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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.
Abstract:
The human leukocyte antigen-C∗06 (HLA-C∗06, formerly HLA-Cw6) is the main genetic biomarker in psoriatic disease. It has been related to several phenotypic traits in psoriatic disease, but its role in relation to cardiometabolic comorbidities is unknown at present. Here, we analyze the potential connections between this biomarker and the cardiometabolic profile of these patients. We carried out a cross-sectional observational study including 400 patients recruited at a single university hospital. Clinical and classical cardiometabolic factors were compared between HLA-C∗06-positive and HLA-C∗06-negative individuals (OR with 95% CI). Multivariate regression analyses were carried out to check for disease traits associated with different cardiometabolic risk factors. The study population included 215 men (53.8%) and 185 women (46.2%), mean age of 46 ± 15 years, and an average disease evolution of 17 ± 12.6 years. Ninety-three (23.3%) patients met CASPAR criteria for psoriatic arthritis. HLA-C∗06 carriers (n: 160, 40%) showed an earlier age at disease onset, psoriasis family history, and more severe skin disease (type I disease). After correcting for age, sex, and disease duration, they also showed less hypertension (13.8% vs. 24.2%, OR 0.7 (95% CI: 0.42-0.78), p = 0.025), lower waist circumference (94.4 ± 13.7 vs. 98.3 ± 13.8 cm), and lower BMI (27 ± 4.4 vs. 28.1 ± 4.8, p < 0.05). We confirmed the well-known association between HLA-C∗06 and type I psoriatic disease. As a novel finding, patients carrying HLA-C∗06 showed a better cardiometabolic profile. In any case, these findings need further confirmation.
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