Lipopolysaccharide-binding protein cannot independently predict type 2 diabetes mellitus: A nested case-control study
Background Cross‐sectional studies have reported a close association between serum lipopolysaccharide‐binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to...
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| Published in | Journal of diabetes Vol. 8; no. 2; pp. 214 - 219 |
|---|---|
| Main Authors | , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Australia
Blackwell Publishing Ltd
01.03.2016
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1753-0393 1753-0407 1753-0407 |
| DOI | 10.1111/1753-0407.12281 |
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| Abstract | Background
Cross‐sectional studies have reported a close association between serum lipopolysaccharide‐binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to investigate the association between serum LBP levels and the risk of developing T2DM.
Methods
A 5‐year nested case‐control study of 3510 individuals was performed as part of the Environment, Inflammation and Metabolic Diseases Study (EIMDS). Clinical data were collected at baseline. Serum levels of LBP and other biochemical factors, such as insulin and high‐sensitivity C‐reactive protein, were detected 5 years later. Subjects were diagnosed as having T2DM on the basis of results of an oral glucose tolerance test (OGTT) and 1998 World Health Organization criteria. Controls were randomly selected to match cases according to age, gender, and body mass index (BMI) in a 1:1 ratio. Odds ratios (OR) for T2DM were calculated using conditional logistic regression analysis.
Results
Over a 5‐year follow‐up period, 255 subjects developed T2DM. There was no significant difference in serum LBP levels between the T2DM and control groups at baseline (19.78 ± 6.40 versus 20.53 ± 6.99 μg/mL; P = 0.207). Subjects were divided into three groups based on tertiles of LBP concentrations (n = 170 in each group; T1 = 1.31–17.16 μg/mL LBP; T2 = 17.21–22.37 μg/mL LBP; T3 = 22.49–40.08 μg/mL LBP). There was no significant association between the risk of developing T2DM and any of the LBP tertiles in either a simple model or after adjusting for general status and biochemical factors.
Conclusion
After matching for gender, age, and BMI, LBP does not improve prediction of the development of T2DM independently.
摘要
背景
既往的横断面研究提示脂多糖结合蛋白(lipopolysaccharide‐binding protein,LBP)与多种代谢紊乱密切相关,然而尚缺乏纵向研究来揭示LBP与2型糖尿病之间的关系。因此,本研究的目的在于探索血清LBP水平与2型糖尿病的发病风险是否相关。
方法
本研究是环境、炎症及代谢性疾病研究(Environment, Inflammation and Metabolic Diseases Study,EIMD)中的一部分。采用巢式病例对照研究的方法,于基线收集临床资料并追踪随访5年,测定基线时血清LBP、超敏C反应蛋白(high sensitive C reactive protein,hs‐CRP)及其他生物学指标水平。分别在基线和随访期间行口服75 g葡萄糖耐量试验(oral glucose tolerance test,OGTT),并根据1998年世界卫生组织(World Health Organization, WHO)标准诊断糖尿病。按1:1选取与新诊断2型糖尿病患者的性别、年龄、体质指数(body mass index,BMI)相匹配的糖耐量正常者作为对照组。采用条件logistic回归分析LBP对2型糖尿病发病风险的影响。
结果
在5年随访期间,2541名受试者中新诊断2型糖尿病为255例,2型糖尿病组与对照组基线血清LBP水平无统计学差异(19.78 ± 6.40 vs. 20.53 ± 6.99 µg/mL,P = 0.207]。根据血清LBP三分位水平将所有研究对象分为三组(每组170人;T1 = 1.31‐17.16 µg/mL LBP;T2 = 17.21‐22.37 µg/mL LBP;T3 = 22.49‐40.08 µg/mL LBP),结果提示随着LBP分位增高,血糖及2型糖尿病发生人数无明显变化。无论是未校正或是校正多因素后,2型糖尿病的发病风险均不随血清LBP水平升高而增加。
结论
在性别、年龄、BMI相匹配的情况下,血清LBP水平升高未增加2型糖尿病的发病风险。 |
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| AbstractList | Cross-sectional studies have reported a close association between serum lipopolysaccharide-binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to investigate the association between serum LBP levels and the risk of developing T2DM.BACKGROUNDCross-sectional studies have reported a close association between serum lipopolysaccharide-binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to investigate the association between serum LBP levels and the risk of developing T2DM.A 5-year nested case-control study of 3510 individuals was performed as part of the Environment, Inflammation and Metabolic Diseases Study (EIMDS). Clinical data were collected at baseline. Serum levels of LBP and other biochemical factors, such as insulin and high-sensitivity C-reactive protein, were detected 5 years later. Subjects were diagnosed as having T2DM on the basis of results of an oral glucose tolerance test (OGTT) and 1998 World Health Organization criteria. Controls were randomly selected to match cases according to age, gender, and body mass index (BMI) in a 1:1 ratio. Odds ratios (OR) for T2DM were calculated using conditional logistic regression analysis.METHODSA 5-year nested case-control study of 3510 individuals was performed as part of the Environment, Inflammation and Metabolic Diseases Study (EIMDS). Clinical data were collected at baseline. Serum levels of LBP and other biochemical factors, such as insulin and high-sensitivity C-reactive protein, were detected 5 years later. Subjects were diagnosed as having T2DM on the basis of results of an oral glucose tolerance test (OGTT) and 1998 World Health Organization criteria. Controls were randomly selected to match cases according to age, gender, and body mass index (BMI) in a 1:1 ratio. Odds ratios (OR) for T2DM were calculated using conditional logistic regression analysis.Over a 5-year follow-up period, 255 subjects developed T2DM. There was no significant difference in serum LBP levels between the T2DM and control groups at baseline (19.78 ± 6.40 versus 20.53 ± 6.99 μg/mL; P = 0.207). Subjects were divided into three groups based on tertiles of LBP concentrations (n = 170 in each group; T1 = 1.31-17.16 μg/mL LBP; T2 = 17.21-22.37 μg/mL LBP; T3 = 22.49-40.08 μg/mL LBP). There was no significant association between the risk of developing T2DM and any of the LBP tertiles in either a simple model or after adjusting for general status and biochemical factors.RESULTSOver a 5-year follow-up period, 255 subjects developed T2DM. There was no significant difference in serum LBP levels between the T2DM and control groups at baseline (19.78 ± 6.40 versus 20.53 ± 6.99 μg/mL; P = 0.207). Subjects were divided into three groups based on tertiles of LBP concentrations (n = 170 in each group; T1 = 1.31-17.16 μg/mL LBP; T2 = 17.21-22.37 μg/mL LBP; T3 = 22.49-40.08 μg/mL LBP). There was no significant association between the risk of developing T2DM and any of the LBP tertiles in either a simple model or after adjusting for general status and biochemical factors.After matching for gender, age, and BMI, LBP does not improve prediction of the development of T2DM independently.CONCLUSIONAfter matching for gender, age, and BMI, LBP does not improve prediction of the development of T2DM independently. Background Cross‐sectional studies have reported a close association between serum lipopolysaccharide‐binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to investigate the association between serum LBP levels and the risk of developing T2DM. Methods A 5‐year nested case‐control study of 3510 individuals was performed as part of the Environment, Inflammation and Metabolic Diseases Study (EIMDS). Clinical data were collected at baseline. Serum levels of LBP and other biochemical factors, such as insulin and high‐sensitivity C‐reactive protein, were detected 5 years later. Subjects were diagnosed as having T2DM on the basis of results of an oral glucose tolerance test (OGTT) and 1998 World Health Organization criteria. Controls were randomly selected to match cases according to age, gender, and body mass index (BMI) in a 1:1 ratio. Odds ratios (OR) for T2DM were calculated using conditional logistic regression analysis. Results Over a 5‐year follow‐up period, 255 subjects developed T2DM. There was no significant difference in serum LBP levels between the T2DM and control groups at baseline (19.78 ± 6.40 versus 20.53 ± 6.99 μg/mL; P = 0.207). Subjects were divided into three groups based on tertiles of LBP concentrations (n = 170 in each group; T1 = 1.31–17.16 μg/mL LBP; T2 = 17.21–22.37 μg/mL LBP; T3 = 22.49–40.08 μg/mL LBP). There was no significant association between the risk of developing T2DM and any of the LBP tertiles in either a simple model or after adjusting for general status and biochemical factors. Conclusion After matching for gender, age, and BMI, LBP does not improve prediction of the development of T2DM independently. 摘要 背景 既往的横断面研究提示脂多糖结合蛋白(lipopolysaccharide‐binding protein,LBP)与多种代谢紊乱密切相关,然而尚缺乏纵向研究来揭示LBP与2型糖尿病之间的关系。因此,本研究的目的在于探索血清LBP水平与2型糖尿病的发病风险是否相关。 方法 本研究是环境、炎症及代谢性疾病研究(Environment, Inflammation and Metabolic Diseases Study,EIMD)中的一部分。采用巢式病例对照研究的方法,于基线收集临床资料并追踪随访5年,测定基线时血清LBP、超敏C反应蛋白(high sensitive C reactive protein,hs‐CRP)及其他生物学指标水平。分别在基线和随访期间行口服75 g葡萄糖耐量试验(oral glucose tolerance test,OGTT),并根据1998年世界卫生组织(World Health Organization, WHO)标准诊断糖尿病。按1:1选取与新诊断2型糖尿病患者的性别、年龄、体质指数(body mass index,BMI)相匹配的糖耐量正常者作为对照组。采用条件logistic回归分析LBP对2型糖尿病发病风险的影响。 结果 在5年随访期间,2541名受试者中新诊断2型糖尿病为255例,2型糖尿病组与对照组基线血清LBP水平无统计学差异(19.78 ± 6.40 vs. 20.53 ± 6.99 µg/mL,P = 0.207]。根据血清LBP三分位水平将所有研究对象分为三组(每组170人;T1 = 1.31‐17.16 µg/mL LBP;T2 = 17.21‐22.37 µg/mL LBP;T3 = 22.49‐40.08 µg/mL LBP),结果提示随着LBP分位增高,血糖及2型糖尿病发生人数无明显变化。无论是未校正或是校正多因素后,2型糖尿病的发病风险均不随血清LBP水平升高而增加。 结论 在性别、年龄、BMI相匹配的情况下,血清LBP水平升高未增加2型糖尿病的发病风险。 Cross-sectional studies have reported a close association between serum lipopolysaccharide-binding protein (LBP) and many metabolic disorders. However, no longitudinal study has explored the relationship between LBP and type 2 diabetes mellitus (T2DM). The aim of the present study was to investigate the association between serum LBP levels and the risk of developing T2DM. A 5-year nested case-control study of 3510 individuals was performed as part of the Environment, Inflammation and Metabolic Diseases Study (EIMDS). Clinical data were collected at baseline. Serum levels of LBP and other biochemical factors, such as insulin and high-sensitivity C-reactive protein, were detected 5 years later. Subjects were diagnosed as having T2DM on the basis of results of an oral glucose tolerance test (OGTT) and 1998 World Health Organization criteria. Controls were randomly selected to match cases according to age, gender, and body mass index (BMI) in a 1:1 ratio. Odds ratios (OR) for T2DM were calculated using conditional logistic regression analysis. Over a 5-year follow-up period, 255 subjects developed T2DM. There was no significant difference in serum LBP levels between the T2DM and control groups at baseline (19.78 ± 6.40 versus 20.53 ± 6.99 μg/mL; P = 0.207). Subjects were divided into three groups based on tertiles of LBP concentrations (n = 170 in each group; T1 = 1.31-17.16 μg/mL LBP; T2 = 17.21-22.37 μg/mL LBP; T3 = 22.49-40.08 μg/mL LBP). There was no significant association between the risk of developing T2DM and any of the LBP tertiles in either a simple model or after adjusting for general status and biochemical factors. After matching for gender, age, and BMI, LBP does not improve prediction of the development of T2DM independently. |
| Author | Zhu, Qibo Hu, Jinbo Wang, Yue Zhen, Qianna Yang, Shumin Gao, Rufei Zhou, Huang Zhang, Yi Lv, Qiong Li, Qifu Liu, Lulu |
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| Keywords | endotoxinemia 内毒素血症 脂多糖结合蛋白 lipopolysaccharide-binding protein 风险 risk 糖尿病 diabetes |
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Arch Intern Med. 2003; 163: 93-99. – volume: 36 start-page: 1442 year: 2012 end-page: 1449 article-title: Circulating lipopolysaccharide‐binding protein (LBP) as a marker of obesity‐related insulin resistance publication-title: Int J Obes (Lond) – volume: 22 start-page: 1971 year: 1999 end-page: 1977 article-title: Body mass index, diabetes, and C‐reactive protein among U.S. adults publication-title: Diabetes Care – volume: 26 start-page: 1745 year: 2003 end-page: 1751 article-title: Inflammatory markers, adiponectin, and risk of type 2 diabetes in the Pima Indian publication-title: Diabetes Care – volume: 15 start-page: 1546 year: 2009 end-page: 1558 article-title: The role of the gut microbiota in energy metabolism and metabolic disease publication-title: Curr Pharm Des – volume: 11 start-page: 69 year: 2005 end-page: 84 article-title: Detoxifying endotoxin: Time, place and person publication-title: J Endotoxin Res – volume: 36 start-page: 166 year: 2013 end-page: 175 article-title: Inflammatory markers and risk of type 2 diabetes publication-title: Diabetes Care – volume: 357 start-page: 1100 year: 2007 end-page: 1106 article-title: Search of type 2 diabetes susceptibility gene on chromosome 20q publication-title: Biochem Biophys Res Commun – volume: 63 start-page: 253 year: 1995 end-page: 258 article-title: Reconstituted high‐density lipoprotein neutralizes Gram‐negative bacterial lipopolysaccharides in human whole blood publication-title: Infect Immun – volume: 31 start-page: 1410 year: 2008 end-page: 1415 article-title: Adipokines and incident type 2 diabetes in an Aboriginal Canadian [corrected] population: The Sandy Lake Health and Diabetes Project publication-title: Diabetes Care – volume: 69 start-page: 6942 year: 2001 end-page: 6950 article-title: Dual role of lipopolysaccharide (LPS)‐binding protein in neutralization of LPS and enhancement of LPS‐induced activation of mononuclear cells publication-title: Infect Immun – volume: 184 start-page: 1601 year: 1996 end-page: 1608 article-title: Antiinflammatory effects of reconstituted high‐density lipoprotein during human endotoxemia publication-title: J Exp Med – volume: 86 start-page: 1286 year: 2007 end-page: 1292 article-title: A high fat meal induces low‐grade endotoxemia: Evidence of a novel mechanism of postprandial inflammation publication-title: Am J Clin Nutr – volume: 95 start-page: 2111 year: 1995 end-page: 2119 article-title: The expression of tumor necrosis factor in human adipose tissue. Regulation by obesity, weight loss and relationship to lipoprotein lipase publication-title: J Clin Invest – volume: 7 start-page: e36868 year: 2012 article-title: Combined use of serum adiponectin and tumor necrosis factor‐alpha receptor 2 levels was comparable to 2‐hour post‐load glucose in diabetes prediction publication-title: PLoS ONE – volume: 8 start-page: e54600 year: 2013 article-title: Determinants of serum concentrations of lipopolysaccharide‐binding protein (LBP) in the adult population: The role of obesity publication-title: PLoS ONE – volume: 851 start-page: 416 year: 1998 end-page: 421 article-title: Limitations of the amebocyte lysate test in demonstrating circulating lipopolysaccharides publication-title: Ann N Y Acad Sci – volume: 108 start-page: 485 year: 2001 end-page: 493 article-title: Plasma CD14 decreases monocyte responses to LPS by transferring cell‐bound LPS to plasma lipoproteins publication-title: J Clin Invest – volume: 30 start-page: 854 year: 2007 end-page: 860 article-title: Sex differences in the prediction of type 2 diabetes by inflammatory markers: Results from the MONICA/KORA Augsburg case‐cohort study, 1984–2002 publication-title: Diabetes Care – volume: 52 start-page: 1040 year: 2009 end-page: 1047 article-title: Association of C‐reactive protein with type 2 diabetes: Prospective analysis and meta‐analysis publication-title: Diabetologia – volume: 15 start-page: 539 year: 1998 end-page: 553 article-title: Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus: Provisional report of a WHO consultation publication-title: Diabet Med – volume: 31 start-page: 785 year: 2003 end-page: 790 article-title: Bactericidal/permeability‐increasing protein (BPI) and lipopolysaccharide‐binding protein (LBP): Structure, function and regulation in host defence against Gram‐negative bacteria publication-title: Biochem Soc Trans – volume: 33 start-page: 1925 year: 2010 end-page: 1932 article-title: A marker of endotoxemia is associated with obesity and related metabolic disorders in apparently healthy Chinese publication-title: Diabetes Care – volume: 286 start-page: 327 year: 2001 end-page: 334 article-title: C‐Reactive protein, interleukin 6, and risk of developing type 2 diabetes mellitus publication-title: JAMA – volume: 163 start-page: 93 year: 2003 end-page: 99 article-title: C‐Reactive protein as a predictor for incident diabetes mellitus among middle‐aged men: Results from the MONICA Augsburg cohort study, 1984–1998 publication-title: Arch Intern Med – volume: 270 start-page: 5320 year: 1995 end-page: 5326 article-title: Lipopolysaccharide (LPS) signal transduction and clearance. Dual roles for LPS binding protein and membrane CD14 publication-title: J Biol Chem – volume: 203 start-page: 494 year: 2009 end-page: 502 article-title: Ethnic and sex differences in circulating endotoxin levels: A novel marker of atherosclerotic and cardiovascular risk in a British multi‐ethnic population publication-title: Atherosclerosis – volume: 264 start-page: 10867 year: 1989 end-page: 10871 article-title: Identification of a lipid A binding site in the acute phase reactant lipopolysaccharide binding protein publication-title: J Biol Chem – volume: 34 start-page: 1809 year: 2011 end-page: 1815 article-title: Bacterial endotoxin activity in human serum is associated with dyslipidemia, insulin resistance, obesity, and chronic inflammation publication-title: Diabetes Care – volume: 1 start-page: 4 year: 2006 end-page: 12 article-title: Recent advances in the relationship between obesity, inflammation, and insulin resistance publication-title: Eur Cytokine Netw – volume: 25 start-page: 1172 year: 2002 end-page: 1176 article-title: C‐Reactive protein, diabetes, and attendance at religious services publication-title: Diabetes Care – volume: 26 start-page: 2754 year: 2003 end-page: 2757 article-title: Elevated C‐reactive protein is a risk factor for the development of type 2 diabetes in Japanese Americans publication-title: Diabetes Care |
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Cross‐sectional studies have reported a close association between serum lipopolysaccharide‐binding protein (LBP) and many metabolic disorders.... Cross-sectional studies have reported a close association between serum lipopolysaccharide-binding protein (LBP) and many metabolic disorders. However, no... |
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| SubjectTerms | Acute-Phase Proteins Aged Body Mass Index C-Reactive Protein - metabolism Carrier Proteins - blood Case-Control Studies diabetes Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - diagnosis endotoxinemia Female Glucose Tolerance Test Humans Insulin - blood lipopolysaccharide-binding protein Logistic Models Male Membrane Glycoproteins - blood Middle Aged Predictive Value of Tests Prognosis risk Risk Assessment Risk Factors Time Factors 内毒素血症 糖尿病 脂多糖结合蛋白 风险 |
| Title | Lipopolysaccharide-binding protein cannot independently predict type 2 diabetes mellitus: A nested case-control study |
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