Spondyloarthritis & psoriatic arthritis

Sex differences in cytokines and adipokines in obese patients with psoriatic arthritis (PsA) and controls undergoing a weight loss intervention

RMD OpenPublished Post hoc analysis of a previously published weight loss intervention study

Authors' conclusion

Women and men with PsA differed with regard to serum levels of cytokines and adipokines before and after weight loss.

Study context

Population
Patients with PsA aged 25–75 years with body mass index (BMI)≥33 kg/m², in a very low energy diet (VLED) weight loss intervention for 12 or 16 weeks (baseline (BL) BMI<40 or ≥40 kg/m²), and obese controls41 PsA, 39 controls
Comparison
Women vs men with PsA, at baseline and 6 months after a VLED weight loss intervention
  • Controlsn = 39
Primary endpoint
Serum cytokine and adipokine levels by sex
Follow-up
BL and M6
Methodological detailsmatched controls (sex, age and weight)
  • Matched controls (sex, age and weight)

Primary result

As reported in the abstract

BL
  • IL-23, leptin and high molecular weight-adiponectin higher in women with PsA than men
  • Interferon (IFN)-γ, IL-12/IL-23 p40 and IL-13 significantly lower in women
  • Serum IL-23 significantly reduced at M6 vs BL in women but not in men with PsA
  • Post hoc analysis

Further findings

Correlations of ∆IL-23 at M6 in women with PsA

∆IL-23 vs ∆DAS28-CRP (rS)
0.486, p=0.016
∆IL-23 vs ∆C reactive protein (CRP) (rS)
0.468, p=0.021
∆IL-23 vs ∆leptin (rS)
0.683, p<0.001
∆IL-23 vs ∆total-adiponectin (rS)
−0.433, p=0.035
  • Spearman's correlation
  • None significant in men with PsA

Correlations of ∆DAPSA in women with PsA · M6

∆DAPSA vs ∆TNF-α (rS)
0.417, p=0.034
∆DAPSA vs ∆IL-1β (rS)
0.550, p=0.034
∆DAPSA vs ∆IFN-γ (rS)
0.414, p=0.035
∆DAPSA vs ∆leptin (rS)
0.410, p=0.038
  • Spearman's correlation
  • None significant in men with PsA

Original publication

Sex differences in cytokines and adipokines in obese patients with PsA and controls undergoing a weight loss intervention. RMD Open. Published 22 March 2024. doi:10.1136/rmdopen-2023-003821

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