Variation of C peptide decay rate in diabetic patients with positive glutamic acid decarboxylase antibody: better discrimination with initial fasting C peptide
© Li et al; licensee BioMed Central Ltd. 2013
Received: 10 October 2012
Accepted: 19 February 2013
Published: 1 March 2013
Diabetic patients with positive glutamic acid decarboxylase antibody (GAD-Ab) could be classified as autoimmune diabetes, which is discriminated into acute-onset classical type 1 diabetes (T1DM) and latent autoimmune diabetes in adults (LADA). However, whether the decay rate of beta cell function is relevant with the mode of onset (acute or latent-onset) is unclear. We aimed to investigate whether initial C peptide levels could help differentiate variation of C peptide decay rate.
Five hundred and twenty-seven newly diagnosed GAD-Ab positive diabetic patients were followed up to assess the natural course of beta cell function. Beta cell function failure was defined as fasting C peptide and postprandial C peptide levels less than 100 pmol/L and 150 pmol/L respectively.
All these diabetic patients were discriminated according to initial fasting C peptide of 300 pmol/L, that is B+ (larger than 300 pmol/L) and B- (less than 300 pmol/L) group. The proportion of developing beta cell function failure was 13.1% in B+ group and 90.5% in B- group, which suggested that fasting C peptide levels made a good distinction of the heterogeneity in autoimmune diabetes. Receiver operator characteristic (ROC) analysis suggested that the fasting C peptide level of 300 pmol/L was optimal for determining beta cell function failure with sensitivity of 90.5% and specificity of 86.9%.
Initial level of fasting C peptide is a good indicator for predicting beta cell function failure in GAD-Ab positive diabetic patients.
The WHO recommendation in 1999 on classification of diabetes is now based more and more on the etiological evidence, with autoimmunity being the most direct and measurable evidence ever since the standardized radioligand assays for islet autoantibodies have been esta blished. So, more and more clinically diagnosed “type 2” diabetes has been re-classified as latent autoimmune diabetes in adults (LADA), a subtype of type 1 diabetes[2, 3]. However, except for the etiology of diabetes, clinicians are paying more attention on the progression of beta cell function. Evidence from UKPDS, DCCT, and other studies has demonstrated that beta cell function decline is closely related with the all-sides glycemic control and the diabetic complications. So, to make a distinction between the different destruction speed of beta cell function in autoimmune diabetes is important and LADA is specially proposed as a subtype for this reason. According to the diagnostic definition proposed by the Immunology of Diabetes Society (IDS), LADA is specially referred to patients over 30 years of age, positive for at least one islet autoantibodies, and not treated with insulin within the first 6 months after diagnosis. So, the age (adult, over 30 years) and mode (latent, no need for insulin at the initial stage) of onset are regarded as discriminative factors for autoimmune diabetes. However, “latent” does not always “adult-onset”, and patients with “latent autoimmune diabetes in the young (LADY)” was also put forward because of the relative slow progression.
Glutamic acid decarboxylase antibody (GAD-Ab) is the most widely used and the most valuable autoimmune markers in diagnosing autoimmune diabetes, especially for Chinese and adult-onset patients.[7, 8]. Previous studies reported that GAD-Ab titer could help identify the heterogeneity of LADA patients with LADA-type 1 and LADA-type 2 diabetes[9, 10]. But for juvenile- and adult-onset autoimmune diabetes, the status and the titer of GAD-Ab is not so helpful. So, to address possible predictors of the discrepancy of beta cell loss, we have conducted a prospective study to characterize the difference of 527 cases of autoimmune diabetes, who have been followed closely and assessed serum C peptide levels repeatedly. Our results indicated that initial beta cell function was the most usefulmarker for differentiating beta cell failure tendency in autoimmune diabetes.
Inclusion of subjects and data collection
This study was carried out according to the Helsinki guidelines. All patients gave informed consent to participation in the study and the protocol was approved by the Research Ethics Committee in Second Xiangya Hospital, Central South University. A total of 4,469 newly diagnosed patients who were hospitalized from July 2002 to July 2006 were screened for GAD-Ab; five hundred and twenty-seven patients with positive GAD-Ab were invited and agreed to participate in this study as they fulfilled the following criteria: (1) diabetes diagnosed according to the report of WHO in 1999; (2) disease duration less than one year; (3) GAD-Ab positive testing twice within one month. The disease onset was defined as the initial diagnosis of diabetes and disease duration was thus calculated.
All patients were treated according to the decision of individual physician and insulin or metformin were applied in accordance with the seriousness of the case and adjusted in line with blood glucose levels,other kinds of hypoglycemic agents including sulfonylureas and thiazolidinediones were not employed. Data from all patients, including age of onset, diabetes duration, body mass index (BMI), ketosis were collected. Serum was collected for measurement of HbA1c, islet autoantibodies and C peptide levels.
We have complied with the recommendations of the Declaration of Helsinki. This study was approved by the ethics committee of Second Xiangya Hospital, Central South University and informed consent was obtained from all participants.
Definition of clinical subtype of autoimmune diabetes
All these autoimmune diabetes were subdivided into two subtypes, that is the acute-onset T1DM and latent-onset LADA. Acute-onset autoimmune T1DM was defined by 1) Requirement of insulin therapy since diagnosis; + 2) positive GAD-Ab. Latent-onset LADA was defined by 1) No ketosis or ketoacidosis during the first 6 months after diagnosis; + 2) no requirement of insulin therapy during the first 6 months after diagnosis; + 3) positive GAD-Ab.
Diabetes associated autoantibody analysis
Serum was analyzed for the presence of GAD-Ab by highly sensitive and specific quantitative radioligand binding assay methods as reported previously. Intra-assay and inter-assay coefficients of variation were 8.9% and 11.2% (n=5) respectively. The cut-off point of GAD-Ab index was determined according to the 99.5% upper limit of 188 healthy Chinese controls. The GAD-Ab index of 0.05 or higher was defined as positive.
Human leukocyte antigen (HLA-DQ) genotyping
DNA was isolated from peripheral blood leukocytes using the phenol–chloroform method. The polymorphic second exons of DQA1, DQB1 were amplified using PCR. The HLA-DQA1 and -DQB1 types were defined by DNA analysis using polymerase chain reaction (sequencing-based typing). The frequencies of HLA-DQA1 and –DQB1 genes were tested; the susceptible and protective haplotypes were defined according to our previous report and HLA-DQA1*03-DQB1*0303, DQA1*05-DQB1*0201 and DQA1*03-DQB1*0401 are susceptible to type 1 diabetes, and HLA- DQA1*0102-DQB1*0602 is protective haplotypes.
Measurement of beta cell function
Beta cell function was assessed in all patients in two ways: 1) fasting plasma C-peptide (FCP) concentration; 2) postprandial C-peptide (PCP): Sera were determined 2 h after a mixed meal (with about 400 cal). C-peptide levels were measured at the time of initial inclusion (after glucotoxicity had been removed) and during the follow-up.
Beta cell function failure was defined as FCP and PCP levels less than 100 pmol/L and 150 pmol/L respectively, and the initial beta cell function was defined as preserved (B+) if FCP level was higher than 300 pmol/L or PCP level higher than 600 pmol/L, and those whose C peptide levels could not meet the above criteria were defined as B-. These cutoff values are determined according to the results previously reported to differentiate normal subjects, type 1 and type 2 diabetic patients.
The statistical analysis was done with SPSS 16.0 software. Data were shown by means ± SD or as indicated. ANOVA was used to assess differences in continuous variables (age, age at diagnosis, HbA1c on admission, BMI, HbA1c, C-peptide levels). When this test indicated that there were significant differences between groups, pair-wise comparisons were made to identify those differences. Chi-square test was used in comparison of classification data. All significance tests were performed as P-value less than 0.05 and were two-tailed.
Patient characteristics and different tendency of beta cell function
Among all the 527 cases of autoimmune diabetes, the mean age was 39.1±19.1 yr, 54.6% were males, with the mean duration of 8.3±1.7 months,and all patients were newly onset diabetes with duration less than one year. One hundred and seventy-eight cases were defined as beta cell function failure (FCP and PCP levels less than 100 pmol/L and 150 pmol/L respectively) at the beginning of the study and thus were not followed up. Forty-nine patients descended to beta cell failure when followed up for 12 months and 24 failure patients at 24 months, 14 at 36 months, 17 at 48 months. Altogether, 104 patients developed beta cell function failure during the 48 months’ follow up.
Difference of beta cell function failure in acute-and latent-onset autoimmune diabetic patients
We tested whether patients in T1DM and LADA had disparate progression of beta cell function. Among all the 258 T1DM cases, 216 patients developed beta cell failure at the onset or during follow-up of the study, with the proportion of 83.7%; while for LADA patients, 24.5% developed beta cell failure at the onset or during follow-up of the study.
Different clinical features in patients with distinct variation of beta cell function
Clinical features in patients with distinct variation of beta cell function
Group 1: Patients with beta cell function failure at the onset of the disease (n=178)
Group 2: Patients who developed beta cell function failure during the follow-up (n=104)
Group 3: Patients who did not develop beta cell function failure during the follow-up (n=245)
Age of onset (yr)
Percentage of T1DM
Percentage of LADA
HLA-DQ susceptible haplotypes
HLA-DQ protective haplotypes
Factors which influence the decline of beta cell function
To evaluate the possible risk factors contributing to the development of beta cell failure, multivariate analysis and a Cox regression analysis was performed (age of onset, diabetes duration, frequency of ketosis, BMI, initial fasting C peptide, GAD-Ab titer, HLA-DQ haplotypes were analyzed as inclusive factors). Multivariate analysis showed that age of onset, the frequency of ketosis, BMI and FCP levels were significantly correlated with distinct outcomes of beta cell function. Subsequently, the results of Cox regression analysis revealed that influencing factor included FCP levels, age of onset and BMI, with the largest coefficient of determination (0.89) for initial FCP levels.
Re-classification of autoimmune diabetes with initial beta cell function
The above results suggested that initial FCP levels maybe the promising predictor of possible beta cell function failure. We arbitrarily defined better preservation of beta cell function (B+) when the FCP levels were more than 300 pmol/L and worse beta cell function (B-) when FCP were less than 300 pmol/L. Follow-up study showed that a dramatic difference of beta cell function was found, 13.1% in B+ group while 90.5% in B- group progressed to beta cell function failure. Considering the proportion of 83.7% in T1DM and 24.5% in LADA progressed to beta cell failure, the results showed that initial serum FCP level made a better distinction of the heterogeneity in autoimmune diabetes than WHO recommendation with LADA sub-typing.
Islet beta cell function plays an important role in the pathogenesis of diabetes mellitus, and the destiny of beta cell function failure leads to the uncontrollable hyperglycemia in long term and diabetic complications. From the patients’ point of view, it is of highest priority to find factors for the discrimination of beta cell function course. For autoimmune diabetes, beta cell function failure is more apparent as the immunity mediated beta cell destruction. However, the heterogeneous tempo of beta cell function failure in autoimmune diabetes was recognized and LADA is subdivided specially[16, 17]. However, the arbitrary classification scheme using onset age to categorize the heterogeneity of autoimmune diabetes has some limitations; 1) the confirmation of the exact onset age is not so certain, 2) the onset age is a continuous parameter, the optimal cut off point is undecided, 3) the term “latent” in LADA could not be reflected by the “late onset”, classical type 1 diabetes in adults is common, and “young onset” could also be “latent”.
So, we aimed to investigate whether initial C peptide levels is useful marker for differentiating variation of C peptide decay rate. There were three different outcomes of beta cell function progression, that is, beta cell function failure at the onset of the disease, failure during the follow-up and no failure during the follow-up, and initial fasting C peptide levels was dramatically different in patients with distinct progressive endings of beta cell function. So, we proposed that the disparate outcomes of beta cell function in autoimmune diabetes could be better discriminated by initial FCP levels. When defined beta cell function as B+ or B- by FCP level of 300 pmol/L, we found 13.1% in B+ group while 90.5% in B- group progressed to beta cell function failure. So, initial FCP levels made a better distinction of the heterogeneity in autoimmune diabetes with the sensitivity of 90.5% and specificity of 86.9%.
Positive islet autoantibodies in autoimmune diabetes patients are thought to indicate a progressive autoimmune disease in the beta cells associated with a gradual decrease in insulin secretion. So, islet autoantibodies (A) was applied as one marker to dissect the heterogeneity of ketosis prone diabetes by Maldonado et al., beta cell function (B) was also used, and four different combination of AB groups with diverse clinical features were found. Therefore, the classification scheme using A (autoantibody) and B (beta cell function) was proposed in discriminating ketosis-prone diabetes.
For antibody positive autoimmune diabetes, it is likely that the beta cell destruction continues after diagnosis, with varying rate until the beta cells are depleted[21, 22]. C-peptide levels at diagnosis, age, gender, titer of GAD-Ab, degree of obesity and puberty, and levels of HbA1c are factors reported to influence beta cell function after diagnosis. In our study, we found that initial beta cell function reflected by fasting C peptide levels might be a good marker for dissection the heterogeneity of autoimmune diabetes. The possible reasons are, 1) the value of FCP levels had a higher sensitivity and specificity in predicting beta cell failure; 2) initial C peptide levels could be a mixed reflection of age onset, predisposing genes, the extent of insulin resistance and insulin deficiency. Consistently, Thunander M et al. followed LADA patients for three years, and determined beta-cell function with early insulin vs conventional treatment, and found only baseline level of C-peptide significantly influenced C-peptide level after 3 years. Other study reported that initial C-peptide is a predicting factor for effectiveness of insulin intervention for LADA. For GAD-Ab positive LADA patients (without classical type 1 diabetes), the same trend of C-peptide declining curve in patients with different initial C-peptide levels, as shown in our Figure 1, had been also reported. So, the use of initial beta cell function may have important implications in predicting the prognosis of autoimmune diabetes.
Based on this study, we conclude that initial level of fasting C peptide, instead of age and mode of onset, is a better criterion for predicting beta cell function failure in GAD-Ab positive autoimmune diabetes.
We would like to thank all the participants in the study. This study was supported by the National Natural Science Foundation of China (Grant No. 81170725,81070672,81100583); the Key Project of Science and Technology Department of Hunan Province of China (2010SK2007); the National Department Public Benefit (Health) Research Foundation of China (Grant No.201002002); program for Changjiang Scholars and Innovative Research Team in University and the European Foundation for the Study of Diabetes (Grant No. EFSD/CDS/Lilly-2010).
- Velloso LA, Kämpe O, Hallberg A, Christmanson L, Betsholtz C, Karlsson FA: Demonstration of GAD-65 as the main immunogenic isoform of glutamate decarboxylase in type 1 diabetes and determination of autoantibodies using a radioligand produced by eukaryotic expression. J Clin Invest. 1993, 91: 2084-2090. 10.1172/JCI116431.View ArticlePubMedPubMed CentralGoogle Scholar
- Leslie RD, Kolb H, Schloot NC, Buzzetti R, Mauricio D, De Leiva A, Yderstraede K, Sarti C, Thivolet C, Hadden D, Hunter S, Schernthaner G, Scherbaum W, Williams R, Pozzilli P: Diabetes classification: grey zones, sound and smoke: action LADA 1. Diabetes Metab Res Rev. 2008, 24: 511-519. 10.1002/dmrr.877.View ArticlePubMedGoogle Scholar
- Qi X, Sun J, Wang J, Wang PP, Xu Z, Murphy M, Jia J, Wang J, Xie Y, Xu W: Prevalence and correlates of latent autoimmune diabetes in adults in Tianjin, China: a population-based cross-sectional study. Diabetes Care. 2011, 34: 66-70. 10.2337/dc10-0488.View ArticlePubMedGoogle Scholar
- Kahn SE: The importance of beta-cell failure in the development and progression of type 2 diabetes. J Clin Endocrinol Metab. 2001, 86: 4047-4058. 10.1210/jc.86.9.4047.PubMedGoogle Scholar
- Xiang Y, Zhou P, Li X, Huang G, Liu Z, Xu A, Leslie RD, Zhou Z: Heterogeneity of altered cytokine levels across the clinical spectrum of diabetes in China. Diabetes Care. 2011, 34: 1639-1641. 10.2337/dc11-0039.View ArticlePubMedPubMed CentralGoogle Scholar
- Lohmann T, Nietzschmann U, Kiess W: “Lady-like”: is there a latent autoimmune diabetes in the young?. Diabetes Care. 2000, 23: 1707-1708. 10.2337/diacare.23.11.1707.View ArticlePubMedGoogle Scholar
- Wang JP, Zhou ZG, Lin J, Huang G, Zhang C, Yang L, Yuan Y, Zhou HF, Zhou M, Hou C, Zhou WD, Peng H, Hagopian WA: Islet autoantibodies are associated with HLA-DQ genotypes in Han Chinese patients with type 1 diabetes and their relatives. Tissue Antigens. 2007, 70: 369-375. 10.1111/j.1399-0039.2007.00916.x.View ArticlePubMedGoogle Scholar
- van Deutekom AW, Heine RJ, Simsek S: The islet autoantibody titres: their clinical relevance in latent autoimmune diabetes in adults (LADA) and the classification of diabetes mellitus. Diabet Med. 2008, 25: 117-125. 10.1111/j.1464-5491.2007.02316.x.View ArticlePubMedGoogle Scholar
- Li X, Zhou ZG, Huang G, Yan X, Yang L, Chen XY, Wang JP: Optimal cutoff point of glutamate decarboxylase antibody titers in differentiating two subtypes of adult-onset latent autoimmune diabetes. Ann N Y Acad Sci. 2004, 1037: 122-126. 10.1196/annals.1337.019.View ArticlePubMedGoogle Scholar
- Buzzetti R, Di Pietro S, Giaccari A, Petrone A, Locatelli M, Suraci C, Capizzi M, Arpi ML, Bazzigaluppi E, Dotta F, Bosi E, Non Insulin Requiring Autoimmune Diabetes Study Group: High titer of autoantibodies to GAD identifies a specific phenotype of adult-onset autoimmune diabetes. Diabetes Care. 2007, 30: 932-938. 10.2337/dc06-1696.View ArticlePubMedGoogle Scholar
- Rewers M: Challenges in Diagnosing Type 1 Diabetes in Different Populations. Diabetes Metab J. 2012, 36: 90-97. 10.4093/dmj.2012.36.2.90.View ArticlePubMedPubMed CentralGoogle Scholar
- Yang L, Luo S, Huang G, Peng J, Li X, Yan X, Lin J, Wenzlau JM, Davidson HW, Hutton JC, Zhou Z: The diagnostic value of zinc transporter 8 autoantibody (ZnT8A) for type 1 diabetes in Chinese. Diabetes Metab Res Rev. 2010, 26: 579-584. 10.1002/dmrr.1128.View ArticlePubMedPubMed CentralGoogle Scholar
- Lin J, Zhou ZG, Wang JP, Zhang C, Huang G: From Type 1, through LADA, to type 2 diabetes: a continuous spectrum ?. Ann N Y Acad Sci. 2008, 1150: 99-102. 10.1196/annals.1447.036.View ArticlePubMedGoogle Scholar
- Törn C: C-peptide and autoimmune markers in diabetes. Clin Lab. 2003, 49: 1-10.PubMedGoogle Scholar
- Zeitler P: Update on nonautoimmune diabetes in children. J Clin Endocrinol Metab. 2009, 94: 2215-2220. 10.1210/jc.2009-0493.View ArticlePubMedGoogle Scholar
- Törn C, Landin-Olsson M, Lernmark A, Palmer JP, Arnqvist HJ, Blohmé G, Lithner F, Littorin B, Nyström L, Scherstén B, Sundkvist G, Wibell L, Ostman J: Prognostic factors for the course of beta cell function in autoimmune diabetes. J Clin Endocrinol Metab. 2000, 85: 4619-4623. 10.1210/jc.85.12.4619.PubMedGoogle Scholar
- Palmer JP, Hampe CS, Chiu H, Goel A, Brooks-Worrell BM: Is latent autoimmune diabetes in adults distinct from type 1 diabetes or just type 1 diabetes at an older age?. Diabetes. 2005, 54: S62-S67. 10.2337/diabetes.54.suppl_2.S62.View ArticlePubMedGoogle Scholar
- Maruyama T, Koyama A, Hampe CS: Latent autoimmune diabetes in an adult. Ann N Y Acad Sci. 2008, 1150: 267-269. 10.1196/annals.1447.022.View ArticlePubMedGoogle Scholar
- Hillman M, Törn C, Landin-Olsson M, DISS study group: The glutamic acid decarboxylase 65 immunoglobulin G subclass profile differs between adult-onset type 1 diabetes and latent autoimmune diabetes in adults (LADA) up to 3 years after clinical onset. Clin Exp Immunol. 2009, 157: 255-260. 10.1111/j.1365-2249.2009.03939.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Maldonado M, Hampe CS, Gaur LK, D'Amico S, Iyer D, Hammerle LP, Bolgiano D, Rodriguez L, Rajan A, Lernmark A, Balasubramanyam A: Ketosis-prone diabetes: dissection of a heterogeneous syndrome using an immunogenetic and beta-cell functional classification, prospective analysis, and clinical outcomes. J Clin Endocrinol Metab. 2003, 88: 5090-5098. 10.1210/jc.2003-030180.View ArticlePubMedGoogle Scholar
- Bonfanti R, Bazzigaluppi E, Calori G, Riva MC, Viscardi M, Bognetti E, Meschi F, Bosi E, Chiumello G, Bonifacio E: Parameters associated with residual insulin secretion during the first year of disease in children and adolescents with Type 1 diabetes mellitus. Diabet Med. 1998, 15: 844-850. 10.1002/(SICI)1096-9136(199810)15:10<844::AID-DIA679>3.0.CO;2-A.View ArticlePubMedGoogle Scholar
- Klingensmith GJ, Pyle L, Arslanian S, Copeland KC, Cuttler L, Kaufman F, Laffel L, Marcovina S, Tollefsen SE, Weinstock RS, Linder B, TODAY Study Group: The presence of GAD and IA-2 antibodies in youth with a type 2 diabetes phenotype: results from the TODAY study. Diabetes Care. 2010, 33: 1970-1975. 10.2337/dc10-0373.View ArticlePubMedPubMed CentralGoogle Scholar
- Jensen RA, Gilliam LK, Törn C, Landin-Olsson M, Karlsson FA, Palmer JP, Kockum I, Akesson K, Lernmark B, Lynch K, Breslow N, Lernmark A, Diabetes Incidence Study in Sweden (DISS) group: Multiple factors affect the loss of measurable C-peptide over 6 years in newly diagnosed 15- to 35-year-old diabetic subjects. J Diabetes Complications. 2007, 21: 205-213. 10.1016/j.jdiacomp.2006.01.004.View ArticlePubMedGoogle Scholar
- Thunander M, Thorgeirsson H, Törn C, Petersson C, Landin-Olsson M: β-cell function and metabolic control in latent autoimmune diabetes in adults with early insulin versus conventional treatment: a 3-year follow-up. Eur J Endocrinol. 2011, 164: 239-245. 10.1530/EJE-10-0901.View ArticlePubMedPubMed CentralGoogle Scholar
- Maruyama T, Tanaka S, Shimada A, Funae O, Kasuga A, Kanatsuka A, Takei I, Yamada S, Harii N, Shimura H, Kobayashi T: Insulin intervention in slowly progressive insulin-dependent (type 1) diabetes mellitus. J Clin Endocrinol Metab. 2008, 93: 2115-2121. 10.1210/jc.2007-2267.View ArticlePubMedGoogle Scholar
- Murao S, Kondo S, Ohashi J, Fujii Y, Shimizu I, Fujiyama M, Ohno K, Takada Y, Nakai K, Yamane Y, Osawa H, Makino H: Anti-thyroid peroxidase antibody, IA-2 antibody, and fasting C-peptide levels predict beta cell failure in patients with latent autoimmune diabetes in adults (LADA)–a 5-year follow-up of the Ehime study. Diabetes Res Clin Pract. 2008, 80: 114-121. 10.1016/j.diabres.2008.01.024.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6823/13/10/prepub
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