Mixed Brain Pathology Is the Most Common Cause of Cognitive Impairment in the Elderly

Article type: Research Article

Authors: Alafuzoff, Irina^{a; *} | Libard, Sylwia^{a; b}

Affiliations: [a] Department of Pathology, Uppsala University Hospital, Sweden | [b] Department of Immunology, Genetics and Pathology, Uppsala University, Sweden

Correspondence: [*] Correspondence to: Irina Alafuzoff, MD, PhD, Uppsala University Hospital, Department of Pathology, Rudbeck Laboratory, Dag Hammarskjölds väg 20, 751 85 Uppsala, Sweden. E-mail: [email protected].

Abstract: Background:Systemic diseases, diabetes mellitus (DM), and cardiovascular disease (CaVD) have been suggested being risk factors for cognitive impairment (CI) and/or influence Alzheimer’s disease neuropathologic change (ADNC). Objective:The purpose was to assess the type and the extent of neuropathological alterations in the brain and to assess whether brain pathology was associated with CaVD or DM related alterations in peripheral organs, i.e., vessels, heart, and kidney. Methods:119 subjects, 15% with DM and 24% with CI, age range 80 to 89 years, were chosen and neuropathological alterations were assessed applying immunohistochemistry. Results:Hyperphosphorylated τ (HPτ) was seen in 99%, amyloid-β (Aβ) in 71%, transactive DNA binding protein 43 (TDP43) in 62%, and α-synuclein (αS) in 21% of the subjects. Primary age related tauopathy was diagnosed in 29% (more common in females), limbic predominant age-related TDP encephalopathy in 4% (14% of subjects with CI), and dementia with Lewy bodies in 3% (14% of subjects with CI) of the subjects. High/intermediate level of ADNC was seen in 47% and the extent of HPτ increased with age. The extent of ADNC was not associated with the extent of pathology observed in peripheral organs, i.e., DM or CaVD. Contrary, brain alterations such as pTDP43 and cerebrovascular lesions (CeVL) were influenced by DM, and CeVL correlated significantly with the extent of vessel pathology. Conclusion:In most (66%) subjects with CI, the cause of impairment was “mixed pathology”, i.e., ADNC combined with TDP43, αS, or vascular brain lesions. Furthermore, our results suggest that systemic diseases, DM and CaVD, are risk factors for CI but not related to ADNC.

Keywords: Aging, α-synuclein, amyloid-β , cardiac pathology, cerebrovascular lesions, hyperphosphorylated-τ , nephrosclerosis, transactive DNA binding protein 43

DOI: 10.3233/JAD-200925

Journal: Journal of Alzheimer's Disease, vol. 78, no. 1, pp. 453-465, 2020