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      Vascular complications in patients with type 2 diabetes: prevalence and associated factors in 38 countries (the DISCOVER study program)

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          Abstract

          Background

          The global prevalence of type 2 diabetes-related complications is not well described. We assessed prevalence of vascular complications at baseline in DISCOVER (NCT02322762; NCT02226822), a global, prospective, observational study program of 15,992 patients with type 2 diabetes initiating second-line therapy, conducted across 38 countries.

          Methods

          Patients were recruited from primary and specialist healthcare settings. Data were collected using a standardized case report form. Prevalence estimates of microvascular and macrovascular complications at baseline were assessed overall and by country and region, and were standardized for age and sex. Modified Poisson regression was used to assess factors associated with the prevalence of complications.

          Results

          The median duration of type 2 diabetes was 4.1 years (interquartile range [IQR]: 1.9–7.9 years), and the median glycated hemoglobin (HbA 1c) level was 8.0% (IQR: 7.2–9.1%). The crude prevalences of microvascular and macrovascular complications were 18.8% and 12.7%, respectively. Common microvascular complications were peripheral neuropathy (7.7%), chronic kidney disease (5.0%), and albuminuria (4.3%). Common macrovascular complications were coronary artery disease (8.2%), heart failure (3.3%) and stroke (2.2%). The age- and sex-standardized prevalence of microvascular complications was 17.9% (95% confidence interval [CI] 17.3–18.6%), ranging from 14.2% in the Americas to 20.4% in Europe. The age- and sex-standardized prevalence of macrovascular complications was 9.2% (95% CI 8.7–9.7%), ranging from 4.1% in South-East Asia to 18.8% in Europe. Factors positively associated with vascular complications included age (per 10-year increment), male sex, diabetes duration (per 1-year increment), and history of hypoglycemia, with rate ratios (95% CIs) for microvascular complications of 1.14 (1.09–1.19), 1.30 (1.20–1.42), 1.03 (1.02–1.04) and 1.45 (1.25–1.69), respectively, and for macrovascular complications of 1.41 (1.34–1.48), 1.29 (1.16–1.45), 1.02 (1.01–1.02) and 1.24 (1.04–1.48), respectively. HbA 1c levels (per 1.0% increment) were positively associated with microvascular (1.05 [1.02–1.08]) but not macrovascular (1.00 [0.97–1.04]) complications.

          Conclusions

          The global burden of microvascular and macrovascular complications is substantial in these patients with type 2 diabetes who are relatively early in the disease process. These findings highlight an opportunity for aggressive early risk factor modification, particularly in regions with a high prevalence of complications.

          Trial registration ClinicalTrials.gov; NCT02322762. Registered 23 December 2014. https://clinicaltrials.gov/ct2/show/NCT02322762. ClinicalTrials.gov; NCT02226822. Registered 27 August 2014. https://clinicaltrials.gov/ct2/show/NCT02226822

          Electronic supplementary material

          The online version of this article (10.1186/s12933-018-0787-8) contains supplementary material, which is available to authorized users.

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          Most cited references25

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          Diabetes and Cardiovascular Disease: A Statement for Healthcare Professionals From the American Heart Association

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            Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs

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              Intensive insulin therapy prevents the progression of diabetic microvascular complications in Japanese patients with non-insulin-dependent diabetes mellitus: a randomized prospective 6-year study

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                Author and article information

                Contributors
                mkosiborod@saint-lukes.org
                mariliabgomes@gmail.com
                nicolucci@coresearch.it
                stuart.pocock@lshtm.ac.uk
                rathmann@ddz.uni-duesseldorf.de
                shestakova.mv@gmail.com
                hwatada@juntendo.ac.jp
                ichi@endmet.med.osaka-u.ac.jp
                HungtaChen@astrazeneca.com
                Javier.Cid@evidera.com
                Peter.Fenici@astrazeneca.com
                Niklas.Hammar@ki.se
                Filip.Surmont@astrazeneca.com
                ftang@saint-lukes.org
                kk22@leicester.ac.uk
                Journal
                Cardiovasc Diabetol
                Cardiovasc Diabetol
                Cardiovascular Diabetology
                BioMed Central (London )
                1475-2840
                28 November 2018
                28 November 2018
                2018
                : 17
                : 150
                Affiliations
                [1 ]ISNI 0000 0004 0383 1037, GRID grid.419820.6, Saint Luke’s Mid America Heart Institute, ; 4401 Wornall Road, Kansas City, MO 64111 USA
                [2 ]ISNI 0000 0001 2179 926X, GRID grid.266756.6, University of Missouri, Kansas City, ; 5100 Rockhill Rd, Kansas City, MO 64110 USA
                [3 ]GRID grid.412211.5, Rio de Janeiro State University, ; Av 28 de Setembro 77, Rio de Janeiro, CEP20555-030 Brazil
                [4 ]Center for Outcomes Research and Clinical Epidemiology, Via Tiziano Vecellio, 2, 65124 Pescara, Italy
                [5 ]ISNI 0000 0004 0425 469X, GRID grid.8991.9, London School of Hygiene and Tropical Medicine, ; Keppel St, Bloomsbury, London, WC1E 7HT UK
                [6 ]ISNI 0000 0004 0492 602X, GRID grid.429051.b, Institute for Biometrics and Epidemiology, , German Diabetes Center, ; Auf’m Hennekamp 65, 40225 Düsseldorf, Germany
                [7 ]GRID grid.465364.6, Endocrinology Research Center, ; Moskvorech’ye Ulitsa, 1, Moscow, 115478 Russian Federation
                [8 ]ISNI 0000 0004 1762 2738, GRID grid.258269.2, Graduate School of Medicine, , Juntendo University, ; 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421 Japan
                [9 ]ISNI 0000 0004 0373 3971, GRID grid.136593.b, Graduate School of Medicine, , Osaka University, ; 2-2 Yamadaoka, Suita, Osaka 565-0871 Japan
                [10 ]GRID grid.418152.b, AstraZeneca, ; 950 Wind River Ln, Gaithersburg, MD 20878 USA
                [11 ]Evidera, Metro Building, 6th Floor, 1 Butterwick, London, W6 8DL UK
                [12 ]ISNI 0000 0004 5929 4381, GRID grid.417815.e, AstraZeneca, ; 132 Hills Rd, Cambridge, CB2 1PG UK
                [13 ]AstraZeneca Gothenburg, Pepparedsleden 1, 431 50 Mölndal, Sweden
                [14 ]ISNI 0000 0004 1937 0626, GRID grid.4714.6, Institute of Environmental Medicine, Karolinska Institutet, ; Solnavägen 1, 171 77 Solna, Sweden
                [15 ]ISNI 0000 0004 5929 4381, GRID grid.417815.e, AstraZeneca, ; 600 Capability Green, Luton, LU1 3LU UK
                [16 ]ISNI 0000 0004 1936 8411, GRID grid.9918.9, University of Leicester, ; University Rd, Leicester, LE1 7RH UK
                Author information
                http://orcid.org/0000-0002-3750-9789
                Article
                787
                10.1186/s12933-018-0787-8
                6260731
                30486889
                ccfe13ef-c26f-428d-8f0c-66d46ddd1aa3
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

                History
                : 30 July 2018
                : 6 November 2018
                Funding
                Funded by: AstraZeneca
                Categories
                Original Investigation
                Custom metadata
                © The Author(s) 2018

                Endocrinology & Diabetes
                type 2 diabetes,vascular complications,observational study
                Endocrinology & Diabetes
                type 2 diabetes, vascular complications, observational study

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