Potential Differences in the Cardiometabolic Risk Profile of Patients with Psoriatic Disease according to Their

Rubén Queiro1,2,3, Pablo Coto-Segura4, Ignacio Braña1

  • 1Rheumatology Division, Hospital Universitario Central de Asturias, Oviedo, Asturias, Spain.

Insights

The human leukocyte antigen-C*06 (HLA-C*06) biomarker is linked to a better cardiometabolic profile in psoriatic disease patients. This genetic marker is associated with earlier onset and more severe skin symptoms but reduced hypertension and lower BMI.

Area of Science:

  • Immunogenetics
  • Dermatology
  • Cardiology
  • Metabolic Health

Background:

  • The human leukocyte antigen-C*06 (HLA-C*06) is a key genetic biomarker in psoriatic disease.
  • Its association with cardiometabolic comorbidities remains largely unexplored.
  • Understanding this link is crucial for comprehensive patient management.

Purpose of the Study:

  • To investigate the association between HLA-C*06 and the cardiometabolic profile in patients with psoriatic disease.
  • To explore potential correlations between this genetic marker and various cardiometabolic risk factors.

Main Methods:

  • A cross-sectional observational study involving 400 psoriatic disease patients.
  • Comparison of clinical and cardiometabolic factors between HLA-C*06-positive and negative individuals.
  • Multivariate regression analyses to identify disease traits associated with cardiometabolic risk factors.

Main Results:

  • HLA-C*06 carriers (40%) exhibited an earlier age of disease onset, family history of psoriasis, and more severe skin disease (Type I).
  • A novel finding revealed that HLA-C*06 carriers had a better cardiometabolic profile.
  • Specifically, HLA-C*06 carriers showed significantly less hypertension, lower waist circumference, and lower BMI compared to non-carriers.

Conclusions:

  • The study confirms the association of HLA-C*06 with Type I psoriatic disease.
  • A significant novel finding is the association of HLA-C*06 with a better cardiometabolic profile in psoriatic disease patients.
  • Further research is warranted to validate these findings and explore underlying mechanisms.

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