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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2020
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/11855
Title: | The link between diabetes mellitus and Alzheimer’s disease |
Authors: | Morozan, Olga |
Keywords: | Alzheimer’s disease;hyperglycaemia;diabetes 2 mellitus;insulin resistance |
Issue Date: | 2020 |
Publisher: | MedEspera |
Citation: | MOROZAN, OLGA. The link between diabetes mellitus and Alzheimer’s disease. In: MedEspera: the 8th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2020, p. 264-265. |
Abstract: | Introduction. Type 2 Diabetes mellitus (T2DM) represents a major public health burden and
a growing prevalent chronic disease around the world. It is known that more than 425 million
people have diabetes, and this number is expected to rise to over 642 million by 2040.
Alzheimer’s disease (AD) is the main cause of dementia, affecting over 26 million people
worldwide, and its prevalence continues to increase. Both conditions are related to age, and in
the last decades, an interesting link between them has appeared from various studies that affirm that individuals with T2DM are 2–4 times more likely to develop AD, but definitive
biochemical mechanisms remain unknown.
Aim of the study. This review has the intention to present that type 2 diabetes mellitus (T2DM)
is a significant risk factor for cognitive dysfunction or dementia, especially those related to
Alzheimer's disease
Materials and methods. For the study were used electronic medical platforms such as PubMed
Databases, Hinary and other scientific libraries like Google Scholar. It have been selected and
analyzed 40 articles including manuscripts, reviews, and publications for the last 10 years.
Results. Of the multiple intersection between T2DM and AD, the most pronounced is the
insulin resistance, characterized by hyperinsulinemia and hyperglycaemia. Insulin resistance
decreases glucose metabolism which in turn hyperphosphorylates tau protein causing
neurofibrillary tangles. In AD, the extracellular accumulation of Aβ plaques, intracellular
aggregation of hyperphosphorylated tau protein in neurofibrillary tangles (NFTs), and neuronal
loss occur in the cortex and hippocampus, where are located insulin-dependent receptor GLUT
4 and insulin-independent receptors GLUT1 and GLUT3. Receptors are affected by the
abnormal glucose metabolism, and not only, including enzymes like GSK-3, Cdk-5, CK-1 and
others. The mechanism of influence does not stop here; hyperglycemia can activate K-ATP
channels that increase cellular excitability and leads to an elevated ISF Aβ. Moreover, insulin
alteration in diabetes can interrupt brain cholesterol metabolism leading to metabolic
dysfunction.
Conclusions. T2DM and AD were earlier considered as two independent metabolic disorders.
However, the present study has clearly stated the presence of common pathophysiological and
epidemiological mechanisms, together with signaling pathways that associates a relation
between these two pathologies. It might be possible that therapeutics for T2DM would be
effective for AD, but in order to prove that, more investigations are needed. Recently, AD has
been called Type 3 Diabetes. |
URI: | https://medespera.asr.md/wp-content/uploads/ABSTRACT-BOOK.pdf http://repository.usmf.md/handle/20.500.12710/11855 |
Appears in Collections: | MedEspera 2020
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