4.3 Article

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study

Journal

CIRCULATION-GENOMIC AND PRECISION MEDICINE
Volume 15, Issue 2, Pages 91-99

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGEN.121.003459

Keywords

cardiovascular disease; communication; genomics; risk factor; weight loss

Funding

  1. Business Finland through the Personalized Diagnostics and Care program [3986/31/2013]
  2. Academy of Finland Centre of Excellence in Complex Disease Genetics [312073]
  3. Finnish Foundation for Cardiovascular Research
  4. Sigrid Juselius Foundation
  5. University of Helsinki HiLIFE Fellow grant
  6. Finnish innovation fund SITRA
  7. Finska Lakaresallskapet
  8. Doctoral Programme in Population Health, University of Helsinki

Ask authors/readers for more resources

Prediction tools that combine polygenic risk scores with clinical factors can improve the prediction and prevention of atherosclerotic cardiovascular disease. Returning personal risk information via web-based communication motivates positive changes in health behavior and the propensity to seek care.
Background: Prediction tools that combine polygenic risk scores with clinical factors provide a new opportunity for improved prediction and prevention of atherosclerotic cardiovascular disease, but the clinical utility of polygenic risk score has remained unclear. Methods: We collected a prospective cohort of 7342 individuals (64% women, mean age 56 years) and estimated their 10-year risk for atherosclerotic cardiovascular disease both by a traditional risk score and a composite score combining the effect of a polygenic risk score and clinical risk factors. We then tested how returning the personal risk information with an interactive web-tool impacted on the participants' health behavior. Results: When reassessed after 1.5 years by a clinical visit and questionnaires, 20.8% of individuals at high (>10%) 10-year atherosclerotic cardiovascular disease risk had seen a doctor, 12.4% reported weight loss, 14.2% of smokers had quit smoking, and 15.4% had signed up for health coaching online. Altogether, 42.6% of persons at high risk had made one or more health behavioral changes versus 33.5% of persons at low/average risk such that higher baseline risk predicted a favorable change (OR [CI], 1.53 [1.37-1.72] for persons at high risk versus the rest, P<0.001), with both high clinical (P<0.001) and genomic risk (OR [CI], 1.10 [1.03-1.17], P=0.003) contributing independently. Conclusions: Web-based communication of personal atherosclerotic cardiovascular disease risk-data including polygenic risk to middle-aged persons motivates positive changes in health behavior and the propensity to seek care. It supports integration of genomic information into clinical risk calculators as a feasible approach to enhance disease prevention.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biochemistry & Molecular Biology

Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA

Anniina Tervi, Nella Junna, Martin Broberg, Samuel E. Jones, Satu Strausz, Hanna-Riikka Kreivi, Caroline A. Heckman, Hanna M. Ollila, FinnGen

Summary: Tuberculosis is a significant public health concern that causes over 1 million deaths worldwide each year. This study identified specific HLA alleles and lifestyle risk factors, such as smoking, that are associated with the risk of tuberculosis.

HUMAN MOLECULAR GENETICS (2023)

Article Biochemistry & Molecular Biology

Genome-wide association study meta-analysis of suicide death and suicidal behavior

Qingqin S. Li, Andrey A. Shabalin, Emily DiBlasi, Srihari Gopal, Carla M. Canuso, Aarno Palotie, Wayne C. Drevets, Anna R. Docherty, Hilary Coon

Summary: This study aimed to identify genetic risk variants associated with suicide death and suicidal behavior. The results showed that a locus in the neuroligin 1 (NLGN1) gene was associated with suicide death, while ROBO2 and ZNF28 genes were associated with suicidal behavior. Additionally, variants near SOX5 and LOC101928519 were found to be associated with suicidal attempts. Suicide death and suicidal behavior showed positive correlations with depression, schizophrenia, pain, and suicidal attempt, and negative correlation with educational attainment.

MOLECULAR PSYCHIATRY (2023)

Article Endocrinology & Metabolism

Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register

Minna Harsunen, Jarno L. T. Kettunen, Taina Harkonen, Om Dwivedi, Mikko Lehtovirta, Paula Vahasalo, Riitta Veijola, Jorma Ilonen, Paivi J. Miettinen, Mikael Knip, Tiinamaija Tuomi

Summary: More than 10% of AAB-negative children with diabetes were found to have monogenic diabetes through genetic testing. Genetic diagnosis can lead to major changes in treatment, therefore, it is recommended to refer all AAB-negative pediatric diabetes patients for genetic testing.

DIABETOLOGIA (2023)

Article Biochemistry & Molecular Biology

Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases

Tuomo Kiiskinen, Pyry Helkkula, Kristi Krebs, Juha Karjalainen, Elmo Saarentaus, Nina Mars, Arto Lehisto, Wei Zhou, Mattia Cordioli, Sakari Jukarainen, Joel T. Ramo, Juha Mehtonen, Kumar Veerapen, Markus Rasanen, Sanni Ruotsalainen, Mutaamba Maasha, Teemu Niiranen, Tiinamaija Tuomi, Veikko Salomaa, Mitja Kurki, Matti Pirinen, Aarno Palotie, Mark Daly, Andrea Ganna, Aki S. Havulinna, Lili Milani, Samuli Ripatti

Summary: A new analysis of large biobanks reveals genetic variants associated with changes in medication for cardiometabolic diseases and presents polygenic scores of medication-use behavior. The study used data from the Finnish nationwide drug purchase registry and performed genome-wide association analyses to identify loci associated with medication use in hyperlipidemia, hypertension, and type 2 diabetes. The findings demonstrate the potential for medication-based strategies to identify cardiometabolic risk loci and provide genome-wide tools for preventing cardiovascular diseases.

NATURE MEDICINE (2023)

Article Multidisciplinary Sciences

Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation

Elmo Saarentaus, Juha T. Karjalainen, Joel Raemoe, Tuomo S. Kiiskinen, Aki Havulinna, Juha Mehtonen, Heidi Hautakangas, Sanni Ruotsalainen, Max Tamlander, Nina Mars, Sanna Toppila-Salmi, Matti Pirinen, Mitja Kurki, Samuli Ripatti, Mark Daly, Tuula Palotie, Antti Makitie, Aarno Palotie

Summary: In this study, researchers analyzed the genomic similarity of upper respiratory diseases and found 41 genetic loci associated with these diseases, including some linked to immune-related diseases. They also discovered a genetic correlation between upper respiratory diseases and autoimmune conditions such as rheumatoid arthritis and autoimmune hypothyroidism. Moreover, the study revealed shared genetics for type 2 immunological reaction in upper respiratory diseases.

NATURE COMMUNICATIONS (2023)

Article Biology

Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population

Pyry Helkkula, Shabbeer Hassan, Elmo Saarentaus, Emilia Vartiainen, Sanni T. Ruotsalainen, Jaakko Leinonen, Aarno Palotie, Juha Karjalainen, Mitja Kurki, Samuli Ripatti, Taru Tukiainen

Summary: A genome-wide association study conducted in a Finnish cohort identified new genetic loci associated with varicose veins, including the connexin gene family member, GJD3, which could be a potential drug target. These findings provide insights into the etiology of varicose veins and emphasize the ability of isolated populations, such as Finns, to discover genetic variants relevant to therapeutic development.

COMMUNICATIONS BIOLOGY (2023)

Article Public, Environmental & Occupational Health

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

Laurence J. Howe, Humaira Rasheed, Paul R. Jones, Dorret Boomsma, David M. Evans, Alexandros Giannelis, Caroline Hayward, John L. Hopper, Amanda Hughes, Hannu Lahtinen, Shuai Li, Penelope A. Lind, Nicholas G. Martin, Pekka Martikainen, Sarah E. Medland, Tim T. Morris, Michel G. Nivard, Jean-Baptiste Pingault, Karri Silventoinen, Jennifer A. Smith, Emily A. Willoughby, James F. Wilson, Bjorn Olav Asvold, Oyvind E. Naess, George Davey Smith, Jaakko Kaprio, Ben Brumpton, Neil M. Davies

Summary: Previous Mendelian randomization (MR) studies suggest that educational attainment has beneficial effects on adult health outcomes. However, these estimates may be biased due to population stratification, assortative mating, and indirect genetic effects. Using both population and within-sibship MR approaches, this study provides evidence that genetic liability to educational attainment is associated with decreased BMI, cigarette smoking, and SBP, and potentially with mortality.

INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2023)

Article Dentistry, Oral Surgery & Medicine

Self-reported sleep bruxism and mortality in 1990-2020 in a nationwide twin cohort

Jari Ahlberg, Frank Lobbezoo, Daniele Manfredini, Maarit Piirtola, Christer Hublin, Jaakko Kaprio

Summary: This study investigated the association between sleep bruxism and mortality and found that self-reported sleep bruxism is associated with increased risk of mortality. However, this association is no longer significant after adjusting for other risk factors, suggesting that bruxism is actually a behavior rather than a disease.

JOURNAL OF ORAL REHABILITATION (2023)

Editorial Material Dentistry, Oral Surgery & Medicine

Smoking cessation is not associated with a decline in reported sleep bruxism in middle-aged Finnish twins: Data revisited

Jari Ahlberg, Frank Lobbezoo, Christer Hublin, Maarit Piirtola, Jaakko Kaprio

JOURNAL OF ORAL REHABILITATION (2023)

Article Nutrition & Dietetics

Antioxidant Nutrients and Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes: A Swedish Case-Control Study and Mendelian Randomization Analysis

Anna-Maria Lampousi, Josefin E. Lofvenborg, Emma Ahlqvist, Tiinamaija Tuomi, Alicja Wolk, Sofia Carlsson

Summary: Antioxidant vitamins C and E are inversely associated with type 1 diabetes (T1D). Among adults, vitamin E may have a protective effect on latent autoimmune diabetes (LADA) with high autoantibody levels, as well as on beta cell function and insulin resistance. However, there is no causal relationship between antioxidants and LADA or type 2 diabetes (T2D).

NUTRIENTS (2023)

Letter Genetics & Heredity

Response to Li and Hopper

Nina Mars, Joni V. Lindbohm, Pietro della Briotta Parolo, Elisabeth Widen, Jaakko Kaprio, Aarno Palotie, Samuli Ripatti

AMERICAN JOURNAL OF HUMAN GENETICS (2023)

Article Gastroenterology & Hepatology

Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

Anil K. Giri, Mervi Aavikko, Linnea Wartiovaara, Toni Lemmetyinen, Juha Karjalainen, Juha Mehtonen, Kimmo Palin, Niko Valimaki, Max Tamlander, Riikka Saikkonen, Auli Karhu, Ekaterina Morgunova, Benjamin Sun, Heiko Runz, Priit Palta, Shuang Luo, Heikki Joensuu, Tomi P. Makela, Iiro Kostiainen, Camilla Schalin-Jantti, Aarno FinnGen, Aarno Palotie, Lauri A. Aaltonen, Saara Ollila, Mark J. Daly

Summary: This study is the largest genome-wide association study on small intestinal neuroendocrine tumors (SI-NETs) to date, and it identified 6 significant loci associated with SI-NET risk. Four of these loci are novel, and one of the top hits is a missense variant in the LGR5 gene, a marker of adult intestinal stem cells.

GASTROENTEROLOGY (2023)

Article Biology

Use of electronic health record data mining for heart failure subtyping

Matti A. Vuori, Tuomo Kiiskinen, Niina Pitkanen, Samu Kurki, Hannele Laivuori, Tarja Laitinen, Sampo Mantylahti, Aarno Palotie, FinnGen, Teemu J. Niiranen

Summary: This study aims to assess whether electronic health record data text mining can be used to improve register-based heart failure subtyping. The results show that quantitative ejection fraction data can be efficiently extracted from electronic health records and used with laboratory data to subtype heart failure with reasonable accuracy, especially for heart failure with reduced ejection fraction.

BMC RESEARCH NOTES (2023)

Review Medicine, General & Internal

Dementia in former amateur and professional contact sports participants: population-based cohort study, systematic review, and meta-analysis

G. David Batty, Philipp Frank, Urho M. Kujala, Seppo J. Sarna, Carlos A. Valencia-Hernandez, Jaakko Kaprio

Summary: This study found that retired amateur athletes have a higher risk of dementia compared to the general population, with professional boxers having the highest risk. Retired wrestlers and soccer players also have an increased risk, although lower in magnitude. Furthermore, professional American football players may have a higher risk compared to amateurs.

ECLINICALMEDICINE (2023)

Article Endocrinology & Metabolism

Genetic and environmental factors underlying parallel changes in body mass index and alcohol consumption: a 36-year longitudinal study of adult twins

Gabin Drouard, Karri Silventoinen, Antti Latvala, Jaakko Kaprio

Summary: This study examined the genetic and environmental factors underlying simultaneous changes in body weight and alcohol consumption. The results showed that both genetic and environmental factors play a role in the changes of these traits. There were significant correlations between baseline body weight and change in alcohol consumption, suggesting a direct relationship between the two.

OBESITY FACTS (2023)

No Data Available