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Lupus (SLE): Symptoms, Causes, Diagnosis, and Treatment
What Is Lupus?
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease where the immune system attacks healthy tissues—joints, skin, kidneys, blood cells, heart, lungs, and brain.
Epidemiology
- 9:1 female‑to‑male ratio.
- Onset typically ages 15–44.
- Higher prevalence in African American, Hispanic, Asian, and Native American populations.
Causes
Multifactorial: genetic susceptibility (HLA‑DR2/DR3, complement deficiencies), environmental triggers (UV light, infections, drugs), and hormonal influences (estrogen).
Common Symptoms
- Fatigue, fever, weight loss
- Malar (“butterfly”) rash, photosensitivity
- Arthralgia/arthritis (non‑erosive)
- Renal involvement (lupus nephritis)
- Serositis (pleuritis, pericarditis)
- Hematologic: anemia, leukopenia, thrombocytopenia
- Neuropsychiatric: seizures, psychosis, cognitive dysfunction
Diagnosis
2019 EULAR/ACR criteria: ANA positivity ≥1:80 plus clinical criteria (weighted scoring). Key labs: anti‑dsDNA, anti‑Sm, complement (C3, C4), urinalysis, biopsy if nephritis suspected.
Treatment
- Hydroxychloroquine (baseline for all).
- Corticosteroids for flares.
- Immunosuppressants: mycophenolate, azathioprine, cyclophosphamide (severe).
- Biologics: belimumab, anifrolumab.
- ACE inhibitors for renal protection.
Prognosis
With modern therapy, 10‑year survival >90%. Regular monitoring prevents irreversible organ damage.
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