PMID- 34217772 OWN - NLM STAT- MEDLINE DCOM- 20211124 LR - 20211124 IS - 1872-8227 (Electronic) IS - 0168-8227 (Linking) VI - 178 DP - 2021 Aug TI - Kinetics of C-peptide during mixed meal test and its value for treatment optimization in monogenic diabetes patients. PG - 108938 LID - S0168-8227(21)00298-9 [pii] LID - 10.1016/j.diabres.2021.108938 [doi] AB - AIM: The mixed meal tolerance test (MMTT) is a gold standard for evaluating beta-cell function. There is limited data on MMTT in monogenic diabetes (MD). Therefore, we aimed to analyze plasma C-peptide (CP) kinetics during MMTT in young MODY and neonatal diabetes patients as a biomarker for beta-cell function. METHODS: We included 41 patients with MD diagnosis (22 GCK, 8 HNF1A, 3 HNF4A, 4 KCNJ11, 2 ABCC8, 1 INS, 1 KLF11). Standardized 3-hour MMTT with glycemia and plasma CP measurements were performed for all individuals. Pancreatic beta-cell response was assessed by the area under the curve CP (AUC(CP)), the baseline CP (CP(Base)) and the peak CP (CP(max)). Threshold points of CP(Base), CP(90), CP(max) and CP(AUC) were determined from analysis of ROC curves. RESULTS: GCK diabetes patients had significantly higher AUC(CP), CP(Base) and CP(max) compared to HNF4A and KCNJ11 patients. In HNF4A, KCNJ11 and ABCC8 patients with all CP levels < 200 pmol/L, the treatment change attempt to sulfonylurea agent was unsuccessful. The ROC analysis showed that CP baseline threshold equal or higher to 133.5 pmol/L could be used to predict successful switch to oral agents. CONCLUSION: A pretreatment challenge with MMTT might be used to guide the optimal treatment after molecular diagnosis of MD. CI - Copyright (c) 2021 The Authors. Published by Elsevier B.V. All rights reserved. FAU - Stankute, Ingrida AU - Stankute I AD - Medical Academy, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. Electronic address: ingrida.stankute@lsmuni.lt. FAU - Verkauskiene, Rasa AU - Verkauskiene R AD - Institute of Endocrinology, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. FAU - Dobrovolskiene, Rimante AU - Dobrovolskiene R AD - Medical Academy, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. FAU - Danyte, Evalda AU - Danyte E AD - Institute of Endocrinology, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. FAU - Jasinskiene, Edita AU - Jasinskiene E AD - Medical Academy, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. FAU - Mockeviciene, Giedre AU - Mockeviciene G AD - Medical Academy, Lithuanian University of Health Sciences, Eiveniu 2, LT-50161 Kaunas, Lithuania. FAU - Schwitzgebel, Valerie M AU - Schwitzgebel VM AD - Pediatric Endocrine and Diabetes Unit, Department of Pediatrics, Gynecology and Obstetrics, University Hospitals of Geneva, 1211 Geneva, Switzerland; Diabetes Center of the Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland. LA - eng PT - Journal Article DEP - 20210701 PL - Ireland TA - Diabetes Res Clin Pract JT - Diabetes research and clinical practice JID - 8508335 RN - 0 (Blood Glucose) RN - 0 (C-Peptide) SB - IM MH - Blood Glucose MH - C-Peptide MH - *Diabetes Mellitus, Type 2 MH - Humans MH - Kinetics MH - Meals OTO - NOTNLM OT - Beta-cell function OT - C-peptide OT - Mixed meal tolerance OT - Monogenic diabetes COIS- Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. EDAT- 2021/07/05 06:00 MHDA- 2021/11/25 06:00 CRDT- 2021/07/04 20:39 PHST- 2021/02/01 00:00 [received] PHST- 2021/06/12 00:00 [revised] PHST- 2021/06/29 00:00 [accepted] PHST- 2021/07/05 06:00 [pubmed] PHST- 2021/11/25 06:00 [medline] PHST- 2021/07/04 20:39 [entrez] AID - S0168-8227(21)00298-9 [pii] AID - 10.1016/j.diabres.2021.108938 [doi] PST - ppublish SO - Diabetes Res Clin Pract. 2021 Aug;178:108938. doi: 10.1016/j.diabres.2021.108938. Epub 2021 Jul 1.