TY - JOUR
T1 - Contribution of Genetic Background, Traditional Risk Factors, and HIV-Related Factors to Coronary Artery Disease Events in HIV-Positive Persons
AU - Rotger, Margalida
AU - Glass, Tracy R.
AU - Junier, Thomas
AU - Lundgren, Jens D.
AU - Neaton, James D.
AU - Poloni, Estella S.
AU - van 't Wout, Angelique B.
AU - Lubomirov, Rubin
AU - Colombo, Sara
AU - Martinez, Raquel
AU - Rauch, Andri
AU - Guenthard, Huldrych F.
AU - Neuhaus, Jacqueline
AU - Wentworth, Deborah
AU - van Manen, Danielle
AU - Gras, Luuk A.
AU - Schuitemaker, Hanneke
AU - Albini, Laura
AU - Torti, Carlo
AU - Jacobson, Lisa P.
AU - Li, Xiuhong
AU - Kingsley, Lawrence A.
AU - Carli, Federica
AU - Guaraldi, Giovanni
AU - Ford, Emily S.
AU - Sereti, Irini
AU - Hadigan, Colleen
AU - Martinez, Esteban
AU - Arnedo, Mireia
AU - Egana-Gorrono, Lander
AU - Gatell, Jose M.
AU - Law, Matthew
AU - Bendall, Courtney
AU - Petoumenos, Kathy
AU - Rockstroh, Juergen
AU - Wasmuth, Jan-Christian
AU - Kabamba, Kabeya
AU - Delforge, Marc
AU - De Wit, Stephane
AU - Berger, Florian
AU - Mauss, Stefan
AU - de Paz Sierra, Mariana
AU - Losso, Marcelo
AU - Belloso, Waldo H.
AU - Leyes, Maria
AU - Campins, Antoni
AU - Mondi, Annalisa
AU - Di Luca, Andrea
AU - Bernardino, Ignacio
AU - Swiss HIV Cohort Study
AU - Lowe, Selwyn
PY - 2013/7/1
Y1 - 2013/7/1
N2 - Persons infected with human immunodeficiency virus (HIV) have increased rates of coronary artery disease (CAD). The relative contribution of genetic background, HIV-related factors, antiretroviral medications, and traditional risk factors to CAD has not been fully evaluated in the setting of HIV infection.In the general population, 23 common single-nucleotide polymorphisms (SNPs) were shown to be associated with CAD through genome-wide association analysis. Using the Metabochip, we genotyped 1875 HIV-positive, white individuals enrolled in 24 HIV observational studies, including 571 participants with a first CAD event during the 9-year study period and 1304 controls matched on sex and cohort.A genetic risk score built from 23 CAD-associated SNPs contributed significantly to CAD (P = 2.9 ? 10(-4)). In the final multivariable model, participants with an unfavorable genetic background (top genetic score quartile) had a CAD odds ratio (OR) of 1.47 (95% confidence interval [CI], 1.05-2.04). This effect was similar to hypertension (OR = 1.36; 95% CI, 1.06-1.73), hypercholesterolemia (OR = 1.51; 95% CI, 1.16-1.96), diabetes (OR = 1.66; 95% CI, 1.10-2.49), ? 1 year lopinavir exposure (OR = 1.36; 95% CI, 1.06-1.73), and current abacavir treatment (OR = 1.56; 95% CI, 1.17-2.07). The effect of the genetic risk score was additive to the effect of nongenetic CAD risk factors, and did not change after adjustment for family history of CAD.In the setting of HIV infection, the effect of an unfavorable genetic background was similar to traditional CAD risk factors and certain adverse antiretroviral exposures. Genetic testing may provide prognostic information complementary to family history of CAD.
AB - Persons infected with human immunodeficiency virus (HIV) have increased rates of coronary artery disease (CAD). The relative contribution of genetic background, HIV-related factors, antiretroviral medications, and traditional risk factors to CAD has not been fully evaluated in the setting of HIV infection.In the general population, 23 common single-nucleotide polymorphisms (SNPs) were shown to be associated with CAD through genome-wide association analysis. Using the Metabochip, we genotyped 1875 HIV-positive, white individuals enrolled in 24 HIV observational studies, including 571 participants with a first CAD event during the 9-year study period and 1304 controls matched on sex and cohort.A genetic risk score built from 23 CAD-associated SNPs contributed significantly to CAD (P = 2.9 ? 10(-4)). In the final multivariable model, participants with an unfavorable genetic background (top genetic score quartile) had a CAD odds ratio (OR) of 1.47 (95% confidence interval [CI], 1.05-2.04). This effect was similar to hypertension (OR = 1.36; 95% CI, 1.06-1.73), hypercholesterolemia (OR = 1.51; 95% CI, 1.16-1.96), diabetes (OR = 1.66; 95% CI, 1.10-2.49), ? 1 year lopinavir exposure (OR = 1.36; 95% CI, 1.06-1.73), and current abacavir treatment (OR = 1.56; 95% CI, 1.17-2.07). The effect of the genetic risk score was additive to the effect of nongenetic CAD risk factors, and did not change after adjustment for family history of CAD.In the setting of HIV infection, the effect of an unfavorable genetic background was similar to traditional CAD risk factors and certain adverse antiretroviral exposures. Genetic testing may provide prognostic information complementary to family history of CAD.
KW - HIV infection
KW - coronary artery disease
KW - genetics
KW - traditional risk factors
KW - antiretroviral therapy
U2 - 10.1093/cid/cit196
DO - 10.1093/cid/cit196
M3 - Article
C2 - 23532479
SN - 1058-4838
VL - 57
SP - 112
EP - 121
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 1
ER -