Non-invasive Estimation of Microvasculopathy & Endothelial Dysfunction in Stem Cell Transplant Recipients and its Relationship with GVHD.

GVHD endothelial dysfunction nailfold capillaroscopy transplant vasculopathy

Journal

Blood cell therapy
ISSN: 2432-7026
Titre abrégé: Blood Cell Ther
Pays: Japan
ID NLM: 9918333884906676

Informations de publication

Date de publication:
25 Aug 2024
Historique:
received: 31 12 2023
accepted: 11 03 2024
medline: 12 9 2024
pubmed: 12 9 2024
entrez: 12 9 2024
Statut: epublish

Résumé

Microvasculopathy and endothelial dysfunction play important roles in the development of post-transplant complications, including graft-versus-host disease (GVHD). We assessed structural microvasculopathy by employing nailfold video capillaroscopy (NFVC) and endothelial dysfunction via flow-mediated dilatation (FMD) of the brachial artery in recipients of hematopoietic stem cell transplantation. Recipients of stem cell transplantation were included in this study post day+100 and divided into two cohorts. The first cohort consisted of 35 recipients of allogeneic hematopoietic stem cell transplantation (HCT) and the second cohort was comprised of 31 recipients of autologous HCT. A third cohort included 35 healthy individuals. NFVC was conducted on the second to fifth fingers of both hands using an Optilia video capillaroscope at 200× magnification, and the images were analyzed according to the European Alliance of Associations for Rheumatology (EULAR) criteria. The following parameters were used to measure vasculopathy: (a) median capillary density, derived from the capillary density of eight fingers, (b) median capillary diameter, derived from maximum capillary apical diameters of eight fingers, and (c) significant neoangiogenesis (neoangiogenesis present in ≥2 fingers). FMD of the right brachial artery was observed by high-resolution ultrasonography using the principle of post-occlusive reactive hyperemia, and video images were analyzed using edge-detecting software. The median capillary diameter was significantly higher in the allo-HCT cohort (20.56±5.17 micrometer) compared to the auto-HCT cohort (16.19±3.31 micrometer; Our findings demonstrate the presence of structural microvasculopathy in allo-HCT recipients and suggest a possible role of alloreactivity in the pathogenesis of post-HCT microvasculopathy.

Identifiants

pubmed: 39263621
doi: 10.31547/bct-2023-041
pmc: PMC11384125
doi:

Types de publication

Journal Article

Langues

eng

Pagination

79-86

Informations de copyright

Copyright Ⓒ2024 Asia-Pacific Blood and Marrow Transplantation Group (APBMT).

Déclaration de conflit d'intérêts

The authors declare no conflict of interest. Disclosure forms provided by the authors are available on the website.

Auteurs

Sayan Sinha Roy (S)

Department of Clinical Hematology and Medical Oncology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Raghuraman Sondararajan (R)

Department of Radiodiagnosis and Imaging, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Arun Sharma (A)

Department of Radiodiagnosis and Imaging, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Manphool Singhal (M)

Department of Radiodiagnosis and Imaging, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Shefali Sharma (S)

Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Pankaj Malhotra (P)

Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Charanpreet Singh (C)

Department of Clinical Hematology and Medical Oncology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Arihant Jain (A)

Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Alka Khadwal (A)

Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Gaurav Prakash (G)

Department of Clinical Hematology and Medical Oncology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Classifications MeSH