Urinary C-Peptide Creatinine Ratio Is a Practical Outpatient Tool for Identifying Hepatocyte Nuclear Factor 1-α/Hepatocyte Nuclear Factor 4-α Maturity-Onset Diabetes of the Young From Long-Duration Type 1 Diabetes

被引:90
作者
Besser, Rachel E. J. [1 ]
Shepherd, Maggie H. [1 ]
McDonald, Timothy J. [1 ,2 ]
Shields, Beverley M. [1 ]
Knight, Bridget A. [1 ]
Ellard, Sian [1 ,3 ]
Hattersley, Andrew T. [1 ]
机构
[1] Univ Exeter, Peninsula Med Sch, Peninsula Natl Inst Hlth Res Clin Res Facil, Exeter, Devon, England
[2] Royal Devon & Exeter Natl Hlth Serv Fdn Trust, Dept Clin Biochem, Exeter, Devon, England
[3] Royal Devon & Exeter Natl Hlth Serv Fdn Trust, Dept Mol Genet, Exeter, Devon, England
基金
美国国家卫生研究院;
关键词
INSULIN SECRETORY RESPONSES; BETA-CELL FUNCTION; MUTATIONS; GENE; MODY3; FACTOR-1-ALPHA; DIAGNOSIS; GLUCOSE; CHILDREN;
D O I
10.2337/dc10-1293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Hepatocyte nuclear factor 1-alpha (HNF1A)/hepatocyte nuclear factor 4-alpha (HNF4A) maturity-onset diabetes of the young (MODY) is frequently misdiagnosed as type 1 diabetes, and patients are inappropriately treated with insulin. Blood C-peptide can aid in the diagnosis of MODY, but practical reasons limit its widespread use. Urinary C-peptide creatinine ratio (UCPCR), a stable measure of endogenous insulin secretion, is a noninvasive alternative. We aimed to compare stimulated UCPCR in adults with HNF1A/4A MODY, type 1 diabetes, and type 2 diabetes. RESEARCH DESIGN AND METHODS-Adults with diabetes for >= 5years, without renal impairment, were studied (HNF1A MODY [n = 54], HNF4A MODY [n = 23], glucokinase MODY [n = 20], type 1 diabetes [n = 69], and type 2 diabetes [n = 54]). The UCPCR was collected in boric acid 120 min after the largest meal of the day and mailed for analysis. Receiver operating characteristic (ROC) curves were used to identify optimal UCPCR cutoffs to differentiate HNF1A/4A MODY from type 1 and type 2 diabetes. RESULTS-UCPCR was lower in type 1 diabetes than HNF1A/4A MODY (median [interquartile range]) (<0.02 nmol/mmol [<0.02 to <0.02] vs. 1.72 nmol/mmol [0.98-2.90]; P < 0.0001). ROC curves showed excellent discrimination (area under curve [AUC] 0.98) and identified a cutoff UCPCR of >= 0.2 nmol/mmol for differentiating HNF1A/4A MODY from type 1 diabetes (97% sensitivity, 96% specificity). UCPCR was lower in HNF1A/4A MODY than in type 2 diabetes (1.72 nmol/mmol [0.98-2.90] vs. 2.47 nmol/mmol [1.4-4.13]); P = 0.007). ROC curves showed a weak distinction between HNF1A/4A MODY and type 2 diabetes (AUC 0.64). CONCLUSIONS-UCPCR is a noninvasive outpatient tool that can be used to discriminate HNF1A and HNF4A MODY from long-duration type 1 diabetes. To differentiate MODY from type 1 diabetes of >5 years' duration, UCPCR could be used to determine whether genetic testing is indicated.
引用
收藏
页码:286 / 291
页数:6
相关论文
共 25 条
[1]   Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12 [J].
Byrne, MM ;
Sturis, J ;
Menzel, S ;
Yamagata, K ;
Fajans, SS ;
Dronsfield, MJ ;
Bain, SC ;
Hattersley, AT ;
Velho, G ;
Froguel, P ;
Bell, GI ;
Polonsky, KS .
DIABETES, 1996, 45 (11) :1503-1510
[2]   ALTERED INSULIN SECRETORY RESPONSES TO GLUCOSE IN SUBJECTS WITH A MUTATION IN THE MODY1 GENE ON CHROMOSOME-20 [J].
BYRNE, MM ;
STURIS, J ;
FAJANS, SS ;
ORTIZ, FJ ;
STOLTZ, A ;
STOFFEL, M ;
SMITH, MJ ;
BELL, GI ;
HALTER, JB ;
POLONSKY, KS .
DIABETES, 1995, 44 (06) :699-704
[3]   An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA [J].
Cervin, C. ;
Axler, O. ;
Holmkvist, J. ;
Almgren, P. ;
Rantala, E. ;
Tuomi, T. ;
Groop, L. ;
Dahlback, B. ;
Karlsson, E. .
JOURNAL OF INTERNAL MEDICINE, 2010, 267 (03) :316-321
[4]   Assays for insulin, proinsulin(s) and C-peptide [J].
Clark, PM .
ANNALS OF CLINICAL BIOCHEMISTRY, 1999, 36 :541-564
[5]  
DCCT Res Grp, 1987, J CLIN ENDOCR METAB, V65, P30
[6]   Mechanisms of disease: Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. [J].
Fajans, SS ;
Bell, GI ;
Polonsky, KS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (13) :971-980
[7]   Mixed-Meal Tolerance Test Versus Glucagon Stimulation Test for the Assessment of β-Cell Function in Therapeutic Trials in Type 1 Diabetes [J].
Greenbaum, Carla J. ;
Mandrup-Poulsen, Thomas ;
Friedenberg, Paula ;
Battelino, Tadej ;
Haastert, Burkhard ;
Ludvigsson, Johnny ;
Pozzilli, Paolo ;
Lachin, John M. ;
Kolb, Hubert .
DIABETES CARE, 2008, 31 (10) :1966-1971
[8]   Novel MODY3 mutations in the hepatocyte nuclear factor-1 alpha gene - Evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation [J].
Hansen, T ;
Eiberg, H ;
Rouard, M ;
Vaxillaire, M ;
Moller, AM ;
Rasmussen, SK ;
Fridberg, M ;
Urhammer, SA ;
Holst, JJ ;
Almind, K ;
Echwald, SM ;
Hansen, L ;
Bell, GI ;
Pedersen, O .
DIABETES, 1997, 46 (04) :726-730
[9]   ISPAD Clinical Practice Consensus Guidelines 2006-2007 - The diagnosis and management of monogenic diabetes in children [J].
Hattersley, Andrew ;
Bruining, Jan ;
Shield, Julian ;
Njolstad, Pal ;
Donaghue, Kim .
PEDIATRIC DIABETES, 2006, 7 (06) :352-360
[10]   QUANTITATION OF HUMAN PANCREATIC BETA-CELL FUNCTION BY IMMUNOASSAY OF C-PEPTIDE IN URINE [J].
HORWITZ, DL ;
RUBENSTEIN, AH ;
KATZ, AI .
DIABETES, 1977, 26 (01) :30-35