Abstract
Original language | English |
---|---|
Pages (from-to) | 491-501 |
Number of pages | 11 |
Journal | European Journal of Cardiovascular Prevention and Rehabilitation |
Volume | 17 |
Issue number | 5 |
DOIs | |
Publication status | Published - Oct 2010 |
Keywords
- Antiretroviral drugs
- cardiovascular risk
- HIV
- prediction model
- abacavir
- high density lipoprotein cholesterol
- indinavir
- lopinavir plus ritonavir
- adult
- age
- article
- cardiovascular disease
- cholesterol blood level
- clinical trial
- controlled study
- diabetes mellitus
- female
- gender
- heart infarction
- human
- Human immunodeficiency virus infection
- ischemic heart disease
- major clinical study
- male
- multicenter study
- prediction
- priority journal
- smoking
- systolic blood pressure
Access to Document
Other files and links
Fingerprint
Dive into the research topics of 'Predicting the risk of cardiovascular disease in HIV-infected patients: The Data collection on Adverse Effects of Anti-HIV Drugs Study: European Journal of Cardiovascular Prevention and Rehabilitation'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
Predicting the risk of cardiovascular disease in HIV-infected patients: The Data collection on Adverse Effects of Anti-HIV Drugs Study : European Journal of Cardiovascular Prevention and Rehabilitation. / Friis-Møller, N.; Thiébaut, R.; Reiss, P. et al.
In: European Journal of Cardiovascular Prevention and Rehabilitation, Vol. 17, No. 5, 10.2010, p. 491-501.Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - Predicting the risk of cardiovascular disease in HIV-infected patients: The Data collection on Adverse Effects of Anti-HIV Drugs Study
T2 - European Journal of Cardiovascular Prevention and Rehabilitation
AU - Friis-Møller, N.
AU - Thiébaut, R.
AU - Reiss, P.
AU - Weber, R.
AU - Monforte, A.D.
AU - De Wit, S.
AU - El-Sadr, W.
AU - Fontas, E.
AU - Worm, S.
AU - Kirk, O.
AU - Phillips, A.
AU - Sabin, C.A.
AU - Lundgren, J.D.
AU - Law, M.G.
AU - Torres, Ferran
N1 - Cited By :277 Export Date: 17 February 2022 CODEN: EJCPB Correspondence Address: Friis-Møller, N.; Copenhagen HIV Programme (CHIP), Blegdamsvej 3B, Copenhagen N DK-2200, Denmark; email: nfm@cphiv.dk Chemicals/CAS: abacavir, 136470-78-5, 188062-50-2; indinavir, 150378-17-9, 157810-81-6, 180683-37-8 Funding details: CT94–1637, CT97–2713 Funding details: FIS 99/0887 Funding details: FIPSE 3171/00 Funding details: National Institutes of Health, NIH, 5U01AI042170–10, 5U01AI046362–03 Funding details: U.S. Food and Drug Administration, FDA Funding details: National Institute of Allergy and Infectious Diseases, NIAID, U01-AI069907 Funding details: amfAR, The Foundation for AIDS Research Funding details: Abbott Laboratories Funding details: Bristol-Myers Squibb, BMS Funding details: Pfizer, CURE/97-46486 Funding details: GlaxoSmithKline, GSK Funding details: Merck Funding details: Roche Funding details: Gilead Sciences Funding details: Boehringer Ingelheim Funding details: Merck Sharp and Dohme, MSD Funding details: Cilag Funding details: European Commission, EC Funding details: Department of Health and Ageing, Australian Government Funding details: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, SNF Funding details: Agence Nationale de Recherches sur le Sida et les Hépatites Virales, ANRS Funding details: Fifth Framework Programme, FP5, QLK2-2000–00773 Funding text 1: The study was supported by the Oversight Committee for The Evaluation of Metabolic Complications of HAART, a collaborative committee with representation from academic institutions, the European Agency for the valuation of Medicinal Products, the Food and Drug Administration, the patient community, and all pharmaceutical companies with licensed anti-HIV drugs in the US market: Abbott, Boehringer Ingelheim, Bristol–Myers Squibb, Gilead Sciences, GlaxoSmithKline, Merck, Pfizer, and Hoffman–LaRoche. Supported by a grant (CURE/97-46486) from the Health Insurance Fund Council, Amstelveen, The Netherlands, to the AIDS Therapy Evaluation Project Netherlands (ATHENA); by a grant from the Agence Nationale de Recherches sur le SIDA (Action Coordonnée no.7, Cohortes), to the Aquitaine Cohort; AHOD is funded by the Australian Government Department of Health and Ageing and is supported in part by grants from the U.S. National Institutes of Health's National Institute of Allergey and Infectious Diseases (NIAID) grant no U01-AI069907, and the Foundation for AIDS Research; by grants from the Fondo de Investigación Sanitaria (FIS 99/0887) and Fundación para la Investigación y la Prevención del SIDA en Espanã (FIPSE 3171/00), to the Barcelona Antiretroviral Surveillance Study (BASS); by the National Institute of Allergy and Infectious Diseases, National Institutes of Health (grants 5U01AI042170–10 and 5U01AI046362–03), to the Terry Beirn Community Programs for Clinical Research on AIDS (CPCRA); by grants from the BIOMED 1 (CT94–1637) and BIOMED 2 (CT97–2713) programs and the fifth framework program (QLK2-2000–00773)of the European Commission and grants from Bristol-Myers Squibb, GlaxoSmithKline, Boehringer Ingelheim, and Roche, to the EuroSIDA study; by unrestricted educational grants of Abbott, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead, GSK, Pfizer, Janssen-Cilag to the Italian Cohort Naive to Antiretrovirals (The ICONA Foundation); and by a grant from the Swiss National Science Foundation, to the Swiss HIV Cohort Study (SHCS). Disclosures: M.G.L. has received research grants, consultancy and/or travel grants from Abbott; Boehringer Ingelheim; Bristol–Myers Squibb; Gilead; GlaxoSmithKline; Janssen-Cilag; Johnson & Johnson; Merck Sharp & Dohme; Pfizer; Roche; CSL Ltd. References: Mary-Krause, M., Cotte, L., Simon, A., Partisani, M., Costagliola, D., Increased risk of myocardial infarction with duration of protease inhibitor therapy in HIV-infected men (2003) AIDS, 17, pp. 2479-2486; Holmberg, S.D., Moorman, A.C., Williamson, J.M., Tong, T.C., Ward, D.J., Wood, K.C., Protease inhibitors and cardiovascular outcomes in patients with HIV-1 (2002) Lancet, 360, pp. 1747-1748; Iloeje, U., Yuan, Y., L'Italien, G., Mauskopf, J., Holmberg, S., Moorman, A., Protease inhibitor exposure and increased risk of cardiovascular disease in HIV-infected patients (2005) HIV Med, 6, pp. 37-44; Risk of myocardial infarction in association with different classes of antiretroviral drugs (2007) N Engl J Med, 356, pp. 1723-1735. , The D:A:D Study group; Sabin, C.A., Worm, S.W., Weber, R., Reiss, P., El-Sadr, W., Dabis, F., Use of nucleoside reverse transcriptase inhibitors and risk of myocardial infarction in HIV-infected patients enrolled in the D:A:D study: A multi-cohort collaboration (2008) Lancet, 371, pp. 1417-1426; Use of nucleoside reverse transcriptase inhibitors and risk of myocardial infarction in HIV-infected patients (2008) AIDS, 22, pp. F17-F24. , Strategies for Management of Anti-Retroviral Therapy/INSIGHT and DAD Study Groups; Worm, S.W., Sabin, C., Weber, R., Reiss, P., El-Sadr, W., Dabis, F., Risk of myocardial infarction in HIV patients exposed to specific antiretroviral drugs from the three major drug classes: The D:A:D study (2009) J Infect Dis, 201, pp. 318-330; Law, M.G., Friis-Moller, N., El-Sadr, W.M., Weber, R., Reiss, P., D'Arminio, M.A., The use of the Framingham equation to predict myocardial infarctions in HIV-infected patients: Comparison with observed events in the D:A:D Study (2006) HIV Med, 7, pp. 218-230; El-Sadr, W.M., Lundgren, J.D., Neaton, J.D., Gordin, F., Abrams, D., Arduino, R.C., CD4 + count-guided interruption of antiretroviral treatment (2006) N Engl J Med, 355, pp. 2283-2296; Combination antiretroviral therapy and the risk of myocardial infarction (2003) N Engl J Med, 349, pp. 1993-2003. , The D:A:D Study group; D'Arminio, A., Sabin, C.A., Phillips, A.N., Reiss, P., Weber, R., Kirk, O., Cardio- and cerebrovascular events in HIV-infected persons (2004) AIDS, 18, pp. 1811-1817; Tunstall-Pedoe, H., Kuulasmaa, K., Amouyel, P., Arveiler, D., Rajakangas, A.M., Pajak, A., Myocardial infarction and coronary deaths in the World Health Organization MONICA Project Registration procedures, event rates, and case-fatality rates in 38 populations from 21 countries in four continents (1994) Circulation, 90, pp. 583-612; (1999) MONICA Manual Part IV Event Registration, , http:/www.ktl.fi/publications/monica/manual/part4/iv-1.htm, WHO MONICA Project Accessed 28 October 2009; Lang, S., Mary-Krause, M., Cotte, L., Gilquin, J., Partisani, M., Simon, A., (abstract #43LB) Impact of specific NRTI and PI exposure on the risk of myocardial infarction: A case-control study nested within FHDH ANRS CO4 (2009) Montreal Canada: 16th Conference on Retroviruses and Opportunistic Infections; Hsue, P.Y., Hunt, P.W., Wu, Y., Schnell, A., Ho, J.E., Hatano, H., Association of abacavir and impaired endothelial function in treated and suppressed HIV-infected patients (2009) AIDS, 23, pp. 2021-2027; Martin, A., Bloch, M., Amin, J., Baker, D., Cooper, D.A., Emery, S., Carr, A., Simplification of antiretroviral therapy with tenofovir-emtricitabine or abacavir-lamivudine: A randomized, 96-week trial (2009) Clin Infect Dis, 49, pp. 1591-1601; Teo, K.K., Ounpuu, S., Hawken, S., Pandey, M.R., Valentin, V., Hunt, D., Tobacco use and risk of myocardial infarction in 52 countries in the INTERHEART study: A case-control study (2006) Lancet, 368, pp. 647-658; Lewington, S., Whitlock, G., Clarke, R., Sherliker, P., Emberson, J., Halsey, J., Blood cholesterol and vascular mortality by age, sex, and blood pressure: A meta-analysis of individual data from 61 prospective studies with 55 000 vascular deaths (2007) Lancet, 370, pp. 1829-1839; Lewington, S., Clarke, R., Qizilbash, N., Peto, R., Collins, R., Age-specific relevance of usual blood pressure to vascular mortality: A meta-analysis of individual data for one million adults in 61 prospective studies (2002) Lancet, 360, pp. 1903-1913; Chirovsky, D.R., Fedirko, V., Cui, Y., Sazonov, V., Barter, P., Prospective studies on the relationship between high-density lipoprotein cholesterol and cardiovascular risk: A systematic review (2009) Eur J Cardiovasc Prev Rehabil, 16, pp. 404-423; Thomsen, T., HeartScore: A new web-based approach to European cardiovascular disease risk management (2005) Eur J Cardiovasc Prev Rehabil, 12, pp. 424-426; Anderson, K.M., Odell, P.M., Wilson, P.W., Kannel, W.B., Cardiovascular disease risk profiles (1991) Am Heart J, 121 (1 PART 2), pp. 293-298; De Visser, C.L., Bilo, H.J., Thomsen, T.F., Groenier, K.H., Meyboom-De Jong, B., Prediction of coronary heart disease: A comparison between the Copenhagen risk score and the Framingham risk score applied to a Dutch population (2003) J Intern Med, 253, pp. 553-562; D'Agostino Sr., R.B., Grundy, S., Sullivan, L.M., Wilson, P., Validation of the Framingham coronary heart disease prediction scores: Results of a multiple ethnic groups investigation (2001) JAMA, 286, pp. 180-187; Royston, P., Parmar, M.K., Sylvester, R., Construction and validation of a prognostic model across several studies, with an application in superficial bladder cancer (2004) Stat Med, 23, pp. 907-926; May, M., Royston, P., Egger, M., Justice, A.C., Sterne, J.A., Development and validation of a prognostic model for survival time data: Application to prognosis of HIV positive patients treated with antiretroviral therapy (2004) Stat Med, 23, pp. 2375-2398; Triant, V.A., Lee, H., Hadigan, C., Grinspoon, S.K., Increased acute myocardial infarction rates and cardiovascular risk factors among patients with human immunodeficiency virus disease (2007) J Clin Endocrinol Metab, 92, pp. 2506-2512; Obel, N., Thomsen, H.F., Kronborg, G., Larsen, C.S., Hildebrandt, P.R., Sorensen, H.T., Gerstoft, J., Ischemic heart disease in HIV-infected and HIV-uninfected individuals: A population-based cohort study (2007) Clin Infect Dis, 44, pp. 1625-1631; Cooper, J.A., Miller, G.J., Humphries, S.E., A comparison of the PROCAM and Framingham point-scoring systems for estimation of individual risk of coronary heart disease in the Second Northwick Park Heart Study (2005) Atherosclerosis, 181, pp. 93-100; Thomsen, T.F., McGee, D., Davidsen, M., Jorgensen, T., A cross-validation of risk-scores for coronary heart disease mortality based on data from the Glostrup Population Studies and Framingham Heart Study (2002) Int J Epidemiol, 31, pp. 817-822; Friis-Moller, N., Weber, R., Reiss, P., Thiebaut, R., Kirk, O., D'Arminio, M.A., Cardiovascular disease risk factors in HIV patients-association with antiretroviral therapy. Results from the DAD study (2003) AIDS, 17, pp. 1179-1193; Benard, A., Tessier, J.F., Rambeloarisoa, J., Bonnet, F., Fossoux, H., Neau, D., HIV infection and tobacco smoking behaviour: Prospects for prevention? ANRS CO3 Aquitaine Cohort (2002) Int J Tuberc Lung Dis, 10, pp. 378-383; Patel, N., Talwar, A., Reichert, V.C., Brady, T., Jain, M., Kaplan, M.H., Tobacco and HIV (2006) Clin Occup Environ Med, 5 (193-207), pp. xi; Effros, R.B., From Hayflick to Walford: The role of T cell replicative senescence in human aging (2004) Exp Gerontol, 39, pp. 885-890; Worm, S.W., De, W.S., Weber, R., Sabin, C.A., Reiss, P., El-Sadr, W., Diabetes mellitus, preexisting coronary heart disease, and the risk of subsequent coronary heart disease events in patients infected with human immunodeficiency virus: The data collection on adverse events of Anti-HIV Drugs (D:A:D Study) (2009) Circulation, 119, pp. 805-811; Barrett-Connor, E.L., Cohn, B.A., Wingard, D.L., Edelstein, S.L., Why is diabetes mellitus a stronger risk factor for fatal ischemic heart disease in women than in men? the Rancho Bernardo Study (1991) JAMA, 265, pp. 627-631; Yusuf, S., Hawken, S., Ounpuu, S., Dans, T., Avezum, A., Lanas, F., Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): Case-control study (2004) Lancet, 364, pp. 937-952; Lee, W.L., Cheung, A.M., Cape, D., Zinman, B., Impact of diabetes on coronary artery disease in women and men: A meta-analysis of prospective studies (2000) Diabetes Care, 23, pp. 962-968; Kaplan, R.C., Kingsley, L.A., Sharrett, A.R., Li, X., Lazar, J., Tien, P.C., Ten-year predicted coronary heart disease risk in HIV-infected men and women (2007) Clin Infect Dis, 45, pp. 1074-1081; May, M., Sterne, J.A., Shipley, M., Brunner, E., D'Agostino, R., Whincup, P., A coronary heart disease risk model for predicting the effect of potent antiretroviral therapy in HIV-1 infected men (2007) Int J Epidemiol, 36, pp. 1309-1318; Kristoffersen, U.S., Kofoed, K., Kronborg, G., Benfield, T., Kjaer, A., Lebech, A.M., Changes in biomarkers of cardiovascular risk after a switch to abacavir in HIV-1-infected individuals receiving combination antiretroviral therapy (2009) HIV Med, 10, pp. 627-633; Friis-Moller, N., Thiebaut, R., Reiss, P., El-Sadr, W., Worm, S., Kirk, O., (abstract 808) Predicting the Risk of Coronary Heart Disease in HIV-infected Patients: The D:A:D Risk Equation (2007) Los Angeles: 14th Conference on Retroviruses and Opportunistic Infections; Lundgren, J.D., Mocroft, A., Gatell, J.M., Ledergerber, B., D'Arminio, M.A., Hermans, P., A clinically prognostic scoring system for patients receiving highly active antiretroviral therapy: Results from the EuroSIDA study (2002) J Infect Dis, 185, pp. 178-187; May, M.T., Sterne, J.A., Costagliola, D., Sabin, C.A., Phillips, A.N., Justice, A.C., HIV treatment response and prognosis in Europe and North America in the first decade of highly active antiretroviral therapy: A collaborative analysis (2006) Lancet, 368, pp. 451-458; Lundgren, J.D., Battegay, M., Behrens, G., De, W.S., Guaraldi, G., Katlama, C., European AIDS Clinical Society (EACS) guidelines on the prevention and management of metabolic diseases in HIV (2008) HIV Med, 9, pp. 72-81
PY - 2010/10
Y1 - 2010/10
N2 - Aims: HIV-infected patients receiving combination antiretroviral therapy may experience metabolic complications, potentially increasing their risk of cardiovascular diseases (CVDs). Furthermore, exposures to some antiretroviral drugs seem to be independently associated with increased CVD risk. We aimed to develop cardiovascular risk-assessment models tailored to HIV-infected patients. Methods AND Results: Prospective multinational cohort study. The data set included 22 625 HIV-infected patients from 20 countries in Europe and Australia who were free of CVD at entry into the Data collection on Adverse Effects of Anti-HIV Drugs Study. Using cross-validation methods, separate models were developed to predict the risk of myocardial infarction, coronary heart disease, and a composite CVD endpoint. Model performance was compared with the Framingham score. The models included age, sex, systolic blood pressure, smoking status, family history of CVD, diabetes, total cholesterol, HDL cholesterol and indinavir, lopinavir/r and abacavir exposure. The models performed well with area under the receiver operator curve statistics of 0.783 (range 0.642-0.820) for myocardial infarction, 0.776 (0.670-0.818) for coronary heart disease and 0.769 (0.695-0.824) for CVD. The models estimated more accurately the outcomes in the subgroups than the Framingham score. Conclusion: Risk equations developed from a population of HIV-infected patients, incorporating routinely collected cardiovascular risk parameters and exposure to individual antiretroviral therapy drugs, might be more useful in estimating CVD risks in HIV-infected persons than conventional risk prediction models. © 2010 The European Society of Cardiology.
AB - Aims: HIV-infected patients receiving combination antiretroviral therapy may experience metabolic complications, potentially increasing their risk of cardiovascular diseases (CVDs). Furthermore, exposures to some antiretroviral drugs seem to be independently associated with increased CVD risk. We aimed to develop cardiovascular risk-assessment models tailored to HIV-infected patients. Methods AND Results: Prospective multinational cohort study. The data set included 22 625 HIV-infected patients from 20 countries in Europe and Australia who were free of CVD at entry into the Data collection on Adverse Effects of Anti-HIV Drugs Study. Using cross-validation methods, separate models were developed to predict the risk of myocardial infarction, coronary heart disease, and a composite CVD endpoint. Model performance was compared with the Framingham score. The models included age, sex, systolic blood pressure, smoking status, family history of CVD, diabetes, total cholesterol, HDL cholesterol and indinavir, lopinavir/r and abacavir exposure. The models performed well with area under the receiver operator curve statistics of 0.783 (range 0.642-0.820) for myocardial infarction, 0.776 (0.670-0.818) for coronary heart disease and 0.769 (0.695-0.824) for CVD. The models estimated more accurately the outcomes in the subgroups than the Framingham score. Conclusion: Risk equations developed from a population of HIV-infected patients, incorporating routinely collected cardiovascular risk parameters and exposure to individual antiretroviral therapy drugs, might be more useful in estimating CVD risks in HIV-infected persons than conventional risk prediction models. © 2010 The European Society of Cardiology.
KW - Antiretroviral drugs
KW - cardiovascular risk
KW - HIV
KW - prediction model
KW - abacavir
KW - high density lipoprotein cholesterol
KW - indinavir
KW - lopinavir plus ritonavir
KW - adult
KW - age
KW - article
KW - cardiovascular disease
KW - cholesterol blood level
KW - clinical trial
KW - controlled study
KW - diabetes mellitus
KW - female
KW - gender
KW - heart infarction
KW - human
KW - Human immunodeficiency virus infection
KW - ischemic heart disease
KW - major clinical study
KW - male
KW - multicenter study
KW - prediction
KW - priority journal
KW - smoking
KW - systolic blood pressure
UR - http://www.ncbi.nlm.nih.gov/pubmed/20543702
U2 - 10.1097/HJR.0b013e328336a150
DO - 10.1097/HJR.0b013e328336a150
M3 - Article
C2 - 20543702
VL - 17
SP - 491
EP - 501
IS - 5
ER -