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A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study

Marjonen, Heidi (author)
University of Helsinki,Finnish National Institute for Health and Welfare
Marttila, Minttu (author)
Finnish National Institute for Health and Welfare
Paajanen, Teemu (author)
University of Helsinki,Finnish National Institute for Health and Welfare
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Vornanen, Marleena (author)
University of Helsinki
Brunfeldt, Minna (author)
Finnish National Institute for Health and Welfare
Joensuu, Anni (author)
Finnish National Institute for Health and Welfare,University of Helsinki
Halmesvaara, Otto (author)
University of Helsinki
Aro, Kimmo (author)
Negen Ltd
Alanne-Kinnunen, Mervi (author)
Finnish National Institute for Health and Welfare
Jousilahti, Pekka (author)
Finnish National Institute for Health and Welfare
Borodulin, Katja (author)
Finnish National Institute for Health and Welfare
Koskinen, Seppo (author)
Finnish National Institute for Health and Welfare
Tuomi, Tiinamaija (author)
Lund University,Lunds universitet,Diabetiska komplikationer,Forskargrupper vid Lunds universitet,Diabetic Complications,Lund University Research Groups,University of Helsinki,Folkhälsan Research Center,Helsinki University Central Hospital
Ilanne-Parikka, Pirjo (author)
Finnish Diabetes Association
Lindström, Jaana (author)
Finnish National Institute for Health and Welfare
Laine, Merja K. (author)
Folkhälsan Research Center,University of Helsinki
Auro, Kirsi (author)
Finnish National Institute for Health and Welfare
Kääriäinen, Helena (author)
Finnish National Institute for Health and Welfare
Perola, Markus (author)
University of Helsinki,Finnish National Institute for Health and Welfare
Kristiansson, Kati (author)
University of Helsinki,Finnish National Institute for Health and Welfare
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 (creator_code:org_t)
2021-10-29
2021
English.
In: Frontiers in Genetics. - : Frontiers Media SA. - 1664-8021. ; 12
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We present a method for communicating personalized genetic risk information to citizens and their physicians using a secure web portal. We apply the method for 3,177 Finnish individuals in the P5 Study where estimates of genetic and absolute risk, based on genetic and clinical risk factors, of future disease are reported to study participants, allowing individuals to participate in managing their own health. Our method facilitates using polygenic risk score as a personalized tool to estimate a person’s future disease risk while offering a way for health care professionals to utilize the polygenic risk scores as a preventive tool in patient care.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

coronary heart disease
finhealth 2017 study
P5 study
polygenic risk sore
precision population health
type 2 diabetes
venous thromboembolism
web portal

Publication and Content Type

art (subject category)
ref (subject category)

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