Changes of serum omentin-1 levels in normal subjects and in patients with impaired glucose regulation and with newly diagnosed and untreated type 2 diabetes

被引:331
作者
Pan, Hong-Yan [1 ]
Guo, Lin [1 ]
Li, Qiang [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Endocrinol & Metab, Harbin 150086, Heilongjiang, Peoples R China
关键词
Omentin-1; Insulin resistance; Type; 2; diabetes; TUMOR-NECROSIS-FACTOR; ADIPOSE-TISSUE; FACTOR-ALPHA; ADIPONECTIN SECRETION; SUSCEPTIBILITY GENES; INSULIN; INTERLEUKIN-6; EXPRESSION; ADIPOKINES; RESISTIN;
D O I
10.1016/j.diabres.2010.01.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To assay the levels of serum omentin-1 in subjects with different levels of glucose regulation and to analyze the relationship between serum omentin-1 levels and body mass index (BMI), glycoslated hemoglobin (HbA1c), plasma glucose, insulin resistance index (HOMA-IR), TNF-alpha and IL-6 levels. Methods: Forty-six patients with impaired glucose regulation (IGR), 55 patients with newly diagnosed and untreated type 2 diabetes mellitus (T2DM), and 50 subjects with normal glucose tolerance (NGT) were enrolled in this study. The levels of serum omentin-1 and plasma glucose at fasting and at 2 h after glucose load and fasting serum levels of TNF-alpha, IL-6, insulin, and HbA1c were measured. HOMA-IR was calculated. Results: The levels of serum omentin-1 were lower in the IGR and T2DM groups than in the NGT group. Within groups, omentin-1 levels were no significant difference before and after glucose load. The level of serum omentin-1 was negatively correlated to BMI, HOMA-IR, fasting insulin, TNF-alpha, IL-6, plasma glucose. HOMA-IR and BMI were independent related factors that influenced the levels of serum omentin-1. Conclusions: Serum omentin-1 levels were decreased in impaired glucose regulation subjects. Lack of omentin-1 may contribute to the development of insulin resistance and T2DM. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:29 / 33
页数:5
相关论文
共 26 条
[1]   Adipokines and the peripheral and neural control of energy balance [J].
Ahima, Rexford S. ;
Lazar, Mitchell A. .
MOLECULAR ENDOCRINOLOGY, 2008, 22 (05) :1023-1031
[2]  
[Anonymous], 1999, WHO/NCD/ NCS/99.2
[3]   Omentin plasma levels and gene expression are decreased in obesity [J].
Batista, Celia M. de Souza ;
Yang, Rong-Ze ;
Lee, Mi-Jeong ;
Glynn, Nicole M. ;
Yu, Dao-Zhan ;
Pray, Jessica ;
Ndubuizu, Kelechi ;
Patil, Susheel ;
Schwartz, Alan ;
Kligman, Mark ;
Fried, Susan K. ;
Gong, Da-Wei ;
Shuldiner, Alan R. ;
Pollin, Toni I. ;
McLenithan, John C. .
DIABETES, 2007, 56 (06) :1655-1661
[4]   Adiponectin gene expression and secretion is inhibited by interleukin-6 in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Kralisch, S ;
Klier, M ;
Lossner, U ;
Bluher, M ;
Klein, J ;
Paschke, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (04) :1045-1050
[5]  
Fu M, 2004, DIABETES, V53, pA59
[6]   RETRACTED: Visfatin: A protein secreted by visceral fat that mimics the effects of insulin (Retracted article, see vol 318, pg 565, 2007) [J].
Fukuhara, A ;
Matsuda, M ;
Nishizawa, M ;
Segawa, K ;
Tanaka, M ;
Kishimoto, K ;
Matsuki, Y ;
Murakami, M ;
Ichisaka, T ;
Murakami, H ;
Watanabe, E ;
Takagi, T ;
Akiyoshi, M ;
Ohtsubo, T ;
Kihara, S ;
Yamashita, S ;
Makishima, M ;
Funahashi, T ;
Yamanaka, S ;
Hiramatsu, R ;
Matsuzawa, Y ;
Shimomura, I .
SCIENCE, 2005, 307 (5708) :426-430
[7]   Total and high-molecular-weight adiponectin and resistin in relation to the risk for type 2 diabetes in women [J].
Heidemann, Christin ;
Sun, Qi ;
van Dam, Rob M. ;
Meigs, James B. ;
Zhang, Cuilin ;
Tworoger, Shelley S. ;
Mantzoros, Christos S. ;
Hu, Frank B. .
ANNALS OF INTERNAL MEDICINE, 2008, 149 (05) :307-W66
[8]   Associations of adiponectin, resistin, and tumor necrosis factor-α with insulin resistance [J].
Hivert, Marie-France ;
Sullivan, Lisa M. ;
Fox, Caroline S. ;
Nathan, David M. ;
Sr, Ralph B. D'Agostino ;
Wilson, Peter W. F. ;
Meigs, James B. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (08) :3165-3172
[9]  
Kern PA, 2001, AM J PHYSIOL-ENDOC M, V280, pE745
[10]   Adipose tissue as an endocrine organ [J].
Kershaw, EE ;
Flier, JS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (06) :2548-2556