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PMID: 18425110 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Human metabolic phenotype diversity and its association with diet and blood pressure.

Nature ·Vol. 453 ·No. 7193 ·2008-05-15 ·Pages 396-400

Holmes E, Loo RL, Stamler J, Bictash M, Yap IK, Chan Q, Ebbels T, De Iorio M, Brown IJ, Veselkov KA, Daviglus ML, Kesteloot H, Ueshima H, Zhao L, Nicholson JK, Elliott P

Abstract

Metabolic phenotypes are the products of interactions among a variety of factors-dietary, other lifestyle/environmental, gut microbial and genetic. We use a large-scale exploratory analytical approach to investigate metabolic phenotype variation across and within four human populations, based on 1H NMR spectroscopy. Metabolites discriminating across populations are then linked to data for individuals on blood pressure, a major risk factor for coronary heart disease and stroke (leading causes of mortality worldwide). We analyse spectra from two 24-hour urine specimens for each of 4,630 participants from the INTERMAP epidemiological study, involving 17 population samples aged 40-59 in China, Japan, UK and USA. We show that urinary metabolite excretion patterns for East Asian and western population samples, with contrasting diets, diet-related major risk factors, and coronary heart disease/stroke rates, are significantly differentiated (P < 10(-16)), as are Chinese/Japanese metabolic phenotypes, and subgroups with differences in dietary vegetable/animal protein and blood pressure. Among discriminatory metabolites, we quantify four and show association (P < 0.05 to P < 0.0001) of mean 24-hour urinary formate excretion with blood pressure in multiple regression analyses for individuals. Mean 24-hour urinary excretion of alanine (direct) and hippurate (inverse), reflecting diet and gut microbial activities, are also associated with blood pressure of individuals. Metabolic phenotyping applied to high-quality epidemiological data offers the potential to develop an area of aetiopathogenetic knowledge involving discovery of novel biomarkers related to cardiovascular disease risk.

MeSH Terms
Adult Alanine/urine Animals Blood Pressure/physiology Cardiovascular Diseases/metabolism China Diet Dietary Proteins/pharmacology Female Hippurates/urine Humans Intestines/microbiology Japan Magnetic Resonance Spectroscopy Male Metabolism/physiology Middle Aged Phenotype Principal Component Analysis Time Factors United Kingdom United States Vegetables/chemistry
Chemicals
Dietary Proteins Hippurates Alanine hippuric acid
Authors & Affiliations
16 authors, click to expand affiliations / ORCID
Holmes Elaine
Biomolecular Medicine, Division of Surgery, Oncology, Reproductive Biology and Anaesthetics (SORA), Faculty of Medicine, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Loo Ruey Leng
Stamler Jeremiah
Bictash Magda
Yap Ivan K S
Chan Queenie
Ebbels Tim
De Iorio Maria
Brown Ian J
Veselkov Kirill A
Daviglus Martha L
Kesteloot Hugo
Ueshima Hirotsugu
Zhao Liancheng
Nicholson Jeremy K
Elliott Paul
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Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2008-05-15
Epub
2008-00-20
Pages
396-400
Language
English
Region
England
NLM ID
0410462
PMCID
PMC6556779
Subset
IM
Grants
NHLBI NIH HHS · R01 HL050490 · United States
NHLBI NIH HHS · R01 HL084228 · United States
NHLBI NIH HHS · R01 HL50490 · United States
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