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dc.contributor.authorZagkos, L-
dc.contributor.authorDib, MJ-
dc.contributor.authorPinto, R-
dc.contributor.authorGill, D-
dc.contributor.authorKoskeridis, F-
dc.contributor.authorDrenos, F-
dc.contributor.authorMarkozannes, G-
dc.contributor.authorElliott, P-
dc.contributor.authorZuber, V-
dc.contributor.authorTsilidis, K-
dc.contributor.authorDehghan, A-
dc.contributor.authorTzoulaki, I-
dc.date.accessioned2023-09-17T08:38:58Z-
dc.date.available2023-09-17T08:38:58Z-
dc.date.issued2022-12-29-
dc.identifierORCID iD: Loukas Zagkos https://orcid.org/0000-0002-7700-8102-
dc.identifierORCID iD: Marie-Joe Dib https://orcid.org/0000-0001-7591-5684-
dc.identifierORCID iD: Rui Pinto https://orcid.org/0000-0002-8527-4873-
dc.identifierORCID iD: Dipender Gill https://orcid.org/0000-0001-7312-7078;-
dc.identifierORCID iD: Fotios Koskeridis https://orcid.org/0000-0002-1253-7556-
dc.identifierORCID iD: Fotios Drenos https://orcid.org/0000-0003-2469-5516-
dc.identifierORCID iD: Georgios Markozannes https://orcid.org/0000-0001-8481-579X-
dc.identifierORCID iD: Paul Elliott https://orcid.org/0000-0002-7511-5684-
dc.identifierORCID iD: Abbas Dehghan https://orcid.org/0000-0001-6403-016X-
dc.identifierORCID iD: Ioanna Tzoulaki https://orcid.org/0000-0002-4275-9328-
dc.identifiere1004141-
dc.identifier.citationZagkos, L. et al (2022) 'Associations of genetically predicted fatty acid levels across the phenome: A mendelian randomisation study', PLoS Medicine, 19 (12), e1004141, pp. 1 - 20. doi: 10.1371/journal.pmed.1004141.en_US
dc.identifier.issn1549-1277-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/27210-
dc.descriptionData Availability: UK Biobank individual level data used in this work can be accessed after applying for access at (https://www.ukbiobank.ac.uk/enable-your-research/apply-for-access). Summary statistics used in the analysis can be openly accessed at the IEU OpenGWAS project (https://gwas.mrcieu.ac.uk/). Additional links to datasets used in our work: UKB fatty acids: https://gwas.mrcieu.ac.uk/ FinnGen dataset: https://finngen.gitbook.io/documentation/v/r7/ GIANT consortium: http://ftp.ebi.ac.uk/pub/databases/gwas/summary_statistics/GCST006001-GCST007000/GCST006900/ IGAP consortium: http://ftp.ebi.ac.uk/pub/databases/gwas/summary_statistics/GCST002001-GCST003000/GCST002245/ CARDIoGRAMplusC4D cohort: http://ftp.ebi.ac.uk/pub/databases/gwas/summary_statistics/GCST003001-GCST004000/GCST003116/ MAGIC cohort: http://ftp.ebi.ac.uk/pub/databases/gwas/summary_statistics/GCST000001-GCST001000/GCST000803/ DIAGRAM cohort: https://diagram-consortium.org/downloads.html Kettunen et al., 2016 dataset: https://www.ebi.ac.uk/gwas/publications/27005778.en_US
dc.description.abstractCopyright: © 2022 Zagkos et al. Background: Fatty acids are important dietary factors that have been extensively studied for their implication in health and disease. Evidence from epidemiological studies and randomised controlled trials on their role in cardiovascular, inflammatory, and other diseases remains inconsistent. The objective of this study was to assess whether genetically predicted fatty acid concentrations affect the risk of disease across a wide variety of clinical health outcomes. Methods and findings: The UK Biobank (UKB) is a large study involving over 500,000 participants aged 40 to 69 years at recruitment from 2006 to 2010. We used summary-level data for 117,143 UKB samples (base dataset), to extract genetic associations of fatty acids, and individual-level data for 322,232 UKB participants (target dataset) to conduct our discovery analysis. We studied potentially causal relationships of circulating fatty acids with 845 clinical diagnoses, using mendelian randomisation (MR) approach, within a phenome-wide association study (PheWAS) framework. Regression models in PheWAS were adjusted for sex, age, and the first 10 genetic principal components. External summary statistics were used for replication. When several fatty acids were associated with a health outcome, multivariable MR and MR-Bayesian method averaging (MR-BMA) was applied to disentangle their causal role. Genetic predisposition to higher docosahexaenoic acid (DHA) was associated with cholelithiasis and cholecystitis (odds ratio per mmol/L: 0.76, 95% confidence interval: 0.66 to 0.87). This was supported in replication analysis (FinnGen study) and by the genetically predicted omega-3 fatty acids analyses. Genetically predicted linoleic acid (LA), omega-6, polyunsaturated fatty acids (PUFAs), and total fatty acids (total FAs) showed positive associations with cardiovascular outcomes with support from replication analysis. Finally, higher genetically predicted levels of DHA (0.83, 0.73 to 0.95) and omega-3 (0.83, 0.75 to 0.92) were found to have a protective effect on obesity, which was supported using body mass index (BMI) in the GIANT consortium as replication analysis. Multivariable MR analysis suggested a direct detrimental effect of LA (1.64, 1.07 to 2.50) and omega-6 fatty acids (1.81, 1.06 to 3.09) on coronary heart disease (CHD). MR-BMA prioritised LA and omega-6 fatty acids as the top risk factors for CHD. Although we present a range of sensitivity analyses to the address MR assumptions, horizontal pleiotropy may still bias the reported associations and further evaluation in clinical trials is needed. Conclusions: Our study suggests potentially protective effects of circulating DHA and omega-3 concentrations on cholelithiasis and cholecystitis and on obesity, highlighting the need to further assess them as prevention treatments in clinical trials. Moreover, our findings do not support the supplementation of unsaturated fatty acids for cardiovascular disease prevention.en_US
dc.description.sponsorshipThis work was supported by Health Data Research UK, which is funded by the UK Medical Research Council, Engineering and Physical Sciences Research Council, Economic and Social Research Council, Department of Health and Social Care (England), Chief Scientist Office of the Scottish Government Health and Social Care Directorates, Health and Social Care Research and Development Division (Welsh Government), Public Health Agency (Northern Ireland), British Heart Foundation and Wellcome (Grant Number CFC1007). PE is the director of the Medical Research Council (MRC) Centre for Environment and Health and acknowledges support from the MRC (MR/L01341X/1; MR/ S019669/1). PE and IT also acknowledge support from the Imperial College British Heart Foundation Centre for Research Excellence (RE/18/4/34215), and the UK Dementia Research Institute at Imperial College London (MC_PC_17114), and Health Data Research UK for London.en_US
dc.format.extent1 - 20-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherPLOSen_US
dc.rightsCopyright: © 2022 Zagkos et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectfatty acidsen_US
dc.subjectgeneticsen_US
dc.subjectmedical risk factorsen_US
dc.subjectgenetics of diseaseen_US
dc.subjectcardiovascular diseasesen_US
dc.subjectcoronary heart diseaseen_US
dc.subjectcholelithiasisen_US
dc.subjectgenome-wide association studiesen_US
dc.titleAssociations of genetically predicted fatty acid levels across the phenome: A mendelian randomisation studyen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pmed.1004141-
dc.relation.isPartOfPLoS Medicine-
pubs.issue12-
pubs.publication-statusPublished-
pubs.volume19-
dc.identifier.eissn1549-1676-
dc.rights.holderZagkos et al.-
Appears in Collections:Dept of Life Sciences Research Papers

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