-test or nonparametric test was used to compare the differences between the two groups,and the relationship between serum ferritin levels and body fat distribution was analyzed by Pearson or Spearman correlation analysis,multiple linear regression and logistic regression.Results The VAI and WC were significantly higher in high serum ferritin group[3.13(2.16,4.58)and(96.66±7.78)cm]than in normal serum ferritin group[2.66(1.66,3.81)and(91.96±9.75)cm,P<0.05].The prevalence of central obesity and dyslipidemia was higher in high serum ferritin group(88.0%and 90.0%)than in normal serum ferritin group(68.3%and 75.2%);and the composition ratios of poor glycemic control and insulin resistance(96.0%and 62.0%)were also higher than in normal serum ferritin group(78.2%and 40.6%)(P<0.05),there were no statistically significant differences in BMI,VFA,and SFA levels,as well as antidiabetic drug use and chronic complications of diabetes mellitus between the two groups(P>0.05).Serum ferritin levels in T2DM patients were positively correlated with VAI,WC,triglyceride(TG),fasting blood glucose(FPG),HbA1c,dyslipidemia and serum creatinine(r=0.171,0.207,0.187,0.243,0.270,0.162,0.162;P<0.05),and negatively correlated with age,sex and diabetes course(r=-0.191,-0.434,-0.352;P<0.05).Multivariate linear regression analysis showed that in male T2DM patients,duration of diabetes and FPG were risk factors for increased levels of serum ferritin.However,WC and VAI did not significantly affect serum ferritin levels.In female patients with T2DM,the course of diabetes,TG and VAI were the factors influencing serum ferritin(P<0.05).Conclusion Dyslipidemia and visceral fat accumulation are risk factors for elevated serum ferritin levels in female T 2DM patients.

陈重阳;吕小羽;赵阳婷;刘露霞;王亚雯;李凯;刘靖芳

兰州大学第一临床医学院,甘肃兰州 730000兰州大学第一临床医学院,甘肃兰州 730000||兰州大学第一医院内分泌科,甘肃兰州 730000

临床医学

糖尿病,2型血清铁蛋白体脂分布内脏肥胖指数胰岛素抵抗

diabetes mellitus,type 2serum ferritinbody fat distributionvisceral obesity indexinsulin resistance

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This work was supported by the National Natural Science Foundation of China(81960155),the Natural Science Foundation of Gansu Province(20JR10RA690),and the Internal Hospital Foundation of the First Hospital of Lanzhou University(ldyyyn2020-01) 国家自然科学基金(81960155);甘肃省自然科学基金(20JR10RA690);兰州大学第一医院院内基金(ldyyyn2020-01)

10.11855/j.issn.0577-7402.2403.2023.1031

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