Dietary Patterns among Asian Indians Living in the United States Have Distinct Metabolomic Profiles That Are Associated with Cardiometabolic Risk.
Abstract
Recent studies, primarily in non-Hispanic whites, suggest that dietary patterns have
distinct metabolomic signatures that may influence disease risk. However, evidence
in South Asians, a group with unique dietary patterns and a high prevalence of cardiometabolic
risk, is lacking.We investigated the metabolomic profiles associated with 2 distinct
dietary patterns among a sample of Asian Indians living in the United States. We also
examined the cross-sectional associations between metabolomic profiles and cardiometabolic
risk markers.We used cross-sectional data from 145 Asian Indians, aged 45-79 y, in
the Metabolic Syndrome and Atherosclerosis in South Asians Living in America (MASALA)
pilot study. Metabolomic profiles were measured from fasting serum samples. Usual
diet was assessed by using a validated food-frequency questionnaire. We used principal
components analysis to derive dietary and metabolomic patterns. We used adjusted general
linear regression models to examine associations between dietary patterns, individual
food groups, metabolite patterns, and cardiometabolic risk markers.We observed 2 major
principal components or metabolite clusters, the first comprised primarily of medium-
to long-chain acylcarnitines (metabolite pattern 1) and the second characterized by
branched-chain amino acids, aromatic amino acids, and short-chain acylcarnitines (metabolite
pattern 2). A "Western/nonvegetarian" pattern was significantly and positively associated
with metabolite pattern 2 (all participants: β ± SE = 0.180 ± 0.090, P = 0.05; participants
without type 2 diabetes: β ± SE = 0.323 ± 0.090, P = 0.0005). In all participants,
higher scores on metabolite pattern 2 were adversely associated with measures of glycemia
(fasting insulin: β ± SE = 2.91 ± 1.29, P = 0.03; 2-h insulin: β ± SE = 22.1 ± 10.3,
P = 0.03; homeostasis model assessment of insulin resistance: β ± SE = 0.94 ± 0.42,
P = 0.03), total adiponectin (β ± SE = -1.46 ± 0.47, P = 0.002), lipids (total cholesterol:
β ± SE = 7.51 ± 3.45, P = 0.03; triglycerides: β ± SE = 14.4 ± 6.67, P = 0.03), and
a radiographic measure of hepatic fat (liver-to-spleen attenuation ratio: β ± SE = -0.83 ± 0.42,
P = 0.05).Our findings suggest that a "Western/nonvegetarian" dietary pattern is associated
with a metabolomic profile that is related to an adverse cardiometabolic profile in
Asian Indians. Public health efforts to reduce cardiometabolic disease burden in this
high-risk group should focus on consuming a healthy plant-based diet.
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https://hdl.handle.net/10161/17281Published Version (Please cite this version)
10.1093/jn/nxy074Publication Info
Bhupathiraju, Shilpa N; Guasch-Ferré, Marta; Gadgil, Meghana D; Newgard, Christopher
B; Bain, James R; Muehlbauer, Michael J; ... Kandula, Namratha R (2018). Dietary Patterns among Asian Indians Living in the United States Have Distinct Metabolomic
Profiles That Are Associated with Cardiometabolic Risk. The Journal of nutrition, 148(7). pp. 1150-1159. 10.1093/jn/nxy074. Retrieved from https://hdl.handle.net/10161/17281.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
James R. Bain
Professor in Medicine
Olga Ilkayeva
Assistant Professor in Medicine
Olga Ilkayeva, Ph.D., is the Director of the Metabolomics Core Laboratory at Duke
Molecular Physiology Institute. She received her Ph.D. training in Cell Regulation
from UT Southwestern Medical Center at Dallas, TX. Her postdoctoral research in the
laboratory of Dr. Chris Newgard at Duke University Medical Center focused on lipid
metabolism and regulation of insulin secretion. As a research scientist at the Stedman
Nutrition and Metabolism Center, Dr. Ilkayeva expanded her studies to include the
Christopher Bang Newgard
W. David and Sarah W. Stedman Distinguished Professor of Nutrition in the School of
Medicine
Over its 16 year history, our laboratory has investigated mechanisms of metabolic
regulation and fuel homeostasis in mammalian systems. Major projects include: 1)
Mechanisms involved in regulation of insulin secretion from pancreatic islet β-cells
by glucose and other metabolic fuels; 2) Development of methods for protection of
β-cells against immune-mediated damage; 3) Studies on spatial organization and
regulation of systems controlling hepatic glucose balance; 4) Studies
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