AI Article Synopsis

  • The study examined the effects of the nutraceutical product Citrolive™ on LDL oxidation and lipid metabolism in individuals with cardiovascular risk factors.
  • Participants were randomly assigned to receive either Citrolive™ or a placebo for three months, and those taking Citrolive™ showed a significant reduction in oxidized LDL levels.
  • Results indicated that Citrolive™ may improve lipid profiles by decreasing oxidized LDL and increasing serum paraoxonase activity in moderate-risk individuals compared to the control group.

Article Abstract

The aim of the study was to assess whether oral intake of a nutraceutical product (Citrolive™) could determine changes in low-density lipoprotein (LDL) oxidation and other parameters of lipid metabolism and plasma atherogenic capacity. Citrolive™ is a commercial extract obtained from the combination of citrus fruit flavonoids and olive leaf extracts. Twenty-three untreated subjects (69.6% males, 30.4% females, mean age 41.9 ± 9.4 years) with cardiovascular risk factors and a total cholesterol level >200 mg/dL and LDL cholesterol (LDL-C) > 130 mg/dL participated in a 3-month randomized double-blind controlled study. Participants in the intervention group (71.4% males, 28.6% females, mean age 42.7 ± 9.7 years) consumed Citrolive™ (500 mg, two capsules/day), and controls (66.7% males, 33.3% females, mean age 40.6 ± 9.4 years) received a matched placebo. At 3 months, oxidized LDL (ox-LDL) decreased significantly in the intervention group from 93.8 ± 19.1 U/L to 62.8 ± 28.7 U/L ( < 0.05), whereas the control group increased from 98.2 ± 23.5 U/L to 105.7 ± 21.9 U/L ( = 0.1). Between-group differences were also significant ( < 0.05). Similar findings in the ox-LDL/LDL-C ratio were observed. Serum paraoxonase activity (PON1) increased significantly in the intervention group from 64.5 ± 15.6 U/L to 78.7 ± 28.8 U/L ( < 0.05) but remained unchanged in controls. Consumption of Citrolive™ for 3 months in treatment-naïve subjects with moderate risk of atherosclerosis was associated with a reduction in oxidized LDL-C and LDL-oxidase/LDL-C ratio as compared to controls.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069525PMC
http://dx.doi.org/10.3390/antiox10040589DOI Listing

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