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End of Grant Report to LUPUS UK



          Prof. I.Giles and Prof. A.rahman

          How are adverse pregnancy outcomes and Factor (F)Xa reactive
          IgG associated with cardiovascular disease (CVD) and endothelial
          dysfunction in patients with systemic lupus erythematosus (SLE)?

          Patients with systemic lupus erythematosus  produced to fight infection. In SLE however,  between these sub-groups. Of the MPs
          (SLE) have an increased risk of developing  an over-activation of the immune system  studied only platelet MPs were found to be
          heart attacks and strokes, known as cardio-  leads to production of autoantibodies that  higher in patients with SLE compared to
          vascular disease (CVD), and pregnancy  target healthy tissue, such as skin or kidneys  healthy controls (p=0.025) but these raised
          complications, such as miscarriage,  and thus cause disease. In SLE, autoanti-  levels did not distinguish the presence of
          compared to the general population. In the  bodies have been identified against  plaque.  We did not find an association
          general population pregnancy compli-  various parts of the body including blood  between pregnancy complications and
          cations and CVD may share common causes  clotting factors Factor Xa (FXa) and  subclinical CVD but almost half the women
          because women with a past-history of  thrombin (Thr). In the general population  (45%) with SLE had no children, more than
          pregnancy complications have an increased  FXa and Thr are thought to contribute to  double the rate expected in UK women of
          risk of developing CVD later on in life. In  the thickening of blood vessels, in a process  the same mean age. A total of 61% had
          SLE however, typical risk factors for CVD,  known as atherosclerotic plaque formation,  APO (adverse pregnancy outcomes) and
          such as smoking and high cholesterol, do  which leads to CVD. So we examined  rates of miscarriage were higher (31%)
          not fully explain its increased risk so we  whether autoantibodies against FXa or Thr  than in the general population (15-20%). A
          examined whether other factors may be  are also associated with CVD in SLE. We  systematic review of relevant published
          important in this project.         also tested whether MPs shed by cells that  work showed an overall reduction in
          We examined whether certain atypical  line blood vessels (endothelial cells), or  fertility and parity in women with SLE but
          factors were associated with the presence  circulating blood cells (platelets, involved in  could not identify the cause. In our study of
          of early CVD that had been detected in  clotting) were associated with CVD in SLE.   low bone mineral density we found 81% of
          blood vessels by ultrasound scans in  In 100 patients with SLE who had  patients had available bone density scans
          patients with SLE who did not have any  undergone ultrasound imaging of blood  and 65% had thin bones but that was not
          symptoms of CVD, known as subclinical  vessels we found 36 had increased  associated with presence of subclinical CVD.
          CVD. These factors included a past history  thickening of blood vessels walls, known as  The main findings of this work are that
          of pregnancy problems, certain immune  atherosclerotic plaque and 64 had no  anti-FXa autoantibodies are found less
          and cellular factors and the presence of  plaque. Overall, 95% were female with a  commonly in patients with subclinical CVD
          osteoporosis (or thin bones) that has also  mean age of 45.2 years.  Anti-FXa   and that these patients have an increased
          been linked with the development of CVD  autoantibodies were found in 44% and  risk of adverse pregnancy outcomes and
          in the general population.
                                             anti-Thr autoantibodies in 31% of all 100  reduced family size. Further LUPUS UK
          The immune and cellular factors we studied  SLE patients. Anti-FXa autoantibodies were  funded research is now underway to
          were linked to activation of the immune  found more frequently in 33/64 (52%) of  understand how anti-FXa autoantibodies
          system causing autoantibody formation and  patients without plaque compared with  influence disease features in SLE and
          cellular products known as microparticles  11/36 (31%) of patients with plaque  exactly how pregnancy impacts upon
          (MP). Antibodies are products of the  (p=0.04), whilst there was no difference in  patients with SLE.
          normal immune system that are normally  the presence of anti-Thr autoantibodies

          LUPUS UK Legacy Guide


          The Guide describes what is vital in the writing of a will and what can happen if people fail to
          record their wishes correctly. Almost 50% of adults have not made a will and their estates could
          thus be disposed of in a way that would not have met with their wishes.
          The luPus uK legacy Guide does not attempt to offer a comprehensive summary of legacy options
          nor does it try to make a thorough and exhaustive resume of present law regarding the drawing-up of
          a will. The Guide is a first step; there is no substitute for taking properly qualified advice on such an
          important issue.
                          If you would like a copy please contact National Office on
                                         01708 731251


                   Use the Awareness Leaflet enclosed to order your

                                 LUPUS AWARENESS MONTH items

                          or order online - www.lupusuk.org.uk/order-patient-information/
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