Correlation between serum resistin level and adiposity in obese individuals

被引:277
作者
Azuma, K
Katsukawa, F
Oguchi, S
Murata, M
Yamazaki, H
Shimada, A
Saruta, T
机构
[1] Keio Univ, Sch Med, Dept Internal Med, Shinjuku Ku, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Sports Med Res Ctr, Tokyo 1608582, Japan
[3] Keio Univ, Sch Med, Dept Lab Med, Tokyo 1608582, Japan
来源
OBESITY RESEARCH | 2003年 / 11卷 / 08期
关键词
resistin; body composition; adiposity; insulin resistance; mean insulin;
D O I
10.1038/oby.2003.137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Resistin is associated with insulin resistance in mice and may play a similar role in humans. The aim of our study was to examine the relationship of serum resistin level to body composition, insulin resistance, and related obesity phenotypes in humans. Research Methods and Procedures: Sixty-four young (age 32 +/- 10 years), obese (BMI 32.9 +/- 5.6), nondiabetic subjects taking no medication, and 15 lean (BMI 21.1 +/- 1.3) volunteers were studied cross-sectionally. Thirty-five of the subjects were also reevaluated after 1.5 years on a weight reduction program entailing dieting and exercise; changes of serum resistin were compared with changes of BMI, body composition, fat distribution, and several indices of insulin sensitivity derived from plasma glucose and serum insulin levels measured during 75-g oral glucose tolerance test. Results: In a cross-sectional analysis, serum resistin was significantly higher in obese subjects than in lean volunteers (24.58 +/- 12.93 ng/mL; n = 64 vs. 12.83 +/- 8.30 ng/mL; n = 15; p < 0.01), and there was a correlation between resistin level and BMI, when the two groups were combined (p = 0.35, p < 0.01). Although cross-sectional analysis in obese subjects revealed no correlation between serum resistin and parameters related to adiposity or insulin resistance, longitudinal analysis revealed change in serum resistin to be positively correlated with changes in BMI, body fat, fat mass, visceral fat area, and mean glucose and insulin (p = 0.39, 0.40, 0.44, 0.50, 0.40, and 0.50; p = 0.02, 0.03, 0.02, <0.01, 0.02, and <0.01, respectively). Discussion: Resistin appears to be related to human adiposity and to be a possible candidate factor in human insulin resistance.
引用
收藏
页码:997 / 1001
页数:5
相关论文
共 19 条
[1]   Resistin release by human adipose tissue explants in primary culture [J].
Fain, JN ;
Cheema, PS ;
Bahouth, SW ;
Hiler, ML .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 300 (03) :674-678
[2]  
HOAG S, 1995, INT J OBESITY, V19, P175
[3]  
Jonke J, 2002, OBES RES, V10, P1
[4]   Genetic variants at the resistin locus and risk of type 2 diabetes in Caucasians [J].
Ma, XW ;
Warram, JH ;
Trischitta, V ;
Doria, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (09) :4407-4410
[5]   HOMEOSTASIS MODEL ASSESSMENT - INSULIN RESISTANCE AND BETA-CELL FUNCTION FROM FASTING PLASMA-GLUCOSE AND INSULIN CONCENTRATIONS IN MAN [J].
MATTHEWS, DR ;
HOSKER, JP ;
RUDENSKI, AS ;
NAYLOR, BA ;
TREACHER, DF ;
TURNER, RC .
DIABETOLOGIA, 1985, 28 (07) :412-419
[6]   Resistin, central obesity, and type 2 diabetes [J].
McTernan, CL ;
McTernan, PG ;
Harte, AL ;
Levick, PL ;
Barnett, AH ;
Kumar, S .
LANCET, 2002, 359 (9300) :46-47
[7]   Increased resistin gene and protein expression in human abdominal adipose tissue [J].
McTernan, PG ;
McTernan, CL ;
Chetty, R ;
Jenner, K ;
Fisher, FM ;
Lauer, M ;
Crocker, J ;
Barnett, AH ;
Kumar, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (05) :2407-2410
[8]   Resistin inhibits glucose uptake in L6 cells independently of changes in insulin signaling and GLUT4 translocation [J].
Moon, B ;
Kwan, JJM ;
Duddy, N ;
Sweeney, G ;
Begum, N .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (01) :E106-E115
[9]   Insulin resistance and Type 2 diabetes are not related to resistin expression in human fat cells or skeletal muscle [J].
Nagaev, I ;
Smith, U .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (02) :561-564
[10]   Resistin is expressed in human macrophages and directly regulated by PPARγ activators [J].
Patel, L ;
Buckels, AC ;
Kinghorn, IJ ;
Murdock, PR ;
Holbrook, JD ;
Plumpton, C ;
Macphee, CH ;
Smith, SA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 300 (02) :472-476