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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Study Design

Type
Randomized Controlled Trial (RCT)
Population
60 healthy postmenopausal women aged 47-70 years
Methods
randomized, double-blinded parallel study design, OLE (250 mg/day) or placebo supplementation for 12 weeks
Blinding
Double-blind
Duration
12 weeks
Funding
Unclear
  • Rigorous Journal
Menopause negatively impacts women's health. Objectives: The aim of this study was to investigate whether an olive leaf extract (OLE) improves postmenopausal symptoms, body composition, handgrip strength and blood lipid profile in postmenopausal women. In a randomized, double-blinded parallel study design, 60 healthy postmenopausal women aged 47-70 years received either OLE (250 mg/day) or placebo supplementation for 12 weeks. Postmenopausal symptoms were assessed with the Menopause-Specific Quality of Life Questionnaire (MENQoL), the Hot Flash Interference scale (HFI), and body composition and bone mineral density (BMD) with a DXA scan; the lipid profile was measured in the blood serum. After six and twelve weeks of OLE supplementation, the overall MENQoL score significantly improved (estimated mean difference [-0.4-0.2], p = 0.027) compared to the placebo. A significant improvement (+0.017 [0.003, 0.030], p = 0.019) was recorded in the BMD in the right arm in the OLE group compared to the placebo. The intervention did not affect other body composition outcomes. TG concentrations and the TG/HDL-C ratio were significantly decreased (-0.1 [-0.2, 0.0], p = 0.010; -0.1 [-0.2, -0.0], p = 0.029, respectively) in the OLE group compared to the placebo. Twelve weeks of daily OLE supplementation improved postmenopausal symptoms. Further studies are needed to elucidate the mechanisms underlying the observed effects.

Research Insights

  • The intervention did not affect other body composition outcomes.

    Effect
    Neutral
    Effect size
    Small
    Dose
    250 mg/day
  • After six and twelve weeks of OLE supplementation, the overall MENQoL score significantly improved (estimated mean difference [95% CI]: -0.2 [-0.4-0.2], p = 0.027) compared to the placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    250 mg/day
  • A significant improvement (+0.017 [0.003, 0.030], p = 0.019) was recorded in the BMD in the right arm in the OLE group compared to the placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    250 mg/day
  • The abstract does not report a significant effect for Hot Flash Interference scale; it is mentioned as an outcome assessed but no specific significant result is provided, implying no significant effect.

    Effect
    Neutral
    Effect size
    Small
    Dose
    250 mg/day
  • TG concentrations ... were significantly decreased (-0.1 [-0.2, 0.0], p = 0.010 ...) in the OLE group compared to the placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    250 mg/day
  • TG/HDL-C ratio were significantly decreased ... (-0.1 [-0.2, -0.0], p = 0.029, respectively) in the OLE group compared to the placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    250 mg/day
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