Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| The Danish Rheumatism Association | OTHER |
| University of Southern Denmark | OTHER |
| Region of Southern Denmark | OTHER |
| Pfizer |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The aim of the study is to evaluate cardiovascular events during long-term follow-up in Rheumatoid Arthritis. The primary outcome "any cardiovascular event" will be evaluated using systematic audits of patient records, and will be associated to low levels of vitamin D at baseline, to investigate the hypothesis that low levels of vitamin D can be part of a prediction model for cardiovascular disease in Rheumatoid Arthritis.
Cardiovascular morbidity and mortality is increased in patients with rheumatoid arthritis (RA), and among these patients, the prevalence of hypo-vitaminosis D is high. Low levels of vitamin D have been associated with elevated cardiovascular risk in healthy subjects. The objective of this study is to evaluate the risk of cardiovascular events in patients having low 25OHD-total levels at baseline compared to patients with sufficient levels, in an aggressively treated closed cohort of early-diagnosed RA patients.
The primary outcome will be the proportion of patients with any cardiovascular event, evaluated using systematic journal audits. Logistic regression models will be applied to test the hypothesis that there are more cardiovascular events in patients enrolled with a low level of vitamin D (< 50 nmol/l). Secondarily, Cox regression models, based on survival analysis, will be applied, to determine the extent to which independent variables (including different levels of vitamin D at baseline) predict not only whether a cardiovascular event occur, but also when it will occur.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Rheumatoid arthritis patients | Participants in the original, parental trial |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Baseline serum vitamin D level below 50 nmol/l | Other | There is no medical intervention. The two groups are simple allocated depending on serum levels of D-total at the time of diagnosis |
| Measure | Description | Time Frame |
|---|---|---|
| Cardiovascular event | Events will be recorded using systematic journal audits. A cardiovascular event will be further subclassified as shown in the secondary outcome measures, but for primary outcome measures; any cardiovascular event, including death, will serve as "an event" | Observed in the time-period from inclusion to October the 10th 2016 |
| Measure | Description | Time Frame |
|---|---|---|
| Acute cardiovascular hospitalisation due to Myocardial Ischamia | Non-fatal or fatal myocardial infarction, defined by National and International Guidelines (Thygesen et al. 1581-98). Fatal myocardial infarction is defined as primary fatal event within 7 days, documented post mortem by autopsy, or by the definition of myocardial infarction according to European Guidelines (Thygesen et al. 1581-98) Death of myocardial infarction as a consequence of medical examination/procedure/surgery will be classified as procedure related death. Acute Coronary Syndrome (ACS) includes acute ischaemic symptoms with eventual elevation in biomarkers or electrocardiographic changes which does not fulfil the criteria of acute myocardial infarction. Angina Pectoris. Revascularisation procedures (Percutaneous Coronary Intervention (PCI) or Coronary bypass Graft (CABG). |
Not provided
Inclusion Criteria: Fulfilling ACR1987 (American College of Rheumatology 1987 classification criteria for Rheumatoid Arthritis) criteria for RA, disease duration < 6 months, 2 or more swollen joints and age between 18 and 75 years -
Exclusion Criteria: Glucocorticoid treatment 4 weeks prior to inclusion, previous use of DMARDs, malignancy, diastolic blood pressure > 90 mm Hg, elevated serum creatinine, infections with parvovirus B19, Hepatitis B, C and HIV, and any condition contraindicating the study medication.
-
Not provided
Not provided
Hundred-and-sixty early diagnosed and treatment-naive RA patients, recruited from five Danish University Clinics (Trial Centres) from October 1999 to October 2002
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Torkell Ellingsen, MD, Phd | Odense University Hospital | Study Chair |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D001172 | Arthritis, Rheumatoid |
| D002318 | Cardiovascular Diseases |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
Not provided
Not provided
| INDUSTRY |
| Odense Patient Data Explorative Network | OTHER |
Not provided
Not provided
Not provided
| Baseline serum vitamin D level at or above 50 nmol/l | Other | There is no medical intervention. The two groups are simple allocated depending on serum levels of D-total at the time of diagnosis |
|
| Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to hearth failure | Patients with non-elective hospitalisation or death, minimum one overnight stay, with symptoms or findings of heart failure. Death due to heart failure is defined as escalating heart failure symptoms prior to death. | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to stroke | Cerebral haemorrhage, cerebral thromboembolism, Transitory Cerebral Ischemia (TCI) and others Stroke is defined as abrupt severe neurologic deficits, eventually with computer tomographic (CT) documentation. Death within 14 days after symptom-onset of stroke, and without other obviously reasons, is classified as caused by stroke | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to arrhythmias | Atrial fibrillation or flutter, supraventricular tachycardia and others. Ventricular tachycardia, ventricular fibrillation and others. Death due to arrhythmia requires documentation, e.g. telemetric transcript, pacemaker or electrocardiogram | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to Procedure-related cardiovascular event | Any cardiovascular event within 24 hours after cardiovascular medical examination/procedure/surgery. | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to other reasons | Hospitalisation caused by other cardiovascular events, e.g. pulmonary embolism, rupture of aortic aneurism etc. | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute cardiovascular hospitalisation due to supposed cardiovascular reason | Hospitalisation without any documented non-cardiovascular cause. All deaths which are not defined by the cardiovascular reasons mentioned above, and who are not caused by well-documented non-cardiovascular death. All deaths without known reason | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to cancer | Acute hospitalisation due to cancer | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to infection | Acute hospitalisation due to infection | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to respiratory disease | Acute hospitalisation due to respiratory disease | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to trauma | Acute hospitalisation due to trauma | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to suicide | Acute - hospitalisation due to suicide | Observed in the time-period from inclusion to October the 10th 2016 |
| Acute non-cardiovascular hospitalisation due to other reasons | Acute hospitalisation du to other non-cardiovascular reasons, than those previous mentioned | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective cardiovascular hospitalisation due to myocardial ischemia | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective cardiovascular hospitalisation due to arrhythmia | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective cardiovascular hospitalisation due to heart failure | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective cardiovascular hospitalisation due to other cardiovascular reasons | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective non-cardiovascular hospitalisation due to cancer | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective non-cardiovascular hospitalisation due to infection | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective non-cardiovascular hospitalisation due to respiratory disease | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective non-cardiovascular hospitalisation due to trauma | Observed in the time-period from inclusion to October the 10th 2016 |
| Elective non-cardiovascular hospitalisation due to suicide | Observed in the time-period from inclusion to October the 10th 2016 |
| Witnessed, sudden cardiovascular death | Death is witnessed and abrupt within one hour after symptom-onset | Observed in the time-period from inclusion to October the 10th 2016 |
| Non-witnessed, sudden cardiovascular death | Non-witnessed death with no obvious non-cardiovascular reasons (found death) | Observed in the time-period from inclusion to October the 10th 2016 |
| Non-sudden cardiovascular death | Death due to any of the cardiovascular caused previously mentioned, more than one hour after symptom-onset | Observed in the time-period from inclusion to October the 10th 2016 |
| D003240 |
| Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |