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Objectives: The gastrointestinal tract (GIT) is frequently involved in systemic sclerosis (SSc) and is responsible for alteration of quality of life. Many complications can occur, including chronic intestinal pseudo-obstruction, digestive haemorrhage and small-intestinal bacterial overgrowth. Since early development of organ failure is associated with poor prognosis, we need to identify risk factors associated with severe GIT involvement to prevent severe forms of the disease.
Methods: We conducted an observational prospective study, which included 90 SSc patients from December 2019 to September 2021. We collected questionnaires about digestive manifestations and quality of life, blood and stool samples, and performed imaging. At inclusion and throughout the study we assessed the occurrence of malnutrition and severe GIT disorders. We performed statistical analysis to highlight eventual risk factors associated with digestive manifestations, including hierarchical cluster analysis.
Results: A majority of our patients had gastro-oesophageal manifestations (93.3%), followed by intestinal manifestations (67.8%) and anorectal manifestations (18.9%). We found a correlation between anorectal disorders and cardiac disease, and between gastro-oesophageal involvement and impaired pulmonary function tests. Smoking was significantly associated with occurrence of severe GIT disorders. Malnutrition was frequent and associated with more cardiac and pulmonary disease. Cluster analysis identified three groups of patients, including one cluster with cardiac and digestive involvement.
Conclusions: GIT manifestations are frequent and severe in SSc. Smoking appears to be associated with severe disease. Anorectal manifestations may be associated with cardiac disease, but we need more studies to validate these results.
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http://dx.doi.org/10.55563/clinexprheumatol/qcnuhv | DOI Listing |
Arthritis Care Res (Hoboken)
September 2025
University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Objective: The objective of this study is to characterize gastrointestinal (GI) manifestations in juvenile-onset systemic sclerosis (jSSc) using the UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract 2.0 (UCLA GIT 2.0) patient-reported outcome (PRO) instrument, and to evaluate its validity and responsiveness in this population.
View Article and Find Full Text PDFSci Rep
August 2025
Rheumatology Department, Faculty of Medicine, Al-Azhar University (Cairo branch), Cairo, Egypt.
To describe various demographic, clinical, laboratory, and capillaroscopic features of Egyptian patients with systemic sclerosis (SSc) and to explore the relation between various capillaroscopic features and internal organ involvement as well as other disease parameters. In this cross-sectional multi-centric prospective analysis, two hundred twenty-two adult patients with SSc were recruited. Data regarding general and rheumatological examination including the modified Rodnan skin score (MRSS), internal organ involvement and related imaging and laboratory investigations were collected.
View Article and Find Full Text PDFComput Biol Med
September 2025
Kyungpook National University, School of Computer Science and Engineering, Buk-gu, Daegu, 41566, Daegu, Republic of Korea. Electronic address:
Motivation: Analogous to the sequence-to-sequence alignment problem in discrete settings, two time-series can be aligned based on their longitudinal similarity. In disease contexts, aligning time-series that represent patient severity levels allows quantifying the similarity in their progression. However, in real-world clinical settings, patients are hospitalized at varying stages, and measurements are taken at irregular intervals, leading to sequences of different lengths and sampling rates.
View Article and Find Full Text PDFBioinformatics
July 2025
Department of Statistics and Data Science, Fudan Univers ity, Shanghai, 200094, China.
Motivation: A critical challenge in observational studies arises from the presence of hidden confounders in high-dimensional data. This leads to biases in causal effect estimation due to both hidden confounding and high-dimensional estimation. Some classical deconfounding methods are inadequate for high-dimensional scenarios and typically require prior information on hidden confounders.
View Article and Find Full Text PDFRheumatology (Oxford)
July 2025
Division of Rheumatology, UTHealth Houston, Houston, TX, USA.
Objectives: Anti- Cytolethal Distending Toxin (CDT) antibodies may serve as biomarkers for post-infectious autoimmunity and aid clinical risk stratification. We aimed to determine the prevalence of anti-CDT antibodies in a large, well-characterized cohort of systemic sclerosis (SSc) patients and examine associations with gastrointestinal (GI) and extraintestinal clinical features and SSc-related antibodies.
Methods: Sera from 130 SSc patients enriched for GI disease were screened for anti-CDT antibodies by ELISA.