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A plasma protein-based risk score to predict hip fractures.
Austin, Thomas R; Nethander, Maria; Fink, Howard A; Törnqvist, Anna E; Jalal, Diana I; Buzkova, Petra; Barzilay, Joshua I; Carbone, Laura; Gabrielsen, Maiken E; Grahnemo, Louise; Lu, Tianyuan; Hveem, Kristian; Jonasson, Christian; Kizer, Jorge R; Langhammer, Arnulf; Mukamal, Kenneth J; Gerszten, Robert E; Psaty, Bruce M; Robbins, John A; Sun, Yan V; Skogholt, Anne Heidi; Kanis, John A; Johansson, Helena; Åsvold, Bjørn Olav; Valderrabano, Rodrigo J; Zheng, Jie; Richards, J Brent; Coward, Eivind; Ohlsson, Claes.
Afiliación
  • Austin TR; Cardiovascular Health Research Unit, University of Washington, Seattle, WA, US.
  • Nethander M; Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Fink HA; Bioinformatics and Data Center, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Törnqvist AE; Geriatric Research Education and Clinical Center, VA Health Care System, Minneapolis, MN, US.
  • Jalal DI; Department of Medicine, University of Minnesota, Minneapolis, MN, US.
  • Buzkova P; Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Barzilay JI; Division of Nephrology, Department of Internal Medicine, Carver College of Medicine, Iowa City, IA, US.
  • Carbone L; Iowa City VA Medical Center, Iowa City, IA, US.
  • Gabrielsen ME; Department of Biostatistics, University of Washington, Seattle, WA, US.
  • Grahnemo L; Division of Endocrinology, Kaiser Permanente of Georgia, Atlanta, GA, US.
  • Lu T; Charlie Norwood VAMC, Augusta, GA, US.
  • Hveem K; Division of Rheumatology, Department of Medicine, Medical College of Georgia, Augusta University, Augusta, GA, US.
  • Jonasson C; HUNT Center for Molecular and Clinical Epidemiology, Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.
  • Kizer JR; Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Langhammer A; Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.
  • Mukamal KJ; Quantitative Life Sciences Program, McGill University, Montreal, Quebec, Canada.
  • Gerszten RE; 5 Prime Sciences Inc, Montreal, Quebec, Canada.
  • Psaty BM; HUNT Center for Molecular and Clinical Epidemiology, Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.
  • Robbins JA; HUNT Research Centre, NTNU, Levanger, Norway.
  • Sun YV; Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.
  • Skogholt AH; HUNT Center for Molecular and Clinical Epidemiology, Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.
  • Kanis JA; Cardiology Section, San Francisco VA Health Care System, San Francisco, CA, US.
  • Johansson H; Department of Medicine, Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, US.
  • Åsvold BO; HUNT Research Centre, NTNU, Levanger, Norway.
  • Valderrabano RJ; Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway.
  • Zheng J; Department of Medicine, Beth Israel Deaconess Medical Center, Brookline, MA, US.
  • Richards JB; Department of Medicine, Beth Israel Deaconess Medical Center, Brookline, MA, US.
  • Coward E; Cardiovascular Health Research Unit, University of Washington, Seattle, WA, US.
  • Ohlsson C; Departments of Medicine, Epidemiology, and Health Systems and Population Health, University of Washington, Seattle, WA, US.
Nat Aging ; 4(8): 1064-1075, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38802582
ABSTRACT
As there are effective treatments to reduce hip fractures, identification of patients at high risk of hip fracture is important to inform efficient intervention strategies. To obtain a new tool for hip fracture prediction, we developed a protein-based risk score in the Cardiovascular Health Study using an aptamer-based proteomic platform. The proteomic risk score predicted incident hip fractures and improved hip fracture discrimination in two Trøndelag Health Study validation cohorts using the same aptamer-based platform. When transferred to an antibody-based proteomic platform in a UK Biobank validation cohort, the proteomic risk score was strongly associated with hip fractures (hazard ratio per s.d. increase, 1.64; 95% confidence interval 1.53-1.77). The proteomic risk score, but not available polygenic risk scores for fractures or bone mineral density, improved the C-index beyond the fracture risk assessment tool (FRAX), which integrates information from clinical risk factors (C-index, FRAX 0.735 versus FRAX + proteomic risk score 0.776). The developed proteomic risk score constitutes a new tool for stratifying patients according to hip fracture risk; however, its improvement in hip fracture discrimination is modest and its clinical utility beyond FRAX with information on femoral neck bone mineral density remains to be determined.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Proteómica / Fracturas de Cadera Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Aging Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Proteómica / Fracturas de Cadera Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Aging Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos