EGb in the Treatment for Patients with VCI: A Systematic Review and Meta-Analysis
Background. Ginkgo biloba extract (EGb) is widely used to treat impairments in memory, cognition, activities of daily living, inflammation, edema, stroke, Alzheimer’s dementia, and aging. Aim. We aimed to evaluate the safety and efficacy of EGb in treating vascular cognitive impairment (VCI). Method...
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Veröffentlicht in: | Oxidative medicine and cellular longevity 2021, Vol.2021 (1), p.8787684-8787684 |
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Zusammenfassung: | Background. Ginkgo biloba extract (EGb) is widely used to treat impairments in memory, cognition, activities of daily living, inflammation, edema, stroke, Alzheimer’s dementia, and aging. Aim. We aimed to evaluate the safety and efficacy of EGb in treating vascular cognitive impairment (VCI). Methods. The systematic review was performed using the latest guidelines. We searched for EGb-related trials up to March 1, 2021, in four Chinese databases, three English databases, and clinical trial registry platforms. Randomized controlled trials (RCTs) were included if the study enrolled participants with VCI. Two reviewers independently extracted the data and critically appraised the study quality. Heterogeneity was quantified with I2. Both sensitivity and subgroup analyses were used to identify the sources of heterogeneity. Publication bias was assessed with funnel plots. We used the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach to rate the evidence quality. Outcomes included assessments using the Activities of Daily Living (ADL), Montreal Cognitive Assessment (MoCA), Mini-Mental State Examination (MMSE), Hasegawa Dementia Scale (HDS), Barthel Index (BI), Functional Activity Questionnaire (FAQ), and adverse events. Results. In this study, a total of 2019 patients in 23 RCTs were included. EGb appeared to be more effective than control conditions as assessed by the results of cognitive function evaluation, including MMSE (MDMMSE,EGb vs.blank=3.04, 95% CI: 0.10-5.98; MDMMSE,EGb vs.drugs for VCI=2.70, 95% CI: 1.39-4.01; MDMMSE,EGb+drugs for VCI vs.blank=5.90, 95% CI: 4.21-7.59; and MDMMSE,EGb+drugs for VCI vs.drugs for VCI=3.14, 95% CI: 2.14-4.15), MoCA (MDMoCA,EGb vs.blank=5.30, 95% CI: 2.15-8.46; MDMoCA,EGb+drugs for VCI vs.blank=2.66, 95% CI: 1.82-3.50; and MDMoCA,EGb+drugs for VCI vs.drugs for VCI=2.56, 95% CI: 1.85-3.27), HDS (MDHDS,EGb vs.blank=6.50; 95% CI: 4.86-8.14; MDHDS,EGb+drugs for VCI vs.drugs for VCI=3.60, 95% CI: 2.50-4.70), ADL (MDADL,EGb vs.blank=7.20, 95% CI: 3.28-11.12; MDADL,EGb+drugs for VCI vs.blank=10.00, 95% CI: 7.51-12.49; and MDADL,EGb+drugs for VCI vs.drugs for VCI=9.20, 95% CI: 7.26-11.14), BI (MDBI,EGb+drugs for VCI vs.drugs for VCI=5.71, 95% CI: 2.99-8.43; MDFAQ,EGb vs.drugs for VCI=−1.43, 95% CI: -2.78 to 0.08), and FAQ (MDFAQ,EGb+drugs for VCI vs.drugs for VCI=−2.17, 95% CI: -4.13 to 0.21). Evidence of certainty ranged from medium certainty to very low certainty. Conclusion. This meta-analysis s |
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ISSN: | 1942-0900 1942-0994 |
DOI: | 10.1155/2021/8787684 |