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Vascular complications in patients with type 2 diabetes: prevalence and associated factors in 38 countries (the DISCOVER study program).
Kosiborod, Mikhail; Gomes, Marilia B; Nicolucci, Antonio; Pocock, Stuart; Rathmann, Wolfgang; Shestakova, Marina V; Watada, Hirotaka; Shimomura, Iichiro; Chen, Hungta; Cid-Ruzafa, Javier; Fenici, Peter; Hammar, Niklas; Surmont, Filip; Tang, Fengming; Khunti, Kamlesh.
Afiliação
  • Kosiborod M; Saint Luke's Mid America Heart Institute, 4401 Wornall Road, Kansas City, MO, 64111, USA. mkosiborod@saint-lukes.org.
  • Gomes MB; University of Missouri, Kansas City, 5100 Rockhill Rd, Kansas City, MO, 64110, USA. mkosiborod@saint-lukes.org.
  • Nicolucci A; Rio de Janeiro State University, Av 28 de Setembro 77, Rio de Janeiro, CEP20555-030, Brazil.
  • Pocock S; Center for Outcomes Research and Clinical Epidemiology, Via Tiziano Vecellio, 2, 65124, Pescara, Italy.
  • Rathmann W; London School of Hygiene and Tropical Medicine, Keppel St, Bloomsbury, London, WC1E 7HT, UK.
  • Shestakova MV; Institute for Biometrics and Epidemiology, German Diabetes Center, Auf'm Hennekamp 65, 40225, Düsseldorf, Germany.
  • Watada H; Endocrinology Research Center, Moskvorech'ye Ulitsa, 1, Moscow, 115478, Russian Federation.
  • Shimomura I; Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.
  • Chen H; Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
  • Cid-Ruzafa J; AstraZeneca, 950 Wind River Ln, Gaithersburg, MD, 20878, USA.
  • Fenici P; Evidera, Metro Building, 6th Floor, 1 Butterwick, London, W6 8DL, UK.
  • Hammar N; AstraZeneca, 132 Hills Rd, Cambridge, CB2 1PG, UK.
  • Surmont F; AstraZeneca Gothenburg, Pepparedsleden 1, 431 50, Mölndal, Sweden.
  • Tang F; Institute of Environmental Medicine, Karolinska Institutet, Solnavägen 1, 171 77, Solna, Sweden.
  • Khunti K; AstraZeneca, 600 Capability Green, Luton, LU1 3LU, UK.
Cardiovasc Diabetol ; 17(1): 150, 2018 11 28.
Article em En | MEDLINE | ID: mdl-30486889
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 (HbA1c) 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. HbA1c 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Angiopatias Diabéticas Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Angiopatias Diabéticas Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article