J Rheum Dis.  2022 Oct;29(4):200-214. 10.4078/jrd.22.0029.

Epidemiology and Treatment of Systemic Sclerosis in Korea

Affiliations
  • 1Department of Internal Medicine, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea
  • 2Division of Rheumatology, Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea

Abstract

Systemic sclerosis (SSc), a rare, chronic progressive systemic autoimmune disease of unknown etiology, is characterized by autoimmunity, tissue fibrosis, and obliterative vasculopathy. SSc can affect all major organs including the skin, blood vessels, lung, heart, kidneys, and gastrointestinal tract. Our understanding of its pathogenesis has increased over the past few decades, leading to improved diagnosis and treatment. However, the mortality rate of SSc remains considerable, mainly due to cardiopulmonary causes. A growing body of evidence suggests that geographical, regional, and ethnic differences could affect the epidemiology, clinical characteristics and prognosis of SSc. Although Korean data of this issue are lacking, a considerable amount of research has been published by many Korean researchers. To establish treatment strategies for Korean patients, extensive Korean research data are needed. This review summarizes the prevalence, incidence, mortality, and clinical and laboratory manifestations of Korean patients with SSc and discusses the current trends in evidence-based treatment and recommendations.

Keyword

Systemic scleroderma; Epidemiology; Korea; Drug therapy

Figure

  • Fig. 1 The frequency of systemic sclerosis specific autoantibodies in patients with systemic sclerosis according to the countries. Scl70: anti-Scl70 antibody, ACA: anti-centromere antibody.


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