Gastrointestinal motility disorder assessment in systemic sclerosis

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Abstract

Objectives: SSc is a clinically heterogeneous and generalized disease, characterized by thickness of the connective tissue of the skin and internal organs, such as the digestive tract, impairing gastrointestinal (GI) motility. Our aim is to evaluate retrospectively abnormalities of oesophageal motility, gastric emptying, oro-cecal transit time (OCTT) and small intestine bacterial overgrowth (SIBO) in a large cohort of SSc patients. Methods: Ninety-nine SSc patients were included in the study. Forty-two patients underwent oesophageal conventional manometry, 45 performed a [13C]octanoic acid breath test to measure gastric emptying time and all 99 patients performed a lactulose breath test in order to evaluate OCTT and SIBO. Data were compared with healthy controls. Results: In SSc patients, median lower oesophageal sphincter (LOS) pressure [14mmHg (25th-75th; 8-19) vs 24mmHg (19-28); P<0.01] and median wave amplitude [30mmHg (16-70) vs 72mmHg (48-96); P<0.01] were lower than in controls. Oesophageal involvement, defined as reduced LOS pressure and ineffective oesophageal motility pattern, was encountered in 70% of SSc patients. A delayed gastric emptying time was present in 38% of SSc patients: mean t1/2 was 141 ± 79 min vs 90 ± 40 min of controls (P<0.01). Also, OCTT was significantly delayed in SSc: median OCTT was 160 min (25th-75th; 135-180) vs 105 min (25th-75th; 90-135) of controls (P<0.01). SIBO was observed in 46% of SSc compared with 5% of controls (P<0.01). Conclusion: GI involvement is very frequent in SSc patients. Oesophagus and small bowel are more frequently impaired, whereas delayed gastric emptying is less common. © The Author 2013. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.

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Savarino, E., Mei, F., Parodi, A., Ghio, M., Furnari, M., Gentile, A., … Gasbarrini, A. (2013). Gastrointestinal motility disorder assessment in systemic sclerosis. Rheumatology (United Kingdom), 52(6), 1095–1100. https://doi.org/10.1093/rheumatology/kes429

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