https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Dementia associated with toxic causes and autoimmune disease https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:524 Wed 11 Apr 2018 10:44:39 AEST ]]> Complement genes contribute sex-biased vulnerability in diverse disorders https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:38872 1, whereas schizophrenia affects men with greater frequency and severity relative to women2. All three illnesses have their strongest common genetic associations in the major histocompatibility complex (MHC) locus, an association that in SLE and Sjögren’s syndrome has long been thought to arise from alleles of the human leukocyte antigen (HLA) genes at that locus3,4,5,6. Here we show that variation of the complement component 4 (C4) genes C4A and C4B, which are also at the MHC locus and have been linked to increased risk for schizophrenia7, generates 7-fold variation in risk for SLE and 16-fold variation in risk for Sjögren’s syndrome among individuals with common C4 genotypes, with C4A protecting more strongly than C4B in both illnesses. The same alleles that increase risk for schizophrenia greatly reduce risk for SLE and Sjögren’s syndrome. In all three illnesses, C4 alleles act more strongly in men than in women: common combinations of C4A and C4B generated 14-fold variation in risk for SLE, 31-fold variation in risk for Sjögren’s syndrome, and 1.7-fold variation in schizophrenia risk among men (versus 6-fold, 15-fold and 1.26-fold variation in risk among women, respectively). At a protein level, both C4 and its effector C3 were present at higher levels in cerebrospinal fluid and plasma8,9 in men than in women among adults aged between 20 and 50 years, corresponding to the ages of differential disease vulnerability. Sex differences in complement protein levels may help to explain the more potent effects of C4 alleles in men, women’s greater risk of SLE and Sjögren’s syndrome and men’s greater vulnerability to schizophrenia. These results implicate the complement system as a source of sexual dimorphism in vulnerability to diverse illnesses.]]> Tue 22 Feb 2022 16:36:25 AEDT ]]> Assessing the care needs of people with Systemic Lupus Erythematosus https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:14422 Tue 04 Jun 2019 16:13:25 AEST ]]> Prevalence and correlates of perceived unmet needs of people with systemic lupus erythematosus https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:487 Thu 25 Jul 2013 09:09:52 AEST ]]> Assessing the unmet needs of people with systemic lupus erythematosus: honoring patient self-report https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:14508 Sat 24 Mar 2018 08:19:43 AEDT ]]> Development and psychometric analysis of the systemic lupus erythematosus needs questionnaire (SLENQ) https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:14459 Sat 24 Mar 2018 08:19:18 AEDT ]]> TSGA10 - A target for autoantibodies in autoimmune polyendocrine syndrome type 1 and systemic lupus erythematosus https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:13249 Sat 24 Mar 2018 08:16:00 AEDT ]]> Persistence of unmet need for care among people with systemic lupus erythematosus: a longitudinal study https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:4904 Sat 24 Mar 2018 07:23:00 AEDT ]]>