• No results found

Genomics and metabolomics insights into cardiovascular disease

N/A
N/A
Protected

Academic year: 2021

Share "Genomics and metabolomics insights into cardiovascular disease"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Genomics and metabolomics insights into cardiovascular disease

Eppinga, Ruben Nathaniël

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from

it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date:

2018

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Eppinga, R. N. (2018). Genomics and metabolomics insights into cardiovascular disease. Rijksuniversiteit

Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Stellingen

behorende bij het proefschrift

Genomics and metabolomics insights into cardiovascular disease

Ruben N. Eppinga - 16 mei 2018

1. Genetic variants associated with higher resting heart rate confer a risk for all-cause mortality (this thesis).

2. Telomere length has a causal link with overall cardiovascular disease, hyperten-sion and common cancers (this thesis).

3. Coronary artery disease and heart failure have a common shared genetic heritability with a genetic correlation of 68%, prevention is better than cure

(this thesis).

4. A genetic risk score may be helpful in discriminating patients with high risk for coronary artery disease and to guide to more intensive preventive therapies

(this thesis).

5. Triglyceride concentrations in high density lipoprotein is superior in predict-ing left ventricular ejection fraction and infarct size after myocardial infarction

compared to high density lipoprotein concentration itself (this thesis). 6. Metformin treatment initiated directly after the acute phase of myocardial infarction elicits a small decrease in low density lipoprotein cholesterol together

with a decrease in low density lipoprotein size (this thesis).

7. High-throughput metabolic profiling is a powerful tool to dissect a drug’s efficacy profile (this thesis).

8. Life is 10% what happens to you and 90% how you react to it (Charles R. Swindoll).

9. Stel dat het leven wel zin had en dat wij die zouden vatten. Dat zou een ware catastrofe zijn (unknown).

Referenties

GERELATEERDE DOCUMENTEN

We further specify the pregnancy risk for mother and foetus in specific severe cardiovascular diseases with high maternal mortality including new onset and pre-existing ischemic

Ja, dus het is niet allemaal flagship en zo maar goed, van belang is natuurlijk altijd dat je een combinatie houdt van grotere merken en kleinere merken, eh eh, hè dat je van

In het Besluit bodemkwaliteit (Bbk) wordt de mogelijkheid geboden voor hergebruik van grond en bagger op of in de bodem of onder oppervlaktewater als grootschalige bodemtoepassing

Ordinal and nominal scales were used to collect the demographic data of respondents, which included age, gender, the number of times a respondent made a purchase with a mobile

Open Will Open Heart Open Mind LISTENING 2: from outside disconfirming [new] data Downloading habits of judgment reconfirming old opinions

Summary MR estimates of the causal association between (a) leisure television watching, (b) leisure computer use and (c) driving on coronary artery disease were derived from the

We performed multivariable Cox regression analyses to test the association of observational caffeine intake per 60 mg caffeine (equivalent to the caffeine content of 1 cup of

I then performed Mendelian randomization analyses using the caffeine trait specific variants as instrumental variants in independent cohorts of coronary artery disease and type