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      Potential clinical biomarkers and perspectives in diabetic cardiomyopathy

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          Abstract

          Diabetic cardiomyopathy (DCM) is a serious cardiovascular complication and the leading cause of death in diabetic patients. Patients typically do not experience any symptoms and have normal systolic and diastolic cardiac functions in the early stages of DCM. Because the majority of cardiac tissue has already been destroyed by the time DCM is detected, research must be conducted on biomarkers for early DCM, early diagnosis of DCM patients, and early symptomatic management to minimize mortality rates among DCM patients. Most of the existing implemented clinical markers are not very specific for DCM, especially in the early stages of DCM. Recent studies have shown that a number of new novel markers, such as galactin-3 (Gal-3), adiponectin (APN), and irisin, have significant changes in the clinical course of the various stages of DCM, suggesting that we may have a positive effect on the identification of DCM. As a summary of the current state of knowledge regarding DCM biomarkers, this review aims to inspire new ideas for identifying clinical markers and related pathophysiologic mechanisms that could be used in the early diagnosis and treatment of DCM.

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          Most cited references147

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          A PGC1α-dependent myokine that drives browning of white fat and thermogenesis

          Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional coactivator PGC1α Here we show that PGC1α expression in muscle stimulates an increase in expression of Fndc5, a membrane protein that is cleaved and secreted as a new hormone, irisin. Irisin acts on white adipose cells in culture and in vivo to stimulate UCP1 expression and a broad program of brown fat-like development. Irisin is induced with exercise in mice and humans, and mildly increased irisin levels in blood cause an increase in energy expenditure in mice with no changes in movement or food intake. This results in improvements in obesity and glucose homeostasis. Irisin could be a protein therapeutic for human metabolic disease and other disorders that are improved with exercise.
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            Cardiac Fibrosis: The Fibroblast Awakens.

            Myocardial fibrosis is a significant global health problem associated with nearly all forms of heart disease. Cardiac fibroblasts comprise an essential cell type in the heart that is responsible for the homeostasis of the extracellular matrix; however, upon injury, these cells transform to a myofibroblast phenotype and contribute to cardiac fibrosis. This remodeling involves pathological changes that include chamber dilation, cardiomyocyte hypertrophy and apoptosis, and ultimately leads to the progression to heart failure. Despite the critical importance of fibrosis in cardiovascular disease, our limited understanding of the cardiac fibroblast impedes the development of potential therapies that effectively target this cell type and its pathological contribution to disease progression. This review summarizes current knowledge regarding the origins and roles of fibroblasts, mediators and signaling pathways known to influence fibroblast function after myocardial injury, as well as novel therapeutic strategies under investigation to attenuate cardiac fibrosis.
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              Role of diabetes in congestive heart failure: the Framingham study.

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                Author and article information

                Contributors
                qiaoaijun@simm.ac.can
                yandw963@126.com
                Journal
                Diabetol Metab Syndr
                Diabetol Metab Syndr
                Diabetology & Metabolic Syndrome
                BioMed Central (London )
                1758-5996
                4 March 2023
                4 March 2023
                2023
                : 15
                : 35
                Affiliations
                [1 ]GRID grid.452847.8, ISNI 0000 0004 6068 028X, Department of Endocrinology, Shenzhen Second People’s Hospital, the First Affiliated Hospital of Shenzhen University, Health Science Center of Shenzhen University, , Shenzhen Clinical Research Center for Metabolic Diseases, ; No. 3002, Sungang West Road, Futian District, Shenzhen, 518035 Guangdong Province China
                [2 ]GRID grid.459428.6, Geriatric Diseases Institute of Chengdu, Center for Medicine Research and Translation, , Chengdu Fifth People’s Hospital, ; Chengdu, 611137 Sichuan Province China
                [3 ]Department of Geriatrics, the Traditional Chinese Medicine Hospital of Wenjiang District, Chengdu, 611130 China
                [4 ]GRID grid.9227.e, ISNI 0000000119573309, Zhongshan Institute for Drug Discovery, , Shanghai Institute of Materia Medica, Chinese Academy of Sciences, ; Zhongshan, 528400 Guangdong Province China
                [5 ]GRID grid.9227.e, ISNI 0000000119573309, Shanghai Institute of Materia Medica, , Chinese Academy of Sciences, ; 555 Zu Chong Zhi Road, Shanghai, 201203 China
                Article
                998
                10.1186/s13098-023-00998-y
                9985231
                36871006
                ee5dceb5-3853-49cd-8ce4-a2e8d1eeb809
                © The Author(s) 2023

                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
                : 24 December 2022
                : 15 February 2023
                Funding
                Funded by: National Social Science Fund of China
                Award ID: 81670759
                Award Recipient :
                Funded by: Basic Research Foundation of Shenzhen
                Award ID: JCYJ20170306092910641
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2023

                Nutrition & Dietetics
                diabetic cardiomyopathy,biomarkers,apelin,irisin,galactin-3,nlrp3 inflammasome
                Nutrition & Dietetics
                diabetic cardiomyopathy, biomarkers, apelin, irisin, galactin-3, nlrp3 inflammasome

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