53 research outputs found
The socioeconomic burden of SLE.
Systemic lupus erythematosus (SLE) is a chronic, relapsing-remitting, multisystemic autoimmune inflammatory disorder that predominantly affects women of childbearing age. Much has been written about the clinical course and long-term damage associated with SLE, as well as the reduced life expectancy of patients with this condition. In addition, studies have emphasized the socioeconomic and psychosocial impact of SLE, although the monetary cost of caring for patients with the disorder has only been evaluated in a modest number of studies and a restricted number of countries. SLE has a negative impact on quality of life and is associated with high health-care costs and significant productivity loss. Factors associated with increased cost of SLE include long disease duration, high disease activity and damage, poor physical and mental health, and high education and employment levels. Similarly, high disease activity and damage, poor physical health, certain disease manifestations, as well as poor family and social support are associated with poor health-related quality of life outcomes. SLE incurs a great burden on both the patient and society. Long-term prospective studies should be encouraged to monitor the costs and psychosocial impact of this condition, and to better understand the factors that are associated with poor outcomes.postprin
Cardiovascular disease in patients with rheumatoid arthritis: results from the QUEST-RA study
Long-term outcome of patients with rheumatoid arthritis and systemic lupus erythematosus with special reference to cardiovascular disease
The aim of this thesis was to assess the long-term prognosis in terms of
mortality, especially from cardiovascular disease, in patients with
rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). By
using the population based Swedish health care registries, large cohorts
with patients with RA and SLE were identified in the nationwide Hospital
Discharge Register from 1964 to 1994.
In a cohort of 46,917 RA patients followed until the end of 1995, overall
mortality was increased 2fold compared with the expected. Cardiovascular
disease comprised 49% of all deaths. Coronary artery disease was the
major cause of death and the relative risk was increased by 80 %. Young
patients with RA had a more than 5 -fold increased risk of coronary
death.
In a cohort of 4,737 SLE patients followed until the end of 1995.
mortality was 3-fold increased compared with the expected. Cardiovascular
disease comprised 42% of all deaths. The relative risk of death from
coronary heart disease was 3-fold and persisted increased even 20 years
after the first discharge. SLE patients diagnosed at young age were at an
additional increased risk for death due to coronary heart disease, which
was 16-fold compared with the expected.
There was a decline in overall mortality during the two last decades in
patients with RA and SLE. This decline was most prominent in the patients
youngest at first discharge. In SLE patients, this decrease was entirely
due to causes attributed to SLE. Despite this decrease in overall
mortality, the risk for cardiovascular death still remained unchanged for
RA and SLE patients.
The risk for cardiovascular death is increased in RA patients, but we did
not know the impact of a familial history of cardiovascular disease, and
whether it is due to common genetic and/or environmental factors shared
in a family. Through the national Multi Generation Register, we
identified a cohort of 14,390 patients with RA and their 57,350
first-degree relatives. RA patients whose parent(s) died from
cardiovascular disease had themselves a 70% higher risk of cardiovascular
death. than patients without such parental history. whereas patients
whose relative(s) also had RA were not at higher risk of death than other
patients. The parents and siblings of RA patients had a barely increased
overall mortality, but a 10% and 30%, respectively, increased risk from
cardiovascular death. The data suggest that the increased cardiovascular
morbidity in RA patients is mainly related to the phenotype of the
disease, possibly disease activity, and thus preventable.
In a cohort of 5.715 SLE patients. 443 cancers were registered during
1964-1995. The overall incidence of cancer overall was increased by 25%
to the expected, mainly due to lymphomas, lung cancer and nonmelanoma
skin cancer (SCC). The inciderce of non-Hodgkin's lymphoma (NHL) was
nearly 3-fold increased compared with the expected
Coronary Heart Disease in Systemic Lupus Erythematosus Is Associated With Interferon Regulatory Factor-8 Gene Variants
Neutrophil subsets and their gene signature associate with vascular inflammation and coronary atherosclerosis in lupus
Impact of parental history on patients' cardiovascular mortality in rheumatoid arthritis
BACKGROUND: Patients with rheumatoid arthritis are at increased risk of death from cardiovascular disease (CVD). This risk is influenced by the inflammatory activity of the rheumatoid arthritis as well as by traditional risk factors for CVD. However, little is known about whether or to what extent hereditary factors for CVD contribute additional risk in patients with rheumatoid arthritis. OBJECTIVE: To assess the clinical impact of a parental history of CVD in patients with rheumatoid arthritis. METHODS: Population based cohort study of 10 805 Swedish patients with rheumatoid arthritis aged 16–67 years during follow up (1990–2000). Parents, and cardiovascular deaths among patients and parents, were identified through register linkages. Relative risk of death v the general population was assessed using standardised mortality ratios (SMR), which were compared by Poisson regression. RESULTS: Rheumatoid patients with a parental history of fatal CVD had an SMR of death from CVD of 2.9 (95% confidence interval, 2.5 to 3.4). By contrast, rheumatoid patients without a parental history of fatal CVD had an SMR of 1.7 (1.2 to 2.3). A parental death from CVD was associated with a 70% increase in the risk of fatal CVD in rheumatoid arthritis (SMR ratio = 1.7 (1.2 to 2.4), and an increase in the 10 year mortality from CVD from 5% to 10% in men and from 2% to 4% in women aged 50 to 67 years. CONCLUSIONS: Parental history of death from CVD is an important (and easily assessable) risk factor for fatal CVD in rheumatoid arthritis
Cardiovascular magnetic resonance evaluation of paediatric patients with systemic lupus erythematosus and cardiac symptoms
Systemic Lupus Erythematosus Patients with and without Neuropsychiatric Manifestations: A Neck and Transcranial Duplex Sonography Study
Cardiovascular Disease Prevention Counseling Program for Systemic Lupus Erythematosus Patients
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