Key result
Psoriasis vulgaris linked to lower blood ACE activity compared to atopic dermatitis and healthy controls.
Why the study?
Emerging evidence suggests the involvement of the renin-angiotensin system in the pathogenesis and progression of autoimmune dermatological diseases.
Does blood ACE activity differ in young males with psoriasis compared to those with atopic dermatitis and healthy controls?
Case-Control (n=14)
No
Does blood ACE activity differ in young males with psoriasis compared to those with atopic dermatitis and healthy controls?
This small pilot study suggests that blood ACE activity is significantly lowered in young men with psoriasis compared to healthy controls and those with atopic dermatitis, challenging previous reports of increased ACE activity in psoriasis.
Should not yet change psoriasis management; leaves open whether ACE differences merit targeted therapies in larger studies.
PURPOSE: Emerging evidence suggests the involvement of the renin-angiotensin system (RAS) in the pathogenesis and progression of autoimmune dermatological diseases. In a small exploratory study, we investigated angiotensin-converting enzyme (ACE) activity in blood obtained from male probands with psoriasis vulgaris (n = 4) and atopic dermatitis (AD, n = 5). METHODS: The degradation capacity of dabsylated synthetic bradykinin (DBK) with and without inhibition was determined using a thin-layer chromatography (TLC)-based neuropeptide reporter assay. RESULTS: We observed a significantly reduced capacity for cleavage of DBK in psoriasis patients compared with that in AD patients and controls. In patient samples, the variation in the measured values was generally greater than that in healthy controls. We could not confirm the increased ACE activity in the circulation in psoriasis patients reported by others, likely because of different study designs and detection methods. We did not include samples of female patients and focused on younger men to avoid hormonal effects and minimize age-related factors. CONCLUSION: This preliminary study of the hypothesis-generating nature lacks power, but it certainly adds a question to the current view of the role of ACE in psoriasis. Treatments targeting specific components of the RAS could ameliorate inflammatory responses; thus, research in this area is becoming increasingly important.
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Osterhus et al. (2026) conducted a case-control in Psoriasis vulgaris and Atopic dermatitis (n=14). Psoriasis vulgaris vs. Healthy controls and Atopic dermatitis patients was evaluated on Degradation capacity of dabsylated synthetic bradykinin (DBK) (p=0.034). Psoriasis vulgaris was associated with a significantly reduced capacity for cleavage of dabsylated bradykinin (P=0.034) compared to atopic dermatitis and healthy controls, indicating lower blood ACE activity.
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