From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

From genome-wide association studies to Mendelian randomization : novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment. / Benn, Marianne; Nordestgaard, Børge G.

I: Cardiovascular Research, Bind 114, Nr. 9, 15.07.2018, s. 1192-1208.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Benn, M & Nordestgaard, BG 2018, 'From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment', Cardiovascular Research, bind 114, nr. 9, s. 1192-1208. https://doi.org/10.1093/cvr/cvy045

APA

Benn, M., & Nordestgaard, B. G. (2018). From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment. Cardiovascular Research, 114(9), 1192-1208. https://doi.org/10.1093/cvr/cvy045

Vancouver

Benn M, Nordestgaard BG. From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment. Cardiovascular Research. 2018 jul. 15;114(9):1192-1208. https://doi.org/10.1093/cvr/cvy045

Author

Benn, Marianne ; Nordestgaard, Børge G. / From genome-wide association studies to Mendelian randomization : novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment. I: Cardiovascular Research. 2018 ; Bind 114, Nr. 9. s. 1192-1208.

Bibtex

@article{8193a1349aa541fe8e14ac1ef58d3049,
title = "From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment",
abstract = "The Mendelian randomization approach is an epidemiological study design incorporating genetic information into traditional epidemiological studies to infer causality of biomarkers, risk factors, or lifestyle factors on disease risk. Mendelian randomization studies often draw on novel information generated in genome-wide association studies on causal associations between genetic variants and a risk factor or lifestyle factor. Such information can then be used in a largely unconfounded study design free of reverse causation to understand if and how risk factors and lifestyle factors cause cardiovascular disease. If causation is demonstrated, an opportunity for prevention of disease is identified; importantly however, before prevention or treatment can be implemented, randomized intervention trials altering risk factor levels or improving deleterious lifestyle factors needs to document reductions in cardiovascular disease in a safe and side-effect sparse manner. Documentation of causality can also inform on potential drug targets, more likely to be successful than prior approaches often relying on animal or cell studies mainly. The present review summarizes the history and background of Mendelian randomization, the study design, assumptions for using the design, and the most common caveats, followed by a discussion on advantages and disadvantages of different types of Mendelian randomization studies using one or more samples and different levels of information on study participants. The review also provides an overview of results on many of the risk factors and lifestyle factors for cardiovascular disease examined to date using the Mendelian randomization study design.",
author = "Marianne Benn and Nordestgaard, {B{\o}rge G}",
year = "2018",
month = jul,
day = "15",
doi = "10.1093/cvr/cvy045",
language = "English",
volume = "114",
pages = "1192--1208",
journal = "Cardiovascular Research",
issn = "0008-6363",
publisher = "Oxford University Press",
number = "9",

}

RIS

TY - JOUR

T1 - From genome-wide association studies to Mendelian randomization

T2 - novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment

AU - Benn, Marianne

AU - Nordestgaard, Børge G

PY - 2018/7/15

Y1 - 2018/7/15

N2 - The Mendelian randomization approach is an epidemiological study design incorporating genetic information into traditional epidemiological studies to infer causality of biomarkers, risk factors, or lifestyle factors on disease risk. Mendelian randomization studies often draw on novel information generated in genome-wide association studies on causal associations between genetic variants and a risk factor or lifestyle factor. Such information can then be used in a largely unconfounded study design free of reverse causation to understand if and how risk factors and lifestyle factors cause cardiovascular disease. If causation is demonstrated, an opportunity for prevention of disease is identified; importantly however, before prevention or treatment can be implemented, randomized intervention trials altering risk factor levels or improving deleterious lifestyle factors needs to document reductions in cardiovascular disease in a safe and side-effect sparse manner. Documentation of causality can also inform on potential drug targets, more likely to be successful than prior approaches often relying on animal or cell studies mainly. The present review summarizes the history and background of Mendelian randomization, the study design, assumptions for using the design, and the most common caveats, followed by a discussion on advantages and disadvantages of different types of Mendelian randomization studies using one or more samples and different levels of information on study participants. The review also provides an overview of results on many of the risk factors and lifestyle factors for cardiovascular disease examined to date using the Mendelian randomization study design.

AB - The Mendelian randomization approach is an epidemiological study design incorporating genetic information into traditional epidemiological studies to infer causality of biomarkers, risk factors, or lifestyle factors on disease risk. Mendelian randomization studies often draw on novel information generated in genome-wide association studies on causal associations between genetic variants and a risk factor or lifestyle factor. Such information can then be used in a largely unconfounded study design free of reverse causation to understand if and how risk factors and lifestyle factors cause cardiovascular disease. If causation is demonstrated, an opportunity for prevention of disease is identified; importantly however, before prevention or treatment can be implemented, randomized intervention trials altering risk factor levels or improving deleterious lifestyle factors needs to document reductions in cardiovascular disease in a safe and side-effect sparse manner. Documentation of causality can also inform on potential drug targets, more likely to be successful than prior approaches often relying on animal or cell studies mainly. The present review summarizes the history and background of Mendelian randomization, the study design, assumptions for using the design, and the most common caveats, followed by a discussion on advantages and disadvantages of different types of Mendelian randomization studies using one or more samples and different levels of information on study participants. The review also provides an overview of results on many of the risk factors and lifestyle factors for cardiovascular disease examined to date using the Mendelian randomization study design.

U2 - 10.1093/cvr/cvy045

DO - 10.1093/cvr/cvy045

M3 - Review

C2 - 29471399

VL - 114

SP - 1192

EP - 1208

JO - Cardiovascular Research

JF - Cardiovascular Research

SN - 0008-6363

IS - 9

ER -

ID: 218178742