Dermal cellular senescence and EndMT in patients with systemic sclerosis undergoing cyclophosphamide or aHSCT treatment

Both aHSCT and iv CYC in dcSSc reduced skin thickening clinically and attenuated EndMT, but affected cellular senescence not significantly different. EndMT and uPAR were associated with fibro-remodelling activity, whereas senescence, CTGF, uPAR and vascularity were associated with treatment response.

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Publication Details

Journal
Lara D. Veeken
Published
2024-12-04
DOI
https://doi.org/10.1093/rheumatology/keae660
Citations
1
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
0.42

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article

Dermal cellular senescence and EndMT in patients with systemic sclerosis undergoing cyclophosphamide or aHSCT treatment

Jeska K de Vries‐Bouwstra, Yu‐Hsiang Chiu, Roel Goldschmeding, Julia Spierings et al.
1 citations
Lara D. Veeken
Systemic Sclerosis and Related Diseases
0.42
article

Dermal cellular senescence and EndMT in patients with systemic sclerosis undergoing cyclophosphamide or aHSCT treatment

Jeska K de Vries‐Bouwstra, Yu‐Hsiang Chiu, Roel Goldschmeding, Julia Spierings, J.M. van Laar, Marijke van Dijk
article en
1 citations

Abstract

Both aHSCT and iv CYC in dcSSc reduced skin thickening clinically and attenuated EndMT, but affected cellular senescence not significantly different. EndMT and uPAR were associated with fibro-remodelling activity, whereas senescence, CTGF, uPAR and vascularity were associated with treatment response.

Lara D. VeekenVol. 64(6)
Tri-Service General Hospital (TW), Utrecht University (NL), Leiden University Medical Center (NL), The Royal Free Hospital (GB), University Medical Center Utrecht (NL), University College London (GB), National Defense Medical Center (TW)
Eli Lilly and Company, Universitair Medisch Centrum Utrecht, Leids Universitair Medisch Centrum
Good health and well-being
Openalex Percentile: Top 32%
Systemic Sclerosis and Related Diseases
0.42
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