| Literature DB >> 31902378 |
Mehri Jamilian1, Zohreh Tabassi2, Željko Reiner3, Ida Panahandeh2, Fatemeh Naderi2, Esmat Aghadavod4, Elaheh Amirani4, Mohsen Taghizadeh4, Rana Shafabakhsh4, Mahbobeh Satari4, Mohammad Ali Mansournia5, Mohammad Reza Memarzadeh4, Zatollah Asemi4.
Abstract
The present study was performed to evaluate the effects of n-3 fatty acids from flaxseed oil on genetic and metabolic profiles in patients with gestational diabetes mellitus (GDM). This randomised, double-blind, placebo-controlled clinical trial was performed in sixty women with GDM. Participants were randomly divided into two groups to intake either 2 × 1000 mg/d n-3 fatty acids from flaxseed oil containing 400 mg α-linolenic acid in each capsule (n 30) or placebo (n 30) for 6 weeks. n-3 Fatty acid intake up-regulated PPAR-γ (P < 0·001) and LDL receptor (P = 0·004) and down-regulated gene expression of IL-1 (P = 0·002) and TNF-α (P = 0·001) in peripheral blood mononuclear cells of subjects with GDM. In addition, n-3 fatty acid supplementation reduced fasting plasma glucose (P = 0·001), insulin levels (P = 0·001) and insulin resistance (P < 0·001) and increased insulin sensitivity (P = 0·005) when compared with the placebo. Additionally, n-3 fatty acid supplementation was associated with a decrease in TAG (P < 0·001), VLDL-cholesterol (P < 0·001), total cholesterol (P = 0·01) and total cholesterol:HDL-cholesterol ratio (P = 0·01) when compared with placebo. n-3 Fatty acid administration was also associated with a significant reduction in high-sensitivity C-reactive protein (P = 0·006) and malondialdehyde (P < 0·001), and an increase in total nitrite (P < 0·001) and total glutathione levels (P = 0·006) when compared with the placebo. n-3 Fatty acid supplementation for 6 weeks to women with GDM had beneficial effects on gene expression related to insulin, lipid and inflammation, glycaemic control, lipids, inflammatory markers and oxidative stress.Entities:
Keywords: Flaxseed oil; Gestational diabetes; Inflammation; Insulin resistance; Metabolic status
Year: 2020 PMID: 31902378 DOI: 10.1017/S0007114519003416
Source DB: PubMed Journal: Br J Nutr ISSN: 0007-1145 Impact factor: 3.718