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      Effect of cocoa ( Theobroma cacao L.) on platelet function testing profiles in patients with coronary artery disease: ECLAIR pilot study

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          Abstract

          Introduction

          This prospective pharmacodynamic nutraceutical study assessed the effect of a 1-week trial of 30 g/day of 65% cocoa (dark chocolate) ( Theobroma cacao L.) consumption intervention on platelet reactivity.

          Methods

          Patients with stable coronary artery disease (CAD) (n=20) who were on maintenance dual antiplatelet therapy of aspirin (ASA) 81 mg/day and clopidogrel 75 mg/day were recruited. Platelet function was evaluated with the VerifyNow P2Y 12 reaction unit (PRU) and aspirin reaction unit (ARU) assays (Werfen, Bedford, Massachusetts, USA) and assessed prior to initiation of and after a 1-week trial of 30 g/day of 65% cocoa consumption intervention. Results were compared with a paired t-test.

          Results

          Cocoa augmented the inhibitory effect of clopidogrel, demonstrated by a reduction of 11.9% (95% CI 5.7% to 18.0%, p value 0.001), significantly decreasing the PRU by 26.85 (95% CI 12.22 to 41.48, p value 0.001). The inhibitory effect of ASA was not impacted by cocoa, reflected by a non-significant reduction in ARU of 17.65 (95% CI 21.00 to 56.3, p value 0.351). No patients experienced any serious adverse events.

          Conclusions

          Cocoa augmented the inhibitory effect of clopidogrel but not ASA. This nutraceutical study could be potentially informative and applicable for patients with stable CAD. Further long-term studies are required to confirm these exploratory findings.

          Trial registration number

          NCT04554901.

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          Most cited references43

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          World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects.

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            Global Burden of Cardiovascular Diseases and Risk Factors, 1990–2019

            Cardiovascular diseases (CVDs), principally ischemic heart disease (IHD) and stroke, are the leading cause of global mortality and a major contributor to disability. This paper reviews the magnitude of total CVD burden, including 13 underlying causes of cardiovascular death and 9 related risk factors, using estimates from the Global Burden of Disease (GBD) Study 2019. GBD, an ongoing multinational collaboration to provide comparable and consistent estimates of population health over time, used all available population-level data sources on incidence, prevalence, case fatality, mortality, and health risks to produce estimates for 204 countries and territories from 1990 to 2019. Prevalent cases of total CVD nearly doubled from 271 million (95% uncertainty interval [UI]: 257 to 285 million) in 1990 to 523 million (95% UI: 497 to 550 million) in 2019, and the number of CVD deaths steadily increased from 12.1 million (95% UI:11.4 to 12.6 million) in 1990, reaching 18.6 million (95% UI: 17.1 to 19.7 million) in 2019. The global trends for disability-adjusted life years (DALYs) and years of life lost also increased significantly, and years lived with disability doubled from 17.7 million (95% UI: 12.9 to 22.5 million) to 34.4 million (95% UI:24.9 to 43.6 million) over that period. The total number of DALYs due to IHD has risen steadily since 1990, reaching 182 million (95% UI: 170 to 194 million) DALYs, 9.14 million (95% UI: 8.40 to 9.74 million) deaths in the year 2019, and 197 million (95% UI: 178 to 220 million) prevalent cases of IHD in 2019. The total number of DALYs due to stroke has risen steadily since 1990, reaching 143 million (95% UI: 133 to 153 million) DALYs, 6.55 million (95% UI: 6.00 to 7.02 million) deaths in the year 2019, and 101 million (95% UI: 93.2 to 111 million) prevalent cases of stroke in 2019. Cardiovascular diseases remain the leading cause of disease burden in the world. CVD burden continues its decades-long rise for almost all countries outside high-income countries, and alarmingly, the age-standardized rate of CVD has begun to rise in some locations where it was previously declining in high-income countries. There is an urgent need to focus on implementing existing cost-effective policies and interventions if the world is to meet the targets for Sustainable Development Goal 3 and achieve a 30% reduction in premature mortality due to noncommunicable diseases.
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              Platelet activation and atherothrombosis.

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                Author and article information

                Journal
                Open Heart
                Open Heart
                openhrt
                openheart
                Open Heart
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2053-3624
                2022
                13 September 2022
                : 9
                : 2
                : e002066
                Affiliations
                [1 ]departmentClinical Medical Sciences , The University of the West Indies , Saint Augustine, Trinidad and Tobago
                [2 ]departmentCocoa Research Centre , The University of the West Indies , Saint Augustine, Trinidad and Tobago
                [3 ]departmentDepartment of Medicine , North Central Regional Health Authority , Champ Fleurs, Trinidad and Tobago
                [4 ]departmentDepartment of Medicine , University of Kansas Medical Center , Wichita, Kansas, USA
                [5 ]departmentCardiology Division , HeartPlace , Dallas, Texas, USA
                [6 ]departmentCardiology Division , Universidad de Murcia , Murcia, Spain
                [7 ]departmentCardiology Division , University of Vermont Medical Center , Burlington, Vermont, USA
                Author notes
                [Correspondence to ] Dr Naveen Anand Seecheran; nseecheran@ 123456gmail.com
                Author information
                http://orcid.org/0000-0002-7779-0181
                Article
                openhrt-2022-002066
                10.1136/openhrt-2022-002066
                9472200
                36100318
                e02410d7-8107-45de-9698-c84d83ceb082
                © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See:  https://creativecommons.org/licenses/by/4.0/.

                History
                : 28 May 2022
                : 30 August 2022
                Funding
                Funded by: The University of the West Indies, St Augustine Campus Research and Publication Fund;
                Award ID: CRP.3.MAR21.03
                Categories
                Coronary Artery Disease
                1506
                Original research
                Custom metadata
                unlocked

                epidemiology,pharmacology, clinical,drug interactions

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