AB0415 SIGNIFICANT REDUCTION OF ABDOMINAL FAT WITH APREMILAST TREATMENT IN PATIENTS WITH PSORIATIC ARTHRITIS (2024)

AB0415 SIGNIFICANT REDUCTION OF ABDOMINAL FAT WITH APREMILAST TREATMENT IN PATIENTS WITH PSORIATIC ARTHRITIS (1)

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AB0415 SIGNIFICANT REDUCTION OF ABDOMINAL FAT WITH APREMILAST TREATMENT IN PATIENTS WITH PSORIATIC ARTHRITIS

  1. B. Dijkshoorn1,
  2. F. Coban1,
  3. E. Van Geel1,
  4. R. Hansildaar1,
  5. R. Bos2,3,
  6. F. Reimann2,
  7. M. Korteweg4,
  8. M. Nurmohamed1,5
  1. 1Amsterdam Rheumatology & Immunology Center Location Reade, Rheumatology, Amsterdam, Netherlands
  2. 2Medical Center Leeuwarden, Rheumatology, Leeuwarden, Netherlands
  3. 3Leiden University Medical Center, Rheumatology, Leiden, Netherlands
  4. 4Amsterdam Rheumatology & Immunology Center Location Reade, Radiology, Amsterdam, Netherlands
  5. 5Amsterdam UMC Location Vrije Universiteit Amsterdam, Rheumatology, Amsterdam, Netherlands

Abstract

Background: Psoriatic arthritis (PsA) is associated with metabolic and cardiovascular comorbidities. Metabolic syndrome is prevalent in 29% of PsA patients. Excess adipose tissue, a symptom of metabolic syndrome, functions as a source of pro-inflammatory cytokines, contributing to low-grade chronic systemic inflammation. Given the substantial prevalence and implications, metabolic and cardiovascular comorbidities might have on morbidity and mortality in PsA patients, understanding and addressing these cardiovascular and metabolic risk factors is clinically relevant. A few data suggested that apremilast, in addition to its anti-inflammatory effects, decreases visceral adiposity and promotes weight loss. These potential effects of apremilast on abdominal fat and cardiometabolic risk factors could help to decrease the burden of cardiometabolic comorbidities.

Objectives: The aim of this study was to examine the effects of apremilast on measures of abdominal fat in PsA patients.

Methods: This multi-center, prospective study included consecutive adults with active PsA in whom apremilast was initiated. Participants received 30 mg administered twice daily after a step-up regimen plan. Assessment of abdominal fat measures was done with Dual Energy X-ray Absorptiometry (DEXA). The values measured comprised android fat mass, arms-legs fat mass, arms-legs lean mass, gynoid fat mass, total body mass, total body fat mass, and truncal fat mass to calculate appendicular lean mass, android to gynoid fat mass ratio, fat mass index, and the percentage of fat distributed to the trunk.

Disease activity was assessed with DAS28-CRP. Measurements were done at baseline, 26, and 52 weeks after initiation of treatment with apremilast. Subsequently, these data were compared using a linear mixed model. The alpha for statistical significance was set at p-values less than 0.05.

Results: Forty four patients (30 females and fourteen males) were included. All patients were included in the intent- to-treat analyses, whereas eighteen (40.8%) of the patients could be included in the, now reported, per protocol analysis. The mean age was 55.6 years (± 11.3) and the median duration of PsA was five years [range 2.0y-12.0y]. At baseline, the participants anthropometric measurements reported a median BMI of 28.2 kg/m2 [range 24.2-33.4 kg/m2], a mean hip circumference of 108.0 cm (±14.0 cm), a mean waist circumference of 98.7 cm (±19.1 cm), a mean waist-to-hip ratio of 0.9 (±0.1 cm) and a mean weight of 86,9 kg (±17,1 kg). An overview of the results is presented in Table 1. Following one year of treatment with apremilast significant reductions in total body mass, total body fat mass, truncal fat mass and fat mass index were observed. Similarly, both android fat mass (-0.5 kg; 95% CI [-0.9 – -0.2]; p=0.002) and gynoid fat mass (-0.8 kg; 95% CI [-1.2 – -0.3]; p= <0.001) decreased significantly, alongside with notable reductions in arms-legs fat mass. While the decline in abdominal fat measures continued between weeks 26 and 52, the additional changes in fat mass did not reach statistical significance. Age, sex, diagnosis of diabetes mellitus (DM), and nausea did not demonstrate a significant impact on body mass. Disease activity improved significantly after 52 weeks of treatment with apremilast. Correlation analysis, using a linear mixed model, revealed a significant association between disease activity and changes in body mass parameters (Table 2).

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Conclusion: The findings indicate that apremilast in PsA patients favorably changes body composition. Treatment with apremilast resulted in a significant reduction in android fat mass, alongside with total body fat mass reduction. Additionally, the observed weight loss correlated with reduced disease activity. These findings imply favorable cardiovascular and metabolic effects of apremilast in psoriatic arthritis patients.

REFERENCES: NIL.

Acknowledgements: NIL.

Disclosure of Interests: Bas Dijkshoorn: None declared, Fatih Coban: None declared, Eva van Geel: None declared, Romy Hansildaar: None declared, Reinhard Bos Galapagos and Janssen, Abbvie, Galapagos, Pfizer, UCB, Galapagos, Sanofi, Floor Reimann: None declared, Mies Korteweg: None declared, Michael Nurmohamed: None declared.

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    AB0415 SIGNIFICANT REDUCTION OF ABDOMINAL FAT WITH APREMILAST TREATMENT IN PATIENTS WITH PSORIATIC ARTHRITIS (2024)

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