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2

Department of Emergency Medicine, University Hospital Galway,

Newcastle road, Galway City,

3

Health Research Board Clinical Research

Facility Galway, National University of Ireland, Galway, Geata an Eolais,

University Road, Galway,

4

Frail Elderly Assessment Team, University

Hospital Galway, Newcastle road, Galway City,

5

Centre for Gerontology

and Rehabilitation, University College Cork, St Finbarrs Hospital, Douglas

Rd, Cork City,

6

PCCC, Shantalla Health Centre, Costello road, Galway City,

Ireland

Introduction:

Although frailty is common among older adults pre-

senting to the Emergency Department (ED), its prevalence is not well

described.

Methods:

We assessed consecutive older adults, aged >70 years,

attending a large university hospital ED, 24-hours/day for a two week

period in March 2016, for frailty using a battery of frailty measures

including the FRAIL Scale, Clinical Frailty Scale, Groningen Frailty

Indicator, Mini-Nutritional Assessment (MNA), body mass index

(BMI), Alzheimer

s disease 8 (AD8) cognitive test, the Euroqol-5D

and the Caregiver Burden Score (CBS).

Results:

In all, 307 patients were available. Of these, 280 were included

with a median (interquartile) age of 78 (83

73 = +/

10) years. Most,

53.6%, were female. The number considered globally frail by physician

assessment was 161, a point prevalence of 58%. Using the FRAIL scale

alone, the point prevalence of frailty (cut-off

3/5) and pre-frailty

(cut-off <3/5 but

1/5), was 29% and 41% respectively. Frail patients

were significantly more likely to be older (p = 0.003), have lower

MNA (p < 0.001), higher AD8 (p < 0.001), poorer Euroqol-5D scores

(p < 0.001), and a higher CBS (p = 0.01), compared to those scoring as

non-frail (pre-frail or robust). There were no differences in gender or

BMI. Pre-frail patients had significantly better MNA, AD8, Euroqol-5D

and CBS scores than frail patients but were similar in age, sex and BMI.

Conclusion:

The point prevalence of frailty and pre-frailty in an Irish

university hospital ED is high. Frail and pre-frail older patients report

more cognitive impairment, are more likely to screen positive for

malnutrition, report lower quality of life and have higher caregiver

burden scores.

P-361

The relationship between frailty, functional capacity, nutritional

status and mobility in males and females aged 70 years or older

C. Kilic

1

, R. Demir

2

, G.B. Ozturk

1

, F. Tufan

1

, N. Erten

1

, G. Baskent

3

,

M.A. Karan

1

.

1

Istanbul University, Istanbul Faculty of Medicine,

Department of Internal Medicine, Division of Geriatrics,

2

Istanbul

University, Cardiology Institute,

3

Istanbul University, Institute of Child

Health, Istanbul, Turkey University, Institute of Child Health, Istanbul,

Turkey

Objectives:

In this study we aimed to investigate the relationship

between frailty, functional capacity, nutritional status and physical

mobility in males and females aged 70 years or older.

Methods:

The patients were recruited from a university hospital

geriatric outpatient clinic. 183 were male (mean age: 78,9) and 277

were female (mean age: 78,2). Frailty status was assessed by FRAIL

questionnaire; functional capacity was assessed by Katz activities of

daily living (ADL) and Lawton-Brody instrumental activities of daily

living (IADL), nutritional status was assessed by mini-nutritional

assessment short form (MNA-SF), physical mobility was assessed by

timed up and go (TUG) test.

Results:

When compared with the males having similar age and

body mass index; ADL (p = 0.004), nutritional status (p = 0.005) and

physical mobility (p < 0.0001) were worse and frailty was more

common (p = 0.001) in the female patients. In both males and

females, there was significant correlation between the frailty scores

and ADL scores (r =

0.37, r =

0.33; p < 0.0001), IADL scores (r =

0.42,

r = -0.50; p < 0.0001), MNA scores (r =

0.52, r =

0.50; p < 0.0001), and

physical mobility scores (r = 0.38, r = 0.43; p < 0.0001), respectively.

Conclusion:

Our results suggest that in both older males and females,

frailty status is significantly associated with worse functional,

nutritional and mobility status.

P-362

The impact of ACE I/D polymorphism in sarcopenia and

osteoporosis

A. Pereira da Silva

1,2,3

, N. Marques

4

, A. Matos

1,2

, Â. Gil

1,2

, M. Bicho

1,2

,

J. Gorjão-Clara

3,5

.

1

Genetics Laboratory and Environmental Institute of

Health, Faculdade de Medicina da Universidade de Lisboa,

2

Instituto

Rocha Cabral, Lisbon,

3

Universitary Geriatric Unit of Faculdade de

Medicina, Universidade de Lisboa, Portugal,

4

Centro Hospitalar Lisboa

Central,

5

Academic Medical Center of Lisbon

North of Lisbon Hospital

Center, Lisboa, Portugal

Objectives:

To evaluate, in a sample of Portuguese centenarians,

the distribution of ACE-genotypes associated with sarcopenia and

osteoporosis.

Methods:

We performed an observational cross-sectional study in

a nationwide population of 253 Centenarians. Sarcopenia was

determined using a muscle mass (MM) index cutoff

16.7 kg/m

2

.

Osteoporosis was defined through estimated bone mass (BM),

according to gender and body weight. Genotyping of Angiotensin

Converting Enzyme (ACE) (rs4646994) was performed through a

high-throughput DNA Microchip platform using iPlex MassArray

system from Sequenom. PCR Malditof mass spectrometry.

Results:

In our study, 230 Centenarians were genotyped (79.1%

women), being 6.5% II-genotype, 48.3% ID-genotype and 45.2%

DD-genotype. Taking in consideration the ID+DD-genotypes (vs.

II-genotype) and DD-genotypes (vs. II + ID-genotypes) we verified

significant differences in relation to the prevalence of sarcopenia

(P = 0.016) and osteoporosis (P = 0.032), respectively. In a univariate

analysis, DD-genotypes centenarians had a significant 5.02-fold

increase to have osteoporosis (95%CI [1.065

6.716], P = 0.036) and

ID + DD-genotype centenarians had a significant 2.67-fold increase

to have sarcopenia (95%CI [1.200

21.045],

P = 0.027).

The

ID + DD-genotypes adjusted for gender, BMI < 18.5 Kg/m

2

, total body

water (TBW, %), osteoporosis and age were risk factors in favor of

sarcopenia (OR = 12.63, CI95% = 1.517

105.065, P = 0.019). Whereas,

the DD-genotype adjusted for BMI < 18.5 Kg/m

2

, TBW, sarcopenia and

TUG-test>12s was a risk factor in favor of osteoporosis (OR = 5.12,

CI95% = 1.151

22.741, P = 0.032).

Conclusions:

Multivariate-analysis for these genetic models

showed that BMI < 18.5 Kg/m

2

and age were independent predictors

of sarcopenia/osteoporosis in centenarians. ACE I/D polymorphism

may be a possible marker associated to sarcopenia and osteoporosis,

being ID + DD-genotypes in favor of sarcopenia and DD-genotype in

favor of osteoporosis.

P-363

Various diagnostic criteria of frailty as predictors for falls, weight

change, quality of life, and mortality

N. Perttila

1,2

, K. Pitkala

1

, H. Kautiainen

1

, R. Tilvis

3

, T. Strandberg

3,4

.

1

Department of General Practice and Unit of Primary Health Care,

University of Helsinki, Helsinki University Central Hospital, Helsinki,

2

City of Vantaa,

3

University of Oulu, Center for Life Course Health

Research, Oulu,

4

University of Helsinki, Clinicum, and Helsinki University

Central Hospital, Helsinki, Finland

Objectives:

Whether various criteria identify the same people as frail

and predict the same outcomes are unknown. To shed light on this

issue, we examined the cohort in the Helsinki Businessmen Study

(HBS), a long-term observational study of men born in 1919

1934.

Methods:

The three criteria compared were the modified Fried criteria

of phenotypic frailty (1) in the HBS and (2) in the Women

s Health

Initiative Observational Study (WHI-OS), and (3) the Frailty Index (FI)

consisting of 20 criteria. We investigated how these three criteria

separated not frail, prefrail, and frail individuals, and predicted

mortality, falls, weight change, and health-related quality of life

(HRQoL, 15D instrument) during a 5-year follow-up. All three criteria

were available for 480 men, whose average age was 73 years at the

start of follow-up.

Poster presentations / European Geriatric Medicine 7S1 (2016) S29

S259

S125