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Multi-ancestry polygenic risk scores for venous thromboembolism.
Jee, Yon Ho; Thibord, Florian; Dominguez, Alicia; Sept, Corriene; Boulier, Kristin; Venkateswaran, Vidhya; Ding, Yi; Cherlin, Tess; Verma, Shefali Setia; Faro, Valeria Lo; Bartz, Traci M; Boland, Anne; Brody, Jennifer A; Deleuze, Jean-Francois; Emmerich, Joseph; Germain, Marine; Johnson, Andrew D; Kooperberg, Charles; Morange, Pierre-Emmanuel; Pankratz, Nathan; Psaty, Bruce M; Reiner, Alexander P; Smadja, David M; Sitlani, Colleen M; Suchon, Pierre; Tang, Weihong; Trégouët, David-Alexandre; Zöllner, Sebastian; Pasaniuc, Bogdan; Damrauer, Scott M; Sanna, Serena; Snieder, Harold; Kabrhel, Christopher; Smith, Nicholas L; Kraft, Peter.
Affiliation
  • Jee YH; Department of Epidemiology, Harvard T.H. Chan School of Public Health, 677 Huntington Ave, Boston, MA 02115, United States.
  • Thibord F; Population Sciences Branch, Division of Intramural Research, National Heart, Lung and Blood Institute, 31 Center Drive, Bethesda, MD 20892, United States.
  • Dominguez A; Framingham Heart Study, Boston University and National Heart, Lung, and Blood Institute, Framingham, 73 Mt. Wayte Ave, Suite #2, Framingham, MA 01702, United States.
  • Sept C; Department of Biostatistics, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48109, United States.
  • Boulier K; Department of Biostatistics, Harvard T.H. Chan School of Public Health, 677 Huntington Ave, Boston, MA 02115, United States.
  • Venkateswaran V; Bioinformatics Interdepartmental Program, University of California Los Angeles, 611 Charles E. Young Drive East, Los Angeles, CA 90095-1570, United States.
  • Ding Y; Department of Oral Biology, University of California Los Angeles School of Dentistry, 13-089 CHS, Box 951668, Box 951570, Los Angeles, CA 90095-1668, United States.
  • Cherlin T; Bioinformatics Interdepartmental Program, University of California Los Angeles, 611 Charles E. Young Drive East, Los Angeles, CA 90095-1570, United States.
  • Verma SS; Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, 3400 Spruce St. Philadelphia, PA 19104-4238, United States.
  • Faro VL; Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, 3400 Spruce St. Philadelphia, PA 19104-4238, United States.
  • Bartz TM; Department of Epidemiology, University of Groningen, University Medical Center Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands.
  • Boland A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Dag Hammarskjölds väg 20751 85 Uppsala, Sweden.
  • Brody JA; Cardiovascular Health Research Unit, Departments of Biostatistics and Medicine, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Deleuze JF; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057 Evry, France.
  • Emmerich J; Laboratory of Excellence in Medical Genomics, GENMED, F-91057 Evry, France.
  • Germain M; Cardiovascular Health Research Unit, Department of Medicine, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Johnson AD; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057 Evry, France.
  • Kooperberg C; Laboratory of Excellence in Medical Genomics, GENMED, F-91057 Evry, France.
  • Morange PE; Centre d'Etude du Polymorphisme Humain, Fondation Jean Dausset, 27 rue Juliette Dodu, 75010 Paris, France.
  • Pankratz N; Department of Vascular Medicine, Paris Saint-Joseph Hospital Group, University of Paris, 75014 Paris, France.
  • Psaty BM; INSERM CRESS UMR 1153, F-75005, Paris, France.
  • Reiner AP; Bordeaux Population Health Research Center, University of Bordeaux, INSERM, UMR 1219, Bordeaux, France.
  • Smadja DM; Population Sciences Branch, Division of Intramural Research, National Heart, Lung and Blood Institute, 31 Center Drive, Bethesda, MD 20892, United States.
  • Sitlani CM; Framingham Heart Study, Boston University and National Heart, Lung, and Blood Institute, Framingham, 73 Mt. Wayte Ave, Suite #2, Framingham, MA 01702, United States.
  • Suchon P; Division of Public Health Sciences, Fred Hutchinbson Cancer Center, PO Box 19024, Seattle, WA 98109, United States.
  • Tang W; Aix-Marseille University, INSERM, INRAE, Centre de Recherche en CardioVasculaire et Nutrition, Laboratory of Haematology, CRB Assistance Publique - Hôpitaux de Marseille, HemoVasc, 27, boulevard Jean Moulin, 13005 Marseille, France.
  • Trégouët DA; Department of Laboratory Medicine and Pathology, University of Minnesota, 420 Delaware Street SE, Minneapolis, MN 55455, United States.
  • Zöllner S; Cardiovascular Health Research Unit, Department of Medicine, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Pasaniuc B; Department of Epidemiology, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Damrauer SM; Department of Health Systems and Population Health, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Sanna S; Division of Public Health Sciences, Fred Hutchinbson Cancer Center, PO Box 19024, Seattle, WA 98109, United States.
  • Snieder H; Department of Epidemiology, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Kabrhel C; Hematology Department and Biosurgical Research Lab (Carpentier Foundation), Assistance Publique Hôpitaux de Paris, Centre-Université de Paris (APHP-CUP), F-75015, Paris, France.
  • Smith NL; Cardiovascular Health Research Unit, Department of Medicine, University of Washington, 4333 Brooklyn Ave, Seattle, WA 98195, United States.
  • Kraft P; Aix-Marseille University, INSERM, INRAE, Centre de Recherche en CardioVasculaire et Nutrition, Laboratory of Haematology, CRB Assistance Publique - Hôpitaux de Marseille, HemoVasc, 27, boulevard Jean Moulin, 13005 Marseille, France.
Hum Mol Genet ; 33(18): 1584-1591, 2024 Sep 03.
Article in En | MEDLINE | ID: mdl-38879759
ABSTRACT
Venous thromboembolism (VTE) is a significant contributor to morbidity and mortality, with large disparities in incidence rates between Black and White Americans. Polygenic risk scores (PRSs) limited to variants discovered in genome-wide association studies in European-ancestry samples can identify European-ancestry individuals at high risk of VTE. However, there is limited evidence on whether high-dimensional PRS constructed using more sophisticated methods and more diverse training data can enhance the predictive ability and their utility across diverse populations. We developed PRSs for VTE using summary statistics from the International Network against Venous Thrombosis (INVENT) consortium genome-wide association studies meta-analyses of European- (71 771 cases and 1 059 740 controls) and African-ancestry samples (7482 cases and 129 975 controls). We used LDpred2 and PRS-CSx to construct ancestry-specific and multi-ancestry PRSs and evaluated their performance in an independent European- (6781 cases and 103 016 controls) and African-ancestry sample (1385 cases and 12 569 controls). Multi-ancestry PRSs with weights tuned in European-ancestry samples slightly outperformed ancestry-specific PRSs in European-ancestry test samples (e.g. the area under the receiver operating curve [AUC] was 0.609 for PRS-CSx_combinedEUR and 0.608 for PRS-CSxEUR [P = 0.00029]). Multi-ancestry PRSs with weights tuned in African-ancestry samples also outperformed ancestry-specific PRSs in African-ancestry test samples (PRS-CSxAFR AUC = 0.58, PRS-CSx_combined AFR AUC = 0.59), although this difference was not statistically significant (P = 0.34). The highest fifth percentile of the best-performing PRS was associated with 1.9-fold and 1.68-fold increased risk for VTE among European- and African-ancestry subjects, respectively, relative to those in the middle stratum. These findings suggest that the multi-ancestry PRS might be used to improve performance across diverse populations to identify individuals at highest risk for VTE.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Venous Thromboembolism / Genetic Risk Score Limits: Female / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Venous Thromboembolism / Genetic Risk Score Limits: Female / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom