Antibodies to Multiple Receptors are Associated with Neuropsychiatric Symptoms and Mortality in Alzheimer's Disease: A Longitudinal Study

J Alzheimers Dis. 2018;64(3):761-774. doi: 10.3233/JAD-170882.

Abstract

Background: Endogenous antibodies to signaling molecules and receptors (Abs) are associated with Alzheimer's disease (AD).

Objectives: To investigate the association of 33 Abs to dopaminergic, serotoninergic, muscarinic, adrenergic, vascular, and immune receptors with cognitive, neuropsychiatric, and mortality outcomes.

Methods: Ninety-one patients with mild AD were followed annually for 5 years with the Mini-Mental State Examination (MMSE) and the Neuropsychiatric Inventory (NPI; composite outcomes: "psychosis" (item 1 + 2), "mood" (item 4 + 5 + 7), and "agitation" (item 3 + 8 + 9)). Abs were quantified in sera obtained at baseline by ELISA and reduced to principal components (PCs). Associations between Abs and outcomes were assessed by a mixed model (MMSE decline), zero-inflated fixed effects count models (composite NPI scores), and Cox regression (mortality). The resulting p-values were adjusted for multiple testing according to a false discovery rate of 0.05 (Benjamini-Hochberg).

Results: The measured levels of the 33 Abs formed four PCs. PC1 (dopaminergic and serotonergic Abs) was associated with increased mortality (Hazard ratio 2.57, p < 0.001), PC2 (serotonergic, immune, and vascular Abs) with decreased agitation symptoms (β - 0.19, p < 0.001), and PC3 (cholinergic receptor Abs) with increased mood symptoms (β 0.04, p = 0.002), over time. There were no associations between Abs and MMSE decline.

Conclusion: The associations between Abs, mortality, and neuropsychiatric symptoms reported in this cohort are intriguing. They cannot, however, be generalized. Validation in independent sample sets is required.

Keywords: Dopaminergic; naturally occurring antibodies; neuropsychiatric inventory; neuropsychiatric symptoms; physiological antibodies; serotonergic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / blood*
  • Alzheimer Disease / complications
  • Alzheimer Disease / mortality*
  • Cognition Disorders / etiology
  • Female
  • Humans
  • Immunoglobulin G / blood*
  • Longitudinal Studies
  • Male
  • Neuropsychological Tests
  • Principal Component Analysis
  • Protein Interaction Maps
  • Psychiatric Status Rating Scales
  • Psychomotor Disorders / etiology
  • Receptors, Biogenic Amine / immunology*

Substances

  • Immunoglobulin G
  • Receptors, Biogenic Amine