IDEAS home Printed from https://ideas.repec.org/a/asi/joasrj/v2y2012i12p949-957id3442.html
   My bibliography  Save this article

Visfatin Between Fact and Fiction; A Marker of Obesity or a New Player in the Pathogenesis of Type 2 Diabetes Mellitus

Author

Listed:
  • Yasser S Sheta
  • El-Sayed A Elgohary
  • Samar Sharaf

Abstract

An adipose-tissue-derived protein termed visfatin was described recently with putative key role in pathogenesis of type 2 diabetes mellitus. It turns out, though, that the molecule was previously identified as a growth factor for early B-lymphocytes termed pre-B cell colony enhancing factor (PBEF). Visfatin was reported to be expressed almost exclusively in visceral adipose tissue and has insulin-like metabolic effects. These findings are very attractive and could provide a hot point of medical research to answer if visfatin provide a novel mechanism by which visceral fat accumulation can promote the development of type 2 diabetes mellitus (T2DM). However, its patho-physiological role in humans remains largely unknown. The Aim of this study is to investigate the role of plasma visfatin as a missing link between obesity and type 2 DM patients. Methods: Plasma visfatin concentrations were measured through ELISA in forty obese patients and compared to forty age and sex matched healthy non-obese subjects. Obese patients further subdivided into two subgroups according to presence of diabetes mellitus. Results: Plasma visfatin was found to be elevated in obese (38.7±13.3 ng/ml) compared to lean subjects (20.8±3.8 ng/ml), (P < 0.01).In obese patients no significant difference was found in diabetic obese patients (39.1± 7.3 ng/ml) in comparison to non diabetic patients (36.9±7.4 ng/ml) .In the other hand; no significant differences between diabetic patients according to diabetic control and line of treatments. Only waist to hip ratio was correlated with plasma visfatin level. Conclusion: Our results indicate that visfatin is elevated in obese patients apart from the presence of diabetes, diabetes control and line of treatments. Visfatin more reasonably to be a marker of obesity as a product of visceral fat cells rather than a new key in pathogenesis of type 2 diabetes mellitus . It seems that visfatin could not be one of the missing links between type 2 diabetes mellitus and its relation to visceral obesity. Further large scale studies are needed to determine its relation to immune status of obese patients and other adipo-cytokines and the effect of weight loss on its level.

Suggested Citation

  • Yasser S Sheta & El-Sayed A Elgohary & Samar Sharaf, 2012. "Visfatin Between Fact and Fiction; A Marker of Obesity or a New Player in the Pathogenesis of Type 2 Diabetes Mellitus," Journal of Asian Scientific Research, Asian Economic and Social Society, vol. 2(12), pages 949-957.
  • Handle: RePEc:asi:joasrj:v:2:y:2012:i:12:p:949-957:id:3442
    as

    Download full text from publisher

    File URL: https://archive.aessweb.com/index.php/5003/article/view/3442/5491
    Download Restriction: no
    ---><---

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:asi:joasrj:v:2:y:2012:i:12:p:949-957:id:3442. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Robert Allen (email available below). General contact details of provider: https://archive.aessweb.com/index.php/5003/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.