Carrying the HLA-C*06:02 allele has been linked to certain features of psoriasis, such as early onset of disease, severe disease, guttate psoriasis, and differential response to therapy with biologics in the past [2–5]. “We, therefore, set out to systematically evaluate and further characterise differences between HLA-C*06:02 positive and negative psoriasis,” Dr Ravi Ramessur (King’s College London, UK) said [1]. To do so, data of people with European ancestry was analysed from 2 British cross-sectional databanks: the Biomarkers of Systemic Treatment Outcomes in Psoriasis (BSTOP) and the UK Biobank [1,2]. BSTOP is an observational study of severe psoriasis containing clinical and genotype data from more than 70 dermatology centres in the UK. The UK Biobank is a population-based biomedical research resource with also genotype and clinical data from questionnaires and healthcare records. In the BSTOP cohort (n=3,767), 43.5% were women, 53.7% were HLA-C*06:02 positive, and the median age of psoriasis onset was 20 years [1]. In contrast, the respective characteristics in the UK Biobank (n=5,519) were 45.7%, 46.3%, and 29 years of age.
“The 2 stand-out observations from our study were: firstly, intriguing sex-specific differences and, secondly, an association with comorbidity,” Dr Ramessur disclosed. In both datasets, HLA-C*06:02-positive participants were significantly more likely to be women and have a younger median age at onset of psoriasis (P<0.0001 for all). BSTOP also provided information on the proportion of those with a family history of psoriasis and this was considerably higher in carriers of the HLA-C*06:02 allele (60.2% vs 42.6%; P<0.0001).
Obesity and hypertension associated with negative HLA-C*06:02 status
HLA-C*06:02 negativity was also associated with higher levels of obesity in terms of waist circumference and BMI, an effect that was more pronounced in women.
Overall, comorbid cardiometabolic disease had a higher prevalence in HLA-C*06:02-negative persons with a consistent trend for traits like ischaemic hypertension, ischaemic heart disease, and dyslipidaemia in both datasets. However, only hypertension demonstrated statistical significance (P<0.0001 for both datasets).
In addition, clinical subtypes were evaluated according to status of positive or negative presence of HLA-C*06:02 in BSTOP. “We confirmed the previously established association of a high prevalence of guttate psoriasis and a lower prevalence of nail involvement in HLA-C*06:02-positive compared with HLA-C*06:02-negative psoriasis,” Dr Ramessur commented.
“These findings are suggestive of a different contribution of genetic effects between the sexes and highlight the importance of considering sex stratification for future genetic analyses to help identify potential sex-specific disease mechanisms,” underlined Dr Ramessur.
- Ramessur R, et al. Differences in clinical features and comorbid burden between HLA-C*06:02 carrier groups in more than 9000 people with psoriasis. FC21, Psoriasis from Gene to Clinic 2021, 9–11 December.
- Douroudis K, et al. J Invest Dermatol. 2021;S0022-202X(21)02473–8.
- Fan X, et al. Acta Derm Venereol. 2007;87(4):335–340.
- Dand N, et al. J Allergy Clin Immunol. 2019;143(6):2120–2130.
- Gudjonsson JE, et al. J Invest Dermatol. 2006;126(4):740–745.
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Table of Contents: PFGC 2021
Featured articles
Letter from the Editor
Guselkumab shows highest drug survival among systemic treatments
Genes in Psoriasis and Psoriatic Arthritis
HLA-C*06:02-positive patients on ustekinumab show higher drug survival in a real-world scenario
Protective factors identified against anti-drug antibody formation to adalimumab in psoriasis
Comorbidity in Psoriasis
Psoriasis associated with a higher cancer risk
Comorbidity and clinical features of psoriasis vary according to HLA-C*06:02 status
Psoriasis patients with cardiovascular comorbidity characterised by high systemic inflammation
Psoriasis Therapy: New Findings
Inhibition of heat shock protein: A novel way to treat psoriasis?
Guselkumab shows highest drug survival among systemic treatments
Tapering biologics: No alarming signs of increased anti-drug antibodies
Intermediate monocytes are possible predictors of response to secukinumab
Gut microbiota of psoriasis patients: less diverse and reduced functionality
COVID-19: What's New
DLQI scores underestimated during lockdowns?
TNF blockers likely beneficial for psoriatic patients with COVID-19
Patients on immunomodulators need 2 COVID-19 vaccinations before seroconversion
Paradoxical Reactions to Biologics
The Yin and Yang of opposing vectors: an explanation for side effects of biologics
Explaining arthropathy development through IL-4 and IL-13 blockade
Best of the Posters
Potential biomarker discovered for treatment response to ustekinumab
TNF inhibitor for immune-mediated inflammatory disease doubles the risk of paradoxical psoriasis
Secukinumab also tolerable in paediatric psoriasis patients
High treatment success with ixekizumab in patients with psoriasis and diabetes
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