Immunohistochemical Expression of Haptoglobin in Skin Lesions of Hidradenitis Suppurativa
- PMID: 40430166
- PMCID: PMC12113320
- DOI: 10.3390/life15050738
Immunohistochemical Expression of Haptoglobin in Skin Lesions of Hidradenitis Suppurativa
Abstract
Background: Meta-inflammation is a hallmark of hidradenitis suppurativa (HS). Research on meta-inflammation in HS is growing, but there is still no research on haptoglobin as an inflammatory protein in lesional HS skin. This study examines the relationship between haptoglobin expression in HS skin lesions and clinical parameters.
Methods: An examination was performed on 44 skin samples from HS patients and 10 healthy skin samples. Clinical parameters were then compared with haptoglobin expression.
Results: Median haptoglobin expression was significantly higher in the Hurley stage III lesions compared with milder stages (H-score: 37.6 versus 17.1, p = 0.028). High haptoglobin expression (≥30.8% positive cells) was associated with advanced disease (Hurley stage III: 80% versus 41.7%, p = 0.01), active smoking (80% versus 50%, p = 0.039), increased pain (visual analogue scale: 5 versus 1.5, p = 0.03), and a higher prevalence of diabetes (35% versus 8.3%, p = 0.029) and hypertension (55% versus 25%, p = 0.042). No significant associations were found with the BMI, disease duration, or CRP levels.
Conclusions: High haptoglobin expression (positive cells ≥ 30.8%) in a skin lesion is associated with higher HS severity, active smoking, more pain and the comorbidities of diabetes mellitus and arterial hypertension in HS patients.
Keywords: HS; diabetes mellitus; haptoglobin; hidradenitis suppurativa; inflammation; meta-inflammation; skin lesion.
Conflict of interest statement
N.A. received funding, travel support, or personal honoraria for lectures from Novartis Pharma, Janssen-Cilag GmbH, Recordati Rare Diseases Germany GmbH, Therakos (UK) Ltd. and Johnson & Johnson that were independent of the work submitted. F.G.B. has received honoraria for participation on advisory boards, in clinical trials, or as a speaker from AbbVie Inc., AbbVie Deutschland GmbH & Co. KG, Acelyrin, Beiersdorf, Boehringer Ingelheim Pharma GmbH & Co. KG, Celltrion, Dr. Wolff, Incyte Corporation, Janssen-Cilag GmbH, Johnson & Johnson, Merck, Mölnlycke, MoonLake, Novartis Pharma GmbH, Sanofi, Sitala and UCB Pharma. E.S. has received lecture fees from Almirall, Leo, Pierre Favre, and Philips. L.O. has received honoraria as a speaker or travel support from Novartis Pharma GmbH, Incyte Biosciences Corporation, and Janssen. T.M. has received honoraria as a speaker from Novartis, Coldplasmatech and Hologic. The other authors (H.T., M.S., D.M., Y.H.) declare no conflicts of interest.
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