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THU0414 The Incidence and Presentation of Systemic Lupus Erythematosus (SLE) in UK Primary Care Using the UK Clinical Practice Research Datalink (CPRD)
  1. A.L. Nightingale1,
  2. J.E. Davidson2,
  3. C.T. Molta3,
  4. H.J. Kan4,
  5. N.J. McHugh1
  1. 1Pharmacy & Pharmacology, University of Bath, Bath
  2. 2Worldwide Epidemiology, GlaxoSmithKline, Stockley Park, United Kingdom
  3. 3U.S. Health Outcomes, GlaxoSmithKline, Research Triangle Park
  4. 4U.S. Medical Affairs, GlaxoSmithKline, Philadelphia, United States


Background The onset of SLE is often described as varied and insidious yet few studies have described the pattern of the onset of symptoms using primary care data. We used the CPRD to investigate the way in which SLE presents in UK primary care.

Objectives To calculate the incidence of SLE in the CPRD population between 1/1/00 and 31/12/12; to describe the presentation of symptoms of SLE and to determine the time from the accumulation of up to five SLE symptoms to SLE diagnosis.

Methods We identified incident cases of SLE using a previously described identification algorithm1. Kaplan-Meier failure curves were constructed looking back from SLE diagnosis to the recording of symptoms related to SLE (i.e. using the presence of symptoms as the failure). The equality of the failure curves were compared for age group (<30, 30-49 and ≥50 yrs) at diagnosis using the Log Rank test.

Results There were 1426 incident cases (170 males, 1256 females) giving age-standardised incidence rates of 0.7/100,000/yr in males (CI950.7,0.8) and 5.4/100,000/yr (CI955.3,5.5) in females. Peak incidence rates were in women aged 30-59 years. The failure curves indicated a gradual onset of symptoms and the median time from first symptom to diagnosis was 5.9yrs (IQR 3.0,9.9). In those aged <30, 30-49 and 50+ at diagnosis the median times from first symptom to diagnosis were 3.3yrs (IQR 2.7,3.9), 4.6yrs (IQR 4.2,5.1) and 6.4yrs (IQR 5.8,6.8); from second symptom to diagnosis1.9yrs (IQR 1.3,2.4), 3.3yrs (2.9,3.6) and 4.2yrs (IQR 3.7,4.7) respectively and from third symptom to diagnosis 1.2yrs (IQR 0.6,1.7), 2.2yrs (IQR 1.9,2.5) and 2.8yrs (IQR 2.4,3.2) respectively. Younger patients were more likely to have constitutional (p<0.001), neurological (p<0.001) and musculoskeletal (p=0.02) symptoms whereas older patients had more cardiorespiratory symptoms and vasculitis (p<0.001) prior to diagnosis. There was a significant difference between the failure curves for the time from the accumulation of one, two and three symptoms of SLE to diagnosis by age group (p<0.001). Musculoskeletal symptoms were the most frequent first symptom in patients aged <30 and 50+ at diagnosis whereas neurological symptoms were most the most common first symptom in those aged 30-49.

Conclusions The presentation of symptoms of SLE is varied and insidious with a long delay from first symptom to SLE diagnosis. Those diagnosed after the age of 50 had a significantly longer time from the presentation of their symptoms to diagnosis (6.4yrs) than those aged <30 (3.3yrs). The longer delay to diagnosis in older patients may be due to a combination of low diagnostic suspicion and a more insidious pattern of onset.


  1. Nightingale AL, Farmer RD, de Vries CS. Incidence of clinically diagnosed systemic lupus erythematosus 1992-1998 using the UK General Practice Research Database. Pharmacoepidemiol Drug Saf 2006; 15(9): 656-661

Acknowledgements Sponsor: GlaxoSmithKline; WEUKBRE6479.

Disclosure of Interest : A. Nightingale Grant/research support: GlaxoSmithKline, J. Davidson Shareholder of: GlaxoSmithKline, Employee of: GlaxoSmithKline, C. Molta Shareholder of: GlaxoSmithKline, Employee of: GlaxoSmithKline, H. Kan Shareholder of: GlaxoSmithKline, Employee of: GlaxoSmithKline, N. McHugh Grant/research support: GlaxoSmithKline, Consultant for: GlaxoSmithKline

DOI 10.1136/annrheumdis-2014-eular.3573

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