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Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial

OBJECTIVE: The effect of lycopene (LycoRed) supplementation was evaluated in healthy postmenopausal women by biochemical markers for cardiovascular protection and osteoporosis protection. STUDY SETTINGS AND DESIGN: This was a multi-centric placebo-controlled double-blind randomized clinical trial th...

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Autores principales: Meeta, Meeta, Sharma, Sudhaa, Unni, Jyothi, Khandelwal, Sunila, Choranur, Ambuja, Malik, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9190964/
https://www.ncbi.nlm.nih.gov/pubmed/35707307
http://dx.doi.org/10.4103/jmh.jmh_61_22
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author Meeta, Meeta
Sharma, Sudhaa
Unni, Jyothi
Khandelwal, Sunila
Choranur, Ambuja
Malik, Sonia
author_facet Meeta, Meeta
Sharma, Sudhaa
Unni, Jyothi
Khandelwal, Sunila
Choranur, Ambuja
Malik, Sonia
author_sort Meeta, Meeta
collection PubMed
description OBJECTIVE: The effect of lycopene (LycoRed) supplementation was evaluated in healthy postmenopausal women by biochemical markers for cardiovascular protection and osteoporosis protection. STUDY SETTINGS AND DESIGN: This was a multi-centric placebo-controlled double-blind randomized clinical trial that screened 198 postmenopausal women at 21 centers across 12 cities in India. Levels of lycopene, lipid profile, high-risk C-reactive protein, and bone turnover markers: amino-terminal propeptide of Type I collagen (P1NP) and C-terminal telopeptide of Type I collagen (β-CTx) were measured at baseline and 6 months postsupplementation with LycoRed or placebo. INTERVENTIONS: The study was completed with 57 of the 100 women on LycoRed 8 mg (antioxidant potency is equivalent to 24 mg of lycopene) and 43 placebos for 6 months by randomization. MAIN OUTCOME MEASURES: Rise in serum lycopene and effect of serum lycopene on surrogate markers of cardiovascular health and bone health. RESULTS: LycoRed supplementation increases lycopene levels and P1NP and nonsignificant fall in β-CTx levels in healthy postmenopausal women. CONCLUSIONS: Lycopene supplementation in Indian menopausal women may confer protection from osteoporosis as shown by the directional change in the surrogate biochemical markers. This study can form a basis for larger studies with different doses to understand the effect of lycopene to prevent and act as adjuvant treatment on clinical endpoints for cardiovascular disease (CVD) and bone health.
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spelling pubmed-91909642022-06-14 Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial Meeta, Meeta Sharma, Sudhaa Unni, Jyothi Khandelwal, Sunila Choranur, Ambuja Malik, Sonia J Midlife Health Original Article OBJECTIVE: The effect of lycopene (LycoRed) supplementation was evaluated in healthy postmenopausal women by biochemical markers for cardiovascular protection and osteoporosis protection. STUDY SETTINGS AND DESIGN: This was a multi-centric placebo-controlled double-blind randomized clinical trial that screened 198 postmenopausal women at 21 centers across 12 cities in India. Levels of lycopene, lipid profile, high-risk C-reactive protein, and bone turnover markers: amino-terminal propeptide of Type I collagen (P1NP) and C-terminal telopeptide of Type I collagen (β-CTx) were measured at baseline and 6 months postsupplementation with LycoRed or placebo. INTERVENTIONS: The study was completed with 57 of the 100 women on LycoRed 8 mg (antioxidant potency is equivalent to 24 mg of lycopene) and 43 placebos for 6 months by randomization. MAIN OUTCOME MEASURES: Rise in serum lycopene and effect of serum lycopene on surrogate markers of cardiovascular health and bone health. RESULTS: LycoRed supplementation increases lycopene levels and P1NP and nonsignificant fall in β-CTx levels in healthy postmenopausal women. CONCLUSIONS: Lycopene supplementation in Indian menopausal women may confer protection from osteoporosis as shown by the directional change in the surrogate biochemical markers. This study can form a basis for larger studies with different doses to understand the effect of lycopene to prevent and act as adjuvant treatment on clinical endpoints for cardiovascular disease (CVD) and bone health. Wolters Kluwer - Medknow 2022 2022-05-02 /pmc/articles/PMC9190964/ /pubmed/35707307 http://dx.doi.org/10.4103/jmh.jmh_61_22 Text en Copyright: © 2022 Journal of Mid-life Health https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Meeta, Meeta
Sharma, Sudhaa
Unni, Jyothi
Khandelwal, Sunila
Choranur, Ambuja
Malik, Sonia
Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title_full Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title_fullStr Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title_full_unstemmed Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title_short Cardiovascular and Osteoporosis Protection at Menopause with Lycopene: A Placebo-Controlled Double-Blind Randomized Clinical Trial
title_sort cardiovascular and osteoporosis protection at menopause with lycopene: a placebo-controlled double-blind randomized clinical trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9190964/
https://www.ncbi.nlm.nih.gov/pubmed/35707307
http://dx.doi.org/10.4103/jmh.jmh_61_22
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