Markers of inflammation and prediction of diabetes mellitus in adults (Atherosclerosis Risk in Communities study): a cohort study

Citation
Mi. Schmidt et al., Markers of inflammation and prediction of diabetes mellitus in adults (Atherosclerosis Risk in Communities study): a cohort study, LANCET, 353(9165), 1999, pp. 1649-1652
Citations number
30
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
LANCET
ISSN journal
01406736 → ACNP
Volume
353
Issue
9165
Year of publication
1999
Pages
1649 - 1652
Database
ISI
SICI code
0140-6736(19990515)353:9165<1649:MOIAPO>2.0.ZU;2-R
Abstract
Background Type 2 diabetes mellitus and atherosclerotic cardiovascular dise ase have common antecedents. Since markers of inflammation predict coronary heart disease and are raised in patients with type 2 diabetes, we investig ated whether they predict whether people will develop type 2 diabetes. Methods 12 330 men and women, aged 45-64 years, were followed up for a mean of 7 years. We analysed the association between different markers of acute inflammation and subsequent diagnosis of diabetes. In a subgroup of 610 in dividuals selected originally for an unrelated atherosclerosis case-control study, we also investigated diabetes associations with total sialic acid a nd orosomucoid, haptoglobin, and alpha(1)-antitrypsin. Findings 1335 individuals had a new diagnosis of diabetes. Adjusted odds ra tios for developing diabetes for quartile extremes were 1.9 (95% CI 1.6-2.3 ) for raised white-cell count, 1.3 (1.0-1.5) for low serum albumin, and 1.2 (1.0-1.5) for raised fibrinogen. In the subgroup analysis, individuals wit h concentrations of orosomucoid and sialic acid of more than the median had odds ratios of 7.9 (2.6-23.7) and 3.7 (1.4-9.8), respectively. Adjustment for body-mass index and waist-to-hip ratio lessened the associations; those for white-cell count (1.5 [1.3-1.8]), orosomucoid (7.1 [2.1-23.7]), and si alic acid (2.8 [1.0-8.1]) remained significant. Interpretation Markers of inflammation are associated with the development of diabetes in middle-aged adults. Although autoimmunity may partly explain these associations, they probably reflect the pathogenesis of type 2 diabe tes.