Symptoms and manifestations which led to PGA≥0.5* despite cSLEDAI-2K=0 in a multicentre cohort of 646 patients with lupus
Patients with PGA≥0.5 and cSLEDAI-2K=0 | 195/646 (30.2%) |
1. Patients with subjective findings without objectifiable clinical manifestations likely due to SLE (condition 1) | 157/195 (80.5%) |
Musculoskeletal domain | 98 |
Arthromyalgias | 95 |
Low back pain | 10 |
Morning stiffness | 8 |
Asthenia/fatigue | 66 |
Paraesthesia | 1 |
Finger stings | 1 |
Shortness of breath | 1 |
Nausea | 1 |
Burning mouth syndrome | 1 |
Ocular pain | 1 |
Dermatitis/urticaria | 1 |
Multiple symptoms (arthromyalgias, asthenia, anxiety, panic attack, hallucinations, demoralisation, sleepiness, confusion, headache, memory deficit, dizziness, insomnia, vision loss, low-grade fever, chronic cough, paraesthesia, finger stings, chronic pharyngodynia, fast heartbeat, chronic itch, influenza syndrome, hand/foot ulcers, constipation, vaginosis and/or effluvium capillorum) | 25 |
2. Patients with objectifiable clinical manifestations likely due to SLE (condition 2) | 38/195 (19.5%) |
Haematological involvement (i.e., lymphopenia, haemolytic anaemia)† | 10 |
Monoarthritis | 10 |
Proteinuria‡ | 6 |
Recurrent infections leading to withdrawal/reduction of immunosuppressive therapy | 6 |
Chilblain lupus erythematosus | 2 |
Lower limbs sensory neuropathy | 1 |
Lymphadenopathy | 1 |
Hand pitting scars | 1 |
Impaired diffusing capacity of the lung for carbon monoxide | 1 |
Tachyarrhythmia | 1 |
Venous thrombosis in secondary antiphospholipid syndrome | 1 |
Hepatic-pancreatic enzyme increase | 1 |
Depression | 1 |
*PGA was scored prior to reviewing complement and anti-DNA antibody test.
†not included in SLEDAI-2K.
‡Proteinuria ≤0.5 gr/day.
cSLEDAI-2K, clinical SLE disease activity index-2000; PGA, physician’s global assessment; SLE, systemic lupus erythematosus.