Article Text

THU0184 Identification of biomarkers in SLE pregnancies using urinary proteomics
  1. K. Schreiber1,
  2. K. Bramham2,
  3. H. Mistry2,
  4. O. Barrutia-Ateka1,
  5. S. Lynham3,
  6. A. Weston3,
  7. M.A. Ward3,
  8. L.M. Bertolaccini1,
  9. L.C. Chappell2,
  10. M.A. Khamashta1
  1. 1Lupus Unit
  2. 2Maternal and Fetal Research Unit, Devision of Women’s Health
  3. 3Proteomics Centre, Institute of Psychiatry, King’s College London, London, United Kingdom


Background Pre-eclampsia affects 2-7% of all pregnancies (1), is a leading cause of maternal morbidity and mortality and increases perinatal mortality five-fold (2). Women with Systemic Lupus Erythematosus (SLE) have a particularly high risk of developing pre-eclampsia (3) and patients with specific organ involvement (i.e. lupus nephritis) are at higher risk of developing pre-eclampsia earlier in their pregnancy (4).

Objectives This study aims to identify human pregnancy biomarkers in the urinary proteome to improve the diagnosis and/or prediction of pre-eclampsia in patients with SLE.

Methods Second trimester urine samples were collected from 3 women with SLE and lupus nephritis who subsequently developed pre-eclampsia, 5 SLE gestation-matched patients who did not develop pre-eclampsia and 6 healthy controls. Samples were prepared following our optimized workflow using in-gel trypsin digestion followed by LC-MS/MS. Spectral abundance of differentially expressed proteins was analysed using minimal stringency settings in Scaffold software.

Results Our preliminary data suggest that pre-eclampsia results in a distinctive urinary proteome in women with lupus nephritis, but also in controls compared to women without pre-eclampsia (Figure 1a and b). One hundred and sixteen proteins were identified; of these, 6 proteins were found to be present only in the SLE pre-eclampsia urine samples (arrow). Furthermore, two proteins were found to be present in SLE pre-eclampsia (arrow), but showed a difference in SLE non-pre-eclampsia urinary samples and were absent in the samples from women with SLE without pre-eclampsia (circled in black) (Figure 1b).

Conclusions Previous work in this group involving pre-eclamptic samples has used targeted mass spectrometry for relative quantitation in a validation sample set. Our study shows differentially expressed proteins, representing potential biomarker candidates of pre-eclampsia in patients with SLE/APS and hence warrant further investigation.

  1. Sibai B et al., Lancet 2005;365:785-99.

  2. Roberts J.M.; Placenta 2002;23:359-72.

  3. Salmon JE et al., PLoS Med. 2011;8:e1001013.

  4. Bramham K et al., J Rheumatol 2011 Jun 1.

Disclosure of Interest K. Schreiber Grant/Research support from: ESF - Biolupus, K. Bramham: None Declared, H. Mistry: None Declared, O. Barrutia-Ateka: None Declared, S. Lynham: None Declared, A. Weston: None Declared, M. Ward: None Declared, L. M. Bertolaccini: None Declared, L. C. Chappell: None Declared, M. Khamashta: None Declared

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