Adipocyte-derived factors in age-related dementia and their contribution to vascular and Alzheimer pathology. Review uri icon

Overview

abstract

  • Age-related dementia is increasingly recognized as having a mixed pathology, with contributions from both cerebrovascular factors and pathogenic factors associated with Alzheimer's disease (AD). Furthermore, there is accumulating evidence that vascular risk factors in midlife, e.g., obesity, diabetes, and hypertension, increase the risk of developing late-life dementia. Since obesity and changes in body weight/adiposity often drive diabetes and hypertension, understanding the relationship between adiposity and age-related dementia may reveal common underlying mechanisms. Here we offer a brief appraisal of how changes in body weight and adiposity are related to both AD and dementia on vascular basis, and examine the involvement of two key adipocyte-derived hormones: leptin and adiponectin. The evidence suggests that in midlife increased body weight/adiposity and subsequent changes in adipocyte-derived hormones may increase the long-term susceptibility to dementia. On the other hand, later in life, decreases in body weight/adiposity and related hormonal changes are early manifestations of disease that precede the onset of dementia and may promote AD and vascular pathology. Understanding the contribution of adiposity to age-related dementia may help identify the underlying pathological mechanisms common to both vascular dementia and AD, and provide new putative targets for early diagnosis and therapy. This article is part of a Special Issue entitled: Vascular Contributions to Cognitive Impairment and Dementia, edited by M. Paul Murphy, Roderick A. Corriveau and Donna M. Wilcock.

publication date

  • November 9, 2015

Research

keywords

  • Adiponectin
  • Adipose Tissue
  • Alzheimer Disease
  • Dementia, Vascular
  • Leptin

Identity

PubMed Central ID

  • PMC4821723

Scopus Document Identifier

  • 84960869778

Digital Object Identifier (DOI)

  • 10.1016/j.bbadis.2015.10.029

PubMed ID

  • 26546479

Additional Document Info

volume

  • 1862

issue

  • 5