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      Role of PAI-1 in hepatic steatosis and dyslipidemia

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          Abstract

          Plasminogen activator inhibitor 1 (PAI-1) is a functional biomarker of the metabolic syndrome. Previous studies have demonstrated that PAI-1 is a mechanistic contributor to several elements of the syndrome, including obesity, hypertension and insulin resistance. Here we show that PAI-1 is also a critical regulator of hepatic lipid metabolism. RNA sequencing revealed that PAI-1 directly regulates the transcriptional expression of numerous genes involved in mammalian lipid homeostasis, including PCSK9 and FGF21. Pharmacologic or genetic reductions in plasma PAI-1 activity ameliorates hyperlipidemia in vivo. These experimental findings are complemented with the observation that genetic deficiency of PAI-1 is associated with reduced plasma PCSK9 levels in humans. Taken together, our findings identify PAI-1 as a novel contributor to mammalian lipid metabolism and provides a fundamental mechanistic insight into the pathogenesis of one of the most pervasive medical problems worldwide.

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          Most cited references41

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          Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity.

          A cluster of risk factors for cardiovascular disease and type 2 diabetes mellitus, which occur together more often than by chance alone, have become known as the metabolic syndrome. The risk factors include raised blood pressure, dyslipidemia (raised triglycerides and lowered high-density lipoprotein cholesterol), raised fasting glucose, and central obesity. Various diagnostic criteria have been proposed by different organizations over the past decade. Most recently, these have come from the International Diabetes Federation and the American Heart Association/National Heart, Lung, and Blood Institute. The main difference concerns the measure for central obesity, with this being an obligatory component in the International Diabetes Federation definition, lower than in the American Heart Association/National Heart, Lung, and Blood Institute criteria, and ethnic specific. The present article represents the outcome of a meeting between several major organizations in an attempt to unify criteria. It was agreed that there should not be an obligatory component, but that waist measurement would continue to be a useful preliminary screening tool. Three abnormal findings out of 5 would qualify a person for the metabolic syndrome. A single set of cut points would be used for all components except waist circumference, for which further work is required. In the interim, national or regional cut points for waist circumference can be used.
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            Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association

            Circulation, 135(10)
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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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                Author and article information

                Contributors
                d-vaughan@northwestern.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                11 January 2021
                11 January 2021
                2021
                : 11
                : 430
                Affiliations
                [1 ]GRID grid.16753.36, ISNI 0000 0001 2299 3507, Department of Medicine, , Northwestern University Feinberg School of Medicine, Arkes Pavilion, ; Suite 2330, 676 N. St. Clair Street, Chicago, IL 60611-2927 USA
                [2 ]GRID grid.5288.7, ISNI 0000 0000 9758 5690, Center for Preventive Cardiology, Knight Cardiovascular Institute, , Oregon Health and Science University, ; Portland, OR USA
                [3 ]GRID grid.280892.9, Department of Medicine, , Jesse Brown VA Medical Center, ; Chicago, IL USA
                [4 ]GRID grid.69566.3a, ISNI 0000 0001 2248 6943, Department of Molecular Medicine and Therapy, United Centers for Advanced Research and Translational Medicine, , Tohoku University Graduate School of Medicine, ; Miyagi, Japan
                Article
                79948
                10.1038/s41598-020-79948-x
                7801442
                33432099
                79c2e6af-a30e-4867-8773-5ddda5ce0dc5
                © The Author(s) 2021

                Open Access This 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/.

                History
                : 26 June 2020
                : 10 December 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100015334, Endocrine Fellows Foundation;
                Funded by: FundRef http://dx.doi.org/10.13039/100000062, National Institute of Diabetes and Digestive and Kidney Diseases;
                Award ID: T32 DK007169
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000968, American Heart Association;
                Award ID: 15CVGPSD27260148
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: RO1HL51387
                Award ID: RO1HL136373
                Award ID: RO1HL132985
                Award ID: RO1HL142761
                Award Recipient :
                Funded by: Irving S. Cutter Endowment
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                metabolic syndrome,dyslipidaemias,non-alcoholic fatty liver disease
                Uncategorized
                metabolic syndrome, dyslipidaemias, non-alcoholic fatty liver disease

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