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. 2017 May 8;8(3):475–487. doi: 10.1007/s13300-017-0265-4

Table 1.

Methods of c-peptide evaluation

Cutoff Positives Negatives Test
<0.2 nmol/l Sensitive, specific, quick, reproducible, correlates with diagnosis Nausea Glucagon stimulation test (GST)
<0.2 nmol/l Sensitive, specific reproducible, correlates with diagnosis Time-consuming, liquid mixed meals not widely available Mixed meal tolerance test (MMTT)
<0.2 nmol/l Practical if at time of diagnostic OGTT Time-consuming, limited evidence of predicting beta cell function Oral glucose tolerance test (OGTT)
<0.2 nmol/l Sensitive Time-consuming, limited evidence of predicting beta cell function Tolbutamide tolerance test (tCP)
<0.075 nmol/l Simple, quick, correlates with diabetes type Insufficient to detect subtle rises in c-peptide Fasting (fCP)
<0.2 nmol/l Easy to perform, quick, simple, correlates with diagnosis If indeterminate, requires confirmation with stimulation testing Random non-fasting (rCP)
<0.2 nmol/mmol Non-invasive, simple, stable for 72 h in boric acid, correlates with insulin deficiency in T2DM Inaccurate in CKD, affected by gender as a result of differences in creatinine concentration Urinary c-peptide creatinine ratio (UCPCR)
<0.2 nmol/l Some evidence of correlation with beta cell function in men with T2DM, stable for 72 h in boric acid Inaccurate in CKD, less sensitive than when expressed as ratio to creatinine (UCPCR) Urinary c-peptide (UCP)
<0.3 nmol/l Non-invasive, useful in detecting insulin deficiency, stable for 72 h in boric acid Inaccurate in CKD, time-consuming, requires good patient compliance. Affected by variations in creatinine 24 h urinary collection (24 h UCP)

T2DM type 2 diabetes mellitus, CKD chronic kidney disease