Transactive DNA Binding Protein 43 Rather Than Other Misfolded Proteins in the Brain is Associated with Islet Amyloid Polypeptide in Pancreas in Aged Subjects with Diabetes Mellitus

• Published in: Journal of Alzheimer's disease Vol. 59; no. 1; pp. 43 - 56
• Main Authors: Leino, Marina, Popova, Svetlana N., Alafuzoff, Irina
• Format: Journal Article
• Language: English
• Published: London, England SAGE Publications 01.01.2017
• Subjects: Age Factors; Aged; Aged, 80 and over; alpha-Synuclein - metabolism; Amyloid beta-Peptides - metabolism; Autopsy; Brain - metabolism; Cohort Studies; Diabetes Mellitus - pathology; DNA-Binding Proteins - metabolism; Female; Humans; Islet Amyloid Polypeptide - metabolism; Male; Middle Aged; Organ Size; Pancreas - metabolism; Phosphorylation; Statistics as Topic; islet amyloid polypeptide; amyloid-β; hyperphosphorylated τ; diabetes mellitus; phosphorylated transactive DNA binding protein 43; α-synuclein
• ISSN: 1387-2877; 1875-8908
• DOI: 10.3233/JAD-170192

A link between diabetes mellitus (DM) related islet amyloid polypeptide (IAPP) and Alzheimer’s disease (AD) related amyloid-β (Aβ) has been suggested in epidemiological and clinical studies. In 2017, proof for existing interaction between type 2 DM and AD on a molecular level was provided based on research carried out in experimental animal models. We assessed aging-related neurodegenerative lesions, i.e., misfolded proteins, associated with dementia such as hyperphosphorylated τ (HPτ), Aβ, α-synuclein (αS), and phosphorylated transactive DNA binding protein 43 (pTDP43) seen in the brain and IAPP seen in the pancreas in subjects with and without DM applying immunohistochemical techniques. HPτ in the brain and IAPP in the pancreas were observed in most subjects. The prevalence and the extent of all misfolded proteins increased with age but this increase was not influenced by DM. Interestingly the extent of misfolded proteins in the brain was higher in non-diabetics when compared with diabetics in demented. A significant correlation was observed between HPτ, Aβ, αS, and pTDP43, whereas IAPP showed no association with HPτ, Aβ, and αS. In subjects with DM, the extent of pTDP43 in brain correlated with the extent of IAPP in pancreas. Thus, there is no evidence of a link between AD-related pathology and DM in humans, whereas an association was found between pTDP43 and IAPP in DM. TDP43 is ubiquitously expressed in all organs but whether TDP43 is phosphorylated in other organs in DM or whether the phosphorylation of TDP43 is influenced by glucose metabolism is yet unknown.