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      The Effects of Menopause Hormone Therapy on Lipid Profile in Postmenopausal Women: A Systematic Review and Meta-Analysis

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          Abstract

          Importance: The incidence of dyslipidemia increases after menopause. Menopause hormone therapy (MHT) is recommended for menopause related disease. However, it is benefit for lipid profiles is inconclusive.

          Objective: To conduct a systematic review and meta-analysis of randomized controlled trials to evaluate the effects of MHT on lipid profile in postmenopausal women.

          Evidence Review: Related articles were searched on PubMed/Medline, EMBASE, Web of Science, and Cochrane Library databases from inception to December 2020. Data extraction and quality evaluation were performed independently by two reviewers. The methodological quality was assessed using the “Cochrane Risk of Bias checklist”.

          Results: Seventy-three eligible studies were selected. The results showed that MHT significantly decreased the levels of TC (WMD: −0.43, 95% CI: −0.53 to −0.33), LDL-C (WMD: −0.47, 95% CI: −0.55 to −0.40) and LP (a) (WMD: −49.46, 95% CI: −64.27 to −34.64) compared with placebo or no treatment. Oral MHT led to a significantly higher TG compared with transdermal MHT (WMD: 0.12, 95% CI: 0.04–0.21). The benefits of low dose MHT on TG was also concluded when comparing with conventional-dose estrogen (WMD: −0.18, 95% CI: −0.32 to −0.03). The results also showed that conventional MHT significantly decreased LDL-C (WMD: −0.35, 95% CI: −0.50 to −0.19), but increase TG (WMD: 0.42, 95%CI: 0.18–0.65) compared with tibolone. When comparing with the different MHT regimens, estrogen (E) + progesterone (P) regimen significantly increased TC (WMD: 0.15, 95% CI: 0.09 to 0.20), LDL-C (WMD: 0.12, 95% CI: 0.07–0.17) and Lp(a) (WMD: 44.58, 95% CI:28.09–61.06) compared with estrogen alone.

          Conclusion and Relevance: MHT plays a positive role in lipid profile in postmenopausal women, meanwhile for women with hypertriglyceridemia, low doses or transdermal MHT or tibolone would be a safer choice. Moreover, E + P regimen might blunt the benefit of estrogen on the lipid profile.

          Clinical Trial Registration: [ https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42018092924], identifier [No. CRD42018092924].

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          The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials

          Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for assessing risk of bias aims to make the process clearer and more accurate
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                12 April 2022
                2022
                : 13
                : 850815
                Affiliations
                [1] 1 Department of Gynecology , The Second Affiliated Hospital of Guangzhou University of Chinese Medicine , Guangzhou, China
                [2] 2 The Second Clinical Medical College of Guangzhou University of Chinese Medicine , Guangzhou, China
                [3] 3 Department of Standardization of Traditional Chinese Medicine , The Second Affiliated Hospital of Guangzhou University of Chinese Medicine , Guangzhou, China
                [4] 4 State Key Laboratory of Dampness Syndrome of Chinese Medicine , The Second Affiliated Hospital of Guangzhou University of Chinese Medicine , Guangzhou, China
                [5] 5 Department of Cardiovascular Medicine , Guangdong Provincial Hospital of Chinese Medicine , Guangzhou, China
                [6] 6 Health Science Center , Shenzhen University , Shenzhen, China
                [7] 7 Department of Gynecology , Peking Union Medical College Hospital , Beijing, China
                Author notes

                Edited by: Changting Xiao, University of Saskatchewan, Canada

                Reviewed by: Željko Reiner, University Hospital Centre Zagreb, Croatia

                Mihnea-Alexandru Găman, Carol Davila University of Medicine and Pharmacy, Romania

                [ † ]

                These authors have contributed equally to this work

                This article was submitted to Drugs Outcomes Research and Policies, a section of the journal Frontiers in Pharmacology

                Article
                850815
                10.3389/fphar.2022.850815
                9039020
                35496275
                f17ed874-e896-4c02-b64b-1d010d9a3c2a
                Copyright © 2022 Nie, Yang, Wang, Liang, Li, Luo, Yang, Liu, Wang, Guo, Yu and Liang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 January 2022
                : 28 February 2022
                Categories
                Pharmacology
                Systematic Review

                Pharmacology & Pharmaceutical medicine
                menopause hormone therapy,lipid profile,meta-analysis,postmenopausal women,system review

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