# Chronic companions: An updated national cross-sectional study of metabolic syndrome comorbidities in outpatient visits for hidradenitis suppurativa

**Authors:** Elaine J. Ma, Alyssa M. Roberts, Peichi Chou, Abigail Katz, Charlotte Y. Jeong, Yvonne Nong, Maria T. Ochoa, April W. Armstrong

PMC · DOI: 10.1371/journal.pone.0333010 · 2025-10-24

## TL;DR

This study finds that patients with hidradenitis suppurativa have higher rates of metabolic issues like hypertension and obesity compared to others.

## Contribution

The study provides updated national data on metabolic comorbidities in hidradenitis suppurativa patients using U.S. outpatient data from 2014 to 2019.

## Key findings

- HS patients had significantly higher odds of hypertension, obesity, and hyperlipidemia compared to non-HS controls.
- No significant association was found between HS and type 2 diabetes or cerebrovascular disease.
- Chronic inflammation in HS may contribute to metabolic dysregulation, with obesity and hyperlipidemia amplifying this effect.

## Abstract

Hidradenitis suppurativa (HS) is a painful, chronic inflammatory skin disease associated with significant physical and psychosocial burden. Increasing evidence suggests HS is linked to systemic metabolic dysfunction, including components of metabolic syndrome such as obesity, hypertension, and hyperlipidemia. This study aimed to assess the prevalence of metabolic comorbidities in patients with HS using data from the National Ambulatory Medical Care Survey (NAMCS), a nationally representative dataset of U.S. outpatient visits from 2014 to 2019. We conducted a cross-sectional analysis comparing HS-related visits to age- and sex-matched non-HS visits, using multivariate logistic regression adjusted for demographic and clinical covariates. Among 1.8 million weighted HS-related visits, the most prevalent metabolic comorbidities were hypertension (15.7%), obesity (8.6%), and hyperlipidemia (7.4%). Compared to non-HS controls, HS visits had significantly higher odds of hypertension (adjusted odds ratio [aOR] 2.90; 95% confidence interval [CI]: 2.88–2.92), obesity (aOR 3.12; 3.10–3.15), and hyperlipidemia (aOR 1.76, 1.74–1.77). No significant association was found between HS and type 2 diabetes mellitus (T2DM) or cerebrovascular disease. Mechanistically, chronic systemic inflammation in HS, driven by elevated cytokines such as TNF-α, IL-6, and IL-17, may contribute to endothelial dysfunction and metabolic dysregulation. Obesity, which is commonly associated with HS, exacerbates the inflammatory state and promotes follicular occlusion, while hyperlipidemia may amplify inflammation through oxidative stress and impaired immune resolution. These findings underscore the importance of recognizing metabolic risk factors in patients with HS, particularly within the context of outpatient settings where early intervention is feasible. Early identification and management of these comorbidities may improve long-term health outcomes. Further longitudinal studies are warranted to clarify causal relationships and support the development of multidisciplinary screening and care strategies for this high-risk population.

## Linked entities

- **Chemicals:** IL-6 (PubChem CID 165368475)
- **Diseases:** Hidradenitis suppurativa (MONDO:0006559), obesity (MONDO:0011122), hyperlipidemia (MONDO:0021187), type 2 diabetes mellitus (MONDO:0005148), cerebrovascular disease (MONDO:0011057)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** Obesity (MESH:D009765), endothelial dysfunction (MESH:D014652), metabolic syndrome (MESH:D024821), chronic systemic inflammation (MESH:D007249), hypertension (MESH:D006973), cerebrovascular disease (MESH:D002561), hyperlipidemia (MESH:D006949), HS (MESH:D017497), T2DM (MESH:D003924), metabolic dysregulation (MESH:D021081), metabolic dysfunction (MESH:D008659), inflammatory skin disease (MESH:D012871)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12551858/full.md

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Source: https://tomesphere.com/paper/PMC12551858