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Cardiovascular disease (CVD) is an important public health problem that affects millions of people worldwide. Associations between risk factors, such as smoking, dyslipidaemia or hypertension, and prevalent CVD are well documented. However, few studies have investigated associations with onset of disease. The initial manifestation of CVD, for example an episode of unstable angina, is important because it influences the prognosis, the quality of life and the management of disease. Furthermore, the extent to which social deprivation, alcohol consumption or atrial fibrillation affects presentation of CVD is poorly understood and deserves further consideration.
Most previous studies have considered CVD as a single entity. However, differences in aetiology between coronary phenotypes suggest that risk factors may not be shared across specific coronary phenotypes and their relative importance is likely to differ for each phenotype. Gaining knowledge of these differences could provide insights into the pathophysiology of specific forms of CVD and could eventually lead to modification of recommendations for patient management and disease prevention.
We propose to use the linkage of the national registry of coronary events to general practice records in the Clinical Practice Research Database (CPRD), to investigate whether demographic, behavioral, and clinico-metabolic risk factors differentially influence the onset of specific types of CVD.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CALIBER Healthy Cohort | We will report findings from the CALIBER (CArdiovascular disease research using Linked BEspoke studies and Electronic Records) collaboration where we linked primary care data (from the General Practice Research Database [GPRD]) to three further sources of electronic health records: the Myocardial Ischemia National Audit Project registry (MINAP),cause specific discharge data from Hospital Episodes Statistics (HES) and cause specific mortality from the Office for National Statistics (ONS). |
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| Measure | Description | Time Frame |
|---|---|---|
| First presentation of cardiovascular disease, as specified in description | First occurrence of the following fatal or non-fatal cardiovascular outcomes: acute myocardial infarction, unstable angina, stable angina, ischemic stroke, hemorrhagic stroke, subarachnoid hemorrhage, transient ischemic attack, abdominal aortic aneurysm, peripheral arterial disease, sudden cardiac death, heart failure | Study follow-up will commence on the earliest date on which a patient fulfils the criteria for study inclusion within the period between 1st January 1997 and 25th March 2010 (maximum of 13 years after enrolment). |
| Measure | Description | Time Frame |
|---|---|---|
| Non CVD specific deaths | Death from non CVD, that is, excluding deaths related to the primary endpoints. | Same as for primary outcomes (maximum of 13 years after follow-up start) |
| Measure | Description | Time Frame |
|---|---|---|
| Cardiovascular heart disease and fatal cardiovascular disease | Cardiovascular heart disease: combination of MI and unheralded coronary death. Cardiovascular disease: combination of fatal cardiovascular heart disease and stroke of any type. Fatal cardiovascular disease: combination of fatal coronary heart disease and fatal cardiovascular death. | Same as for primary endpoint (maximum of 13 years after follow-up start) |
Inclusion Criteria:
Exclusion Criteria:
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The study population will include all patients aged ≥30yrs old, registered in CPRD practices in England consenting to data linkage, with at least 1 year of up-to-standard pre-study follow-up and no history of any of the CVD endpoints considered. Follow-up for endpoints will commence on the earliest date on which a patient fulfils the criteria, within the period between 1st January 1997 and 25th March 2010.
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 26312908 | Derived | Dinesh Shah A, Langenberg C, Rapsomaniki E, Denaxas S, Pujades-Rodriguez M, Gale CP, Deanfield J, Smeeth L, Timmis A, Hemingway H. Type 2 diabetes and incidence of a wide range of cardiovascular diseases: a cohort study in 1.9 million people. Lancet. 2015 Feb 26;385 Suppl 1:S86. doi: 10.1016/S0140-6736(15)60401-9. | |
| 25466521 | Derived |
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| Shah AD, Langenberg C, Rapsomaniki E, Denaxas S, Pujades-Rodriguez M, Gale CP, Deanfield J, Smeeth L, Timmis A, Hemingway H. Type 2 diabetes and incidence of cardiovascular diseases: a cohort study in 1.9 million people. Lancet Diabetes Endocrinol. 2015 Feb;3(2):105-13. doi: 10.1016/S2213-8587(14)70219-0. Epub 2014 Nov 11. |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D000789 | Angina, Unstable |
| D060050 | Angina, Stable |
| D000083242 | Ischemic Stroke |
| D020521 | Stroke |
| D013345 | Subarachnoid Hemorrhage |
| D002546 | Ischemic Attack, Transient |
| D017544 | Aortic Aneurysm, Abdominal |
| D058729 | Peripheral Arterial Disease |
| D003645 | Death, Sudden |
| D006323 | Heart Arrest |
| D006333 | Heart Failure |
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D050197 | Atherosclerosis |
| D001161 | Arteriosclerosis |
| D010335 | Pathologic Processes |
| D009203 | Myocardial Infarction |
| D017202 | Myocardial Ischemia |
| D007238 | Infarction |
| D009336 | Necrosis |
| D000787 | Angina Pectoris |
| D002637 | Chest Pain |
| D010146 | Pain |
| D012816 | Signs and Symptoms |
| D007511 | Ischemia |
| D000083302 | Hemorrhagic Stroke |
| D000783 | Aneurysm |
| D001014 | Aortic Aneurysm |
| D001018 | Aortic Diseases |
| D016491 | Peripheral Vascular Diseases |
| D014652 | Vascular Diseases |
| D016757 | Death, Sudden, Cardiac |
| ID | Term |
|---|---|
| D009461 | Neurologic Manifestations |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D020300 | Intracranial Hemorrhages |
| D006470 | Hemorrhage |
| D002545 | Brain Ischemia |
| D001157 | Arterial Occlusive Diseases |
| D003643 | Death |
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