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
. 2024 Mar 4:15:1354593.
doi: 10.3389/fimmu.2024.1354593. eCollection 2024.

Effects of tumor necrosis factor-alpha inhibitors on lipid profiles in patients with psoriasis: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Effects of tumor necrosis factor-alpha inhibitors on lipid profiles in patients with psoriasis: a systematic review and meta-analysis

Liang Su et al. Front Immunol. .

Abstract

Background: There is no consensus on the effect of tumor necrosis factor-alpha (TNF-alpha) inhibitors on lipid profiles in patients with psoriasis. This study aimed to investigate the effects of TNF-alpha inhibitors on lipid profiles (triglycerides, total cholesterol, low-density lipoprotein, or high-density lipoprotein) in patients with psoriasis.

Methods: We searched PubMed, Embase, and Cochrane Library databases for articles published before October 17, 2023. Four TNF-alpha inhibitors (infliximab, etanercept, adalimumab, and certolizumab) were included in our study. (PROSPERO ID: CRD42023469703).

Results: A total of twenty trials were included. Overall results revealed that TNF-alpha inhibitors elevated high-density lipoprotein levels in patients with psoriasis (WMD = 2.31; 95% CI: 0.96, 3.67; P = 0.001), which was supported by the results of sensitivity analyses excluding the effect of lipid-lowering drugs. Subgroup analyses indicated that high-density lipoprotein levels were significantly increased in the less than or equal to 3 months group (WMD = 2.88; 95% CI: 1.37, 4.4; P < 0.001), the etanercept group (WMD = 3.4; 95% CI = 1.71, 5.09, P < 0.001), and the psoriasis group (WMD = 2.52; 95% CI = 0.57, 4.48, P = 0.011). Triglyceride levels were significantly increased in the 3 to 6-month group (WMD = 4.98; 95% CI = 1.97, 7.99, P = 0.001) and significantly decreased in the 6-month and older group (WMD = -19.84; 95% CI = -23.97, -15.7, P < 0.001). Additionally, Triglyceride levels were significantly increased in the psoriasis group (WMD = 5.22; 95% CI = 2.23, 8.21, P = 0.001).

Conclusion: Our results revealed that TNF-alpha inhibitors might temporarily increase high-density lipoprotein levels in patients with psoriasis. However, changes in triglycerides were not consistent among the different durations of treatment, with significant increases after 3 to 6 months of treatment. Future prospective trials with long-term follow-up contribute to confirming and extending our findings.

Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42023469703.

Keywords: lipid profiles; meta-analysis; psoriasis; systematic review; tumor necrosis factor alpha (TNF-alpha); tumor necrosis factor alpha inhibitors.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Flow diagram for the study selection process.
Figure 2
Figure 2
Forest plot for the effect of TNF-alpha inhibitors on triglycerides in patients with psoriasis (weighted mean difference).
Figure 3
Figure 3
Forest plot for the effect of TNF-alpha inhibitors on total cholesterol in patients with psoriasis (weighted mean difference).
Figure 4
Figure 4
Forest plot for the effect of TNF-alpha inhibitors on high-density lipoprotein in patients with psoriasis (weighted mean difference).
Figure 5
Figure 5
Forest plot for the effect of TNF-alpha inhibitors on low-density lipoprotein in patients with psoriasis (weighted mean difference).

References

    1. Takeshita J, Grewal S, Langan SM, Mehta NN, Ogdie A, Van Voorhees AS, et al. . Psoriasis and comorbid diseases: epidemiology. J Am Acad Dermatol. (2017) 76:377–90. doi: 10.1016/j.jaad.2016.07.064 - DOI - PMC - PubMed
    1. Li L, Lu J, Liu J, Wu J, Zhang X, Meng Y, et al. . Immune cells in the epithelial immune microenvironment of psoriasis: emerging therapeutic targets. Front Immunol. (2023) 14:1340677. doi: 10.3389/fimmu.2023.1340677 - DOI - PMC - PubMed
    1. Korman NJ. Management of psoriasis as a systemic disease: what is the evidence? Br J Dermatol. (2020) 182:840–8. doi: 10.1111/bjd.18245 - DOI - PMC - PubMed
    1. Maurelli M, Gisondi P, Girolomoni G. Advanced glycation end products and psoriasis. Vaccines (Basel). (2023) 11:617. doi: 10.3390/vaccines11030617 - DOI - PMC - PubMed
    1. Purzycka-Bohdan D, Kisielnicka A, Bohdan M, Szczerkowska-Dobosz A, Sobalska-Kwapis M, Nedoszytko B, et al. . Analysis of the potential genetic links between psoriasis and cardiovascular risk factors. Int J Mol Sci. (2021) 22:9063. doi: 10.3390/ijms22169063 - DOI - PMC - PubMed

Publication types

MeSH terms