Effects of Biologic Therapy on Laboratory Indicators of Cardiometabolic Diseases in Patients with Psoriasis
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Published on: March 1, 2024
Teppei Hagino1, Hidehisa Saeki2, Eita Fujimoto3
1Department of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Inzai 270-1694, Japan.
Insights
Biologic therapies targeting tumor necrosis factor-alpha (TNF-α), interleukin-23 (IL-23), and IL-17 may improve psoriasis and associated cardiometabolic conditions. TNF-α inhibitors showed potential in improving hyperuricemia and dyslipidemia in patients.
Area of Science:
- Dermatology and Immunology
- Cardiology and Metabolic Diseases
Background:
- Psoriasis is linked to cardiometabolic and cardiovascular diseases.
- Biologic therapies targeting TNF-α, IL-23, and IL-17 may offer benefits beyond skin improvement, potentially impacting cardiometabolic health.
Purpose of the Study:
- To retrospectively evaluate the impact of biologic therapies on cardiometabolic disease indicators in patients with psoriasis.
- To assess changes in body mass index, metabolic markers, and blood pressure following treatment with biologics.
Main Methods:
- Retrospective analysis of 165 psoriasis patients treated with TNF-α, IL-17, or IL-23 biologics from January 2010 to September 2022.
- Collected data on body mass index, HbA1c, lipid profiles (total cholesterol, HDL-C, LDL-C, TG), uric acid (UA), and blood pressure at baseline, week 12, and week 52.
- Correlated baseline Psoriasis Area and Severity Index (PASI) with cardiometabolic parameters.
Main Results:
- Baseline PASI positively correlated with TG and UA, and negatively with HDL-C.
- Infliximab (IFX) treatment showed increased HDL-C at week 12.
- Adalimumab (ADA) treatment resulted in decreased UA levels at week 12.
- Secukinumab (IXE) treatment led to decreased HDL-C at week 52.
- TNF-α inhibitors demonstrated increased HDL-C at week 12 and decreased UA at week 52, though results varied between time points.
Conclusions:
- Biologic therapy, particularly TNF-α inhibitors, may offer benefits for hyperuricemia and dyslipidemia in psoriasis patients.
- While specific outcomes varied by drug and time point, the study suggests a potential positive influence on cardiometabolic health.
- Further research is warranted to elucidate the precise mechanisms and long-term effects of these biologics on cardiometabolic disease indicators.
Abstract:
Psoriasis is associated with cardiometabolic and cardiovascular diseases. Biologic therapy targeting tumor necrosis factor (TNF)-α, interleukin (IL)-23, and IL-17 may improve not only psoriasis but also cardiometabolic diseases. We retrospectively evaluated whether biologic therapy improved various indicators of cardiometabolic disease. Between January 2010 and September 2022, 165 patients with psoriasis were treated with biologics targeting TNF-α, IL-17, or IL-23. The patients' body mass index; serum levels of HbA1c, total cholesterol, high-density lipoprotein-cholesterol (HDL-C), low-density lipoprotein-cholesterol, triglyceride (TG), and uric acid (UA); and systolic and diastolic blood pressures were recorded at weeks 0, 12, and 52 of the treatment. Baseline psoriasis area and severity index (week 0) positively correlated with TG and UA levels but negatively correlated with HDL-C levels, which increased at week 12 of IFX treatment compared to those at week 0. UA levels decreased at week 12 after ADA treatment compared with week 0. HDL-C levels decreased 52 weeks after IXE treatment. In patients treated with TNF-α inhibitors, HDL-C levels increased at week 12, and UA levels decreased at week 52, compared to week 0. Thus, the results at two different time points (at weeks 12 and 52) were inconsistent. However, the results still indicated that TNF-α inhibitors may improve hyperuricemia and dyslipidemia.
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