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Updated: Jan 14, 2026

The Goeckerman Regimen for the Treatment of Moderate to Severe Psoriasis
Published on: July 11, 2013
Biologic Therapies and Major Cardiovascular Events in Psoriasis: Updated Systematic Review and Meta-analysis
Varitsara Mangkorntongsakul1, J S Joseph2, James P Pham3,4
1Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
Insights
Biologic therapies for severe plaque psoriasis do not increase the risk of major adverse cardiovascular events (MACE). This systematic review found no significant difference in MACE risk between biologics and placebo in psoriatic patients.
Area of Science:
- Dermatology and Immunology
- Cardiology
- Pharmacology
Background:
- Psoriasis is frequently associated with cardiovascular disease.
- Biologic therapies are effective for severe plaque psoriasis, but their cardiovascular safety is not fully understood.
Purpose of the Study:
- To investigate the impact of biologic therapies on the risk of major adverse cardiovascular events (MACE) in patients with chronic plaque psoriasis.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs) published up to May 10, 2022.
- Included RCTs compared licensed biologic therapies with placebo or other biologics in adults with moderate-to-severe plaque psoriasis.
- Adherence to Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines.
Main Results:
- Analysis of 43 RCTs found no statistically significant difference in MACE risk between biologic therapies and placebo (Peto odds ratio [POR] 1.26, 95% CI 0.53-3.01, P=0.59).
- Specific biologic classes, including TNF-alpha, IL-17, IL-12/23, and IL-23 inhibitors, did not show a significant association with increased MACE risk.
Conclusions:
- Anti-psoriatic biologic therapies are not associated with an increased risk of MACE in patients with psoriasis.
- Longer-term studies and post-marketing surveillance are necessary to fully elucidate the cardiovascular safety profile of these treatments.
Introduction:
Cardiovascular disease is a leading co-morbidity in psoriasis patients. The cutaneous benefits of biologic therapies for severe plaque psoriasis are well-established, but the impact of biologics on major adverse cardiovascular events (MACE) in psoriatic patients requires further elucidation. This study aimed to investigate the impact of biologic therapies on the risk of MACE in patients with chronic plaque psoriasis.
Methods:
We conducted a systematic review and meta-analysis on 10 May 2022, using Medline, PubMed, Cochrane Central Register of Controlled Trials (CCTR), Cochrane Database of Systematic Reviews (CDSR) and EMBASE databases for relevant studies. The Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) methodology was applied, and all studies were critically appraised. All studies selected for inclusion were randomised control trials (RCTs) that contained data on MACE and compared licensed biologic therapies with placebo or other biologics in adults with moderate-severe plaque psoriasis.
Results:
The search of the databases revealed 36 papers (reporting on 43 RCTs) which met the inclusion criteria. No statistically significant difference in the risk for MACE between biologic therapies and placebo was found [Peto odds ratio (POR) 1.26, 95% confidence interval (CI) 0.53-3.01, P = 0.59]. A comparison of specific types of biologics also revealed no significant effect in adult patients with moderate-to-severe plaque psoriasis: tumour necrosis factor (TNF)-alpha inhibitors (adalimumab, infliximab, etanercept) (POR 1.13, 95% CI 0.29-4.32 P = 0.86), interleukin (IL)-17 inhibitors (secukinumab, ixekizumab, brodalumab, bimekizumab) (POR 0.60, 95% CI 0.16-2.25, P = 0.45); IL 12/23 inhibitors (usetekinumab) (POR 3.80, 95% CI 0.37-39.44, P = 0.26) and IL-23 (guselkumab, risankizumab, tildrakizumab) (POR 1.75, 95% CI 0.25-12.43 P = 0.58).
Conclusions:
Anti-psoriatic biologics were not associated with an increased risk of MACE in psoriasis patients. Given that most included RCTs were of relatively short duration, longer-term studies and post-marketing surveillance are needed to clarify the cardiovascular safety profile of biologic therapies. Further large-scale studies with extended follow-up are warranted.
Study Registration:
This study was prospectively registered on PROSPERO (identification number CRD42022325792).
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