Clinical features of Systemic Lupus Erythematosus (SLE) patients attending the SLE outpatient clinic at the Universitas Hospital in Bloemfontein, SA.

  • Robyn Carey University of the Free State
  • Shereez Simmons University of the Free State
  • Megan Malherbe University of the Free State
  • Johan Jansen van Rensburg University of the Free State
  • Gina Joubert University of the Free State
Keywords: Systemic Lupus Erythematosus, profile, clinical features, SLE

Abstract

Background: Systemic lupus erythematosus (SLE) is an autoimmune disease, a type of self-allergy, whereby the patient’s immune system creates antibodies that attack the person’s own body tissues instead of protecting the body from bacteria and viruses. In most cases the cause of SLE is unknown, although it is believed that many factors may be involved, including genetic predisposition and environmental factors such as excessive sun exposure, infections, antibiotics (especially those in the sulpha and penicillin groups), extreme stress, certain drugs, and hormones. Currently, there is no single laboratory test that can determine whether a person has lupus or not. To assist the physician in the diagnosis of lupus, the American College of Rheumatology (ACR) has compiled a list of 11 symptoms or signs of which a person should have four or more to be classified as SLE. The genetic pool and environmental factors differ in different regions. The Free State and Northern Cape are known for a dry and sunny climate, as well as cold winters. The aim of this study was to determine the most common features of patients with systemic lupus erythematosus attending the outpatient clinic at Universitas Hospital in Bloemfontein, South Africa. Methods: For this descriptive study, the study population included all patients attending the SLE clinic at Universitas Hospital diagnosed with SLE according to the ACR classification criteria. Patients were only included if they had at least one follow-up visit. Patients who had discoid lupus were excluded. Data were collected from patient files using a confidential and anonymous data form. Results: Data were obtained from 76 patients: 71 females (94.7%) and five males (5.3%). African patients accounted for 61.3% of the study population, whites for 33.9%, Asians for 1.6% and coloureds for 3.2%. Patients most frequently had immunological (90.8%), mucocutaneous (86.9%), musculoskeletal (85.5%) and cardiovascular problems (77.6%). Conclusion: Most of the findings correlate with similar studies worldwide. However, mucocutaneous manifestations and Raynaud’s phenomenon were more prevalent in our study population. From this it can be deduced that the climate may play an important role. Further research needs to be conducted to investigate this hypothesis.

Author Biographies

Robyn Carey, University of the Free State
Medical Student School of Medicine
Shereez Simmons, University of the Free State
Medical Student School of Medicine
Megan Malherbe, University of the Free State
Medical Student (deceased) School of Medicine
Johan Jansen van Rensburg, University of the Free State
MBChB, MMed Consultant in Rheumatology Department of Internal Medicine
Gina Joubert, University of the Free State
BA, MSc Head of Department Department of Biostatistics
Published
2008-01-17
Section
Original Research