Random non‐fasting C–peptide: bringing robust assessment of endogenous insulin secretion to the clinic
Open accessAbstract
Background: Measuring endogenous insulin secretion using C–peptide can assist diabetes management, but standard stimulation tests are impractical for clinical use. Random non‐fasting C–peptide assessment would allow testing when a patient is seen in clinic. Methods: We compared C–peptide at 90 min in the mixed meal tolerance test (sCP) with random non‐fasting blood C–peptide (rCP) and random non‐fasting urine C–peptide creatinine ratio (rUCPCR) in 41 participants with insulin‐treated diabetes [median age 72 (interquartile range 68–78); diabetes duration 21 (14–31) years]. We assessed sensitivity and specificity for previously reported optimal mixed meal test thresholds for severe insulin deficiency (sCP < 200 pmol//l) and Type 1 diabetes/inability to withdraw insulin (< 600 pmol//l), and assessed the impact of concurrent glucose. Results: rCP and sCP levels were similar (median 546 and 487 pmol//l, P = 0.92). rCP was highly correlated with sCP, r = 0.91, P < 0.0001, improving to r = 0.96 when excluding samples with concurrent glucose < 8 mmol//l. An rCP cut‐off of 200 pmol//l gave 100% sensitivity and 93% specificity for detecting severe insulin deficiency, with area under the receiver operating characteristic curve of 0.99. rCP < 600 pmol//l gave 87% sensitivity and 83% specificity to detect sCP < 600 pmol//l. Specificity improved to 100% when excluding samples with concurrent glucose < 8 mmol//l. rUCPCR (0.52 nmol/mmol) was also well‐correlated with sCP, r = 0.82, P < 0.0001. A rUCPCR cut‐off of < 0.2 nmol/ mmol gave sensitivity and specificity of 83% and 93% to detect severe insulin deficiency, with area under the receiver operating characteristic curve of 0.98. Conclusions: Random non‐fasting C–peptide measures are strongly correlated with mixed meal C–peptide, and have high sensitivity and specificity for identifying clinically relevant thresholds. These tests allow assessment of C–peptide at the point patients are seen for clinical care.
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Random C-peptide measurements are highly correlated with the gold-standard mixed meal test assessment of endogenous insulin secretion.
“Random C-peptide measurements are highly correlated with the gold-standard mixed meal test assessment of endogenous insulin secretion70.”
From The epidemiology of type 1 diabetes mellitus in older adults (2025) · cites this paper as [70]
Random measurements of levels of C-peptide are more powerful than assessment of post-glucagon and fasting blood levels of C-peptide in distinguishing type 1 diabetes mellitus from type 2 diabetes mellitus.
“Random measurements of levels of C-peptide are more powerful than assessment of post-glucagon and fasting blood levels of C-peptide in distinguishing T1DM from T2DM70 and should therefore be used where possible in the diagnostic work-up of suspected adult-onset T1DM.”
From The epidemiology of type 1 diabetes mellitus in older adults (2025) · cites this paper as [70]
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Cites
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A practical review of C-peptide testing in diabetes
Leighton, E., Sainsbury, C. A., & Jones, G. C. (2017) · Diabetes Therapy · doi:10.1007/s13300-017-0265-4 · Cited by 773 · see citing works
Thomas, N. J., Lynam, A. L., Hill, A. V., Weedon, M. N., Shields, B. M., Oram, R. A., McDonald, T. J., Hattersley, A. T., & Jones, A. G. (2019) · Diabetologia · doi:10.1007/s00125-019-4863-8 · Cited by 183 · see citing works
Approach to the patient with mody-monogenic diabetes
Broome, D. T., Pantalone, K. M., Kashyap, S. R., & Philipson, L. H. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa710 · Cited by 159 · see citing works
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The epidemiology of type 1 diabetes mellitus in older adults
Tomic, D., Harding, J. L., Jenkins, A. J., Shaw, J. E., & Magliano, D. J. (2025) · Nature Reviews Endocrinology · doi:10.1038/s41574-024-01046-z · Cited by 58 · see citing works
- Authors
- Hope, S. V., Knight, B. A., Shields, B. M., Hattersley, A. T., McDonald, T. J., & Jones, A. G.
- Affiliations
- University of Exeter (GB)
- Corresponding author
- Jones, A. G.
- Venue
- Diabetic Medicine
- Publisher
- Wiley
- Published
- 2016-05-26
- Volume
- 33
- Issue
- 11
- Pages
- 1554-1558
- ISSN
- 0742-3071 (ISSN-L)
- 1464-5491
- PMC
- PMC5226330
- OpenAlex
- W2341387423
- Cited by
- 68
- References
- 3
- Citations by year
- 2026: 2 · 2025: 7 · 2024: 7 · 2023: 6 · 2022: 8 · 2021: 7 · 2020: 13 · 2019: 4 · 2018: 9 · 2017: 5
- FWCI
- 6.03
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Diabetic Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Open Research Exeter (University of Exeter) (acceptedVersion)
- Figshare (submittedVersion)
- Royal Devon and Exeter Research Repository (Royal Devon and Exeter) (submittedVersion)
- Funders
- Northcott Devon Medical Foundation
- NIHR Exeter Clinical Research Facility
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Keywords
- C-peptide, endogenous insulin secretion, mixed meal tolerance test, type 1 diabetes, insulin-treated diabetes, sensitivity and specificity, point-of-care testing
- MeSH terms
- Insulin Secretion, Aged, C-Peptide, Diabetes Mellitus, Type 1, Diagnostic Techniques, Endocrine, Fasting, Female, Glucose Tolerance Test, Humans, Insulin, Male, Clinical Laboratory Techniques, Meals
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