Literature DB >> 24399159

Transforming growth factor-β and inflammation in vascular (type IV) Ehlers-Danlos syndrome.

Rachel Morissette1, Florian Schoenhoff, Zhi Xu, David A Shilane, Benjamin F Griswold, Wuyan Chen, Jiandong Yang, Jie Zhu, Justyna Fert-Bober, Leslie Sloper, Jason Lehman, Natalie Commins, Jennifer E Van Eyk, Nazli B McDonnell.   

Abstract

BACKGROUND: Vascular Ehlers-Danlos syndrome (VEDS) causes reduced life expectancy because of arterial dissections/rupture and hollow organ rupture. Although the causative gene, COL3A1, was identified >20 years ago, there has been limited progress in understanding the disease mechanisms or identifying treatments. METHODS AND
RESULTS: We studied inflammatory and transforming growth factor-β (TGF-β) signaling biomarkers in plasma and from dermal fibroblasts from patients with VEDS. Analyses were done in terms of clinical disease severity, genotype-phenotype correlations, and body composition and fat deposition alterations. VEDS subjects had increased circulating TGF-β1, TGF-β2, monocyte chemotactic protein-1, C-reactive protein, intercellular adhesion molecule-1, vascular cell adhesion molecule-1, and leptin and decreased interleukin-8 versus controls. VEDS dermal fibroblasts secreted more TGF-β2, whereas downstream canonical/noncanonical TGF-β signaling was not different. Patients with COL3A1 exon skipping mutations had higher plasma intercellular adhesion molecule-1 and vascular cell adhesion molecule-1, and VEDS probands had abnormally high plasma C-reactive protein versus affected patients identified through family members before any disease manifestations. Patients with VEDS had higher mean platelet volumes, suggesting increased platelet turnover because of ongoing vascular damage, as well as increased regional truncal adiposity.
CONCLUSIONS: These findings suggest that VEDS is a systemic disease with a major inflammatory component. C-reactive protein is linked to disease state and may be a disease activity marker. No changes in downstream TGF-β signaling and increased platelet turnover suggest that chronic vascular damage may partially explain increased plasma TGF-β1. Finally, we found a novel role for dysregulated TGF-β2, as well as adipocyte dysfunction, as demonstrated through reduced interleukin-8 and elevated leptin in VEDS.

Entities:  

Keywords:  Ehlers-Danlos syndrome; aneurysm; biomarkers; extracellular matrix; inflammation

Mesh:

Substances:

Year:  2014        PMID: 24399159     DOI: 10.1161/CIRCGENETICS.113.000280

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  23 in total

Review 1.  The Ehlers-Danlos syndromes.

Authors:  Fransiska Malfait; Marco Castori; Clair A Francomano; Cecilia Giunta; Tomoki Kosho; Peter H Byers
Journal:  Nat Rev Dis Primers       Date:  2020-07-30       Impact factor: 52.329

Review 2.  Eosinophilic Esophagitis: A Primary Disease of the Esophageal Mucosa.

Authors:  J Pablo Abonia; Jonathan M Spergel; Antonella Cianferoni
Journal:  J Allergy Clin Immunol Pract       Date:  2017-03-28

3.  Histone Deacetylase 3 Coordinates Deacetylase-independent Epigenetic Silencing of Transforming Growth Factor-β1 (TGF-β1) to Orchestrate Second Heart Field Development.

Authors:  Sara L Lewandowski; Harish P Janardhan; Chinmay M Trivedi
Journal:  J Biol Chem       Date:  2015-09-29       Impact factor: 5.157

4.  Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia.

Authors:  Rachel Morissette; Wuyan Chen; Ashley F Perritt; Jennifer L Dreiling; Andrew E Arai; Vandana Sachdev; Hwaida Hannoush; Ashwini Mallappa; Zhi Xu; Nazli B McDonnell; Martha Quezado; Deborah P Merke
Journal:  J Clin Endocrinol Metab       Date:  2015-06-15       Impact factor: 5.958

5.  Editorial: Molecular Mechanisms of Heritable Connective Tissue Disorders.

Authors:  Fransiska Malfait; Antonella Forlino; Gerhard Sengle; Tom Van Agtmael
Journal:  Front Genet       Date:  2022-04-27       Impact factor: 4.772

6.  Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome.

Authors:  Keren Machol; Urszula Polak; Monika Weisz-Hubshman; I-Wen Song; Shan Chen; Ming-Ming Jiang; Yuqing Chen-Evenson; Mary Ann E Weis; Douglas R Keene; David R Eyre; Brendan H Lee
Journal:  Hum Mol Genet       Date:  2022-04-22       Impact factor: 5.121

7.  Vascular Ehlers-Danlos syndrome: exploring the role of inflammation in arterial disease.

Authors:  Dianna M Milewicz; Amy J Reid; Alana C Cecchi
Journal:  Circ Cardiovasc Genet       Date:  2014-02

8.  Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-β expression and connective tissue features.

Authors:  Santhi K Ganesh; Rachel Morissette; Zhi Xu; Florian Schoenhoff; Benjamin F Griswold; Jiandong Yang; Lan Tong; Min-Lee Yang; Kristina Hunker; Leslie Sloper; Shinie Kuo; Rafi Raza; Dianna M Milewicz; Clair A Francomano; Harry C Dietz; Jennifer Van Eyk; Nazli B McDonnell
Journal:  FASEB J       Date:  2014-04-14       Impact factor: 5.191

Review 9.  Pathophysiology of Eosinophilic Esophagitis.

Authors:  Benjamin P Davis
Journal:  Clin Rev Allergy Immunol       Date:  2018-08       Impact factor: 8.667

10.  Targeted next-generation sequencing makes new molecular diagnoses and expands genotype-phenotype relationship in Ehlers-Danlos syndrome.

Authors:  Ruwan A Weerakkody; Jana Vandrovcova; Christina Kanonidou; Michael Mueller; Piyush Gampawar; Yousef Ibrahim; Penny Norsworthy; Jennifer Biggs; Abdulshakur Abdullah; David Ross; Holly A Black; David Ferguson; Nicholas J Cheshire; Hanadi Kazkaz; Rodney Grahame; Neeti Ghali; Anthony Vandersteen; F Michael Pope; Timothy J Aitman
Journal:  Genet Med       Date:  2016-03-24       Impact factor: 8.822

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