Abstract
Objective Systemic sclerosis (SSc) gastrointestinal disease is heterogeneous in presentation, with individual symptoms lacking specificity for specific anatomical and functional abnormalities. We used factor analysis to investigate whether latent subgroups of SSc gastrointestinal symptoms can be detected.
Methods Using SCTC UCLA Gastrointestinal 2.0 Questionnaire (GIT 2.0) data from 773 Australian Scleroderma Cohort Study participants, we performed a factor analysis of firstly, GIT 2.0 domains scores and then, individual GIT 2.0 question responses to identify latent factors. A subsequent cluster analysis was performed to explore whether clinically definable SSc phenotypes were associated with specific gastrointestinal symptoms.
Results SSc gastrointestinal symptoms were highly correlated. Factor analysis of individual GIT 2.0 question responses revealed four latent factors within the dataset that could be clinically described as upper gastrointestinal tract symptoms, bloating, diarrhoea and incontinence, and constipation. Cluster analysis revealed two patient clusters, distinguished by disease duration and severity of gastrointestinal manifestations. Anti-centromere antibodies and pulmonary arterial hypertension were more common in participants with severe gastrointestinal disease.
Conclusion Despite the high correlation between gastrointestinal manifestations, it is possible to detect subgroups of SSc gastrointestinal symptoms. Improved understanding of these subgroups of SSc gastrointestinal disease may advance the discovery of targeted interventions to improve the daily function and quality of life of those living with SSc.
