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Association between partial remission phase in type 1 diabetes and vitamin D receptor Fok1 rs2228570 polymorphism.
Masoud, Randa Mahmoud; Abdel-Kader, Nour Mohamed; Abdel-Ghaffar, Abdel-Rahman B; Moselhy, Said Salama; Elhenawy, Yasmine Ibrahim.
Afiliação
  • Masoud RM; Biochemistry Departments, Faculty of Science, 68791 Ain Shams University , Cairo, Egypt.
  • Abdel-Kader NM; Biochemistry Departments, Faculty of Science, 68791 Ain Shams University , Cairo, Egypt.
  • Abdel-Ghaffar AB; Biochemistry Department, School of Life and Medical Sciences, University of Hertfordshire Hosted by Global Academic Foundation, Nasr City, Cairo, Egypt.
  • Moselhy SS; Biochemistry Departments, Faculty of Science, 68791 Ain Shams University , Cairo, Egypt.
  • Elhenawy YI; Biochemistry Departments, Faculty of Science, 68791 Ain Shams University , Cairo, Egypt.
Article em En | MEDLINE | ID: mdl-39237104
ABSTRACT

OBJECTIVES:

The aim of the current study was to assess the natural course of partial remission (PR) phase of type 1 diabetes (T1D) and to highlight the putative association between vitamin D receptor (VDR) (Fok1) gene polymorphism and PR phase.

METHODS:

Ninety participants with newly diagnosed T1D were followed up for a total of 12 months. The VDR (Fok1) rs2228570 gene polymorphism was genotyped using allelic discrimination (AD) assay.

RESULTS:

Fifty-four patients (60 %) reached PR with an average duration of 5.63 ± 2.9 months. Among remitters, the frequency of CC "FF" genotype and allelic frequency of C "F" were significantly higher (p<0.001). Furthermore, participants expressing "CC" genotype had earlier onset of PR and spent a significantly longer duration in remission (p<0.001). Younger age (p<0.001; OR 41.6; CI 12.12-142.99), absence of DKA (p<0.001; OR 16, CI 4.36-50.74), higher C-peptide levels (p<0.001; OR 19.55; CI 6.52-58.63), and presence of CC "FF" genotype of VDR (p<0.001; OR 6.74; CI 2.41-18.86) best predicted the overall occurrence of PR.

CONCLUSIONS:

Younger age, less extent of metabolic derangements, and expression of a CC "FF" genotype were found to influence the occurrence of PR. Data from the current study showed that the "C" allele could have a protective role on preserving residual ß-cell mass and could predict both onset and duration of PR among newly diagnosed T1D. These findings support the growing concept of future tailored precision medicine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Pediatr Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / PEDIATRIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Pediatr Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / PEDIATRIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito País de publicação: Alemanha