Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2020 Aug 31;21(17):6290.
doi: 10.3390/ijms21176290.

Effects of IL-6 Signaling Pathway Inhibition on Weight and BMI: A Systematic Review and Meta-Analysis

Affiliations
Meta-Analysis

Effects of IL-6 Signaling Pathway Inhibition on Weight and BMI: A Systematic Review and Meta-Analysis

Olivia Patsalos et al. Int J Mol Sci. .

Abstract

Inhibitors of the IL-6 signaling pathway, such as tocilizumab, are frequently administered for the treatment of immune diseases, e.g., rheumatoid arthritis and multicentric Castleman's disease. The aim of this systematic review and meta-analysis was to ascertain the effects of IL-6 pathway inhibitors on weight and body mass index (BMI). Using PRISMA guidelines, we systematically reviewed relevant articles from three databases (PubMed, OVID, EMBASE). A random effects model was used to estimate standardized mean change (SMCC). Ten studies with a total of 1531 patients were included in the meta-analysis for weight and ten studies with a total of 1537 patients were included in the BMI meta-analysis. The most commonly administered IL-6 pathway inhibitor was tocilizumab. IL-6 pathway inhibitors were associated with increases in weight (SMCC = 0.09, p = 0.016, 95% CI [0.03, 0.14]) and BMI (SMCC = 0.10, p = 0.0001, 95% CI [0.05, 0.15]). These findings suggest that the IL-6 pathway is involved in weight regulation. Modulating IL-6 signaling may be a potential future therapeutic avenue used as an adjunct for the treatment of disorders associated with weight changes, such as cancer cachexia and anorexia nervosa.

Keywords: BMI; IL-6; obesity; rheumatoid arthritis; siltuximab; spondyloarthritis; tocilizumab; weight.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Forest plot of standardized mean change in body weight from nine datasets (n = 1531). Zero indicates no effect, whereas points to the right indicate an increase in weight when comparing baseline with follow-up values post-treatment with an IL-6 signaling pathway inhibitor.
Figure 2
Figure 2
Forest plot of standardized mean change in body mass index (BMI) from nine datasets (n = 1537). Zero indicates no effect, whereas points to the right indicate an increase in weight when comparing values at baseline and after treatment with an IL-6 signaling pathway inhibitor.
Figure 3
Figure 3
PRISMA flow diagram.

Similar articles

Cited by

References

    1. Kristiansen O.P., Mandrup-Poulsen T. Interleukin-6 and Diabetes: The good, the bad, or the indifferent? Diabetes. 2005;54:S114–S124. doi: 10.2337/diabetes.54.suppl_2.S114. - DOI - PubMed
    1. Dubiński A., Zdrojewicz Z. The role of interleukin-6 in development and progression of atherosclerosis. Polski Merkur. Lek. Organ Polskiego Towar. Lek. 2007;22:291–294. - PubMed
    1. Dowlati Y., Herrmann N., Swardfager W., Liu H., Sham L., Reim E.K., Lanctôt K.L. A meta-analysis of cytokines in major depression. Boil. Psychiatry. 2010;67:446–457. doi: 10.1016/j.biopsych.2009.09.033. - DOI - PubMed
    1. Schoels M.M., Van Der Heijde D., Breedveld F.C., Burmester G.R., Dougados M., Emery P., Ferraccioli G., Gabay C., Gibofsky A., Gomez-Reino J.J., et al. Blocking the effects of interleukin-6 in rheumatoid arthritis and other inflammatory rheumatic diseases: Systematic literature review and meta-analysis informing a consensus statement. Ann. Rheum. Dis. 2012;72:583–589. doi: 10.1136/annrheumdis-2012-202470. - DOI - PMC - PubMed
    1. Yoshizaki K., Murayama S., Ito H., Koga T. The role of interleukin-6 in castleman disease. Hematol. Clin. N. Am. 2018;32:23–36. doi: 10.1016/j.hoc.2017.09.003. - DOI - PubMed