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 (CPBase) and the peak CP (CPmax). Threshold points of CPBase, CP90, CPmax and CPAUC were determined from analysis of ROC curves. Results: GCK diabetes patients had significantly higher AUC(CP), CPBase and CPmax 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. (C) 2021 The Authors. Published by Elsevier B.V.
机构:
Peoples Hosp Fengxian Cty, Dept Endocrinol, Fengxian, Jiangsu, Peoples R ChinaPeoples Hosp Fengxian Cty, Dept Endocrinol, Fengxian, Jiangsu, Peoples R China
Shi, Aixian
Shuai, Ying
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China Japan Friendship Hosp, Dept Endocrinol, Beijing, Peoples R ChinaPeoples Hosp Fengxian Cty, Dept Endocrinol, Fengxian, Jiangsu, Peoples R China
机构:
Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, EnglandUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
Besser, Rachel E. J.
Ludvigsson, Johnny
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Linkoping Univ, Div Pediat, Dept Clin & Expt Med, Linkoping, SwedenUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
Ludvigsson, Johnny
Jones, Angus G.
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Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, EnglandUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
Jones, Angus G.
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McDonald, Timothy J.
Shields, Beverley M.
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Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, EnglandUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
Shields, Beverley M.
Knight, Bridget A.
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Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, EnglandUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
Knight, Bridget A.
Hattersley, Andrew T.
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Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, EnglandUniv Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
机构:
UNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZILUNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZIL
Pozzan, R
Dimetz, T
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UNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZILUNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZIL
Dimetz, T
Gazzola, HM
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UNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZILUNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZIL
Gazzola, HM
Gomes, MB
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UNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZILUNIV ESTADO RIO DE JANEIRO, DEPT MED INTERNA, LAB ENDOCRINOL, DISCIPLINA DIABET, RIO DE JANEIRO, BRAZIL