Impact of visual impairment on physical activity in early and late age-related macular degeneration.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 26 03 2019
accepted: 20 08 2019
entrez: 22 10 2019
pubmed: 22 10 2019
medline: 12 3 2020
Statut: epublish

Résumé

Modifiable risk factors for age-related macular degeneration (AMD) include smoking, nutrition and likely physical activity (PA). Levels of PA, however, are impacted by any visual impairment which makes the assessment of any association with AMD difficult. To assess the impact of visual impairment under both high and low luminance conditions on levels of PA in early and late AMD. Ninety participants with early to late AMD underwent a clinical assessment including conventional best-corrected visual acuity, low luminance visual acuity, contrast sensitivity and the Moorfields acuity test. PA was recorded using a wrist-worn accelerometer (GENEActiv, Activeinsights) on seven consecutive days. Patient characteristics were compared with the Wilcoxon rank-sum test and determinants of moderate-to-vigorous-PA (MVPA) were assessed using linear regression models. Mean age was 73.9 ± 8.5 years (range 50-89) and 47 subjects (52.2%) were women. Average MVPA time was longer in the early (355.1 ± 252.0 minutes/week) compared to the late AMD group (162.2 ± 134.6 minutes/week; p<0.001). Using linear regression, age [β = -0.25; 95% confidence interval (CI): -12.9; -0.8, p = 0.028] and AMD stage (β = -0.28; 95% CI: -230.9, -25.0; p = 0.015) but not visual impairment on any of the employed tests were associated with MVPA (minutes/week). We found late AMD to be associated with reduced PA. As performance on any of the visual tests was not associated with PA, this association cannot entirely be explained by functional impairment. More research is needed to further explore the association of PA and AMD as PA may be a potentially modifiable risk factor.

Sections du résumé

BACKGROUND
Modifiable risk factors for age-related macular degeneration (AMD) include smoking, nutrition and likely physical activity (PA). Levels of PA, however, are impacted by any visual impairment which makes the assessment of any association with AMD difficult.
PURPOSE
To assess the impact of visual impairment under both high and low luminance conditions on levels of PA in early and late AMD.
METHODS
Ninety participants with early to late AMD underwent a clinical assessment including conventional best-corrected visual acuity, low luminance visual acuity, contrast sensitivity and the Moorfields acuity test. PA was recorded using a wrist-worn accelerometer (GENEActiv, Activeinsights) on seven consecutive days. Patient characteristics were compared with the Wilcoxon rank-sum test and determinants of moderate-to-vigorous-PA (MVPA) were assessed using linear regression models.
RESULTS
Mean age was 73.9 ± 8.5 years (range 50-89) and 47 subjects (52.2%) were women. Average MVPA time was longer in the early (355.1 ± 252.0 minutes/week) compared to the late AMD group (162.2 ± 134.6 minutes/week; p<0.001). Using linear regression, age [β = -0.25; 95% confidence interval (CI): -12.9; -0.8, p = 0.028] and AMD stage (β = -0.28; 95% CI: -230.9, -25.0; p = 0.015) but not visual impairment on any of the employed tests were associated with MVPA (minutes/week).
CONCLUSIONS
We found late AMD to be associated with reduced PA. As performance on any of the visual tests was not associated with PA, this association cannot entirely be explained by functional impairment. More research is needed to further explore the association of PA and AMD as PA may be a potentially modifiable risk factor.

Identifiants

pubmed: 31634374
doi: 10.1371/journal.pone.0222045
pii: PONE-D-19-08628
pmc: PMC6802830
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0222045

Déclaration de conflit d'intérêts

The department received financial research support and/or imaging devices from Heidelberg Engineering, Carl Zeiss MediTec, CentreVue, Optos. F.G. Holz has received honoraria as a consultant for Heidelberg Engineering, Carl Zeiss MedicTec, Allergan, Alcon/Novartis, Genentech/Roche, Bayer, Acucela, Boehringer Ingelheim; R.P. Finger has received honoraria as a consultant for Bayer, Novartis, Genentech/Roche, Santen, Opthea, Novelion, Oxford Innovation, Santhera, Alimera. There are no patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials.

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Auteurs

Manuel Heinemann (M)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Susanne G Welker (SG)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Jeany Q Li (JQ)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Maximilian W M Wintergerst (MWM)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Gabrielle N Turski (GN)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Christopher A Turski (CA)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Jan H Terheyden (JH)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Matthias M Mauschitz (MM)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Frank G Holz (FG)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

Robert P Finger (RP)

University of Bonn, Department for Ophthalmology, Ernst- Abbe- Straße, Bonn, Germany.

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