TY - JOUR
T1 - Dietary amino acids and risk of stroke subtypes
T2 - a prospective analysis of 356,000 participants in seven European countries
AU - Tong, Tammy Y.N.
AU - Clarke, Robert
AU - Schmidt, Julie A.
AU - Huybrechts, Inge
AU - Noor, Urwah
AU - Forouhi, Nita G.
AU - Imamura, Fumiaki
AU - Travis, Ruth C.
AU - Weiderpass, Elisabete
AU - Aleksandrova, Krasimira
AU - Dahm, Christina C.
AU - van der Schouw, Yvonne T.
AU - Overvad, Kim
AU - Kyrø, Cecilie
AU - Tjønneland, Anne
AU - Kaaks, Rudolf
AU - Katzke, Verena
AU - Schiborn, Catarina
AU - Schulze, Matthias B.
AU - Mayen-Chacon, Ana Lucia
AU - Masala, Giovanna
AU - Sieri, Sabina
AU - de Magistris, Maria Santucci
AU - Tumino, Rosario
AU - Sacerdote, Carlotta
AU - Boer, Jolanda M.A.
AU - Verschuren, W. M.Monique
AU - Brustad, Magritt
AU - Nøst, Therese Haugdahl
AU - Crous-Bou, Marta
AU - Petrova, Dafina
AU - Amiano, Pilar
AU - Huerta, José María
AU - Moreno-Iribas, Conchi
AU - Engström, Gunnar
AU - Melander, Olle
AU - Johansson, Kristina
AU - Lindvall, Kristina
AU - Aglago, Elom K.
AU - Heath, Alicia K.
AU - Butterworth, Adam S.
AU - Danesh, John
AU - Key, Timothy J.
N1 - Funding Information:
This work was supported by a Nuffield Department of Population Health Intermediate Fellowship (TYNT), the UK Medical Research Council (MR/M012190/1), Cancer Research UK (C8221/A19170 and 570/A16491), and the Wellcome Trust (Our Planet Our Health, Livestock Environment and People 205212/Z/16/Z). EPIC-CVD has been supported by the European Union Framework 7 (HEALTH-F2-2012-279233), the European Research Council (268834), the UK Medical Research Council (G0800270 and MR/L003120/1), the British Heart Foundation (SP/09/002 and RG/08/014 and RG13/13/30194), and the UK National Institute of Health Research. The establishment of the study subcohort was supported by the EU Sixth Framework Programme (FP6) (grant LSHM_CT_2006_037197 to the InterAct project) and the Medical Research Council Epidemiology Unit (grants MC_UU_12015/1 and MC_UU_12015/5). The coordination of the European Prospective Investigation into Cancer and Nutrition (EPIC) is financially supported by the International Agency for Research on Cancer (IARC) and also by the Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London which has additional infrastructure support provided by the NIHR Imperial Biomedical Research Centre (BRC). The national cohorts are supported by: Danish Cancer Society (Denmark); Ligue Contre le Cancer, Institut Gustave Roussy, Mutuelle Générale de l’Education Nationale, Institut National de la Santé et de la Recherche Médicale (INSERM) (France); German Cancer Aid, German Cancer Research Center (DKFZ), German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Federal Ministry of Education and Research (BMBF) (Germany); Associazione Italiana per la Ricerca sul Cancro-AIRC-Italy, Compagnia di SanPaolo and National Research Council (Italy); Dutch Ministry of Public Health, Welfare and Sports (VWS), LK Research Funds, Dutch Prevention Funds, Dutch ZON (Zorg Onderzoek Nederland), World Cancer Research Fund (WCRF) (The Netherlands), and Statistics Netherlands is acknowledged for providing the causes of death; Health Research Fund (FIS)—Instituto de Salud Carlos III (ISCIII), Regional Governments of Andalucía, Asturias, Basque Country, Murcia and Navarra, and the Catalan Institute of Oncology—ICO (Spain); Swedish Cancer Society, Swedish Research Council and County Councils of Skåne and Västerbotten and the funds supporting the Northern Sweden Diet Database (Sweden); Cancer Research UK (14136 to EPIC-Norfolk; C8221/A29017 to EPIC-Oxford), Medical Research Council (1000143 to EPIC-Norfolk; MR/M012190/1 to EPIC-Oxford) (United Kingdom). The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. For the purpose of open access, the author(s) has applied a Creative Commons Attribution (CC BY) licence to any Author Accepted Manuscript version arising.
Publisher Copyright:
© 2023, The Author(s).
PY - 2024/2
Y1 - 2024/2
N2 - Purpose: Previously reported associations of protein-rich foods with stroke subtypes have prompted interest in the assessment of individual amino acids. We examined the associations of dietary amino acids with risks of ischaemic and haemorrhagic stroke in the EPIC study. Methods: We analysed data from 356,142 participants from seven European countries. Dietary intakes of 19 individual amino acids were assessed using validated country-specific dietary questionnaires, calibrated using additional 24-h dietary recalls. Multivariable-adjusted Cox regression models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) of ischaemic and haemorrhagic stroke in relation to the intake of each amino acid. The role of blood pressure as a potential mechanism was assessed in 267,642 (75%) participants. Results: After a median follow-up of 12.9 years, 4295 participants had an ischaemic stroke and 1375 participants had a haemorrhagic stroke. After correction for multiple testing, a higher intake of proline (as a percent of total protein) was associated with a 12% lower risk of ischaemic stroke (HR per 1 SD higher intake 0.88; 95% CI 0.82, 0.94). The association persisted after mutual adjustment for all other amino acids, systolic and diastolic blood pressure. The inverse associations of isoleucine, leucine, valine, phenylalanine, threonine, tryptophan, glutamic acid, serine and tyrosine with ischaemic stroke were each attenuated with adjustment for proline intake. For haemorrhagic stroke, no statistically significant associations were observed in the continuous analyses after correcting for multiple testing. Conclusion: Higher proline intake may be associated with a lower risk of ischaemic stroke, independent of other dietary amino acids and blood pressure.
AB - Purpose: Previously reported associations of protein-rich foods with stroke subtypes have prompted interest in the assessment of individual amino acids. We examined the associations of dietary amino acids with risks of ischaemic and haemorrhagic stroke in the EPIC study. Methods: We analysed data from 356,142 participants from seven European countries. Dietary intakes of 19 individual amino acids were assessed using validated country-specific dietary questionnaires, calibrated using additional 24-h dietary recalls. Multivariable-adjusted Cox regression models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) of ischaemic and haemorrhagic stroke in relation to the intake of each amino acid. The role of blood pressure as a potential mechanism was assessed in 267,642 (75%) participants. Results: After a median follow-up of 12.9 years, 4295 participants had an ischaemic stroke and 1375 participants had a haemorrhagic stroke. After correction for multiple testing, a higher intake of proline (as a percent of total protein) was associated with a 12% lower risk of ischaemic stroke (HR per 1 SD higher intake 0.88; 95% CI 0.82, 0.94). The association persisted after mutual adjustment for all other amino acids, systolic and diastolic blood pressure. The inverse associations of isoleucine, leucine, valine, phenylalanine, threonine, tryptophan, glutamic acid, serine and tyrosine with ischaemic stroke were each attenuated with adjustment for proline intake. For haemorrhagic stroke, no statistically significant associations were observed in the continuous analyses after correcting for multiple testing. Conclusion: Higher proline intake may be associated with a lower risk of ischaemic stroke, independent of other dietary amino acids and blood pressure.
KW - Amino acids
KW - Dietary protein
KW - Haemorrhagic stroke
KW - Ischaemic stroke
KW - Nutritional epidemiology
KW - Prospective cohort
UR - http://www.scopus.com/inward/record.url?scp=85173723528&partnerID=8YFLogxK
U2 - 10.1007/s00394-023-03251-4
DO - 10.1007/s00394-023-03251-4
M3 - Article
C2 - 37804448
AN - SCOPUS:85173723528
SN - 1436-6207
VL - 63
SP - 209
EP - 220
JO - European Journal of Nutrition
JF - European Journal of Nutrition
IS - 1
ER -