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Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health.
Young, Mary-Anne; Yanes, Tatiane; Cust, Anne E; Dunlop, Kate; Limb, Sharne; Newson, Ainsley J; Purvis, Rebecca; Thiyagarajan, Lavvina; Scott, Rodney J; Verma, Kunal; James, Paul A; Steinberg, Julia.
Affiliation
  • Young MA; Garvan Institute of Medical Research, Sydney, NSW, Australia.
  • Yanes T; St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Sydney, New South Wales, Australia.
  • Cust AE; Dermatology Research Centre, Frazer Institute, The University of Queensland, Brisbane, Queensland, Australia.
  • Dunlop K; The Melanoma Institute Australia, The University of Sydney, NSW, Australia.
  • Limb S; The Daffodil Centre, The University of Sydney, a joint venture with Cancer Council NSW, Sydney, New South Wales, Australia.
  • Newson AJ; The Daffodil Centre, The University of Sydney, a joint venture with Cancer Council NSW, Sydney, New South Wales, Australia.
  • Purvis R; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and Royal Melbourne Hospitals, Melbourne, Victoria, Australia.
  • Thiyagarajan L; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia.
  • Scott RJ; The University of Sydney, Faculty of Medicine and Health, Sydney School of Public Health, Sydney Health Ethics. Sydney, New South Wales, Australia.
  • Verma K; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and Royal Melbourne Hospitals, Melbourne, Victoria, Australia.
  • James PA; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia.
  • Steinberg J; The University of New South Wales, Sydney, New South Wales, Australia.
Twin Res Hum Genet ; 26(1): 40-48, 2023 02.
Article in En | MEDLINE | ID: mdl-36950972
Considerable progress continues to be made with regards to the value and use of disease associated polygenic scores (PGS). PGS aim to capture a person's genetic liability to a condition, disease, or a trait, combining information across many risk variants and incorporating their effect sizes. They are already available for clinicians and consumers to order in Australasia. However, debate is ongoing over the readiness of this information for integration into clinical practice and population health. This position statement provides the viewpoint of the Human Genetics Society of Australasia (HGSA) regarding the clinical application of disease-associated PGS in both individual patients and population health. The statement details how PGS are calculated, highlights their breadth of possible application, and examines their current challenges and limitations. We consider fundamental lessons from Mendelian genetics and their continuing relevance to PGS, while also acknowledging the distinct elements of PGS. Use of PGS in practice should be evidence based, and the evidence for the associated benefit, while rapidly emerging, remains limited. Given that clinicians and consumers can already order PGS, their current limitations and key issues warrant consideration. PGS can be developed for most complex conditions and traits and can be used across multiple clinical settings and for population health. The HGSA's view is that further evaluation, including regulatory, implementation and health system evaluation are required before PGS can be routinely implemented in the Australasian healthcare system.
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Full text: 1 Database: MEDLINE Main subject: Multifactorial Inheritance / Population Health Limits: Humans Country/Region as subject: Oceania Language: En Journal: Twin Res Hum Genet Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: Australia

Full text: 1 Database: MEDLINE Main subject: Multifactorial Inheritance / Population Health Limits: Humans Country/Region as subject: Oceania Language: En Journal: Twin Res Hum Genet Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: Australia