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
. 2022 Sep 21:2022:2442603.
doi: 10.1155/2022/2442603. eCollection 2022.

Risk of Candida Infection and Serious Infections in Patients with Moderate-to-Severe Psoriasis Receiving Biologics: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Affiliations
Meta-Analysis

Risk of Candida Infection and Serious Infections in Patients with Moderate-to-Severe Psoriasis Receiving Biologics: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Yue Feng et al. Int J Clin Pract. .

Abstract

Background: Biological agents used to treat moderate-to-severe plaque psoriasis have been associated with Candida infection and other serious infections. It is, however, necessary to verify whether biologic agents increase the risk of Candida infection and serious infections and whether these risks vary among biologics.

Methods: PubMed, EMBASE, and Cochrane Library were searched for eligible randomized controlled trials (RCTs) from their inception to December 2021. Results from individual RCT were pooled using Peto's method with a fixed-effects model, and I 2 was calculated to assess the heterogeneity. A Cochrane collaboration tool was used to examine bias risk, and Grades of Recommendation, Assessment, Development, and Evaluation (GRADE) were used to assess the quality of evidence.

Results: This study included 48 published articles with data from 52 RCTs involving 27297 participants. The anti-interleukin (IL)-17 agents (95% confidence interval (CI) = 1.54-3.45, P < 0.0001) and anti-IL-12/23 agents (95% CI = 1.69-3.83, P < 0.0001) were associated with an increased risk of Candida infection compared with placebos, but there was no difference in Candida infection risk between anti-IL-17 agents and tumor necrosis factor inhibitors (TNFi) (95% CI = 0.92-3.07, P=0.09). There was no evidence that the biological agents increased the risk of serious infections in adult psoriasis (95% CI = 0.93-2.06, P=0.11) or that the biologics differed in the risk of serious infections.

Conclusions: Our results indicated that anti-IL-17 agents, especially secukinumab, were associated with the increased risk of Candida infection. The clinically used biological agents did not increase the risk of serious infections.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
PRISMA flowchart of randomized controlled trials (RCTs) included in the analysis.
Figure 2
Figure 2
Forest plot of pooled data regarding Candida infections between anti-interleukin (IL)-17 agents and placebos. CI, confidence interval.
Figure 3
Figure 3
Forest plot of pooled data regarding Candida infections between anti-interleukin (IL)-17 agents and anti-IL-12/23 agents. CI, confidence interval.
Figure 4
Figure 4
Forest plot of pooled data regarding Candida infections between anti-interleukin (IL)-17 agents and tumor necrosis factor inhibitors (TNFi). CI, confidence interval.
Figure 5
Figure 5
Forest plot of pooled data regarding serious infections between biological agents and placebos. CI, confidence interval.

References

    1. Nestle F. O., Kaplan D. H., Barker J. Psoriasis. New England Journal of Medicine . 2009;361(5):496–509. doi: 10.1056/nejmra0804595. - DOI - PubMed
    1. Michalek I. M., Loring B., John S. M. A systematic review of worldwide epidemiology of psoriasis. Journal of the European Academy of Dermatology and Venereology . 2017;31(2):205–212. doi: 10.1111/jdv.13854. - DOI - PubMed
    1. Macleod T., Bridgewood C., Hyde I., et al. Molecular and cellular regulation of psoriatic inflammation. Clinical Science . 2022;136(12):935–952. doi: 10.1042/cs20210916. - DOI - PubMed
    1. Kovitwanichkanont T., Chong A. H., Foley P. Beyond skin deep: addressing comorbidities in psoriasis. Medical Journal of Australia . 2020;212(11):528–534. doi: 10.5694/mja2.50591. - DOI - PubMed
    1. AlQassimi S., AlBrashdi S., Galadari H., Hashim M. J. Global burden of psoriasis - comparison of regional and global epidemiology, 1990 to 2017. International Journal of Dermatology . 2020;59(5):566–571. doi: 10.1111/ijd.14864. - DOI - PubMed

MeSH terms