Publications by authors named "C Cazalets"
Objective: The objective of this study was to explore the etiologies and contributing factors of synovial and tenosynovial involvement in SSc, as well as to assess the phenotype of patients with these synovial and tenosynovial features.
Methods: 171 SSc patients with hand manifestations (either vascular, skin or joint manifestations) who underwent standard X-rays of both hands and hand ultrasound (US), were included. Two independent evaluators recorded the presence or absence of acro-osteolysis, calcinosis, microcrystalline and degenerative rheumatisms, including osteophytosis on X-Rays.
Introduction: Systemic sclerosis (SSc) is an autoimmune disease characterized by antinuclear antibody production, which has been linked to an excess of apoptotic cells, normally eliminated by macrophages through efferocytosis. Additionally, circulating levels of CXCL4, a novel SSc biomarker, correlate with more severe fibrotic manifestations of the disease. Considering the defective efferocytosis of macrophages in SSc and the CXCL4-related M4 macrophage phenotype, we hypothesized that CXCL4 could be involved in the alteration of phagocytic functions of macrophages in SSc, including LC3-associated phagocytosis (LAP), another phagocytic process requiring autophagy proteins and contributing to immune silencing.
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- The study aimed to explore the characteristics of Systemic sclerosis (SSc) patients experiencing sicca symptoms, by analyzing major salivary glands through ultrasound, minor salivary gland biopsies, and clinical evaluations, while comparing these to patients with Sjögren's Disease (SjD) and other causes of sicca symptoms.
- A total of 60 SSc patients with sicca symptoms and additional groups including SSc patients without symptoms and SjD patients were examined, revealing that many SSc patients showed objective abnormalities in salivary gland function, even if they didn't report symptoms.
- The findings indicated that SjD-SSc patients had more severe salivary gland involvement compared to those with isolated conditions, highlighting the need for future
SSc is an auto-immune disease characterized by life-threatening manifestations such as lung fibrosis or pulmonary arterial hypertension. Symptoms with a detrimental impact on quality of life are also reported and sicca syndrome (xerostomia, xeropthalmia) is present in up to 80% of patients with SSc. Sicca syndrome can occur in the absence of overlap with Sjögren's disease and recent studies highlight that fibrosis of minor and major salivary glands, directly linked to the pathogenesis of SSc, could be a major contributor of xerostomia in SSc.
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