Circulating cellular adhesion molecules and risk of diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA)

Autor: Paul A. Decker, S. J. Bielinski, Naomi Q. Hanson, James S. Pankow, Alka M. Kanaya, Weihong Tang, Michael Y. Tsai, Nicholas B. Larson, Christina L. Wassel, Michèle M. Sale, C. Berardi
Rok vydání: 2016
Předmět:
Oncology
Male
Aging
Endocrinology
Diabetes and Metabolism

030204 cardiovascular system & hematology
Cardiovascular
Cohort Studies
0302 clinical medicine
Endocrinology
Psychology
Prospective Studies
Endothelial dysfunction
L-Selectin
Prospective cohort study
biology
Cell adhesion molecule
Incidence
Hazard ratio
Diabetes
Middle Aged
Cadherins
Intercellular Adhesion Molecule-1
CD
P-Selectin
Public Health and Health Services
L-selectin
Female
E-Selectin
Type 2
Risk
medicine.medical_specialty
Clinical Sciences
Vascular Cell Adhesion Molecule-1
030209 endocrinology & metabolism
Article
03 medical and health sciences
Endocrinology & Metabolism
Antigens
CD

Clinical Research
Internal medicine
Diabetes mellitus
Internal Medicine
medicine
Diabetes Mellitus
Humans
Antigens
Cell adhesion
Metabolic and endocrine
Proportional Hazards Models
Nutrition
Proportional hazards model
business.industry
Prevention
medicine.disease
Atherosclerosis
United States
Diabetes Mellitus
Type 2

Immunology
biology.protein
business
Zdroj: Diabetic medicine : a journal of the British Diabetic Association, vol 33, iss 7
Popis: Aims To test the hypothesis that soluble cellular adhesion molecules would be positively and independently associated with risk of diabetes. Methods Soluble levels of six cellular adhesion molecules (ICAM-1, E-selectin, VCAM-1, E-cadherin, L-selectin and P-selectin) were measured in participants in the Multi-Ethnic Study of Atherosclerosis, a prospective cohort study. Participants were then followed for up to 10 years to ascertain incident diabetes. Results Sample sizes ranged from 826 to 2185. After adjusting for age, sex, race/ethnicity, BMI and fasting glucose or HbA1c, four cellular adhesion molecules (ICAM-1, E-selectin, VCAM-1 and E-cadherin) were positively associated with incident diabetes and there was a statistically significant trend across quartiles. Comparing the incidence of diabetes in the highest and lowest quartiles of each cellular adhesion molecule, the magnitude of association was largest for E-selectin (hazard ratio 2.49; 95% CI 1.26–4.93) and ICAM-1 (hazard ratio 1.76; 95% CI 1.22–2.55) in fully adjusted models. Tests of effect modification by racial/ethnic group and sex were not statistically significant for any of the cellular adhesion molecules (P > 0.05). Conclusions The finding of significant associations between multiple cellular adhesion molecules and incident diabetes may lend further support to the hypothesis that microvascular endothelial dysfunction contributes to risk of diabetes.
Databáze: OpenAIRE