TY - JOUR
T1 - Extensive diversity in circadian regulation of plasma lipids and evidence for different circadian metabolic phenotypes in humans
AU - Chua, Eric Chern Pin
AU - Shui, Guanghou
AU - Lee, Ivan Tian Guang
AU - Lau, Pauline
AU - Tan, Luuan Chin
AU - Yeo, Sing Chen
AU - Lam, Buu Duyen
AU - Bulchand, Sarada
AU - Summers, Scott A.
AU - Puvanendran, Kathiravelu
AU - Rozen, Steven G.
AU - Wenk, Markus R.
AU - Gooley, Joshua J.
PY - 2013/8/27
Y1 - 2013/8/27
N2 - The circadian system regulates daily rhythms in lipid metabolism and adipose tissue function. Although disruption of circadian clock function is associated with negative cardiometabolic end points, very little is known about interindividual variation in circadianregulated metabolic pathways. Here, we used targeted lipidomicsbased approaches to profile the time course of 263 lipids in blood plasma in 20 healthy individuals. Over a span of 28 h, blood was collected every 4 h and plasma lipids were analyzed by HPLC/MS. Across subjects, about 13% of lipid metabolites showed circadian variation. Rhythmicity spanned all metabolite classes examined, suggesting widespread circadian control of lipid-mediated energy storage, transport, and signaling. Intersubject agreement for lipids identified as rhythmic was only about 20%, however, and the timing of lipid rhythms ranged up to 12 h apart between individuals. Healthy subjects therefore showed substantial variation in the timing and strength of rhythms across different lipid species. Strong interindividual differences were also observed for rhythms of blood glucose and insulin, but not cortisol. Using consensus clustering with iterative feature selection, subjects clustered into different groups based on strength of rhythmicity for a subset of triglycerides and phosphatidylcholines, suggesting that there are different circadian metabolic phenotypes in the general population. These results have potential implications for lipid metabolism disorders linked to circadian clock disruption.
AB - The circadian system regulates daily rhythms in lipid metabolism and adipose tissue function. Although disruption of circadian clock function is associated with negative cardiometabolic end points, very little is known about interindividual variation in circadianregulated metabolic pathways. Here, we used targeted lipidomicsbased approaches to profile the time course of 263 lipids in blood plasma in 20 healthy individuals. Over a span of 28 h, blood was collected every 4 h and plasma lipids were analyzed by HPLC/MS. Across subjects, about 13% of lipid metabolites showed circadian variation. Rhythmicity spanned all metabolite classes examined, suggesting widespread circadian control of lipid-mediated energy storage, transport, and signaling. Intersubject agreement for lipids identified as rhythmic was only about 20%, however, and the timing of lipid rhythms ranged up to 12 h apart between individuals. Healthy subjects therefore showed substantial variation in the timing and strength of rhythms across different lipid species. Strong interindividual differences were also observed for rhythms of blood glucose and insulin, but not cortisol. Using consensus clustering with iterative feature selection, subjects clustered into different groups based on strength of rhythmicity for a subset of triglycerides and phosphatidylcholines, suggesting that there are different circadian metabolic phenotypes in the general population. These results have potential implications for lipid metabolism disorders linked to circadian clock disruption.
KW - Chronobiology
KW - Metabolomics
UR - http://www.scopus.com/inward/record.url?scp=84883365545&partnerID=8YFLogxK
U2 - 10.1073/pnas.1222647110
DO - 10.1073/pnas.1222647110
M3 - Article
C2 - 23946426
AN - SCOPUS:84883365545
SN - 0027-8424
VL - 110
SP - 14468
EP - 14473
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 35
ER -