Systemic Lupus Erythematosus
Conditions
Keywords
Immune mediators, Immune metabolites, cardio vascular diseases, Systemic Lupus Erythematosus
Brief summary
Accelerated atherosclerosis is an established complication of systemic autoimmune diseases, particularly SLE. Young female patients with SLE are more likely to develop myocardial infarction than matched healthy controls, and CVD is nowadays one of the most common causes of death (27%) in lupus patients. While traditional CV risk factors cannot explain such increased CV morbidity associated with SLE, common disease factors shared between SLE, atherosclerosis and treatment exposure may be of outmost importance in this process. Our group made 3 findings of particular interest that could link SLE pathogenesis and atherosclerosis-associated immune dysregulation: 1/ the investigators identified specific immunometabolites (circulating nucleotide-derived metabolites adenine and N4-acetylcytidine), which are increased in the circulation of SLE patients. These immunometabolites trigger a constitutive inflammasome activation resulting in aberrant IL1-β production. Given that IL1-β inhibition was reported to significantly reduce CV events without altering lipid levels, the investigators propose that these immunometabolites may represent novel candidate biomarkers of CV risk stratification in SLE. 2/ the investigators identified OX40L as an important costimulatory molecule implicated in follicular helper T cell (Tfh) activation in SLE. Interestingly, OX40L polymorphism has been associated to both SLE and atherosclerosis, and Tfh have been recently shown to accelerate atherosclerosis progression. 3/ Immune complexes-activated platelets sustain aberrant immune response in SLE and block immunosuppressive functions of regulatory T cells (Tregs) in a P-selectin/PSGL1 dependent manner. Selectins and Tregs cell dysfunction are well accepted players in atherosclerosis pathogenesis. Thus there are multiple pathways that are shared between SLE and atherosclerosis and that may results in an increased risk of CV-associated morbidity in SLE patients. Exploring these interconnected pathways in SLE patients together with traditional and other well-established disease-related factors, might lead to a better stratification of CV risk in SLE. The aim of this study is to investigate the accuracy, predictive value and utility of immunological disease-related biomarkers in stratifying CV risk in patients with SLE.
Interventions
BIOLOGICALblood sample
35 ml whole blood for Peripheral blood mononuclear cell (PBMC), serum and plasma
assessment of atherosclerotic plaques and measurement of carotid intima-media thickness (cIMT)
BEHAVIORALquestionnaires
Food and exercise questionnaires validated by the American heart Association
Sponsors
University Hospital, Bordeaux
Foundation for Research in Rheumatology (FOREUM)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patient aged over 18 years old. * SLE diagnosis according to the 2019 European League Against Rheumatism (EULAR) / American College of Rheumatology (ACR) Classification Criteria for Systemic Lupus Erythematosus * Having signed an informed consent (at the latest on the day of inclusion and before any examination required by research).
Exclusion criteria
* Pregnancy or breast-feeding for woman. * Person concerned by articles L 1121-5 to L 1121-8 (persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients who show atherosclerotic plaque progression defined by the absence of carotid plaque in patients at baseline and its subsequent development at follow-up evaluated by semi-automated 3D vascular ultrasound | At baseline (Day 0) and 18 months from baseline |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of patients who present a history of peripheral artery disease | At baseline (Day 0) and 18 months from baseline | — |
| Change in waist size in centimeters | At baseline (Day 0) and 18 months from baseline | — |
| Change in blood glucose levels in milligram per deciliter | At baseline (Day 0) and 18 months from baseline | — |
| Change in total cholesterol levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in HDL cholesterol levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in LDL cholesterol levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in triglycerides levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in Very Low Density Lipoprotein (VLDL) levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in C-Reactive protein levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in insulin levels | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients with hypertension | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients with Body Mass Index around 30 or more | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients who are smokers or past-smokers | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients who present a history of ischemic heart disease | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients who show carotid Intima Media Thickness (cIMT) progression measured in the common carotid artery, at the bulb and the origin of the internal carotid artery | At baseline (Day 0) and 18 months from baseline | defined as an increase of 0.1mm or more evaluated by vascular ultrasound. |
| Proportion of patients with atherosclerotic plaques | At baseline (Day 0) and 18 months from baseline | — |
| Change in lupus disease activity according to Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) | At baseline (Day 0) and 18 months from baseline | score (Min value: 0 - Max value: 105), with higher values mean higher disease activity. |
| Change in lupus disease activity according to Systemic Lupus International Collaborating Clinics /American College of Rheumatology (SLICC/ACR) damage index | At baseline (Day 0) and 18 months from baseline | (Min value: 0 - Max value: 47), with higher values mean more important damages. |
| Change in glucocorticoids intake | At baseline (Day 0) and 18 months from baseline | — |
| Change in platelets-derived biomarkers (P-selectin, sCD154) in micrograms per milliliter, evaluated by Western Blot analysis. | At baseline (Day 0) and 18 months from baseline | — |
| Change in neutrophils-derived biomarkers Proteins S100A8, A9, A8/9, and A12, IL-6 in micrograms per milliliter, evaluated by Western Blot analysis. | At baseline (Day 0) and 18 months from baseline | — |
| Change in interleukin-6 levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in interleukin-12 levels | At baseline (Day 0) and 18 months from baseline | — |
| Change in T-Follicular Helpers lymphocytes | At baseline (Day 0) and 18 months from baseline | — |
| Proportion of patients who present a history of cerebral vascular accident | At baseline (Day 0) and 18 months from baseline | — |
| Change in myeloperoxidase-conjugated DNA levels in fluorescence intensity evaluated by fluorometric assay. | At baseline (Day 0) and 18 months from baseline | — |
Countries
France, Germany
Contacts
PRINCIPAL_INVESTIGATORPierre DUFFAU, Prof
University Hospital, Bordeaux
STUDY_DIRECTORPatrick BLANCO, Prof
University Hospital, Bordeaux
Outcome results
None listed