Journal
JOURNAL OF VETERINARY INTERNAL MEDICINE
Volume 29, Issue 6, Pages 1569-1577Publisher
WILEY
DOI: 10.1111/jvim.13633
Keywords
Amyloid-beta; Canine; Dementia; Geriatric; Longitudinal
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BackgroundCanine cognitive dysfunction (CCD) is an age-dependent neurodegenerative condition dominated by changes in behavioral patterns. Cohort studies investigating cognitive status in dogs are lacking. ObjectivesTo investigate cognitive function, progression of age-related behavioral changes, survival, and possible biomarkers of CCD in aged dogs. AnimalsFifty-one dogs >8 years old; 21 with no cognitive deficits, 17 with mild cognitive impairments (MCI) and 13 with CCD. MethodsLongitudinal study. Recruitment period of 12 months and an observational period of 24 months including a baseline and 3 planned subsequent assessments. Cognitive status was determined using validated questionnaires. Plasma A-peptides were quantified using commercial ELISA assays and cytokines by a validated immunoassay. ResultsSigns characterizing dogs with CCD were aimless wandering, staring into space, avoid getting patted, difficulty finding dropped food and anxiety. Thirty-three percent of dogs with a normal cognitive status progressed to MCI and 22% classified as MCI progressed to CCD during the study period. For 6 dogs diagnosed with CCD, signs of cognitive dysfunction increased with time. A diagnosis of CCD did not affect survival. The level of plasma A(42) was significantly increased (P < .05) in the CCD group (92.8 24.0 pg/mL) compared to the MCI (77.0 +/- 12.3 pg/mL) and normal group (74.9 +/- 10.0 pg/mL), but no significant differences in concentrations of systemic inflammatory markers were detected. ConclusionsCanine cognitive dysfunction is a progressive disorder with an individual variability in the rate of cognitive decline and clinical signs. Plasma A(42) seems to be an interesting plasma biomarker of CCD.
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