RT Journal
A1 Wilson RS, Krueger KR, Arnold SE, et al
T1 LOneliness and risk of alzheimer disease
JF Archives of General Psychiatry
JO Archives of General Psychiatry
YR 2007
FD February 1
VO 64
IS 2
SP 234
OP 240
DO 10.1001/archpsyc.64.2.234
UL http://dx.doi.org/10.1001/archpsyc.64.2.234
AB Context 
    Social isolation in old age has been associated with risk of developing dementia, but the risk associated with perceived isolation, or loneliness, is not well understood.Objective 
    To test the hypothesis that loneliness is associated with increased risk of Alzheimer disease (AD).Design 
    Longitudinal clinicopathologic cohort study with up to 4 years of annual in-home follow-up.Participants 
    A total of 823 older persons free of dementia at enrollment were recruited from senior citizen facilities in and around Chicago, Ill. Loneliness was assessed with a 5-item scale at baseline (mean ± SD, 2.3 ± 0.6) and annually thereafter. At death, a uniform postmortem examination of the brain was conducted to quantify AD pathology in multiple brain regions and the presence of cerebral infarctions.Main Outcome Measures 
    Clinical diagnosis of AD and change in previously established composite measures of global cognition and specific cognitive functions.Results 
    During follow-up, 76 subjects developed clinical AD. Risk of AD was more than doubled in lonely persons (score 3.2, 90th percentile) compared with persons who were not lonely (score 1.4, 10th percentile), and controlling for indicators of social isolation did not affect the finding. Loneliness was associated with lower level of cognition at baseline and with more rapid cognitive decline during follow-up. There was no significant change in loneliness, and mean degree of loneliness during the study was robustly associated with cognitive decline and development of AD. In 90 participants who died and in whom autopsy of the brain was performed, loneliness was unrelated to summary measures of AD pathology or to cerebral infarction.Conclusion 
    Loneliness is associated with an increased risk of late-life dementia but not with its leading causes.