Omentin plasma levels and gene expression are decreased in obesity

被引:610
作者
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.
机构
[1] Univ Maryland, Sch Med, Dept Med, Div Endocrinol Diabet & Nutr, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[3] Univ Maryland Baltimore Cty, Dept Biol, Baltimore, MD 21228 USA
[4] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[5] Univ Maryland, Sch Med, Dept Surg, Div Gen Surg, Baltimore, MD 21201 USA
[6] Vet Affairs Med Ctr, Ctr Geriatr Res Educ & Clin, Baltimore, MD USA
关键词
D O I
10.2337/db06-1506
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central obesity and the accumulation of visceral fat are risk factors for the development of type 2 diabetes and cardiovascular disease. Omentin is a protein expressed and secreted from visceral but not subcutaneous adipose tissue that increases insulin sensitivity in human adipocytes. To determine the impact of obesity-dependent insulin resistance on the regulation of two omentin isoforms, gene expression and plasma levels were measured in lean, overweight, and obese subjects. Omentin I was shown to be the major circulating isoform in human plasma. Lean subjects had significantly higher plasma omentin 1 levels than obese and overweight subjects. In addition, higher plasma omentin I levels were detected in women compared with men. Plasma omentin 1 levels were inversely correlated with BMI, waist circumference, leptin levels, and insulin resistance as measured by homeostasis model assessment and positively correlated with adiponectin and HDL levels. Both omentin I and omentin 2 gene expression were decreased with obesity and were highly correlated with each other in visceral adipose tissue. In summary, decreased omentin levels are associated with increasing obesity and insulin resistance. Therefore, omentin levels may be predictive of the metabolic consequences or co-morbidities associated with obesity.
引用
收藏
页码:1655 / 1661
页数:7
相关论文
共 43 条
  • [1] Production of plasminogen activator inhibitor 1 by human adipose tissue - Possible link between visceral fat accumulation and vascular disease
    Alessi, MC
    Peiretti, F
    Morange, P
    Henry, M
    Nalbone, G
    JuhanVague, I
    [J]. DIABETES, 1997, 46 (05) : 860 - 867
  • [2] Multipoint quantitative-trait linkage analysis in general pedigrees
    Almasy, L
    Blangero, J
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) : 1198 - 1211
  • [3] Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity
    Arita, Y
    Kihara, S
    Ouchi, N
    Takahashi, M
    Maeda, K
    Miyagawa, J
    Hotta, K
    Shimomura, I
    Nakamura, T
    Miyaoka, K
    Kuriyama, H
    Nishida, M
    Yamashita, S
    Okubo, K
    Matsubara, K
    Muraguchi, M
    Ohmoto, Y
    Funahashi, T
    Matsuzawa, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) : 79 - 83
  • [4] Plasma visfatin concentrations and fat depot-specific mRNA expression in humans
    Berndt, J
    Klöting, N
    Kralisch, S
    Kovacs, P
    Fasshauer, M
    Schön, MR
    Stumvoll, M
    Blüher, M
    [J]. DIABETES, 2005, 54 (10) : 2911 - 2916
  • [5] METABOLIC IMPLICATIONS OF BODY-FAT DISTRIBUTION
    BJORNTORP, P
    [J]. DIABETES CARE, 1991, 14 (12) : 1132 - 1143
  • [6] Brunzell JD, 1999, DIABETES CARE, V22, pC10
  • [7] A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians
    Elbein, SC
    Hoffman, MD
    Teng, K
    Leppert, MF
    Hasstedt, SJ
    [J]. DIABETES, 1999, 48 (05) : 1175 - 1182
  • [8] Pathways from obesity to diabetes
    Felber, JP
    Golay, A
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2002, 26 (Suppl 2) : S39 - S45
  • [9] FRIED SK, 2005, HDB OBESITY
  • [10] Fu M, 2004, DIABETES, V53, pA59