CETP activity is not associated with carotid intima-media thickness in patients with poorly controlled type 2 diabetes.


Journal

Acta diabetologica
ISSN: 1432-5233
Titre abrégé: Acta Diabetol
Pays: Germany
ID NLM: 9200299

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 24 01 2019
accepted: 01 04 2019
pubmed: 14 4 2019
medline: 14 8 2019
entrez: 14 4 2019
Statut: ppublish

Résumé

The impact of cholesteryl ester transfer protein (CETP) on atherosclerotic development in humans remains unclear. Plasma cholesteryl ester transfer was shown to be associated with carotid intima-media thickness in type 2 diabetic (T2D) patients with adequate metabolic control. Since glycation of CETP may influence cholesteryl ester transfer processes, it is important to determine if plasma cholesteryl ester transfer is still a determinant of carotid intima-media thickness (IMT) in patients with poorly controlled diabetes. The aim of the present study was to determine whether CETP activity influences carotid IMT in T2D patients with poor metabolic control. In 110 individuals with T2D, we measured CETP mass concentration with ELISA, CETP activity with a radioactivity method and carotid intima-media thickness with high-resolution real-time B-mode ultrasonography. The mean HbA1C was 8.8 ± 1.7%. Carotid IMT did not correlate with CETP activity in the total population. In T2D patients with HbA1C < 8% (n = 33), mean HbA1C was 6.9% and the correlation between carotid IMT and CETP activity was not significant (p = 0.09). In a multivariable analysis that included the total population, carotid intima-media thickness was positively associated with diabetes duration (p = 0.02) but not with CETP activity or HbA1C. We observed no correlation between carotid intima-media thickness, a marker of early atherosclerosis, and CETP activity in T2D patients with poor metabolic control. Disease duration, which reflects accumulated metabolic abnormalities, may have blunted the potential effect of CETP on atherosclerosis. Metabolic control appears essential to determine the pro- or anti-atherogenic influence of CETP in patients with T2D.

Identifiants

pubmed: 30980187
doi: 10.1007/s00592-019-01340-7
pii: 10.1007/s00592-019-01340-7
doi:

Substances chimiques

Blood Glucose 0
CETP protein, human 0
Cholesterol Ester Transfer Proteins 0
Glycated Hemoglobin A 0
hemoglobin A1c protein, human 0

Types de publication

Journal Article

Langues

eng

Pagination

749-754

Subventions

Organisme : CHU Dijon
ID : AOI

Auteurs

Benjamin Bouillet (B)

Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, Dijon, France. benjamin.bouillet@chu-dijon.fr.
INSERM Unit, LNC-UMR 1231, University of Burgundy, Dijon, France. benjamin.bouillet@chu-dijon.fr.

T Gautier (T)

INSERM Unit, LNC-UMR 1231, University of Burgundy, Dijon, France.

B Terriat (B)

Angiology Department, Dijon University Hospital, Dijon, France.

L Lagrost (L)

INSERM Unit, LNC-UMR 1231, University of Burgundy, Dijon, France.

B Verges (B)

Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, Dijon, France.
INSERM Unit, LNC-UMR 1231, University of Burgundy, Dijon, France.

J M Petit (JM)

Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, Dijon, France.
INSERM Unit, LNC-UMR 1231, University of Burgundy, Dijon, France.

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Classifications MeSH