Polygenic Risk Scores for Prediction of Subclinical Coronary Artery Disease in Persons With Human Immunodeficiency Virus (HIV): The Swiss HIV Cohort Study.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
06 01 2023
Historique:
received: 07 06 2022
pubmed: 14 9 2022
medline: 11 1 2023
entrez: 13 9 2022
Statut: ppublish

Résumé

In people with human immunodeficiency virus (HIV) (PWH), individual polygenic risk scores (PRSs) are associated with coronary artery disease (CAD) events. Whether PRSs are associated with subclinical CAD is unknown. In Swiss HIV Cohort Study participants of European descent, we defined subclinical CAD as presence of soft, mixed, or high-risk plaque (SMHRP) on coronary computed tomography (CT) angiography, or as participants in the top tertile of the study population's coronary artery calcium (CAC) score, using noncontrast CT. We obtained univariable and multivariable odds ratios (ORs) for subclinical CAD endpoints based on nongenetic risk factors, and validated genome-wide PRSs built from single nucleotide polymorphisms associated with CAD, carotid intima-media thickness (IMT), or longevity in the general population. We included 345 genotyped participants (median age, 53 years; 89% male; 96% suppressed HIV RNA); 172 and 127 participants had SMHRP and CAC, respectively. CAD-associated PRS and IMT-associated PRS were associated with SMHRP and CAC (all P < .01), but longevity PRS was not. Participants with unfavorable CAD-PRS (top quintile) had an adjusted SMHRP OR = 2.58 (95% confidence interval [CI], 1.18-5.67), and a CAC OR = 3.95 (95% CI, 1.45-10.77) vs. bottom quintile. Unfavorable nongenetic risk (top vs. bottom quintile) was associated with adjusted SMHRP OR = 24.01 (95% CI, 9.75-59.11), and a CAC-OR = 65.07 (95% CI, 18.48-229.15). Area under the receiver operating characteristic curve increased when we added CAD-PRS to nongenetic risk factors (SMHRP: 0.75 and 0.78, respectively; CAC: 0.80 and 0.83, respectively). In Swiss PWH, subclinical CAD is independently associated with an individual CAD-associated PRS. Combining nongenetic and genetic cardiovascular risk factors provided the most powerful subclinical CAD prediction.

Sections du résumé

BACKGROUND
In people with human immunodeficiency virus (HIV) (PWH), individual polygenic risk scores (PRSs) are associated with coronary artery disease (CAD) events. Whether PRSs are associated with subclinical CAD is unknown.
METHODS
In Swiss HIV Cohort Study participants of European descent, we defined subclinical CAD as presence of soft, mixed, or high-risk plaque (SMHRP) on coronary computed tomography (CT) angiography, or as participants in the top tertile of the study population's coronary artery calcium (CAC) score, using noncontrast CT. We obtained univariable and multivariable odds ratios (ORs) for subclinical CAD endpoints based on nongenetic risk factors, and validated genome-wide PRSs built from single nucleotide polymorphisms associated with CAD, carotid intima-media thickness (IMT), or longevity in the general population.
RESULTS
We included 345 genotyped participants (median age, 53 years; 89% male; 96% suppressed HIV RNA); 172 and 127 participants had SMHRP and CAC, respectively. CAD-associated PRS and IMT-associated PRS were associated with SMHRP and CAC (all P < .01), but longevity PRS was not. Participants with unfavorable CAD-PRS (top quintile) had an adjusted SMHRP OR = 2.58 (95% confidence interval [CI], 1.18-5.67), and a CAC OR = 3.95 (95% CI, 1.45-10.77) vs. bottom quintile. Unfavorable nongenetic risk (top vs. bottom quintile) was associated with adjusted SMHRP OR = 24.01 (95% CI, 9.75-59.11), and a CAC-OR = 65.07 (95% CI, 18.48-229.15). Area under the receiver operating characteristic curve increased when we added CAD-PRS to nongenetic risk factors (SMHRP: 0.75 and 0.78, respectively; CAC: 0.80 and 0.83, respectively).
CONCLUSIONS
In Swiss PWH, subclinical CAD is independently associated with an individual CAD-associated PRS. Combining nongenetic and genetic cardiovascular risk factors provided the most powerful subclinical CAD prediction.

Identifiants

pubmed: 36097729
pii: 6696567
doi: 10.1093/cid/ciac758
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

48-56

Subventions

Organisme : Swiss National Science Foundation
ID : 177499
Pays : Switzerland

Investigateurs

I Abela (I)
K Aebi-Popp (K)
A Anagnostopoulos (A)
M Battegay (M)
E Bernasconi (E)
D L Braun (DL)
H C Bucher (HC)
A Calmy (A)
M Cavassini (M)
A Ciuffi (A)
G Dollenmaier (G)
M Egger (M)
L Elzi (L)
J Fehr (J)
J Fellay (J)
H Furrer (H)
C A Fux (CA)
H F Günthard (HF)
A Hachfeld (A)
D Haerry (D)
B Hasse (B)
H H Hirsch (HH)
M Hoffmann (M)
I Hösli (I)
M Huber (M)
C R Kahlert (CR)
L Kaiser (L)
O Keiser (O)
T Klimkait (T)
R D Kouyos (RD)
H Kovari (H)
K Kusejko (K)
G Martinetti (G)
B Martinez de Tejada (B)
C Marzolini (C)
K J Metzner (KJ)
N Müller (N)
J Nemeth (J)
D Nicca (D)
P Paioni (P)
G Pantaleo (G)
M Perreau (M)
A Rauch (A)
P Schmid (P)
R Speck (R)
M Stöckle (M)
P Tarr (P)
A Trkola (A)
G Wandeler (G)
S Yerly (S)

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interest. I. C. S.'s institution received a lecture fee from ViiV, outside the submitted work. P. E. T.'s institution reports grants, advisory fees, and support for educational activities from Gilead, ViiV, MSD, and Sankyo Daiichi, outside the submitted work. B. L. received personal fees from Kantonsspital Baselland, Liestal, Switzerland, during the conduct of the study, and reports personal fees from Gilead (for lectures), and ViiV (for participation on Advisory Board), outside the submitted work. R. R. B. reports speaker honoraria from Pfizer (personal <2000 CHF), Sanofi-Aventis (personal 2000 CHF), and GE Healthcare (personal <2000 CHF); support for attending meetings from Pfizer for Registration EAMN Congress 2021; and unpaid roles as Chair of the Nuclear Certification Sub-committee of the European Association of Cardiovascular Imaging and Programme committee member for the annual congress of the European Association of Cardiology; and Research contract with Department of Nuclear Medicine, University Hospital Zurich, Switzerland from GE Healthcare. D. L. B. reports honoraria for advisory boards, lectures and travel grants from AbbVie, Gilead, MSD, and ViiV; and consulting fees from ViiV, MSD, Gilead, Pfizer, and AstraZeneka. AC reports educational grants from AbbVie, MSD, Gilead, and ViiV healthcare; and payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or education events from Gilead Sciences (unrestricted), MSD, and ViiV healthcare (educational grant to institution). R. N. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or education events from Pfizer. P. A. K. reports payment for Advisory Board meeting (Date 02/05/21; Focus: myocardial perfusion tracer) from GE Healthcare; unpaid role as Vice Chair of the Swiss Society of Nucleaer Medicine; and research contract with Department of Nuclear Medicine, University Hospital Zurich, Switzerland from GE Healthcare. All other authors report no potential conflicts. All authors have prepared ICMJE forms for disclosure of potential conflicts of interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Isabella C Schoepf (IC)

Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.
Hepatology, Department for Visceral Surgery and Medicine, Bern University Hospital, University of Bern, Bern, Switzerland.
University Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.

Christian W Thorball (CW)

Precision Medicine Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

Helen Kovari (H)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Bruno Ledergerber (B)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Ronny R Buechel (RR)

Department of Nuclear Medicine, Cardiac Imaging, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Alexandra Calmy (A)

Division of Infectious Disease, Geneva University Hospital, Geneva, Switzerland.

Rainer Weber (R)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Philipp A Kaufmann (PA)

Department of Nuclear Medicine, Cardiac Imaging, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

René Nkoulou (R)

Division of Cardiology, University Hospital Geneva, University of Geneva, Geneva, Switzerland.

Johannes M Schwenke (JM)

University Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.

Dominique L Braun (DL)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Jacques Fellay (J)

Precision Medicine Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

Philip E Tarr (PE)

University Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.

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