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      Association of serum hemoglobin level with the risk of carotid plaque beyond metabolic abnormalities among asymptomatic adults without major adverse clinical events: a cross-sectional cohort study

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          Abstract

          Background

          The serum hemoglobin (Hb) level is closely related to adverse clinical outcomes. However, data on the association of Hb levels with subclinical atherosclerosis beyond metabolic abnormalities are limited.

          Methods

          This study evaluated the association among serum Hb level, metabolic syndrome (MetS), and the risk of carotid plaque formation in asymptomatic adults without a history of major adverse clinical events.

          Results

          A total of 2560 participants (mean age: 60 ± 8 years, 32.9% men) were stratified into four groups based on Hb quartiles, as follows: ≤ 12.8 g/dL (group I), 12.9–13.6 g/dL (group II), 13.7–14.5 g/dL (group III), and ≥ 14.6 g/dL (group IV). The overall prevalence of MetS and carotid plaque was 37.2% and 33.4%, respectively. The prevalence of MetS increased with increasing Hb level (group I: 27.4% vs. group II: 35.9% vs. group III: 42.6% vs. group IV: 44.1%, p < 0.001). The prevalence of carotid plaque was 34.3%, 28.1%, 32.8%, and 39.5% in groups I, II, III, and IV, respectively. Univariate logistic regression analysis showed that MetS was associated with an increased risk of carotid plaque (odds ratio [OR] 1.568, 95% confidence interval [CI] 1.326–1.856, p < 0.001). Only group II showed a lower risk of carotid plaque than group I (OR 0.750, 95% CI 0.596–0.943, p = 0.014). Multiple logistic regression models showed consistent results after adjusting for clinical factors, including MetS and its individual components.

          Conclusion

          Serum Hb level is associated with the risk of carotid plaque beyond MetS and its components in a relatively healthy adult population.

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          Most cited references34

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          Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement.

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            Prevalence of the Metabolic Syndrome Among US Adults

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              Increasing Prevalence of Metabolic Syndrome in Korea

              OBJECTIVE The number of people with metabolic syndrome is increasing worldwide, and changes in socioenvironmental factors contribute to this increase. Therefore, investigation of changes in metabolic syndrome and its components in South Korea, where rapid socioenvironmental changes have occurred in recent years, would be foundational in setting up an effective strategy for reducing this increasing trend. RESEARCH DESIGN AND METHODS We compared the prevalence and pattern of metabolic syndrome among participants in the Korean National Health and Nutrition Examination Surveys for 1998, 2001, 2005, and 2007. In each survey, stratified, multistage, probability–sampling designs and weighting adjustments were conducted to represent the entire Korean population. The revised National Cholesterol Education Program criteria were used as the definition of metabolic syndrome. All biochemical parameters were measured in a central laboratory. RESULTS A total of 6,907 (mean ± SE age 45.0 ± 0.2 years), 4,536 (45.5 ± 0.2), 5,373 (47.1 ± 0.2), and 2,890 (49.9 ± 0.3) Koreans over 20 years of age have participated in the studies in 1998, 2001, 2005, and 2007, respectively. The age-adjusted prevalence of metabolic syndrome increased significantly from 24.9% in 1998, 29.2% in 2001, and 30.4% in 2005 to 31.3% in 2007. Among the five components, the level of low HDL cholesterol increased the most, by 13.8% over the 10 years. Abdominal obesity and hypertriglyceridemia followed, with 8.7 and 4.9% increases, respectively. CONCLUSIONS Because dyslipidemia and abdominal obesity were major factors in increasing the prevalence of metabolic syndrome in Koreans for the past 10 years, lifestyle interventions should be conducted at the national level to reduce the burden and consequences of metabolic syndrome.
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                Author and article information

                Contributors
                0733274@uuh.ulsan.kr
                kbwon@uuh.ulsan.kr
                khh3822@naver.com
                hjchang@yuhs.ac
                Journal
                BMC Cardiovasc Disord
                BMC Cardiovasc Disord
                BMC Cardiovascular Disorders
                BioMed Central (London )
                1471-2261
                2 March 2021
                2 March 2021
                2021
                : 21
                : 35
                Affiliations
                [1 ]GRID grid.267370.7, ISNI 0000 0004 0533 4667, Division of Hematology and Oncology, , Ulsan University Hospital, University of Ulsan College of Medicine, ; Ulsan, Republic of Korea
                [2 ]GRID grid.267370.7, ISNI 0000 0004 0533 4667, Division of Cardiology, , Ulsan University Hospital, University of Ulsan College of Medicine, ; Ulsan, Republic of Korea
                [3 ]GRID grid.15444.30, ISNI 0000 0004 0470 5454, Division of Cardiology, , Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, ; 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722 South Korea
                [4 ]GRID grid.411947.e, ISNI 0000 0004 0470 4224, Division of Pulmonary, Critical Care and Sleep Medicine, College of Medicine, , The Catholic University of Korea, ; Seoul, Republic of Korea
                [5 ]GRID grid.267370.7, ISNI 0000 0004 0533 4667, Division of Pulmonary, Critical Care and Sleep Medicine, , Ulsan University Hospital, University of Ulsan College of Medicine, ; 877 Bangeojinsunhwando-ro, Dong-gu, Ulsan, 44033 Republic of Korea
                Author information
                http://orcid.org/0000-0001-5860-9407
                Article
                1852
                10.1186/s12872-021-01852-7
                7923602
                33648442
                a773a658-5824-460a-a521-70afc7120f1f
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 13 April 2020
                : 4 January 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003052, Ministry of Trade, Industry and Energy;
                Award ID: 10075266
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2021

                Cardiovascular Medicine
                hemoglobin,metabolic syndrome,carotid plaque,atherosclerosis
                Cardiovascular Medicine
                hemoglobin, metabolic syndrome, carotid plaque, atherosclerosis

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