TY - JOUR
T1 - Effects of dietary eicosapentaenoic acid and docosahexaenoic acid supplementation on metabolic syndrome
T2 - A systematic review and meta-analysis of data from 33 randomized controlled trials
AU - Zhang, Hui Jun
AU - Gao, Xiang
AU - Guo, Xiao Fei
AU - Li, Ke Lei
AU - Li, Shan
AU - Sinclair, Andrew J.
AU - Li, Duo
N1 - Funding Information:
This work was supported by the Key Scientific Research Projects in Shandong Province China ( 2017YYSP007 ), the National Natural Science Foundation of China ( 81773433 ).
Publisher Copyright:
© 2021 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - Background & aims: Previous randomized controlled trials (RCTs) have compared the effects of pure preparations of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in reducing metabolic syndrome (MetS) risk factors, but the results were inconsistent. The present study aimed to clarify whether EPA and DHA have differential effects on MetS features in humans. Methods: A systematic literature search was conducted in CNKI, PubMed, Embase and Scopus updated to February 2021. The mean changes in the characteristics of MetS were calculated as weighted mean differences by using a random-effects model. Thirty-three RCTs were included. Results: The results showed that both EPA and DHA were effective at lowering serum triglycerides (TG) levels. EPA supplementation decreased the serum levels of total cholesterol (TC) (WMD = −0.24 mmol/L; 95% CI, −0.43, −0.05 mmol/L), TG (WMD = −0.77 mmol/L; 95% CI, −1.54, −0.00 mmol/L) and low density lipoprotein-cholesterol (LDL-C) (WMD = −0.13 mmol/L; 95% CI, −0.25, −0.01 mmol/L), while DHA increased the serum levels of TC (WMD = 0.14 mmol/L; 95% CI, 0.03, 0.25 mmol/L), LDL-C (WMD = 0.26 mmol/L; 95% CI, 0.15, 0.38 mmol/L) and high density lipoprotein-cholesterol (HDL-C) (WMD = 0.07 mmol/L; 95% CI, 0.04, 0.09 mmol/L). Moreover, DHA increased the serum levels of insulin compared with EPA, especially in subgroups whose mean age was <60 years (0.43 mU/L; 95% CI: 0.04, 0.81 mU/L) and duration of DHA supplementation < 3 months (0.39 mU/L; 95% CI: 0.01, 0.77 mU/L). Conclusions: The present meta-analysis provides evidence that EPA and DHA have different effects on risk factors of MetS.
AB - Background & aims: Previous randomized controlled trials (RCTs) have compared the effects of pure preparations of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in reducing metabolic syndrome (MetS) risk factors, but the results were inconsistent. The present study aimed to clarify whether EPA and DHA have differential effects on MetS features in humans. Methods: A systematic literature search was conducted in CNKI, PubMed, Embase and Scopus updated to February 2021. The mean changes in the characteristics of MetS were calculated as weighted mean differences by using a random-effects model. Thirty-three RCTs were included. Results: The results showed that both EPA and DHA were effective at lowering serum triglycerides (TG) levels. EPA supplementation decreased the serum levels of total cholesterol (TC) (WMD = −0.24 mmol/L; 95% CI, −0.43, −0.05 mmol/L), TG (WMD = −0.77 mmol/L; 95% CI, −1.54, −0.00 mmol/L) and low density lipoprotein-cholesterol (LDL-C) (WMD = −0.13 mmol/L; 95% CI, −0.25, −0.01 mmol/L), while DHA increased the serum levels of TC (WMD = 0.14 mmol/L; 95% CI, 0.03, 0.25 mmol/L), LDL-C (WMD = 0.26 mmol/L; 95% CI, 0.15, 0.38 mmol/L) and high density lipoprotein-cholesterol (HDL-C) (WMD = 0.07 mmol/L; 95% CI, 0.04, 0.09 mmol/L). Moreover, DHA increased the serum levels of insulin compared with EPA, especially in subgroups whose mean age was <60 years (0.43 mU/L; 95% CI: 0.04, 0.81 mU/L) and duration of DHA supplementation < 3 months (0.39 mU/L; 95% CI: 0.01, 0.77 mU/L). Conclusions: The present meta-analysis provides evidence that EPA and DHA have different effects on risk factors of MetS.
KW - Docosahexaenoic acid
KW - Eicosapentaenoic acid
KW - Meta-analysis
KW - Metabolic syndrome
KW - Randomized controlled trial
UR - http://www.scopus.com/inward/record.url?scp=85109028227&partnerID=8YFLogxK
U2 - 10.1016/j.clnu.2021.05.025
DO - 10.1016/j.clnu.2021.05.025
M3 - Article
C2 - 34229258
AN - SCOPUS:85109028227
SN - 0261-5614
VL - 40
SP - 4538
EP - 4550
JO - Clinical Nutrition
JF - Clinical Nutrition
IS - 7
ER -