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HERO ID
4106766
Reference Type
Journal Article
Title
Impact of weight loss diet associated with flaxseed on inflammatory markers in men with cardiovascular risk factors: a clinical study
Author(s)
Cassani, RS; Fassini, PG; Silvah, JH; Lima, CM; Marchini, JS
Year
2015
Is Peer Reviewed?
1
Journal
Nutrition Journal
ISSN:
1475-2891
Volume
14
Page Numbers
5
Language
English
PMID
25577201
DOI
10.1186/1475-2891-14-5
Web of Science Id
WOS:000348815500001
Relationship(s)
has retraction
4099673
Retraction Note:
Abstract
BACKGROUND:
Flaxseed has received attention for its anti-inflammatory and antioxidant role. The present study hypothesizes if flaxseed added to a weight loss diet could improve the lipid and metabolic profiles and decrease risk factors related to cardiovascular disease.
METHODS:
In a prospective, single blinded 42 days protocol, subjects were allocated into two groups with low carbohydrates intake: GriceLC (35% of carbohydrate and 60g of raw rice powder per day) and GflaxLC (32% of carbohydrate and 60g of flaxseed powder per day). Blood pressure, anthropometric measures and serum levels of isoprostane, C-reactive protein, Tumor Necrosis Factor-alpha, glucose, lipidic profile, uric acid, adiponectin, leptin and insulin were measured at baseline and at the end of interventions. Serum and urinary enterodiol and enterolactione were also measured.
RESULTS:
A total of 27 men with cardiovascular risk factors were evaluated, with mean age of 33 ± 10 years to GriceLC and 40 ± 9 years to GflaxLC. Both groups experienced weight loss and systolic blood pressure reduction. A decrease in inflammatory markers (CRP and TNF-α) was observed after flaxseed intake (mean decrease of 25% and 46% for GflaxLC respectively). All groups also showed improvement in levels of total cholesterol, LDL-c, uric acid and adiponectin. Only GflaxLC group showed a decrease in triglyceride levels.
CONCLUSION:
This study suggests that flaxseed added to a weight loss diet could be an important nutritional strategy to reduce inflammation markers such as CRP and TNF-α.
TRIAL REGISTRATION:
ClinicalTrials.gov NCT02132728.
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