参考文献/References:
[1] van Schouwenburg IM,Gansevoort RT,Mahmoodi BK,et al.?Increased risk of arterial thromboembolism after a prior episode of venous thromboembolism:results from the Prevention of Renal and Vascular end stage Disease PREVEND,Study[J].?Br J Haematol,2012,159(2):216-222.
[2] Naess IA,Christiansen SC,Romundstad P,et al. Incidence and mortality of venous thrombosis:a population-based study[J].?J Thromb Haemost,2007,5(4):692-699.
[3] Silverstein MD,Heit JA,Mohr DN,et al. Trends in the incidence of deep vein thrombosis and pulmonary embolism:a 25-year population-based study[J].?Arch Intern Med,1998,158(6):585-593.
[4] Klemen ND,Feingold PL,Hashimoto B,et al. Mortality risk associated with venous thromboembolism:a systematic review and Bayesian meta-analysis[J].?Lancet Haematol,2020,7(8):e583-e593.
[5] Cohen AT,Agnelli G,Anderson FA,et al. Venous thromboembolism VTE,in Europe. The number of VTE events and associated morbidity and mortality[J].?Thromb Haemost,2007,98(4):756-764.
[6] White RH. The epidemiology of venous thromboembolism[J].?Circulation,2003,107(1):I4-I8.
[7] Spencer FA,Gore JM,Lessard D,et al. Patient outcomes after deep vein thrombosis and pulmonary embolism:the Worcester Venous Thromboembolism Study[J].?Arch Intern Med,2008,168(4):425-430.
[8] Mensah GA,Roth GA,Fuster V. The Global Burden of Cardiovascular Diseases and Risk?Factors:2020 and Beyond[J].?J Am Coll Cardiol,2019,74(20):2529-2532.
[4] Floch MH. Intestinal microecology in health and wellness[J].?J Clin Gastroenterol,2011,45(supp 1):108-S110.
[9] Kiouptsi K,Reinhardt C. Contribution of the commensal microbiota to atherosclerosis and arterial thrombosis[J].?Br J Pharmacol,2018,175(24):4439-4449.
[10] Dunzendorfer S,Lee HK,Tobias PS. Flow-dependent regulation of endothelial Toll-like receptor 2 expression through inhibition of SP1 activity[J].?Circ Res,2004,95(7):684-691.
[11] Andonegui G,Kerfoot SM,McNagny K,et al. Platelets express functional Toll-like receptor-4[J].?Blood,2005,106(7):2417-2423.
[12] Dauphinee SM,Karsan A. Lipopolysaccharide signaling in endothelial cells[J].?Lab Invest, 2006 ,86(1):9-22.
[13] Zhu W,Gregory JC,Org E,et al. Gut microbial metabolite TMAO enhances platelet hyperreactivity and thrombosis risk[J].?Cell,2016,165(1):111-124.
[14] Komatsu S,Berg RD,Russell JM,et al. Enteric microflora contribute to constitutive ICAM-1 expression on vascular endothelial cells[J].?Am J Physiol Gastrointest Liver Physiol,2000,279(1):G186-G191.
[15] J?ckel S,Kiouptsi K,Lillich M,et al. Gut microbiota regulate hepatic von Willebrand factor synthesis and arterial thrombus formation via Toll-like receptor-2[J]. Blood,2017,130(4):542-553.
[16] Burgess S,Butterworth A,Thompson SG. Mendelian randomization analysis with multiple genetic variants using summarized data[J].?Genet Epidemiol,2013,37(7):658-665.
[17] Smith GD,Ebrahim S. ’Mendelian randomization’:can genetic epidemiology contribute to understanding environmental determinants of disease? [J].?Int J Epidemiol,2003,32(1):1-22.
[18] Davies NM,Holmes MV,Davey Smith G. Reading Mendelian randomisation studies:a guide,glossary,and checklist for clinicians[J].?BMJ,2018,362:k601.
[19] RRhee EP,Ho JE,Chen MH,et al. A genome-wide association study of the human metabolome in a community-based cohort[J].?Cell Metab,2013,18(1):130-143.
[20] Hemani G,Zheng J,Elsworth B,et al. The MR-Base platform supports systematic causal inference across the human phenome[J].?Elife,2018,7:e34408.
[21] Palmer TM,Lawlor DA,Harbord RM,et al. Using multiple genetic variants as instrumental variables for modifiable risk factors[J].?Stat Methods Med Res,2012,21(3):223-242.
[22] Yang J,Ferreira T,Morris AP,et al. Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits[J].?Nat Genet,2012,44(4):369-S3.
[23] Ren W,Liang Z,He S,et al. Hybrid of restricted and penalized maximum likelihood method for efficient genome-wide association study[J]. Genes(Basel),2020,11(11):1286.
[24] Bowden J,Davey Smith G,Burgess S. Mendelian randomization with invalid instruments:effect estimation and bias detection through Egger regression[J].?Int J Epidemiol,2015,44(2):512-525.
[25] Bowden J,Davey Smith G,Haycock PC,et al. Consistent estimation in Mendelian randomization with some invalid instruments using a weighted median estimator[J].?Genet Epidemiol,2016,40(4):304-314.
[26] Verbanck M,Chen CY,Neale B,et al. Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases[J].?Nat Genet,2018,50(5):693-698.
[27] Burgess S,Thompson SG. Erratum to:interpreting findings from Mendelian randomization using the MR-Egger method[J].?Eur J Epidemiol,2017,32(5):391-392.
[28] Tripathi A,Debelius J,Brenner DA,et al. The gut-liver axis and the intersection with the microbiome[J].?Nat Rev Gastroenterol Hepatol,2018,15(7):397-411.
[29] Zhu W,Wang Z,Tang WHW,et al. Gut microbe-generated trimethylamine?N-oxide from dietary choline is prothrombotic in subjects[J].?Circulation,2017,135(17):1671-1673.
[30] Wang Z,Klipfell E,Bennett BJ,et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease[J].?Nature,2011,472(17):57-63.
[31] Qiao J,Arthur JF,Gardiner EE,et al. Regulation of platelet activation and thrombus formation by reactive oxygen species[J].?Redox Biol,2018,14:126-130.
[32] Seldin MM,Meng Y,Qi H,et al. Trimethylamine N-oxide promotes vascular inflammation through signaling of mitogen-activated protein kinase and nuclear factor-κB[J].?J Am Heart Assoc,2016,5(2):e002767.
[33] Chen ML,Zhu XH,Ran L,et al. Trimethylamine-N-oxide induces vascular inflammation by activating the NLRP3 inflammasome through the SIRT3-SOD2-mtROS signaling pathway[J].?J Am Heart Assoc,2017,6(11):e006347.
[34] Bennett JA,Mastrangelo MA,Ture SK,et al. The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function[J].?Nat Commun,2020,11(1):3479.