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Serum Carnosinase 1 Is Not Associated with Insulin Resistance or Glucose Metabolism in a Type 1 Diabetes Cohort

ORCID
0000-0002-9835-8398
Affiliation
5th Medical Department, University Hospital Mannheim, Heidelberg University, 68167 Mannheim, Germany;(J.Q.);(B.A.Y.);(B.K.K.)
Qiu, Jiedong;
ORCID
0000-0003-3451-3122
Affiliation
5th Medical Department, University Hospital Mannheim, Heidelberg University, 68167 Mannheim, Germany;(J.Q.);(B.A.Y.);(B.K.K.)
Yard, Benito A.;
ORCID
0000-0002-1718-2918
Affiliation
5th Medical Department, University Hospital Mannheim, Heidelberg University, 68167 Mannheim, Germany;(J.Q.);(B.A.Y.);(B.K.K.)
Krämer, Bernhard K.;
ORCID
0000-0002-6670-1577
Affiliation
Department of Pathology and Medical Biology, University Medical Centre Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands;
van Goor, Harry;
ORCID
0000-0002-9702-6551
Affiliation
Department of Endocrinology, University Medical Centre Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands
van Dijk, Peter R.;
ORCID
0000-0002-5197-2286
Affiliation
5th Medical Department, University Hospital Mannheim, Heidelberg University, 68167 Mannheim, Germany;(J.Q.);(B.A.Y.);(B.K.K.)
Kannt, Aimo

Background/Objectives : Preclinical studies suggest that the deleterious effect of a high serum carnosinase 1 (CN1) concentration is attributed to its adverse effects on insulin sensitivity and glucose metabolism. However, there is little evidence for a modulating role of CN1 in glucose metabolism in humans. Methods : We measured serum CN1 concentration in an observational type 1 diabetes cohort of 172 patients in whom glucose variability (MAGE, MODD, SD of individual blood glucose, mean, and CV) was recorded by blinded continuous glucose monitoring for 5–7 days. Furthermore, insulin dose per kg body weight was compared. Results : Insulin sensitivity (insulin dosage) and glucose variability parameters did not differ between different CN1 tertiles ( p > 0.05). Conclusions : There was no association of serum CN1 with indices of glucose variability in this type 1 diabetes cohort.

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