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A randomized, controlled clinical trial demonstrates improved owner-assessed cognitive function in senior dogs receiving a senolytic and NAD+ precursor combination.
Simon, Katherine E; Russell, Katharine; Mondino, Alejandra; Yang, Chin-Chieh; Case, Beth C; Anderson, Zachary; Whitley, Christine; Griffith, Emily; Gruen, Margaret E; Olby, Natasha J.
Affiliation
  • Simon KE; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Russell K; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Mondino A; Southeast Veterinary Neurology, Miami, FL, USA.
  • Yang CC; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Case BC; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Anderson Z; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Whitley C; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Griffith E; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
  • Gruen ME; Department of Statistics, College of Sciences, North Carolina State University, Raleigh, NC, USA.
  • Olby NJ; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
Sci Rep ; 14(1): 12399, 2024 05 29.
Article in En | MEDLINE | ID: mdl-38811634
ABSTRACT
Age-related decline in mobility and cognition are associated with cellular senescence and NAD + depletion in dogs and people. A combination of a novel NAD + precursor and senolytic, LY-D6/2, was examined in this randomized controlled trial. Seventy dogs with mild to moderate cognitive impairment were enrolled and allocated into placebo, low or full dose groups. Primary outcomes were change in cognitive impairment measured with the owner-reported Canine Cognitive Dysfunction Rating (CCDR) scale and change in activity measured with physical activity monitors. Fifty-nine dogs completed evaluations at the 3-month primary endpoint, and 51 reached the 6-month secondary endpoint. There was a significant difference in CCDR score across treatment groups from baseline to the primary endpoint (p = 0.02) with the largest decrease in the full dose group. No difference was detected between groups using in house cognitive testing. There were no significant differences between groups in changes in measured activity. The proportion of dogs that improved in frailty and owner-reported activity levels and happiness was higher in the full dose group than other groups, however this difference was not significant. Adverse events occurred equally across groups. All groups showed improvement in cognition, frailty, and activity suggesting placebo effect and benefits of trial participation. We conclude that LY-D6/2 improves owner-assessed cognitive function over a 3-month period and may have broader, but more subtle effects on frailty, activity and happiness as reported by owners.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cognition / Cognitive Dysfunction / NAD Limits: Animals / Female / Humans / Male Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cognition / Cognitive Dysfunction / NAD Limits: Animals / Female / Humans / Male Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom