Relationship Between C-Peptide Levels, Clinical Features, and Serum Data in a Brazilian Type 1 Diabetes Population with Large Variations in Genomic Ancestry.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
    • Publication Information:
      Original Publication: Basel, Switzerland : MDPI, [2000-
    • Subject Terms:
    • Abstract:
      Type 1 diabetes (T1D) is a chronic disease characterized by the immune-mediated destruction of the pancreatic beta cells responsible for insulin production. The secreted insulin and C-peptide are equimolar. Due to its longer half-life, C-peptide has become a safer means of assessing the pancreatic reserve. C-peptide levels were evaluated in a population of patients with T1D, focusing on the relationship between this variable and other factors. In addition, the influence of C-peptide on metabolic control and microvascular complications was investigated. This cross-sectional study included 95 patients who had been diagnosed with T1D at least five years earlier. These patients were evaluated using a clinical demographic survey, anthropometric data, laboratory tests, and fundoscopy. This study showed that 29.5% of patients had residual insulin secretion, which correlated directly with their age at diagnosis. No statistically significant differences in metabolic control or microvascular complications were observed between the C-peptide level groups. In addition, our results indicate that ancestry does not influence the persistence of residual C-peptide function in our highly mixed population. It is recommended that future research consider incorporating new variables, such as HLA and pancreatic autoimmunity, as factors that may influence residual β-cell function.
    • References:
      Diabetes Obes Metab. 2014 Mar;16(3):262-7. (PMID: 24118704)
      Diabet Med. 2015 Oct;32(10):1346-53. (PMID: 26172028)
      PLoS One. 2012;7(1):e29684. (PMID: 22272242)
      Nat Rev Endocrinol. 2019 Nov;15(11):635-650. (PMID: 31534209)
      J Clin Invest. 2021 Apr 15;131(8):. (PMID: 33759815)
      Diabetes. 2010 Nov;59(11):2846-53. (PMID: 20699420)
      Arq Bras Endocrinol Metabol. 2010;54(5):449-54. (PMID: 20694405)
      Am J Hum Genet. 2020 Mar 5;106(3):303-314. (PMID: 32059761)
      Diabetes Care. 2020 Jan;43(1):5-12. (PMID: 31753960)
      Diabetol Metab Syndr. 2023 Mar 20;15(1):51. (PMID: 36935525)
      Diabetes Metab Res Rev. 2024 Feb;40(2):e3770. (PMID: 38450851)
      Diabetes. 2022 Jul 1;71(7):1591-1596. (PMID: 35499624)
      Lancet Diabetes Endocrinol. 2022 Aug;10(8):597-608. (PMID: 35724677)
      Front Immunol. 2023 Apr 27;14:1176403. (PMID: 37180128)
      J Diabetes Complications. 2019 Sep;33(9):657-661. (PMID: 31239235)
      J Diabetes Investig. 2022 Mar;13(3):552-559. (PMID: 34637185)
      J Clin Endocrinol Metab. 1987 Jul;65(1):30-6. (PMID: 2884229)
      JAMA. 2021 Aug 24;326(8):717-727. (PMID: 34427600)
      Diabetologia. 2014 Jan;57(1):187-91. (PMID: 24121625)
      Diabetologia. 2020 Jun;63(6):1258-1267. (PMID: 32172310)
      Diabet Med. 2013 Jul;30(7):803-17. (PMID: 23413806)
      Front Med (Lausanne). 2022 Jul 12;9:932086. (PMID: 35903316)
      Diabetes Care. 2015 Mar;38(3):476-81. (PMID: 25519448)
      Diabetes Care. 2012 Mar;35(3):465-70. (PMID: 22355018)
      Ann Transl Med. 2021 Apr;9(8):650. (PMID: 33987348)
      Sci Rep. 2021 Jul 8;11(1):14157. (PMID: 34239025)
      Diabetes. 2014 Feb;63(2):739-48. (PMID: 24089509)
    • Contributed Indexing:
      Keywords: C-peptide; genomic ancestry; microvascular complication; type 1 diabetes
    • Accession Number:
      0 (C-Peptide)
      0 (Insulin)
    • Publication Date:
      Date Created: 20241026 Date Completed: 20241026 Latest Revision: 20241028
    • Publication Date:
      20241028
    • Accession Number:
      PMC11508759
    • Accession Number:
      10.3390/ijms252011144
    • Accession Number:
      39456927