Antidiabetic drugs and cognitive impairment in type 2 diabetes

被引:0
作者
Matveeva, Mariia, V [1 ,2 ]
Samoilova, Yulia G. [1 ,2 ,3 ]
Zhukova, Natalia G. [1 ,4 ]
Oleynik, Oxana A. [1 ,2 ]
Rotkank, Mariya A. [1 ,3 ]
Leiman, Olga P. [1 ,3 ]
Kudlay, Dmitry A. [5 ]
机构
[1] Siberian State Med Univ, 2 Moskovskytrakt, Tomsk 634050, Russia
[2] Dept Endocrinol & Diabetol, 2 Moskovskytrakt, Tomsk 634050, Russia
[3] Dept Pediat, 2 Moskovskytrakt, Tomsk 634050, Russia
[4] Dept Neurol & Neurosurg, 2 Moskovskytrakt, Tomsk 634050, Russia
[5] Lab Personalized Med & Mol Immunol, Inst Immunol, Moscow 115522, Russia
关键词
Type; 2; diabetes; antidiabetic medication; cognitive impairment; IMPROVED GLYCEMIC CONTROL; INSULIN; MELLITUS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Type 2 diabetes is a metabolic disease that is a risk factor for cognitive impairment, some antidiabetic medication may be associated with the survival of neurons. Objective: To study the association of antidiabetic medication and cognitive functions in patients with type 2 diabetes. Materials and methods: we examined 240 patients with type 2 diabetes. The patients were divided into 4 groups depending on glucose-lowering therapy: group 1 - insulin, group 2 - tableting medication, group 3 - combined therapy, group 4 - analogues of glucagon-like peptide 1. All patients underwent general clinical examination, cognitive functions test based on the Montreal scale. Statistical analysis was performed using the R-system software package. Results: The overall score of the MoCA test was higher in the group of patients receiving glucagon-like peptide-1 compared with the patients in groups 1, 2 and 3, whose cognitive functions declined. Patients receiving only biguanides medication performed the cognitive test significantly better. The correlation analysis revealed that cognitive functions are affected by age, disease duration, complications presence, and HbA1c level. Conclusion: In type 2 diabetes glucagon-like peptide-1 and biguanides treatment is accompanied by better performance of the cognitive function assessment tests.
引用
收藏
页码:369 / 374
页数:6
相关论文
共 16 条
  • [1] Insulin in the brain: There and back again
    Banks, William A.
    Owen, Joshua B.
    Erickson, Michelle A.
    [J]. PHARMACOLOGY & THERAPEUTICS, 2012, 136 (01) : 82 - 93
  • [2] Biessels GJ, 2018, BMC NEUROL, V18, DOI [10.1186/s12883-018-1014-7, 10.1186/S12883-018-1014-7]
  • [3] Comparative efficacy and acceptability of antidiabetic agents for Alzheimer's disease and mild cognitive impairment: A systematic review and network meta-analysis
    Cao, Bing
    Rosenblat, Joshua D.
    Brietzke, Elisa
    Park, Caroline
    Lee, Yena
    Musial, Natalie
    Pan, Zihang
    Mansur, Rodrigo B.
    McIntyre, Roger S.
    [J]. DIABETES OBESITY & METABOLISM, 2018, 20 (10) : 2467 - 2471
  • [4] DPP4 Inhibitors Can Be a Drug of Choice for Type 3 Diabetes: A Mini Review
    Chalichem, Nehru Sai Suresh
    Gonugunta, Chaitanya
    Krishnamurthy, Praveen Thaggikuppe
    Duraiswamy, Basavan
    [J]. AMERICAN JOURNAL OF ALZHEIMERS DISEASE AND OTHER DEMENTIAS, 2017, 32 (07): : 444 - 451
  • [5] Insulin and neurodegenerative disease: shared and specific mechanisms
    Craft, S
    Watson, GS
    [J]. LANCET NEUROLOGY, 2004, 3 (03) : 169 - 178
  • [6] Dedov II, 2017, DIABETES MELLIT, V20, P1, DOI 10.14341/DM20171S8
  • [7] VERBAL-LEARNING AND OR MEMORY IMPROVES WITH GLYCEMIC CONTROL IN OLDER SUBJECTS WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS
    GRADMAN, TJ
    LAWS, A
    THOMPSON, LW
    REAVEN, GM
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1993, 41 (12) : 1305 - 1312
  • [8] Herath PM, 2016, EFFECT DIABETES MEDI, V2016
  • [9] The effects of sitagliptin, a DPP-4 inhibitor, on cognitive functions in elderly diabetic patients with or without Alzheimer's disease
    Isik, Ahmet Turan
    Soysal, Pinar
    Yay, Adnan
    Usarel, Cansu
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 2017, 123 : 192 - 198
  • [10] Cognitive dysfunction and diabetes mellitus
    Kodl, Christopher T.
    Seaquist, Elizabeth R.
    [J]. ENDOCRINE REVIEWS, 2008, 29 (04) : 494 - 511