IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0122026.html
   My bibliography  Save this article

Association between Complement C3 and Prevalence of Fatty Liver Disease in an Adult Population: A Cross-Sectional Study from the Tianjin Chronic Low-Grade Systemic Inflammation and Health (TCLSIHealth) Cohort Study

Author

Listed:
  • Qiyu Jia
  • Chunlei Li
  • Yang Xia
  • Qing Zhang
  • Hongmei Wu
  • Huanmin Du
  • Li Liu
  • Chongjin Wang
  • Hongbin Shi
  • Xiaoyan Guo
  • Xing Liu
  • Shaomei Sun
  • Xing Wang
  • Ming Zhou
  • Honglin Zhao
  • Kun Song
  • Yuntang Wu
  • Kaijun Niu

Abstract

Activation of the innate immune system plays a key role in the development of fatty liver disease (FLD). The complement system is a major humoral component of the innate immune response and complement C3 plays a central role, implying that C3 may be a powerful predictor or therapeutic target for FLD. However, few studies have assessed the association between C3 and FLD in a large population. Here we use a cross-sectional study to investigate the link between serum C3 levels and FLD. Participants were recruited from Tianjin Medical University’s General Hospital-Health Management Centre. Serum C3 was measured using immunoturbidimetry method and FLD was diagnosed by liver ultrasonography. Multiple logistic regression analysis was used to examine the association between quartiles of C3 and FLD prevalence. The overall prevalence of nonalcoholic fatty liver disease (NAFLD) and alcoholic fatty liver disease (AFLD) were 37.3% and 10.1%, respectively. After adjusting for covariates, the odds ratio of having NAFLD or AFLD (only in males) in the fourth quartile of C3 compared with the first quartile was 4.13 times greater (95% confidence interval, 2.97-5.77) (trend P values

Suggested Citation

  • Qiyu Jia & Chunlei Li & Yang Xia & Qing Zhang & Hongmei Wu & Huanmin Du & Li Liu & Chongjin Wang & Hongbin Shi & Xiaoyan Guo & Xing Liu & Shaomei Sun & Xing Wang & Ming Zhou & Honglin Zhao & Kun Song , 2015. "Association between Complement C3 and Prevalence of Fatty Liver Disease in an Adult Population: A Cross-Sectional Study from the Tianjin Chronic Low-Grade Systemic Inflammation and Health (TCLSIHealth," PLOS ONE, Public Library of Science, vol. 10(4), pages 1-10, April.
  • Handle: RePEc:plo:pone00:0122026
    DOI: 10.1371/journal.pone.0122026
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0122026
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0122026&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0122026?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    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:plo:pone00:0122026. 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: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    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.