Incidence rates and predictors of microvascular and macrovascular complications in patients with type 2 diabetes: Results from the longitudinal global discover study.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
01 2022
Historique:
received: 28 04 2021
accepted: 02 10 2021
pubmed: 20 10 2021
medline: 8 4 2022
entrez: 19 10 2021
Statut: ppublish

Résumé

Micro- and macrovascular complications are a major cause of morbidity and mortality in people with type 2 diabetes (T2D). We sought to understand the global incidence rates and predictors of these complications. We examined the incidence of vascular complications over 3 years of follow-up in the DISCOVER study-a global, observational study of people with T2D initiating second-line glucose-lowering therapy. Hierarchical Cox proportional hazards regression models examined factors associated with development of micro- and macrovascular complications during follow-up. Among 11,357 people with T2D from 33 countries (mean age 56.9 ± 11.7 years, T2D duration 5.7 ± 5.1 years, HbA1c 8.4 ± 1.7%), 19.0% had a microvascular complication at enrolment (most commonly neuropathy), and 13.2% had a macrovascular complication (most commonly coronary disease). Over 3 years of follow-up, 16.0% developed an incident microvascular complication, and 6.6% had an incident macrovascular complication. At the end of 3 years of follow-up, 31.5% of patients had at least one microvascular complication, and 16.6% had at least one macrovascular complication. Higher HbA1c and smoking were associated with greater risk of both incident micro- and macrovascular complications. Known macrovascular complications at baseline was the strongest predictor for development of new microvascular complications (HR 1.40, 95% CI 1.21 -1.61) and new macrovascular complications (HR 3.39, 95% CI 2.84 -4.06). In this global study, both the prevalence and 3-year incidence of vascular complications were high in patients with relatively short T2D duration, highlighting the need for early risk-factor modification.

Sections du résumé

BACKGROUND
Micro- and macrovascular complications are a major cause of morbidity and mortality in people with type 2 diabetes (T2D). We sought to understand the global incidence rates and predictors of these complications.
METHODS
We examined the incidence of vascular complications over 3 years of follow-up in the DISCOVER study-a global, observational study of people with T2D initiating second-line glucose-lowering therapy. Hierarchical Cox proportional hazards regression models examined factors associated with development of micro- and macrovascular complications during follow-up.
RESULTS
Among 11,357 people with T2D from 33 countries (mean age 56.9 ± 11.7 years, T2D duration 5.7 ± 5.1 years, HbA1c 8.4 ± 1.7%), 19.0% had a microvascular complication at enrolment (most commonly neuropathy), and 13.2% had a macrovascular complication (most commonly coronary disease). Over 3 years of follow-up, 16.0% developed an incident microvascular complication, and 6.6% had an incident macrovascular complication. At the end of 3 years of follow-up, 31.5% of patients had at least one microvascular complication, and 16.6% had at least one macrovascular complication. Higher HbA1c and smoking were associated with greater risk of both incident micro- and macrovascular complications. Known macrovascular complications at baseline was the strongest predictor for development of new microvascular complications (HR 1.40, 95% CI 1.21 -1.61) and new macrovascular complications (HR 3.39, 95% CI 2.84 -4.06).
CONCLUSIONS
In this global study, both the prevalence and 3-year incidence of vascular complications were high in patients with relatively short T2D duration, highlighting the need for early risk-factor modification.

Identifiants

pubmed: 34666013
pii: S0002-8703(21)00433-6
doi: 10.1016/j.ahj.2021.10.181
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

232-239

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Suzanne V Arnold (SV)

Division of Cardiology, Saint Luke's Mid America Heart Institute, Kansas City, Missouri; Department of Medicine, University of Missouri, Kansas City, Missouri.

Kamlesh Khunti (K)

Diabetes Research Centre, University of Leicester, Leicester.

Fengming Tang (F)

Division of Cardiology, Saint Luke's Mid America Heart Institute, Kansas City, Missouri.

Hungta Chen (H)

AstraZeneca, Gaithersburg, Maryland.

Javier Cid-Ruzafa (J)

Evidera, Barcelona, Spain.

Andrew Cooper (A)

AstraZeneca, Cambridge.

Peter Fenici (P)

AstraZeneca, Cambridge.

Marilia B Gomes (MB)

Departamento de Medicina Interna, Rio de Janeiro State University, Rio de Janeiro, Brazil.

Niklas Hammar (N)

Institute of Environmental Medicine, AstraZeneca Gothenburg, Mölndal, Sweden and Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

Linong Ji (L)

Department of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.

Gabriela Luporini Saraiva (GL)

AstraZeneca, Gaithersburg, Maryland.

Jesús Medina (J)

AstraZeneca, Madrid, Spain.

Antonio Nicolucci (A)

Center for Outcomes Research and Clinical Epidemiology, Pescara, Italy.

Larisa Ramirez (L)

AstraZeneca, Luton.

Wolfgang Rathmann (W)

Leibniz Center for Diabetes Research at Heinrich Heine University, German Diabetes Center, Düsseldorf, Germany.

Marina V Shestakova (MV)

Endocrinology Research Centre, Diabetes Institute, Moscow, Russian Federation.

Iichiro Shimomura (I)

Graduate School of Medicine, Osaka University, Osaka, Japan.

Filip Surmont (F)

Departamento de Medicina Interna, Rio de Janeiro State University, Rio de Janeiro, Brazil.

Jiten Vora (J)

Department of Diabetes and Endocrinology, Royal Liverpool University Hospital, Liverpool.

Hirotaka Watada (H)

Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Mikhail Kosiborod (M)

Division of Cardiology, Saint Luke's Mid America Heart Institute, Kansas City, Missouri; Department of Medicine, University of Missouri, Kansas City, Missouri; The George Institute for Global Health and University of New South Wales, Sydney, Australia.

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