Correlation between brain volume and retinal photoreceptor outer segment volume in normal aging and neurodegenerative diseases.
Aged
Aging
/ pathology
Brain
/ diagnostic imaging
Female
Humans
Linear Models
Magnetic Resonance Imaging
Male
Middle Aged
Multivariate Analysis
Neurodegenerative Diseases
/ diagnostic imaging
Organ Size
Retinal Photoreceptor Cell Outer Segment
/ pathology
Retinal Pigment Epithelium
/ diagnostic imaging
Tomography, Optical Coherence
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
28
01
2020
accepted:
19
07
2020
entrez:
4
9
2020
pubmed:
4
9
2020
medline:
21
10
2020
Statut:
epublish
Résumé
To investigate the association between outer retinal layer metrics, including photoreceptor outer segment volume, on spectral-domain optical coherence tomography (OCT) and brain volume on MRI in normal aging, Alzheimer's disease and Parkinson's disease. This was an exploratory analysis of a cross-sectional cohort study that was approved by the Cleveland Clinic Institutional Review Board to evaluate neurodegenerative disorders. Subjects aged ≥ 50 were recruited. A comprehensive neurological exam, brain MRI with volumetric evaluation, and OCT were performed for each subject. Outer retinal layer parameters, including ellipsoid zone (EZ) to retinal pigment epithelium (RPE) volume (i.e., surrogate for panmacular photoreceptor outer segment volume), were evaluated with a novel OCT analysis platform. Of 85 subjects, 64 eyes of 64 subjects met MRI and OCT quality control criteria. Total brain volume (%ICV) significantly correlated with EZ-RPE volume in the normal cognition control group (n = 31, Pearson correlation coefficient 0.514, P < .01), the Parkinson's disease group (n = 19, Pearson correlation coefficient 0.482, P = .04), and the Alzheimer's dementia group (n = 14, Pearson correlation coefficient 0.526, P = .05). Multiple linear regression analysis revealed that photoreceptor outer segment (i.e., EZ-RPE) volume was an independent, influential factor on total brain volume in all study subjects (Coefficient 15.2, 95% confidence interval 7.8-22.6, P < .001). Outer retinal parameters on OCT may serve as a novel biomarker related to brain volume. This correlation was noted in control subjects suggesting a possible developmental link between retina and brain volume. This relationship was also maintained with atrophic neurodegenerative disorders. Further research is needed to explore possible threshold differences for underlying neurodegenerative disorders.
Identifiants
pubmed: 32881874
doi: 10.1371/journal.pone.0237078
pii: PONE-D-20-02616
pmc: PMC7470418
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0237078Subventions
Organisme : NIA NIH HHS
ID : K23 AG055685
Pays : United States
Organisme : NEI NIH HHS
ID : K23 EY022947
Pays : United States
Déclaration de conflit d'intérêts
I have read journal's policy and the authors of this manuscript have the following financial disclosures, AU: None; JP: None; RB: Biogen (C), Novartis (C), Genzyme (C), Mallickrodt (C), Biogen (F), JBL: Avid (C), Axovant (C), GE Healthcare (C, F), Genzyme/Sanofi (F), Takeda (C); HF: Medical Communications Media; Pfizer (C); SEJ: Biogen (F), Siemens (R), Monteris (R); SKS: Allergan (F), Bausch and Lomb (C),Bioptigen (P), Santen (C), Gilead (F); JPE: Bioptigen/Leica (C, P), Thrombogenics (C, F), Genentech (F, C), Zeiss (C), Alcon (C, F), Regeneron (C, F), Novartis (C, F), Aerpio (C, F), Allergan (C, F). This does not alter our adherence to PLOS ONE policies on sharing data and materials.
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