Safety of conjugated linoleic acid (CLA) in overweight or obese human volunteers
Autor: | Jan Wadstein, Erling Thom, Grethe Berven, Henrietta Blankson, Amund Bye, Hans Fagertun, Ola Gudmundsen, Ottar Hals |
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Rok vydání: | 2000 |
Předmět: |
business.industry
Conjugated linoleic acid Placebo-controlled study Vital signs Physiology General Chemistry Overweight medicine.disease Placebo Obesity Industrial and Manufacturing Engineering chemistry.chemical_compound Biochemistry chemistry Medicine medicine.symptom business Adverse effect Body mass index Food Science Biotechnology |
Zdroj: | European Journal of Lipid Science and Technology. 102:455-462 |
ISSN: | 1438-9312 1438-7697 |
DOI: | 10.1002/1438-9312(200008)102:7<455::aid-ejlt455>3.0.co;2-v |
Popis: | The main objective of the study was to investigate the safety of conjugated linoleic acid (CLA) in healthy volunteers. The effect of CLA on body composition was also investigated. The trial design was a randomized, double-blind placebo controlled study including 60 overweight or obese volunteers (body mass index (BMI) 27.5—39.0 kg/m2). The subjects were divided into two groups receiving 3.4 g CLA or placebo (4.5 g olive oil) daily for 12 weeks. The safety was evaluated by analysis of blood parameters and by clinical examinations at baseline and week 12. Vital signs and adverse events were registered at baseline, week 6, and week 12. Bio Impedance Assessment was applied for body composition measurements. 55 subjects completed the study. Adverse events occurred in 10% of the subjects. No difference in adverse events or other safety parameters was found between the treatment groups. Small changes in the laboratory safety data were not regarded as clinically significant. Moreover, no clinically significant changes in vital signs were observed in any of the groups. In the CLA group, mean weight was reduced by 1.1 kg (paired t-test p = 0.005), while mean BMI was reduced by 0.4 kg/m2(p = 0.007). However, the overall treatment effect of CLA on body weight and BMI was not significant. There were no differences found between the groups with regard to efficacy parameters. The results indicate that CLA in the given dose is a safe substance in healthy populations with regard to the safety parameters investigated. |
Databáze: | OpenAIRE |
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