Table 1.
Characteristics of the 31 eligible meta-analyses that examined biomarkers for cardiovascular risk and included data from at least one observational study (OS) and one randomised controlled trial (RCT)
| Analysis ID, reference, and biomarker examined | Clinical setting | Recommended for clinical use in guidelines | Type of meta-analysis | No of studies | Total No of events | RCT names | |||
|---|---|---|---|---|---|---|---|---|---|
| OS | RCT | OS | RCT | ||||||
| 139, selenium | No history of CVD | No | Published literature | 11 | 2 | 1934 | 302 | PHS, NITL | |
| 237, C reactive protein | Vascular surgery patients† | Yes18 20 23 | Published literature | 1 | 1 | 1 | 3 | AAART | |
| 334, serum albumin | Haemodialysis patients‡ | No | Published literature | 7 | 1 | NA | NA | HEMO Study | |
| 433, C reactive protein | No history of CVD | Yes15-17 23 | Individual participant data | 26 | 5 | 9171 | 1170 | AFTCAPS, WHS, MRFIT, PROSPER, WOSCOPS | |
| 535, triglycerides | No history of CVD | Yes15-17 | Individual participant data | 61 | 7 | 10 341 | 2444 | AFTCAPS, WHS, MRFIT, PROSPER, WOSCOPS, ALLHAT, LEADER | |
| 635, non-HDL cholesterol | No history of CVD | Yes17 | Individual participant data | 61 | 7 | 10341 | 2444 | AFTCAPS, WHS, MRFIT, PROSPER, WOSCOPS, ALLHAT, LEADER | |
| 736, Lp(a) lipoprotein | No history of CVD | Yes15 22 | Individual participant data | 25 | 5 | 8285 | 1036 | AFTCAPS, WHS, MRFIT, WOSCOPS,* PHS | |
| 832, lipoprotein associated phospholipase A2 activity | General | Yes15 | Individual participant data | 10 | 2 | 1798 | 2165 | PROSPER, HPS | |
| 932, lipoprotein associated phospholipase A2 mass | General | Yes15 | Individual participant data | 9 | 3 | 1821 | 2540 | PROSPER, HPS, WOSCOPS | |
| 1045, serum amyloid A | No history of CVD | No | Published literature | 1 | 1 | 506 | 85 | WHS | |
| 1145, serum amyloid A | Pre-existing CVD | No | Published literature | 1 | 1 | 75 | 391 | CARE trial | |
| 1245, serum albumin | No history of CVD | No | Published literature | 6 | 1 | 3320 | 450 | MRFIT† | |
| 1345, leucocyte count | No history of CVD | No | Published literature | 12 | 2 | 5402 | 562 | WOSCOPS, HHS | |
| 1445, leucocyte count | Pre-existing CVD | No | Published literature | 3 | 2 | 222 | 1043 | CDS,* PAR | |
| 1544, Chlamydia pneumoniae IgG titre | General | No | Published literature | 12 | 3 | 2639 | 530 | PHS, WHS, HHS | |
| 1643, homocysteine | General | Yes16 17 | Published literature | 27 | 2 | NA | NA | PHS,‡ MRFIT† | |
| 1742, D-dimer | No history of CVD | No | Published literature | 4 | 1 | 998 | 296 | PHS | |
| 1810, apolipoprotein B | General | No | Published literature | 16 | 3 | 5442 | 891 | AFTCAPS, PHS, WHS | |
| 1940, apolipoprotein A I | General | No | Published literature | 18 | 3 | 5429 | 891 | AFTCAPS, PHS, WHS | |
| 2040, apolipoprotein B:A I ratio | General | Yes17 | Published literature | 5 | 2 | 3085 | 645 | AFTCAPS, WHS | |
| 2138, fasting insulin | General | No | Published literature | 13 | 1 | 26 251 | 208 | MRFIT | |
| 2231, apolipoprotein(a) isoforms | General | No | Published literature | 29 | 1 | 7187 | 195 | MRFIT | |
| 2330, post-load glucose | No history of diabetes | Yes21 | Published literature | 14 | 1 | 11 851 | 801 | PHS | |
| 2441, fibrinogen | General | No | Individual participant data | 29 | 2 | 5319 | 1799 | Throm Prev, WOSCOPS | |
| 2550, tissue plasminogen activator antigen | General | No | Published literature | 6 | 1 | 1438 | 231 | PHS | |
| 2646, night time ambulatory blood pressure | High blood pressure | Yes24 | Published literature | 6 | 2 | 922 | 337 | Syst-Eur trial,* ASCOT BPLA | |
| 2746, daytime ambulatory blood pressure | High blood pressure | Yes24 | Published literature | 6 | 2 | 922 | 337 | Syst-Eur trial,* ASCOT BPLA | |
| 2847, B-type natriuretic peptide | General population or stable CVD | Yes20 | Published literature | 30 | 10 | 4005 | 6620 | Steno-2, LIFE, AASK, FRISC II, PROVE IT TIMI-22, PROGRESS, LIPID, PEACE, HOPE, HPS | |
| 2948, coronary artery calcium | General population | Yes15 | Published literature | 11 | 2 | 1729 | 174 | INSIGHT, St Francis Heart Study* | |
| 3049, troponin T/I | Acute coronary syndrome patients (non-ST elevation) | Yes18 | Published literature | 11 | 5 | 132 | 140 | GUSTO-IIa, TIMI-IIIb, TRIM, TIMI-11a, CAPTURE* | |
| 3149, troponin T/I | Acute coronary syndrome patients (ST elevation) | Yes18 | Published literature | 1 | 2 | 8 | 1322 | GUSTO-IIa, GUSTO-III | |
CVD=cardiovascular disease, HDL=high density lipoprotein, NA=data not available.
Names of trials: WOSCOPS=West of Scotland Coronary Prevention Study, PHS=Physicians Health Study, NITL=Nutrition Intervention Trial in Linxian, AAART=Abdominal aortic aneurysm repair trial, HEMO=Hemodialysis study, WHS=Women’s Health Study, CARE trial=Cholesterol and Recurrent Events trial, MRFIT=Multiple Risk Factor Intervention Trial, CDS=Coronary Drug Study, PAR=Persantin-Aspirin Reinfarction Study, HHS=Helsinki Heart Study, AFTCAPS=Air Force/Texas Coronary Atherosclerosis Prevention Study, Throm Prev=Thrombosis Prevention, PROSPER=Prospective Study of Pravastatin in the Elderly at Risk, ALLHAT=Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial, LEADER=Lower Extremity Arterial Disease Event Reduction Trial, HPS=Heart Protection Study, LIFE=Losartan Intervention For Endpoint, AASK=African American Study of Kidney Disease and Hypertension, FRISC II=Fragmin and fast Revascularisation during InStability in Coronary artery disease, LIPID=Long-term Intervention with Pravastatin in Ischemic Disease, PROGRESS=Perindopril Protection Against Recurrent Stroke Study, PEACE=Prevention of Events with Angiotensin Converting Enzyme Inhibition, HOPE=Heart Outcomes Prevention Evaluation, INSIGHT=International Nifedipine Study Intervention as Goal for Hypertension Therapy, GUSTO=Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries, TIMI=Thrombolysis in Myocardial Ischemia Trial, TRIM=Thrombin Inhibition in Myocardial ischemia, CAPTURE=c7E3 Fab Antiplatelet Therapy in Unstable Refractory Angina, Syst-Eur trial=Systolic Hypertension in Europe, ASCOT-BPLA=Anglo-Scandinavian cardiac outcomes trial-blood pressure lowering arm.
*Only placebo arm analysed.
†MRFIT analysed as 2 different cohorts.
‡PHS analysed as 4 different cohorts.