Brain-derived neurotrophic factor Val66Met polymorphism is associated with mild cognitive impairment in elderly patients with type 2 diabetes: a case-controlled study
Background Brain-derived neurotrophic factor ( BDNF) Val66Met polymorphism is reported to be associated with cognitive dysfunction, an important comorbidity factor in patients with type 2 diabetes mellitus (T2DM), especially in elderly populations, however, the underlying pathophysiological mechanis...
Gespeichert in:
Veröffentlicht in: | Aging clinical and experimental research 2021-06, Vol.33 (6), p.1659-1666 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background
Brain-derived neurotrophic factor
(
BDNF)
Val66Met polymorphism is reported to be associated with cognitive dysfunction, an important comorbidity factor in patients with type 2 diabetes mellitus (T2DM), especially in elderly populations, however, the underlying pathophysiological mechanisms are unclear.
Aim
This study was performed to investigate the association between
BDNF
Val66Met polymorphism and mild cognitive impairment (MCI) in elderly patients with T2DM.
Methods
In total, 105 MCI and 105 normal cognition controls of T2DM patients were enrolled; all of the patients underwent neuropsychological assessments.
BDNF
Val66Met polymorphism was genotyped via TaqMan SNP genotyping assay. Data from clinical and laboratory-based examinations were collected.
Results
The frequency of the
BDNF
Met allele was significantly higher in the MCI group than in the controls. Multiple regression analysis indicated an association of the Met allele with MCI in patients with T2DM (OR = 2.54; 95% CI 1.33–4.84;
p
= 0.005). Stratified by educational level, the
BDNF
Met allele was significantly associated with MCI in elderly T2DM patients (OR = 3.29; 95% CI 1.26–8.57;
p
= 0.015) among the group of low educational levels ( |
---|---|
ISSN: | 1720-8319 1594-0667 1720-8319 |
DOI: | 10.1007/s40520-020-01687-w |