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Alzheimer's Association International Conference 2026

July 12-15, 2026 | London, United Kingdom, and Online

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Trajectories Of Cognitive Functioning In Adults With Down Syndrome Based On Residence

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Longitudinal Trajectories of Cognitive Functioning in Adults with Down Syndrome based on Residence

Introduction: 

•Genetic Foundation: Triplication of chromosome 21 causes APP over-expression, leading to near-universal Alzheimer’s Disease (AD) neuropathology by midlife (Wiseman et al., 2015; Rafii et al., 2025).
•Heterogeneity: While average decline begins in the 40s or 50s, symptom onset spans a 30-year range, suggesting lifestyle factors could influence timing (Fortea et al., 2021; McCarron et al., 2017). 
•Residence & Cognitive Reserve: Living arrangements heavily dictate daily routines and social engagement, directly shaping the cognitive reserve required to compensate for underlying AD pathology. (Mihaila et al., 2020).
•Transition: Residential moves are major life stressors associated with functional decline and increased mortality, potentially overwhelming remaining reserve (Aneshensel et al., 2000; Melrose, 2019).
 
Current Study:
•Aim: To compare cognitive trajectories across residential settings and evaluate the impact of residential transitions using a large, multi-site cohort.
•Hypothesis: Residential transitions will act as significant stressors, leading to accelerated cognitive decline compared to stable living arrangements.
 

Methods

Participants

-N = 529 adults with DS (age > 25)
-Residential Groups
-With Parent (n = 220)
-With Sibling (n = 32)
-Independently (n = 66)
-Group Home/Facility (n = 161)
-Transition (n = 50)
 
Key Measures

Down Syndrome Mental Status Examination

(DSMSE; Haxby, 1989)

Modified Cued Recall Test

(mCRT; Devenny et al., 2002)

Dementia Questionnaire for People with Learning Disabilities Scale, Cognitive Subscale

(DLD; Evenhuis et al., 1992)

National Task Group–Early Detection Screen for Dementia

(NTG; Esralew et al., 2013)

 
Longitudinal Change by Residence Group

What the Data Shows

Stable parental and independent living are associated with cognitive and functional stability, whereas individuals in group homes or those undergoing residential relocations exhibit significant decline, with transitioning cohorts experiencing the sharpest, most rapid deterioration across all metrics.

Interpretation

Disparities are dual-driven: "selection effects" reflect pre-existing medical conditions, baseline functioning, or changes in parental care capacity that dictate placement, while "environmental effects" capture variations in daily social, cognitive, and physical activities that build or deplete cognitive reserve.

Transition Group: The "Move Effect"

What the Data Shows

Piecewise models reveal statistical stability immediately prior to relocation followed by a sharp, abrupt post-move drop across all outcomes, occurring universally regardless of move direction.

Interpretation

This inflection point represents a dual dynamic: relocation may act as a stressor whose high cognitive and adaptation demands exhaust remaining reserve (causality), or the transition itself is a reactive measure prompted by early, subtle functional changes preceding formal clinical detection (reaction).

Discussion

Reserve vs. Disruption: Stable family settings provide a protective "environmental reserve" that preserves cognitive function longer. Conversely, relocation disrupts automatic routines and introduces intense adaptation demands that exhaust remaining cognitive reserve, though moves can also be reactive to early, unmeasured functional shifts.

 

Clinical Action: Clinicians must flag residential transitions as periods of acute cognitive risk requiring proactive monitoring. Structural mitigation should utilize "phased integration" (e.g., visual schedules, reminders) alongside targeted resource toolkits for sibling caregivers. 

Future Directions: Future research must examine specific move triggers (e.g., parental health) and contexts (planned vs. crisis) to refine clinical risk profiles.

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