Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Oct 6;61(10):4024-4034.
doi: 10.1093/rheumatology/keac118.

Gastrointestinal symptom severity and progression in systemic sclerosis

Affiliations

Gastrointestinal symptom severity and progression in systemic sclerosis

Nina M van Leeuwen et al. Rheumatology (Oxford). .

Abstract

Objectives: To evaluate the severity and evolution of patient-reported gastrointestinal tract (GIT) symptoms in systemic sclerosis (SSc) patients, assess predictive factors for progression and determine the impact of standard of care treatment.

Methods: SSc patients from the Leiden and Oslo cohorts were included. We assessed clinical data and patient-reported GIT symptoms measured by the validated University of California, Los-Angeles Gastrointestinal-tract (UCLA-GIT) score at baseline and annually. GIT severity and progression was determined. Logistic regression was applied to identify risk factors associated with baseline GIT symptom severity. Linear mixed-effect models were applied to assess progression in GIT symptom burden and to identify predictive factors. We repeated all analysis in patients with early disease (inception cohort) to exclude the effect of longstanding disease and increase insights in development of GIT symptom burden early in the disease course.

Results: We included 834 SSc patients with baseline UCLA GIT scores, 454 from Leiden and 380 from Oslo. In the total cohort, 28% reported moderate-severe GIT symptoms at baseline, with increased risk for severity conferred by ACA, smoking and corticosteroid use, while use of calcium channel blockers appeared protective. In the inception cohort, 23% reported moderate-severe GIT symptoms at baseline, with increased risk for females and with smoking. Over time, symptom burden increased mainly for reflux/bloating. Female sex and ACA predicted GIT symptom progression.

Conclusion: High GIT symptom burden is present early in SSc disease course. Both for prevalence and for progression of GIT symptom burden, female sex and smoking were identified as risk factors.

Keywords: SSc; gastrointestinal symptoms.

PubMed Disclaimer

Figures

<sc>Fig</sc>. 1
Fig. 1
Severity of gastrointestinal involvement at baseline in the total cohort and the inception cohort Disease severity at baseline according to the UCLA GIT 2.0 score on every subdomain in the total and the inception cohort. This figure shows the percentage of SSc patients with non-mild, moderate and severe gastro-intestinal involvement for each subdomain at baseline.
<sc>Fig</sc>. 2
Fig. 2
Mean scores per GIT subdomain over the follow-up period in the inception cohort and the total cohort Mean scores per GIT subdomain over the follow-up period in the inception and the total cohort. Higher scores indicate worse GIT symptoms, lower scores indicate lesser GIT symptoms.
<sc>Fig</sc>. 3
Fig. 3
Progressors (inception) for the total GIT score after 1 year stratified for immunomodulatory treatment Percentage of progressors in inception cohort. Inception patients with available UCLA GIT after one year (n = 118); n = 71 remained treatment-naïve, n = 47 started with immune-modulating therapy. No treatment are those patients who remained treatment-naïve.

References

    1. Butt S, Emmanuel A.. Systemic sclerosis and the gut. Expert Rev Gastroenterol Hepatol 2013;7:331–9. - PubMed
    1. Nagaraja V, McMahan ZH, Getzug T, Khanna D.. Management of gastrointestinal involvement in scleroderma. Curr Treat Options Rheumatol 2015;1:82–105. - PMC - PubMed
    1. Khanna D, Hays RD, Park GS. et al. Development of a preliminary scleroderma gastrointestinal tract 1.0 quality of life instrument. Arthritis Rheum 2007;57:1280–6. - PubMed
    1. Steen VD, Medsger TA Jr.. Severe organ involvement in systemic sclerosis with diffuse scleroderma. Arthritis Rheum 2000;43:2437–44. - PubMed
    1. Richard N, Hudson M, Wang M. et al. Severe gastrointestinal disease in very early systemic sclerosis is associated with early mortality. Rheumatology 2019;58:636–44. - PMC - PubMed

Substances