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Gastrointestinal involvement in systemic sclerosis: An updated review
Mahmoud Nassar1, Victoria Ghernautan1, Nso Nso1
1Department of Medicine, Icahn School of Medicine at Mount Sinai, NYC Health+Hospitals, Queens, NY, USA.
Systemic scleroderma (SSc) frequently impacts the gastrointestinal tract, leading to severe complications and increased mortality. Effective multidisciplinary management and targeted therapies are crucial for improving patient outcomes and quality of life.
Area of Science:
- Gastroenterology and Immunology
- Rheumatology
Background:
- Systemic scleroderma (SSc) significantly affects the gastrointestinal (GI) tract, second only to the skin.
- GI manifestations are linked to elevated morbidity and mortality rates in SSc patients.
- The incidence of SSc is approximately 19.3 per million adults in the US, with higher prevalence in females aged 44-55.
Approach:
- This article provides a comprehensive overview of GI pathology in SSc.
- It summarizes epidemiology, clinical manifestations, complications, and current treatment strategies.
- Highlights the need for multidisciplinary management and prospective studies for targeted therapies.
Key Points:
- Esophageal and intestinal involvement affects 90% and 40-70% of SSc patients, respectively.
- Small bowel hypomotility and bacterial overgrowth cause malabsorption, malnutrition, and contribute to a 50% mortality rate.
- Fecal incontinence is a common symptom, potentially leading to depression and reduced quality of life.
Conclusions:
- Gastrointestinal complications in SSc profoundly impact daily life and prognosis.
- Multidisciplinary approaches are essential for managing these complex GI issues.
- Further research into targeted therapies is needed to improve SSc patient recovery and outcomes.
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