Evidence map›Paper›PMID 25411619›Full record

ArticleJournal of diabetes investigation2014

Postprandial C-peptide to glucose ratio as a predictor of β-cell function and its usefulness for staged management of type 2 diabetes.

Eun Young Lee, Sena Hwang, Seo Hee Lee, Yong-Ho Lee, A Ra Choi, Youngki Lee, Byung-Wan Lee, Eun Seok Kang, Chul Woo Ahn, Bong Soo Cha and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Eun Young LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Sena HwangDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea ; International Health Care Center Yonsei Medical Health System Seoul Korea.
Seo Hee LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Yong-Ho LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
A Ra ChoiDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Youngki LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Byung-Wan LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Eun Seok KangDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Chul Woo AhnDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Bong Soo ChaDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.
Hyun Chul LeeDepartment of Internal Medicine Yonsei University College of Medicine Seoul Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionType 2 diabetes is characterized by progressive deterioration of β-cell function. Recently, it was suggested that the C-peptide-to-glucose ratio after oral glucose ingestion is a better predictor of β-cell mass than that during fasting. We investigated whether postprandial C-peptide-to-glucose ratio (PCGR) reflects β-cell function, and its clinical application for management of type 2 diabetes. MATERIALS AND

methodsWe carried out a two-step retrospective study of 919 Korean participants with type 2 diabetes. In the first step, we evaluated the correlation of PCGR level with various markers for β-cell function in newly diagnosed and drug-naïve patients after a mixed meal test. In the second step, participants with well-controlled diabetes (glycated hemoglobin <7%) were divided into four groups according to treatment modality (group I: insulin, group II: sulfonylurea and/or dipeptityl peptidase IV inhibitor, group III: metformin and/or thiazolidinedione and group IV: diet and exercise group).

resultsIn the first step, PCGR was significantly correlated with various insulin secretory indices. Furthermore, PCGR showed better correlation with glycemic indices than homeostatic model assessment of β-cell function (HOMA-β). In the second step, the PCGR value significantly increased according to the following order: group I, II, III, and IV after adjusting for age, sex, body mass index and duration of diabetes. The cut-off values of PCGR for separating each group were 1.457, 2.870 and 3.790, respectively (P < 0.001).

conclusionsWe suggest that PCGR might be a useful marker for β-cell function and an ancillary parameter in the choice of antidiabetic medication in type 2 diabetes.

Indexed as

C‐peptidePancreatic β‐cellType 2 diabetes mellitus

Identifiers

PMID25411619
PMCPMC4188109

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.