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P452 Poster Presentations: P1

P1-256 MEMORY DIFFICULTIES AND SITTING SCREEN done using random effects models. The population attributable
TIME IN THE ELDERLY risk (PAR) was also estimated. Egger’s regression coefficient
Richard F. Gillum1,2, Julius S. Ngwa3, Isaac M.E. Dodd3,
and visual inspection of the funnel plot was used to assess pub-
Thomas O. Obisesan3, 1Howard University Hospital, Washington, DC, lication bias. I-square statistics quantified heterogeneity across
USA; 2Howard University College of Medicine, Washington, DC, USA; studies, and multivariable meta-regression analysis examined
3
Howard University College of Medicine, Washington, DC, USA. the effect of possible influential factors (sex, mean age, sample
Contact e-mail: isaac.dodd@bison.howard.edu size and study quality). Results: Twenty-five publications that
Background: Lack of physical activity and exercise is associated met the selection and final inclusion/exclusion criteria for the
with poorer memory and a greater risk of dementia and mortality study were included in the systematic review. Collectively, sig-
in the elderly. Daily hours spent sitting or viewing TV is associ- nificant evidence exist and show that OSA is associated with
ated with adverse physical health outcome and mortality. Studies AD, cognitive decline and AD pathology. Altogether, 7 observa-
associating sitting and memory are lacking. We examined data tional studies (n ¼ 13,328 participants) that provided 26 RR esti-
from a national US survey to evaluate the hypothesis that mates were included for the meta-analysis. Results showed that
increased daily sitting hours is associated with greater prevalence OSA increased AD, or cognitive decline by 70% (RR: 1.70,
of difficulty with memory and confusion in persons aged 60 95% CI: 1.25-2.31), and almost 3% of AD could be attributed
years and over. Methods: In NHANES 2005-2006 survey, partici- to OSA. I-square was 72% suggesting heterogeneity, however,
pants were asked the following: (1) “{Are you/Is SP} limited in this was not explained by the subgroup meta-analyses. None of
any way because of difficulty remembering or because {you/s/ the studied factors in the meta-regression analysis significantly
he} experience{s} periods of confusion?” (2) “Over the past 30 influenced the effect size between OSA and AD. Conclusions:
days, on average about how many hours per day did {you/SP} sit This meta-analysis substantiated the association between OSA
and watch TV or videos?” (3) “Over the past 30 days, on average and AD and, for the first time, quantified its magnitude. Since
about how many hours per day did {you/SP} use a computer or OSA is of increasing concern in the population, these findings
play computer games?” TV/video and computer hours were are of interest for both AD researchers and caregivers.
summed to estimate sitting screen-hours. We assessed the associa-
tion of sitting screen-hours and memory/confusion in persons aged
60 years and over. Results: Among 1,356 persons with complete
data, 194 (14%) reported limitations due to memory/confusion. P1-258 POST-MENOPAUSAL HORMONE THERAPY AND
The median number of screen-hours was 3 per day. Among persons ALZHEIMER’S DISEASE: A PROSPECTIVE
with memory/confusion problems, the mean screen-hours was 3.28 COHORT STUDY
compared to 3.10 in others (p¼0.27). In a logistic regression model Bushra Imtiaz1, Anna-Maija Tolppanen1, Hilkka Soininen1,
controlling for age, gender, race and fair/poor health status, screen- Miia Kivipelto2, Marjo Tuppurainen3, Heikki Kr€oger3, 1University of
hours was not significantly associated with memory/confusion Eastern Finland, Kuopio, Finland; 2Karolinska Institute, Stockholm,
problems: odds ratio 1.04 (95% confidence interval 0.96-1.13). Per- Sweden; 3Kuopio University Hospital, Kuopio, Finland.
Contact e-mail: bushra.imtiaz@uef.fi
sons with >3 screen-hours per day had odds ratio of 1.16 (0.84-
1.59) relative to others. Conclusions: In persons aged 60 and over, Background: Association between Alzheimer’s disease (AD) and
more hours sitting before a screen was not significantly associated type and duration of use of post-menopausal hormone therapy
with more difficulty with memory/confusion. Studies in larger sam- (HT) is vague. We explored this interplay by using two different
ples may be warranted. methodologies for data collection i.e. self-administered question-
naires and register-based data in the same cohort while control-
ling for various life-style and socio-demographic variables.
Methods: This study is based on 20 years follow-up (1989-2009)
P1-257 OBSTRUCTIVE SLEEP APNEA AND of Kuopio Osteoporosis Risk factor and Prevention (OSTPRE)
ALZHEIMER’S DISEASE: A SYSTEMATIC study cohort. First self-administered questionnaire was sent in
REVIEW AND META-ANALYTIC APPROACH 1989 to all women resident of Kuopio province Eastern Finland,
Omonigho Michael Bubu, Ovie Utuama, Ogie Queen Umasabor-Bubu, aged 47-56 years. It was followed by a new questionnaire every
Skai Schwartz, University of South Florida, Tampa, FL, USA. 5th year till 2009. Data on use of self-reported HT was calculated
Contact e-mail: obubu@health.usf.edu as number of months of use per year since 1989-2009. While regis-
Background: Evidence from several epidemiologic studies tered based information on HT was available since 1995 from Na-
suggest that apnea recurrence and nocturnal hypoxemia may be tional prescription register. AD cases diagnosed according to
a risk factor for Alzheimer’s disease (AD) in Obstructive Sleep NINCS-ADRDA and DSM-IV criteria were identified from special
apnea (OSA) patients, however, the magnitude of the risk is un- reimbursement register since 1999-2009. While data on life-style
clear. In that regard, a systematic review and meta-analysis to and socio-demographic variables was collected in all question-
quantify the effect of OSA on AD, cognitive decline or dementia naires. Results: Long term use of post-menopausal HT i.e. >10
was conducted. Methods: We searched four bibliographic data- years was found to be protective against incident AD (HR /95%
bases, including PubMed, Embase, Web of Science, and the CI) (0.47/0.28-0.80). However no specific type or duration of HT
Cochrane Central Register of Controlled Trials, from their was associated with AD significantly. Results were almost similar
onset until and including November, 2014 and identified orig- when results on use of estrogen were compared between registers
inal published literature assessing any association of Obstruc- and self-administered questionnaires. Among other risk factors:
tive Sleep apnea with AD, or cognitive decline. Pooling of older age, lack of occupation and smoking increased likelihood
the effect estimates of the individual studies and calculations of AD while high physical activity and higher education was pro-
of relative risks (RR) and 95% confidence intervals (CI) was tective against AD. Conclusions: Our findings support protective

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