Ann Pediatr Endocrinol Metab.  2014 Jun;19(2):80-85. 10.6065/apem.2014.19.2.80.

Fasting serum C-peptide is useful for initial classification of diabetes mellitus in children and adolescents

Affiliations
  • 1Department of Pediatrics, Chonbuk National University Medical School, Jeonju, Korea. children@jbnu.ac.kr
  • 2Department of Pediatrics, Chonnam National University Medical School, Gwangju, Korea.
  • 3Department of Pediatrics, Chosun University School of Medicine, Gwangju, Korea.
  • 4Department of Pediatrics, Wonkwang University College of Medicine, Iksan, Korea.
  • 5Department of Pediatrics, Kwangju Christian Hospital, Gwangju, Korea.

Abstract

PURPOSE
With rising obesity rates in children, it is increasingly difficult to differentiate between type 1 and type 2 diabetes mellitus (T1DM, T2DM) on clinical grounds alone. Using C-peptide as a method of classifying diabetes mellitus (DM) has been suggested. This study aimed to find a correlation between fasting C-peptide level and DM types in children and adolescents.
METHODS
A total of 223 diabetic children, newly diagnosed at 5 hospitals between January 2001 and December 2012, were enrolled in this study. Initial DM classification was based on clinical and laboratory data including fasting C-peptide at diagnosis; final classification was based on additional data (pancreatic autoantibodies, human leukocyte antigen type, and clinical course).
RESULTS
Of 223 diabetic children, 140 were diagnosed with T1DM (62.8%) and the remaining 83 with T2DM (37.2%). The mean serum C-peptide level was significantly lower in children with T1DM (0.80 ng/mL) than in children with T2DM (3.91 ng/mL). Among 223 children, 54 had a serum C-peptide level <0.6 ng/mL; they were all diagnosed with T1DM. The proportion of children with T2DM increased in accordance with C-peptide level. Forty-nine of 223 children had a C-peptide level >3.0 ng/mL; 48 of them (97.9%) were diagnosed with T2DM.
CONCLUSION
In this study, we found that if the C-peptide level was <0.6 ng/mL at diagnosis, T2DM could be excluded; if C-peptide level was >3.0 ng/mL, a T1DM diagnosis is unlikely. This finding suggests that serum fasting C-peptide level is useful for classifying DM type at the time of diagnosis in youth.

Keyword

C-peptide; Classification; Diabetes mellitus; Child

MeSH Terms

Adolescent*
Autoantibodies
C-Peptide*
Child*
Classification*
Diabetes Mellitus*
Diabetes Mellitus, Type 2
Diagnosis
Fasting*
Humans
Leukocytes
Obesity
Autoantibodies
C-Peptide

Figure

  • Fig. 1 Initial and final classification of 223 children with diabetes mellitus (DM). T1DM, type 1 DM; T2DM, type 2 DM.

  • Fig. 2 Distribution of C-peptide level in type 1 (T1DM) and type 2 diabetes mellitus (T2DM).


Cited by  2 articles

Clinical and Laboratory Characteristics of Childhood Diabetes Mellitus: A Single-Center Study from 2000 to 2013
Tae Hyun Park, Min Sun Kim, Dae-Yeol Lee
Chonnam Med J. 2016;52(1):64-69.    doi: 10.4068/cmj.2016.52.1.64.

Clinical features of childhood diabetes mellitus focusing on latent autoimmune diabetes
Seung Ho Lee, Jeesuk Yu
Ann Pediatr Endocrinol Metab. 2016;21(4):212-218.    doi: 10.6065/apem.2016.21.4.212.


Reference

1. Daneman D. Type 1 diabetes. Lancet. 2006; 367:847–858. PMID: 16530579.
Article
2. Gungor N, Hannon T, Libman I, Bacha F, Arslanian S. Type 2 diabetes mellitus in youth: the complete picture to date. Pediatr Clin North Am. 2005; 52:1579–1609. PMID: 16301084.
Article
3. Harron KL, Feltbower RG, McKinney PA, Bodansky HJ, Campbell FM, Parslow RC. Rising rates of all types of diabetes in south Asian and non-south Asian children and young people aged 0-29 years in West Yorkshire, U.K., 1991-2006. Diabetes Care. 2011; 34:652–654. PMID: 21278139.
Article
4. American Diabetes Association. Type 2 diabetes in children and adolescents. Pediatrics. 2000; 105(3 Pt 1):671–680. PMID: 10699131.
5. Katz LE, Jawad AF, Ganesh J, Abraham M, Murphy K, Lipman TH. Fasting c-peptide and insulin-like growth factor-binding protein-1 levels help to distinguish childhood type 1 and type 2 diabetes at diagnosis. Pediatr Diabetes. 2007; 8:53–59. PMID: 17448127.
Article
6. Ludvigsson J, Carlsson A, Forsander G, Ivarsson S, Kockum I, Lernmark A, et al. C-peptide in the classification of diabetes in children and adolescents. Pediatr Diabetes. 2012; 13:45–50. PMID: 21910810.
Article
7. Hattersley A, Bruining J, Shield J, Njolstad P, Donaghue K. International Society for Pediatric and Adolescent Diabetes. ISPAD Clinical Practice Consensus Guidelines 2006-2007. The diagnosis and management of monogenic diabetes in children. Pediatr Diabetes. 2006; 7:352–360. PMID: 17212604.
Article
8. Pearson ER, Starkey BJ, Powell RJ, Gribble FM, Clark PM, Hattersley AT. Genetic cause of hyperglycaemia and response to treatment in diabetes. Lancet. 2003; 362:1275–1281. PMID: 14575972.
Article
9. Byrne MM, Sturis J, Fajans SS, Ortiz FJ, Stoltz A, Stoffel M, et al. Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20. Diabetes. 1995; 44:699–704. PMID: 7789636.
Article
10. Besser RE. Determination of C-peptide in children: when is it useful? Pediatr Endocrinol Rev. 2013; 10:494–502. PMID: 23957200.
11. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997; 20:1183–1197. PMID: 9203460.
12. D'Adamo E, Caprio S. Type 2 diabetes in youth: epidemiology and pathophysiology. Diabetes Care. 2011; 34(Suppl 2):S161–S165. PMID: 21525449.
13. Garcia-Webb P, Bonser A, Welborn TA. Correlation between fasting serum C-peptide and B cell insulin secretory capacity in diabetes mellitus. Diabetologia. 1982; 22:296. PMID: 7047275.
Article
14. Webb PG, Bonser AM. Basal C-peptide in the discrimination of type I from type II diabetes. Diabetes Care. 1981; 4:616–619. PMID: 6751738.
Article
15. Service FJ, Rizza RA, Zimmerman BR, Dyck PJ, OBrien PC, Melton LJ 3rd. The classification of diabetes by clinical and C-peptide criteria. A prospective population-based study. Diabetes Care. 1997; 20:198–201. PMID: 9118774.
Article
16. Hother-Nielsen O, Faber O, Sorensen NS, Beck-Nielsen H. Classification of newly diagnosed diabetic patients as insulin-requiring or non-insulin-requiring based on clinical and biochemical variables. Diabetes Care. 1988; 11:531–537. PMID: 3203569.
Article
17. Gjessing HJ, Matzen LE, Froland A, Faber OK. Correlations between fasting plasma C-peptide, glucagon-stimulated plasma C-peptide, and urinary C-peptide in insulin-treated diabetics. Diabetes Care. 1987; 10:487–490. PMID: 3304899.
Article
18. The Korean Society of Pediatric Endocrinology. Pediatric endocrinology. Seoul: Kwangmoon Press;1996.
19. Park J, Oh J, Yu J. Autoantibody positivity and clinical characteristics of diabetes mellitus in childhood. J Korean Soc Pediatr Endocrinol. 2011; 16:119–127.
Article
20. Hur J, Lee HS, Hwang JS. Clinical characteristics of type 1 diabetes mellitus at initial Diagnosis. J Korean Soc Pediatr Endocrinol. 2006; 11:177–184.
21. Lee CW, Shin HJ, Kim DH. Prevalence of autoimmune antibodies in type i diabetic children and their siblings. J Korean Soc Pediatr Endocrinol. 1999; 4:78–87.
22. Hong EH, Park JS, Lee HS, Cho MH, Ko CW. Clinical characteristics and laboratory findings of children who were newly diagnosed with diabetes mellitus (from 2001 to 2008). J Korean Soc Pediatr Endocrinol. 2009; 14:110–115.
23. Yu J, Shin CH, Yang SW, Park MH, Eisenbarth GS. Analysis of children with type 1 diabetes in Korea: high prevalence of specific anti-islet autoantibodies, immunogenetic similarities to Western populations with "unique" haplotypes, and lack of discrimination by aspartic acid at position 57 of DQB. Clin Immunol. 2004; 113:318–325. PMID: 15507397.
Article
24. Ludvigsson J, Heding LG. C-peptide in children with juvenile diabetes: a preliminary report. Diabetologia. 1976; 12:627–630. PMID: 1001852.
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