# Phenotype-associated microvascular differences in pediatric Behçet’s disease revealed by nailfold videocapillaroscopy

**Authors:** Ufuk Furkan Ozdemir, Elif Kucuk, Lutfiye Koru, Feray Kaya, Zelal Aydin, Serpil Meric Toprak, Betul Aysegul Ayyildiz, Hatice Kubra Dursun, Eda Nur Dizman, Merve Ozen Balci, Kubra Ozturk, Fatih Haslak

PMC · DOI: 10.1007/s00431-026-06804-x · European Journal of Pediatrics · 2026-02-23

## TL;DR

This study finds that children with Behçet’s disease show distinct microvascular changes, with more severe changes in those with complete disease phenotype.

## Contribution

The study reveals measurable microvascular abnormalities in pediatric Behçet’s disease using nailfold videocapillaroscopy, with differences between complete and incomplete disease phenotypes.

## Key findings

- Complete BD patients showed significantly lower capillary density and more abnormal capillary features than incomplete BD.
- BD patients had lower capillary density and higher intercapillary distance compared to healthy children.
- Microvascular changes in BD were more pronounced in complete phenotype, suggesting cumulative vascular burden.

## Abstract

Behçet’s disease (BD) is a chronic multisystem vasculitis that may begin in childhood. Microvascular dysfunction is central to its pathogenesis, yet pediatric data are scarce. This study evaluated nailfold videocapillaroscopy (NVC) findings in children with BD using standardized methodology and compared microvascular parameters between complete and incomplete disease phenotypes, as well as with age-matched healthy reference data. In this cross-sectional study, pediatric BD patients fulfilling the pediatric Behçet’s disease (PEDBD) criteria underwent NVC following the European Alliance of Associations for Rheumatology (EULAR) microcirculation protocol. Capillary density, morphology, and microhemorrhages were compared between complete and incomplete BD and with age-matched healthy reference data. Associations between NVC parameters and clinical or laboratory findings were analyzed. Complete BD patients (n = 15, 40.5%) had significantly lower capillary density and higher apical loop width, tortuosity, dilatation, abnormal capillaries, and microhemorrhage scores than incomplete BD (n = 22, 59.5%). Compared with healthy peers, BD patients showed significantly lower capillary density, arterial and venous diameters, and capillary length but higher intercapillary distance and width.

Conclusion: Pediatric BD is associated with distinct NVC abnormalities compared with healthy reference data. Differences in capillary density and morphology were observed between complete and incomplete phenotypes. These findings provide a descriptive overview of phenotype-associated microvascular features in pediatric BD.
What Is Known:• Nailfold videocapillaroscopy (NVC) can detect microvascular abnormalities in adult Behçet’s disease, but pediatric data are extremely limited.• Childhood-onset Behçet’s disease often evolves over time from incomplete to complete phenotype, and reliable objective markers reflecting vascular involvement are lacking.What Is New:• Pediatric Behçet’s disease shows measurable NVC abnormalities compared with healthy children, even in the absence of clinically overt vascular involvement.• Microvascular alterations are significantly more pronounced in complete phenotype than incomplete phenotype, suggesting cumulative vascular burden independent of disease activity scores.

What Is Known:

• Nailfold videocapillaroscopy (NVC) can detect microvascular abnormalities in adult Behçet’s disease, but pediatric data are extremely limited.

• Childhood-onset Behçet’s disease often evolves over time from incomplete to complete phenotype, and reliable objective markers reflecting vascular involvement are lacking.

What Is New:

• Pediatric Behçet’s disease shows measurable NVC abnormalities compared with healthy children, even in the absence of clinically overt vascular involvement.

• Microvascular alterations are significantly more pronounced in complete phenotype than incomplete phenotype, suggesting cumulative vascular burden independent of disease activity scores.

The online version contains supplementary material available at 10.1007/s00431-026-06804-x.

## Linked entities

- **Diseases:** Behçet’s disease (MONDO:0007191)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Raynaud's phenomenon (MESH:D011928), systemic vasculitis (MESH:D056647), uveitis (MESH:D014605), BDCAF (MESH:D001528), pseudofolliculitis (MESH:C563016), scleroderma (MESH:D012595), aphthae (MESH:D013281), capillary abnormalities (OMIM:163000), connective tissue disease (MESH:D003240), Microvascular dysfunction (MESH:D017566), NVC abnormalities (MESH:D000014), thrombotic (MESH:D013927), nailbed trauma (MESH:D014947), erythema nodosum (MESH:D004893), Vasculitis (MESH:D014657), inflammation (MESH:D007249), genital ulcer (MESH:D014456), Rheumatic Diseases (MESH:D012216), vascular injury (MESH:D057772), involvement (MESH:C564676), antiphospholipid syndrome (MESH:D016736), endothelial dysfunction (MESH:D014652), acneiform lesion (MESH:D017486), infection (MESH:D007239)
- **Chemicals:** colchicine (MESH:D003078), PVAS (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12929361