C-Peptide Decline in Type 1 Diabetes Has Two Phases: An Initial Exponential Fall and a Subsequent Stable Phase

被引:85
作者
Shields, Beverley M. [1 ]
McDonald, Timothy J. [2 ]
Oram, Richard [1 ]
Hill, Anita [1 ]
Hudson, Michelle [1 ]
Leete, Pia [3 ]
Pearson, Ewan R. [4 ]
Richardson, Sarah J. [3 ]
Morgan, Noel G. [3 ]
Hattersley, Andrew T. [1 ]
机构
[1] Univ Exeter, Natl Inst Hlth Res, Exeter Clin Res Facil, Med Sch, Exeter, Devon, England
[2] Royal Devon & Exeter NHS Fdn Trust, Blood Sci, Exeter, Devon, England
[3] Univ Exeter, Med Sch, Islet Biol Exeter IBEx, Inst Biomed & Clin Sci, Exeter, Devon, England
[4] Univ Dundee, Sch Med, Div Mol & Clin Med, Dundee, Scotland
基金
英国惠康基金;
关键词
BETA-CELL FUNCTION; DIAGNOSIS; DURATION; AGE; POPULATION; ONSET; CHILDREN; YOUNG;
D O I
10.2337/dc18-0465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVEThe decline in C-peptide in the 5 years after diagnosis of type 1 diabetes has been well studied, but little is known about the longer-term trajectory. We aimed to examine the association between log-transformed C-peptide levels and the duration of diabetes up to 40 years after diagnosis.RESEARCH DESIGN AND METHODSWe assessed the pattern of association between urinary C-peptide/creatinine ratio (UCPCR) and duration of diabetes in cross-sectional data from 1,549 individuals with type 1 diabetes using nonlinear regression approaches. Findings were replicated in longitudinal follow-up data for both UCPCR (n = 161 individuals, 326 observations) and plasma C-peptide (n = 93 individuals, 473 observations).RESULTSWe identified two clear phases of C-peptide decline: an initial exponential fall over 7 years (47% decrease/year [95% CI -51, -43]) followed by a stable period thereafter (+0.07%/year [-1.3, +1.5]). The two phases had similar durations and slopes in patients above and below the median age at diagnosis (10.8 years), although levels were lower in the younger patients irrespective of duration. Patterns were consistent in both longitudinal UCPCR (n = 162; 7 years duration: -48%/year [-55, -38]; >7 years duration -0.1% [-4.1, +3.9]) and plasma C-peptide (n = 93; >7 years duration only: -2.6% [-6.7, +1.5]).CONCLUSIONSThese data support two clear phases of C-peptide decline: an initial exponential fall over a 7-year period, followed by a prolonged stabilization where C-peptide levels no longer decline. Understanding the pathophysiological and immunological differences between these two phases will give crucial insights into understanding -cell survival.
引用
收藏
页码:1486 / 1492
页数:7
相关论文
共 26 条
[1]   Age-dependent decline of β-cell function in type 1 diabetes after diagnosis: a multi-centre longitudinal study [J].
Barker, A. ;
Lauria, A. ;
Schloot, N. ;
Hosszufalusi, N. ;
Ludvigsson, J. ;
Mathieu, C. ;
Mauricio, D. ;
Nordwall, M. ;
Van der Schueren, B. ;
Mandrup-Poulsen, T. ;
Scherbaum, W. A. ;
Weets, I. ;
Gorus, F. K. ;
Wareham, N. ;
Leslie, R. D. ;
Pozzilli, P. .
DIABETES OBESITY & METABOLISM, 2014, 16 (03) :262-267
[2]   Lessons From the Mixed-Meal Tolerance Test Use of 90-minute and fasting C-peptide in pediatric diabetes [J].
Besser, Rachel E. J. ;
Shields, Beverley M. ;
Casas, Rosaura ;
Hattersley, Andrew T. ;
Ludvigsson, Johnny .
DIABETES CARE, 2013, 36 (02) :195-201
[3]   Urine C-Peptide Creatinine Ratio Is a Noninvasive Alternative to the Mixed-Meal Tolerance Test in Children and Adults With Type 1 Diabetes [J].
Besser, Rachel E. J. ;
Ludvigsson, Johnny ;
Jones, Angus G. ;
McDonald, Timothy J. ;
Shields, Beverley M. ;
Knight, Bridget A. ;
Hattersley, Andrew T. .
DIABETES CARE, 2011, 34 (03) :607-609
[4]   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 [J].
Besser, Rachel E. J. ;
Shepherd, Maggie H. ;
McDonald, Timothy J. ;
Shields, Beverley M. ;
Knight, Bridget A. ;
Ellard, Sian ;
Hattersley, Andrew T. .
DIABETES CARE, 2011, 34 (02) :286-291
[5]   Insulitis and -Cell Mass in the Natural History of Type 1 Diabetes [J].
Campbell-Thompson, Martha ;
Fu, Ann ;
Kaddis, John S. ;
Wasserfall, Clive ;
Schatz, Desmond A. ;
Pugliese, Alberto ;
Atkinson, Mark A. .
DIABETES, 2016, 65 (03) :719-731
[6]   Clinical evolution of beta cell function in youth with diabetes: the SEARCH for Diabetes in Youth study [J].
Dabelea, D. ;
Mayer-Davis, E. J. ;
Andrews, J. S. ;
Dolan, L. M. ;
Pihoker, C. ;
Hamman, R. F. ;
Greenbaum, C. ;
Marcovina, S. ;
Fujimoto, W. ;
Linder, B. ;
Imperatore, G. ;
D'Agostino, R., Jr. .
DIABETOLOGIA, 2012, 55 (12) :3359-3368
[7]   Prevalence of Detectable C-Peptide According to Age at Diagnosis and Duration of Type 1 Diabetes [J].
Davis, Asa K. ;
DuBose, Stephanie N. ;
Haller, Michael J. ;
Miller, Kellee M. ;
DiMeglio, Linda A. ;
Bethin, Kathleen E. ;
Goland, Robin S. ;
Greenberg, Ellen M. ;
Liljenquist, David R. ;
Ahmann, Andrew J. ;
Marcovina, Santica M. ;
Peters, Anne L. ;
Beck, Roy W. ;
Greenbaum, Carla J. .
DIABETES CARE, 2015, 38 (03) :476-481
[8]   Fall in C-Peptide During First 2 Years From Diagnosis Evidence of at Least Two Distinct Phases From Composite Type 1 Diabetes Trial Net Data [J].
Greenbaum, Carla J. ;
Beam, Craig A. ;
Boulware, David ;
Gitelman, Stephen E. ;
Gottlieb, Peter A. ;
Herold, Kevan C. ;
Lachin, John M. ;
McGee, Paula ;
Palmer, Jerry P. ;
Pescovitz, Mark D. ;
Krause-Steinrauf, Heidi ;
Skyler, Jay S. ;
Sosenko, Jay M. .
DIABETES, 2012, 61 (08) :2066-2073
[9]   Fall in C-Peptide During First 4 Years From Diagnosis of Type 1 Diabetes: Variable Relation to Age, HbA1c, and Insulin Dose [J].
Hao, Wei ;
Gitelman, Steven ;
DiMeglio, Linda A. ;
Boulware, David ;
Greenbaum, Carla J. .
DIABETES CARE, 2016, 39 (10) :1664-1670
[10]   Random non-fasting C-peptide: bringing robust assessment of endogenous insulin secretion to the clinic [J].
Hope, S. V. ;
Knight, B. A. ;
Shields, B. M. ;
Hattersley, A. T. ;
McDonald, T. J. ;
Jones, A. G. .
DIABETIC MEDICINE, 2016, 33 (11) :1554-1558